Co-reporter:Tang Zhu, Chao Cai, Jing Guo, Rong Wang, Ning Zhao, and Jian Xu
ACS Applied Materials & Interfaces March 22, 2017 Volume 9(Issue 11) pp:10224-10224
Publication Date(Web):March 2, 2017
DOI:10.1021/acsami.7b00149
Polypropylene (PP), including isotactic PP (i-PP) and atactic PP (a-PP) with distinct tacticity, is one of the most widely used general plastics. Herein, ultra water repellent PP coatings with tunable adhesion to water were prepared via a simple casting method. The pure i-PP coating shows a hierarchical morphology with micro/nanobinary structures, exhibiting a water contact angle (CA) larger than 150° and a sliding angle less than 5° (for 5 μL water droplet). In contrast, the pure a-PP coating has a less rough morphology with a water contact angle of about 130°, and the water droplets stick on the coating at any tilted angles. For the composite i-PP/a-PP coatings, however, ultra water repellency with CA > 150° but water adhesion tailorable from slippery to sticky can be realized, depending on the contents of a-PP and i-PP. The different wetting behaviors are due to the various microstructures of the composite coatings resulting from the distinct crystallization ability of a-PP and i-PP. Furthermore, the existence of a-PP in the composite coatings enhances the mechanical properties compared to the i-PP coating. The proposed method is feasible to modify various substrates and potential applications in no-loss liquid transportation, slippery surfaces, and patterned superhydrophobic surfaces are demonstrated.Keywords: adhesion; crystallization; microstructure; polypropylene; water repellent;
Co-reporter:Wen-Xing Liu, Chi Zhang, Huan Zhang, Ning Zhao, Zhi-Xiang Yu, and Jian Xu
Journal of the American Chemical Society June 28, 2017 Volume 139(Issue 25) pp:8678-8678
Publication Date(Web):May 30, 2017
DOI:10.1021/jacs.7b03967
Polyurethanes (PUs) have many applications resulting from their preeminent properties, but being commonly used toxic catalysts, and the lack of processability for PU thermosets cause limitations. Herein, we report a new class of the PU-like dynamic covalent polymers, poly(oxime-urethanes) (POUs), which are prepared from the uncatalyzed polyaddition of multifunctional oximes and hexamethylene diisocyanate (HDI) at ambient temperature. Kinetics studies reveal that almost complete polymerization (∼99% conversion) can be achieved in 3 h at 30 °C in dichloromethane (DCM), the most effective among the solvents evaluated, producing linear POUs with comparable molecular weights to the catalyzed PUs. We find that the oxime-carbamate structures are reversible at about 100 °C through oxime-enabled transcarbamoylation via a thermally dissociative mechanism. The cross-linked POUs based on oxime–carbamate bonds show efficient catalyst-free healable/recyclable properties. Density functional theory (DFT) calculations suggest that the fast oxime-urethanation and the mild thermoreversible nature are mediated by the characteristic nitrone tautomer of the oxime. Given widespread urethane-containing materials, POUs are of promising potential in applications because of the excellent mechanical performances, facile preparation, and dynamic property without using catalysts.
Co-reporter:Dongdong Li, Heng Shen, Chao Cai, Tongbing Sun, Yiping Zhao, Li Chen, Ning Zhao, and Jian Xu
ACS Omega April 2017? Volume 2(Issue 4) pp:1738-1738
Publication Date(Web):April 28, 2017
DOI:10.1021/acsomega.7b00039
Catkin, a natural hollow fiber, is used as a template to fabricate light, flexible, and electrically conductive silver microtubes with a high aspect ratio. The template is functionalized with tannic acid (TA)–Fe coordination complexes. Because of the metal ion chelating ability and reducibility of TA, silver nanoparticles (Ag NPs) can be formed in situ on the fiber’s surface. The as-formed Ag NPs can act as nucleation sites in subsequent electroless silver plating, leading to the formation of a compact and uniform silver coating on the microtube. The coating is constructed by densely packed Ag NPs of only 15 ± 5 nm in diameter. Because of the tight accumulation and small size of the Ag NPs, the resulting silver-coated microtubes, without any post-treatment, show an electrical resistivity of 1500 mΩ·cm at a bulk density of 0.6 g·cm–3. We find that the in situ formed nucleation sites and the stirring speed in the electroless plating play important roles in the formation of a silver coating with a high electrical conductivity. This method may be extended to fabricate conductive nanocoatings on other substrates.Topics: Coating materials; Deposition process; Electric properties; Electric transport processes and properties; Organic compounds and Functional groups;
Co-reporter:Ke-Jian Cui;Cai-Zhen Zhu;Huan Zhang;Qin Xuan;Wei-Zhi Zou;Zhi-Yan Zhang;Xue-Chun Lin;Jian Xu
Journal of Materials Chemistry C 2017 vol. 5(Issue 46) pp:12035-12038
Publication Date(Web):2017/11/30
DOI:10.1039/C7TC04303A
Herein, a promising application of blue LD-initiated photosensitive resins in 3D printing is developed. Compared with traditional UV 3D printing, a safer and inexpensive light source, higher polymerization efficiency, and more available precursors are presented.
Co-reporter:Chao Cai;Tang Zhu;Dongdong Li;Yun Ran;Haixia Dong;Jian Xu
CrystEngComm (1999-Present) 2017 vol. 19(Issue 14) pp:1888-1895
Publication Date(Web):2017/04/03
DOI:10.1039/C7CE00127D
In this paper, tannic acid (TA) was used to assist the fabrication of spherically aggregated Cu2O–TA hybrid sub-microparticles with good chemical stability and controllable sizes. TA exhibited multiple functions in the synthesis: the reductant for the formation of Cu2O crystal seeds, the stabilizer of the primary Cu2O crystals and the protector against the oxidation of Cu2O. A probable mechanism was presumed, including 1) seed formation and TA encapsulation, 2) primary crystal nucleation and growth, and 3) aggregation into spheres. We found that pH played a key role in determining the final morphology of the product while the precursor concentration strongly influenced the size of the particles. At a suitable pH, hierarchically structured Cu2O–TA sub-microspheres with nanocrystals as building blocks were produced. The size of the spheres can be tuned from 130 to 670 nm by adjusting the precursor concentration. Cu2O–TA hybrids exhibited excellent chemical stability against water and oxygen. The method reported here possessed many advantages like cost-effectiveness, facility of preparation, environmental friendliness, chemical stability and excellent adjustability. The properties of the prepared Cu2O particles might facilitate their applications in marine antifouling paints, adsorption materials and antibacterial agents.
Co-reporter:Rong Wang, Yuhua Long, Tang Zhu, Jing Guo, Chao Cai, Ning Zhao, Jian Xu
Journal of Colloid and Interface Science 2017 Volume 498(Volume 498) pp:
Publication Date(Web):15 July 2017
DOI:10.1016/j.jcis.2017.03.035
Wrinkles exist widely in nature and our life. In this paper, wrinkles on polydopamine (PDA)/polystyrene (PS) bilayer films were formed by thermal annealing due to the different thermal coefficients of expansion of each layer. The factors that influenced the dimensions of wrinkles were studied. We found that oriented wrinkles could be formed if the bilayer films were patterned with micro-grooves, and the degree of the orientation depended on the thickness of the PDA and the dimensions of the grooves. Combined with the strong adhesion, biocompatibility and reactivity of PDA, the oriented wrinkles on PDA/PS patterned bilayers may find potential application in diffraction gratings, optical sensors and microfluidic devices.Download high-res image (45KB)Download full-size image
Co-reporter:Dong Wang;Huan Zhang;Jing Guo;Beichen Cheng;Yuan Cao;Shengjun Lu;Jian Xu
Macromolecular Rapid Communications 2016 Volume 37( Issue 7) pp:655-661
Publication Date(Web):
DOI:10.1002/marc.201500637
Co-reporter:Heng Shen, Chao Cai, Jing Guo, Zhenchao Qian, Ning Zhao and Jian Xu
RSC Advances 2016 vol. 6(Issue 20) pp:16489-16494
Publication Date(Web):29 Jan 2016
DOI:10.1039/C6RA00980H
Thermal interface materials are widely used in thermal management, and usually require a high thermal conductivity, low coefficient of thermal expansion (CTE) and adequate softness. Herein, hBN/PDMS composites are fabricated by the infiltration of a PDMS prepolymer in the hBN scaffolds followed by a thermal curing process. The scaffolds are prepared by an ice templating method with hBN microplatelets, leading to a good alignment of hBN platelets along the z direction in the PDMS matrix. This unique structure results in a high thermal conductivity, which is about 3 times higher than that of the composites fabricated by a casting method, and the thermal conductivity is as high as 1.4 W m−1 K−1 along the z direction at ∼20 wt% of hBN microplatelets. The composites also possess low CTEs which are <100 ppm K−1 along the z direction and maintain an adequate softness.
Co-reporter:Zhen Wang, Zhenchao Qian, Yuan Cao, Xiangzhi Zhang, Renzhong Tai, Haixia Dong, Ning Zhao and Jian Xu
RSC Advances 2016 vol. 6(Issue 26) pp:21571-21576
Publication Date(Web):17 Feb 2016
DOI:10.1039/C5RA22733J
Creating hollow structures in microspheres is attracting increasing interest because of the notable large capacity, high porosity, low density and extended surface area of the hollow microspheres prepared. Herein, facile preparation of bridged silsesquioxane (BSQ) microspheres with interconnected multi-cavities and open-hole structures is presented. The well-developed multi-cavities are derived from the configuration of the water-in-oil-in-water emulsion of the precursor. The condensation of the precursor in the emulsion results in the transition of the liquid precursor to solid BSQ resin, which preserves the emulsion structure and induces the formation of voids. The resultant hollow BSQ microspheres show advantages in controllable cargo delivery.
Co-reporter:Dong Wang;Huan Zhang;Beichen Cheng;Zhenchao Qian;Wenxing Liu;Jian Xu
Journal of Polymer Science Part A: Polymer Chemistry 2016 Volume 54( Issue 10) pp:1357-1366
Publication Date(Web):
DOI:10.1002/pola.27983
ABSTRACT
A facile cross-linking strategy of using small molecules as physcial crosslinkers to facilitate recyclable polybutadiene (PB) elastomer with excellent toughness and stretchability is demonstrated. Carboxylic acid groups were incorporated along the PB backbone via thiol-ene reaction, and then the polymer can be cross-linked by ionic hydrogen bonds between the carboxylic acid groups from PB and the amine groups of the cross-linkers. The ionic hydrogen bonds can dynamiclly break and reconstruct upon deformation, thus endowing the resultant polymer with not only high toughness and stretchability (∼1800%), but also good self-recovery and enhanced damping properties. Remarkably, the dynamically cross-linked PB elastomer can be thermally recycled owing to the thermal reversibility of the ionic hydrogen bonds and the mechanical properties can be largely recovered after reprocessing. © 2015 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2016, 54, 1357-1366
Co-reporter:Yi Hou;Chun-ting Duan 赵宁;Huan Zhang
Chinese Journal of Polymer Science 2016 Volume 34( Issue 10) pp:1234-1239
Publication Date(Web):2016 October
DOI:10.1007/s10118-016-1828-y
Separation of oil/water mixtures, especially for the emulsified oil/water mixtures, is important because of the frequent occurrence of oil spill accidents. Utilizing superwetting porous membrane has become a promising approach to separate either surfactant-free or surfactant-stabilized emulsions. Herein we report a facile and versatile strategy for preparing hydrophobic/under-oil superhydrophobic membranes by coating the skeletons of the membranes with the poly[(3,3,3-trifluoropropyl)methylsiloxane] (PTFPMS) nanoparticles. The obtained membranes could be used to separate various waterin- oil emulsions with high flux and separation efficiency. In addition, owning to the outstanding resistance of PTFPMS to the most organic solvents or oils, the modified membranes exhibited the excellent reusability and the antifouling properties that were critical in the practical applications. Many commercially available membranes can be modified by such a simple method.
Co-reporter:Dong Wang, Jing Guo, Huan Zhang, Beichen Cheng, Heng Shen, Ning Zhao and Jian Xu
Journal of Materials Chemistry A 2015 vol. 3(Issue 24) pp:12864-12872
Publication Date(Web):11 May 2015
DOI:10.1039/C5TA01915J
A strategy for combining covalent and non-covalent cross-links to construct multifunctional rubber materials with intelligent self-healing and shape memory ability is demonstrated. Rubbers were prepared by self-assembly of complementary polybutadiene oligomers bearing carboxylic acid and amine groups through reversible ionic hydrogen bonds via the acid–base reaction, and then further covalently cross-linked by tri-functional thiol via the thiol-ene reaction. The resulting polymers exhibit self-healing and shape memory functions owing to the reversible ionic hydrogen bonds. The covalent cross-linking density can be tuned to achieve tailorable mechanical and stimuli-responsive properties: a low covalent cross-linking density maintains the remarkable self-healing capability of rubber at ambient temperature without any external stimulus, while a high covalent cross-linking density improves the mechanical strength and induces shape memory behavior, but effective self-healing needs to be triggered at high temperature. This strategy might open a promising pathway to fabricate intelligent multifunctional polymers with versatile functions.
Co-reporter:Heng Shen, Chunting Duan, Jing Guo, Ning Zhao and Jian Xu
Journal of Materials Chemistry A 2015 vol. 3(Issue 32) pp:16663-16669
Publication Date(Web):09 Jul 2015
DOI:10.1039/C5TA04188K
An environmentally friendly and facile approach was developed to synthesize boron nitride nanosheet/Ag nanoparticle hybrids (BNNS/Ag) in aqueous solution at room temperature without additional reductants. BNNSs were modified with a thin layer of tannic acid–ferric ion (TA–Fe) complex. Silver nanoparticles with a uniform diameter of approximately 7 nm were in situ formed on the surface of the modified BNNSs due to the strong reducibility of TA. The resultant nanohybrids showed excellent catalytic activity in reduction of 4-nitrophenol. BNNS/Au and BNNS/Pd nanohybrids can also be fabricated by this means, implying its extensive promise in catalytic, bio-medical and sensing fields.
Co-reporter:Chao Cai, Xiaoli Yang, Zhen Wang, Haixia Dong, Hongwei Ma, Ning Zhao and Jian Xu
Journal of Materials Chemistry A 2015 vol. 3(Issue 17) pp:4254-4259
Publication Date(Web):30 Mar 2015
DOI:10.1039/C5TC00357A
This paper demonstrates a facile and effective improvement of abrasion resistance of silica nanoparticle (NP) based anti-reflective coatings via capillary condensation of 3-aminopropyl triethoxysilane (APTES). The quartz crystal microbalance (QCM) is used to test the abrasion resistance property. The versatility of this developed method is further illustrated by the successful application to the poor heat-resistant polymer substrates.
Co-reporter:Yi Hou, Zhen Wang, Jing Guo, Heng Shen, Huan Zhang, Ning Zhao, Yiping Zhao, Li Chen, Songmiao Liang, Yan Jin and Jian Xu
Journal of Materials Chemistry A 2015 vol. 3(Issue 46) pp:23252-23260
Publication Date(Web):06 Oct 2015
DOI:10.1039/C5TA05612H
Utilizing superhydrophobic porous materials in oil/water separation has attracted increasing research interest, however, most of these materials are usually complicated to fabricate or easily lose their functions in harsh circumstances. In this study, dispersion of poly[(3,3,3-trifluoropropyl)methylsiloxane] (PTFPMS) micro–nano aggregations in acetone/water was facially prepared via a simple phase separation method. The aggregations can be easily coated on the skeletons of various 2D and 3D porous substrates, endowing the porous materials with superhydrophobicity. The prepared superhydrophobic materials show excellent resistance to chemical erosion, mechanical abrasion, and high temperature (up to 400 °C). This robust superhydrophobicity promises application of the resultant porous materials in harsh environments, and examples of using these superhydrophobic porous materials to separate oil/water mixtures have been demonstrated. This simple and universal method is suitable for the large-scale preparation of porous materials with robust superhydrophobicity.
Co-reporter:Tang Zhu, Chao Cai, Chunting Duan, Shuai Zhai, Songmiao Liang, Yan Jin, Ning Zhao, and Jian Xu
ACS Applied Materials & Interfaces 2015 Volume 7(Issue 25) pp:13996
Publication Date(Web):June 10, 2015
DOI:10.1021/acsami.5b03056
A simple, rapid (10 s) and scalable method to fabricate superhydrophobic polypropylene (PP) fabrics is developed by swelling the fabrics in cyclohexane/heptane mixture at 80 °C. The recrystallization of the swollen macromolecules on the fiber surface contributes to the formation of submicron protuberances, which increase the surface roughness dramatically and result in superhydrophobic behavior. The superhydrophobic PP fabrics possess excellent repellency to blood, urine, milk, coffee, and other common liquids, and show good durability and robustness, such as remarkable resistances to water penetration, abrasion, acidic/alkaline solution, and boiling water. The excellent comprehensive performance of the superhydrophobic PP fabrics indicates their potential applications as oil/water separation materials, protective garments, diaper pads, or other medical and health supplies. This simple, fast and low cost method operating at a relatively low temperature is superior to other reported techniques for fabricating superhydrophobic PP materials as far as large scale manufacturing is considered. Moreover, the proposed method is applicable for preparing superhydrophobic PP films and sheets as well.Keywords: fabrics; polypropylene; recrystallization; superhydrophobic; swelling;
Co-reporter:Chunting Duan, Tang Zhu, Jing Guo, Zhen Wang, Xiaofang Liu, Hao Wang, Xun Xu, Yan Jin, Ning Zhao, and Jian Xu
ACS Applied Materials & Interfaces 2015 Volume 7(Issue 19) pp:10475
Publication Date(Web):April 28, 2015
DOI:10.1021/acsami.5b01901
The separation and removal of oil or organic pollutants from water is highly imperative. The oil phases in surfactant-free oil-in-water emulsions or in free oil/water mixtures can be smartly enriched and transported by using superhydrophobic/superoleophilic iron particles (SHIPs) under a magnetic field. For water-in-oil emulsion, SHIPs-based composite membranes selectively allow the oil to pass through. Their convenient and scalable preparation, excellent separation performance, and good reusability are of great advantages for practical applications in wastewater treatment, the cleanup of oil spills, emulsion concentration, and fuel purification.Keywords: magnetic particles; nanostructured; oil/water separation; superhydrophobicity; superoleophilicity;
Co-reporter:Heng Shen, Jing Guo, Hao Wang, Ning Zhao, and Jian Xu
ACS Applied Materials & Interfaces 2015 Volume 7(Issue 10) pp:5701
Publication Date(Web):February 24, 2015
DOI:10.1021/am507416y
With the development of microelectronic technology, the demand of insulating electronic encapsulation materials with high thermal conductivity is ever growing and much attractive. Surface modification of chemical inert h-BN is yet a distressing issue which hinders its applications in thermal conductive composites. Here, dopamine chemistry has been used to achieve the facile surface modification of h-BN microplatelets by forming a polydopamine (PDA) shell on its surface. The successful and effective preparation of h-BN@PDA microplatelets has been confirmed by SEM, EDS, TEM, Raman spectroscopy, and TGA investigations. The PDA coating increases the dispersibility of the filler and enhances its interaction with PVA matrix as well. Based on the combination of surface modification and doctor blading, composite films with aligned h-BN@PDA are fabricated. The oriented fillers result in much higher in-plane thermal conductivities than the films with disordered structures produced by casting or using the pristine h-BN. The thermal conductivity is as high as 5.4 W m–1 K–1 at 10 vol % h-BN@PDA loading. The procedure is eco-friendly, easy handling, and suitable for the practical application in large scale.Keywords: aligned structure; hexagonal boron nitride; polydopamine; thermal conductivity
Co-reporter:Zhen Wang, Dong Wang, Zhenchao Qian, Jing Guo, Haixia Dong, Ning Zhao, and Jian Xu
ACS Applied Materials & Interfaces 2015 Volume 7(Issue 3) pp:2016
Publication Date(Web):January 5, 2015
DOI:10.1021/am5077765
Aerogels are a family of highly porous materials whose applications are commonly restricted by poor mechanical properties. Herein, thiol-ene chemistry is employed to synthesize a series of novel bridged silsesquioxane (BSQ) precursors with various alkoxy groups. On the basis of the different hydrolyzing rates of the methoxy and ethoxy groups, robust superhydrophobic BSQ aerogels with tailorable morphology and mechanical performances have been prepared. The flexible thioether bridge contributes to the robustness of the as-formed aerogels, and the property can be tuned on the basis of the distinct combinations of alkoxy groups with the density of the aerogels almost unchanged. To the best of our knowledge, the lowest density among the ambient pressure dried aerogels is obtained. Further, potential application of the aerogels for oil/water separation and acoustic materials has also been presented.Keywords: aerogel; alkoxy group; bridged silsesquioxane; oil/water separation; robustness
Co-reporter:Heng Shen;Yuhua Long;Xiaoli Yang;Jian Xu
Polymer International 2015 Volume 64( Issue 8) pp:986-991
Publication Date(Web):
DOI:10.1002/pi.4913
Abstract
A facile method of fabricating metal oxide hollow spheres using polydopamine (PDA) nanoparticles as active templates is reported. Monodisperse PDA nanoparticles were prepared by the polymerization of dopamine in Tris buffer solution containing various amounts of poly(ethylene oxide)–poly(propylene oxide)–poly(ethylene oxide) (PEO-PPO-PEO). The diameter of the resultant PDA nanoparticles decreased from about 180 to 80 nm with an increase of PEO-PPO-PEO concentration from 0 to 1.25 mg mL−1. The active groups of PDA and also the PEO-PPO-PEO adsorbed on the PDA spheres can chelate with various metal ions. It was found that when PDA spheres with diameter below 100 nm were used as templates, diverse metal oxide hollow spheres like CeO2, NiO and Cr2O3 could be obtained after calcination, demonstrating the diversity of this method for fabricating various metal oxide hollow spheres. © 2015 Society of Chemical Industry
Co-reporter:Zhen Wang;Zhen Dai;Xiaoli Zhang
Journal of Sol-Gel Science and Technology 2015 Volume 75( Issue 3) pp:519-529
Publication Date(Web):2015 September
DOI:10.1007/s10971-015-3722-4
A novel bridged silsesquioxane (BSQ) monomer was synthesized from 3-(2,3-epoxypropoxy)propyltrimethoxysilane and (3-aminopropyl)trimethoxysilane based on the reaction between epoxy and amine groups. The monomer was used to fabricate aerogels with excellent mechanical properties via sol–gel processes followed by supercritical CO2 drying. The influence of the sol–gel conditions on the chemical structure, morphology and mechanical property of the aerogels was investigated by NMR, TGA, SEM, nitrogen sorption analysis and DMA. BSQ aerogels prepared from the optimal sol–gel procedure showed excellent properties with high mechanical performance (compression modulus of 20.4 MPa) and low density (0.22 g cm−3), which are of great advantage for practical applications. Further, SiO2/BSQ composite aerogels with significantly improved mechanical performance than SiO2 aerogels can be obtained by co-condensing of BSQ monomer and tetraethoxysilane. The abundant hydroxyl groups in the BSQ precursor are believed to contribute to the robustness of BSQ and SiO2/BSQ composite aerogels due to the strengthened skeleton via the intermolecular H-bonds.
Co-reporter:Ning Zhao;Zhen Wang;Chao Cai;Heng Shen;Feiyue Liang;Dong Wang;Chunyan Wang;Tang Zhu;Jing Guo;Yongxin Wang;Xiaofang Liu;Chunting Duan;Hao Wang;Yunzeng Mao;Xin Jia;Haixia Dong;Xiaoli Zhang ;Jian Xu
Advanced Materials 2014 Volume 26( Issue 41) pp:6994-7017
Publication Date(Web):
DOI:10.1002/adma.201401718
The surprising properties of biomaterials are the results of billions of years of evolution. Generally, biomaterials are assembled under mild conditions with very limited supply of constituents available for living organism, and their amazing properties largely result from the sophisticated hierarchical structures. Following the biomimetic principles to prepare manmade materials has drawn great research interests in materials science and engineering. In this review, we summarize the recent progress in fabricating bioinspired materials with the emphasis on mimicking the structure from one to three dimensions. Selected examples are described with a focus on the relationship between the structural characters and the corresponding functions. For one-dimensional materials, spider fibers, polar bear hair, multichannel plant roots and so on have been involved. Natural structure color and color shifting surfaces, and the antifouling, antireflective coatings of biomaterials are chosen as the typical examples of the two-dimensional biomimicking. The outstanding protection performance, and the stimuli responsive and self-healing functions of biomaterials based on the sophisticated hierarchical bulk structures are the emphases of the three-dimensional mimicking. Finally, a summary and outlook are given.
Co-reporter:Hao Wang, Junjie Wu, Chao Cai, Jing Guo, Haosen Fan, Caizhen Zhu, Haixia Dong, Ning Zhao, and Jian Xu
ACS Applied Materials & Interfaces 2014 Volume 6(Issue 8) pp:5602
Publication Date(Web):March 31, 2014
DOI:10.1021/am406052u
Inspired by the remarkable adhesion of mussel, dopamine, a mimicking adhesive molecule, has been widely used for surface modification of various materials ranging from organic to inorganic. However, dopamine and its derivatives are expensive which impede their application in large scale. Herein, we replaced dopamine with low-cost catechol and polyamine (only 8% of the cost of dopamine), which could be polymerized in an alkaline solution and deposited on the surfaces of various materials. By using this cheap and simple modification method, polypropylene (PP) separator could be transformed from hydrophobic to hydrophilic, while the pore structure and mechanical property of the separator remained intact. The uptake of electrolyte increased from 80% to 270% after the hydrophilic modification. Electrochemical studies demonstrated that battery with the modified PP separator had a better Coulombic efficiency (80.9% to 85.3%) during the first cycle at a current density of 0.1 C, while the discharging current density increased to 15 C and the discharge capacity increased by 1.4 times compared to the battery using the bare PP separator. Additionally, the modification allowed excellent stability during manifold cycles. This study provides new insights into utilizing low-cost chemicals to mimic the mussel adhesion and has potential practical application in many fields.Keywords: bioinspired; catechol; Li-ion battery; mussel; polyamine; separator;
Co-reporter:Haosen Fan, Hao Wang, Jing Guo, Ning Zhao, Jian Xu
Journal of Colloid and Interface Science 2014 Volume 414() pp:46-49
Publication Date(Web):15 January 2014
DOI:10.1016/j.jcis.2013.09.042
•2D leaf-like PANI was prepared using SDBS as dopant.•SDBS plays a dual role in serving as soft template and improving hydrophobic property.•Good hydrophobicity is mainly due to the hydrophobic long dodecyl groups of SDBS dopant.Leaf-like hierarchical polyaniline (PANI) structure with interlaced nanofibers on the surface was prepared by chemical oxidation polymerization of aniline assisted by sodium dodecyl benzene sulfonate (SDBS). The chemical structure and the composition of the leaf-like PANI obtained were characterized by FTIR, UV–vis, XRD and XPS. In order to investigate the formation mechanism of such micro/nanostructures, some micro/nanostructures of PANI polymerized at different polymerization times were synthesized and observed for comparison. The results show that the PANI micro/nanostructures originate from PANI microleaves due to SDBS as soft template, which then covered with interlaced nanofibers on the surface. The leaf-like PANI micro/nanostructures exhibit good hydrophobic property with a water contact angle of 134.3° resulted from the hydrophobic long dodecyl groups of SDBS dopant.
Co-reporter:Xiaofeng Li, Liang Zhang, Xinglin Guo, Caizhen Zhu, Zhong-Zhen Yu, Ning Zhao and Jian Xu
RSC Advances 2014 vol. 4(Issue 91) pp:49861-49865
Publication Date(Web):17 Sep 2014
DOI:10.1039/C4RA06155A
Band-like folds with high aspect ratio and birefringence behavior were observed on an in situ formed thin poly(vinyl alcohol) (PVA) hydrogel film via freezing–thawing treatment of PVA aqueous solution coated on glass. The crystallites generated during the freezing of the PVA solution cross-linked the PVA to form the hydrogel film. The volume expansion of the hydrogel film due to the absorption of condensed water in thawing induced the formation of folds. These folds show interesting birefringence behavior. The morphology, crystallization and birefringence behavior of the folds were characterized by polarized optical microscopy, scanning electron microscopy, Fourier transform infrared spectroscopy and X-ray diffraction. A plausible principle for the fold formation is also discussed. It has been found that the moderate interaction between the hydrogel film and the substrate and the existence of condensed water on the frozen hydrogel film play important roles in the appearance of the folds.
Co-reporter:Zhen Wang;Zhen Dai;Junjie Wu;Jian Xu
Advanced Materials 2013 Volume 25( Issue 32) pp:4494-4497
Publication Date(Web):
DOI:10.1002/adma.201301617
Co-reporter:Xiaoli Yang, Ning Zhao, Qingzhu Zhou, Chao Cai, Xiaoli Zhang and Jian Xu
Journal of Materials Chemistry A 2013 vol. 1(Issue 20) pp:3359-3366
Publication Date(Web):26 Mar 2013
DOI:10.1039/C3TC30324A
This paper describes a straightforward method to precisely prepare monodisperse ZrO2@SiO2 core–shell nanoparticles (CSNs) by sol–gel polymerization of TEOS in the presence of ZrO2 cores without additional capping agents. We studied the morphology and composition of CSNs by Scanning Electron Microscopy (SEM), Transmission Electron Microscopy (TEM) and X-ray Diffraction (XRD). It has been found that the citric acid groups adsorbed onto the ZrO2 surface during the preparation of ZrO2 as well as the slow hydrolysis and condensation of TEOS in isopropanol are crucial for the selective growth of silica on the surface of ZrO2 cores. The thickness of the silica shell can be facilely controlled from about 4 to 30 nm by varying the concentration of TEOS, with the refractive indices of the prepared CSNs tuned accordingly from about 1.2 to 1.9. The coated silica shell, which can be well dispersed in solvents such as methanol and ethanol, can improve the dispersibility of pure ZrO2 nanoparticles which can only be dispersed in water. Moreover, the formation of the silica shell improved the chemical reactivity of pure ZrO2 nanoparticles. After modifying with methyltriethoxysilane (MTES), the CSNs can be well dispersed in various organic solvents, such as dimethylbenzene, chloroform and isoamyl alcohol, which may find applications in optically transparent resins with controllable refractive index or organic silicon packaging materials with high refractive index for LED and so on. Additionally, other silane coupling agents can also be applied to modify the surface chemical properties of CSNs, which may provide more potential applications.
Co-reporter:Haosen Fan, Hao Wang, Jing Guo, Ning Zhao, Jian Xu
Journal of Colloid and Interface Science 2013 Volume 409() pp:255-258
Publication Date(Web):1 November 2013
DOI:10.1016/j.jcis.2013.07.056
•Star-shaped and leaf-shaped PANIs were prepared using lithium triflate as dopant.•Star-shaped and leaf-shaped PANIs both exhibit good superhydrophobicity.•The good superhydrophobicity is due to the special nanoweb structure and low surface tension of dopant.Star-shaped and leaf-shaped polyaniline (PANI) hierarchical structures with interlaced nanofibers on the surface were successfully prepared by chemical polymerization of aniline in the presence of lithium triflate (LT). Chemical structure and composition of the star-like PANI obtained were characterized by FTIR and UV–vis spectra. PANI 2D architectures can be tailored from star-shaped to leaf-shaped structures by change the concentration of LT. The synthesized star-like and leaf-like polyaniline show good superhydrophobicity with water contact angles of both above 150° due to the combination of the rough nanoweb structure and the low surface tension of fluorinated chain of dopant. This method is a facile and applicable strategy for a large-scale fabrication of 2D PANI micro/nanostructures. Many potential applications such as self-cleaning and antifouling coating can be expected based on the superhydrophobic PANI micro/nanostructures.
Co-reporter:Fangfang Si, Ning Zhao, Li Chen, Jian Xu, Qingsheng Tao, Jinyong Li, Chunbo Ran
Journal of Colloid and Interface Science 2013 Volume 407() pp:482-487
Publication Date(Web):1 October 2013
DOI:10.1016/j.jcis.2013.06.068
•Hybrid molecule STA-APTES was obtained by the reaction between STA and APTES.•A superhydrophobic coating can be obtained by casting the STA-APTES solution.•The coating can be cross-linked by the APTES moieties under alkaline atmosphere.•The cross-linked STA-APTES coating shows enhanced thermal and solvent resistance.The chemical originals of natural superhydrophobic surfaces are based on botanic or animal wax or fat, which have poor chemical and thermal resistance. Herein, we report a simple chemical modification of stearic acid (STA) with γ-aminopropyl triethoxysilane (APTES), to obtain an organic–inorganic molecular hybrid STA-APTES compound. A flower-like hierarchically structured surface with superhydrophobicity can be obtained simply by casting the STA-APTES solution under ambient circumstance. The crystallization of the hydrocarbon chain from STA leads to the formation of the binary microstructure and reduces the surface tension, contributing to the superhydrophobicity of the as-formed surface. In addition, the condensation of Si(OCH2CH3)3 from APTES can lead to the cross-linking of the resultant surface, which endows the as-formed superhydrophobic surface with high performances, such as excellent thermal and solvent resistance, etc. This superhydrophobic surface prepared is superior to its many analogs in nature, promising a wide application especially in harsh circumstance.Graphical abstract
Co-reporter:Xiaoyan Zhang, Wangyang Fu, Chunting Duan, Hong Xiao, Meiwu Shi, Ning Zhao, Jian Xu
Applied Surface Science 2013 Volume 266() pp:225-229
Publication Date(Web):1 February 2013
DOI:10.1016/j.apsusc.2012.11.153
Abstract
Superhydrophobicity is commonly regarded as a surface property that has important consequences for self-cleaning applications. Here we show interestingly that the superhydrophobicity is closely connected to the bulk buoyancy performance of kapok fiber aggregates, a natural material endowed with superhydrophobicity and extraordinary high porosity. First of all, we have determined the superhydrophobicity of a single kapok fiber, which can be ascribed to its micro-nano-binary structure (MNBS) and the thin hydrophobic paraffinic wax layer covered on the surface. Second, based on classic capillary and wicking theory, the buoyancy performance of the kapok fiber aggregates can be modeled and we demonstrate that their buoyancy performance is actually determined by the superhydrophobicity of individual kapok fibers. Our results also suggest an optimized density ∼0.015 g cm−3 for using kapok fiber aggregates as the lightest natural buoyancy.
Co-reporter:Haosen Fan, Ning Zhao, Hao Wang, Xiaofeng Li, Jian Xu
Materials Letters 2013 Volume 92() pp:115-118
Publication Date(Web):1 February 2013
DOI:10.1016/j.matlet.2012.10.081
A novel multidimensional architecture of tremella-like polyaniline (PANI) has been synthesized in the presence of oxalic acid (OA) by a template-free method. The PANI tremella is about 3–5 μm in average diameter and consist of petals of interlaced sheets with a thickness of about 20 nm. Chemical structures of obtained PANI were characterized by Fourier transform infrared spectroscopy (FTIR) and Ultraviolet and visible spectroscopy (UV–vis). It is found the micro-nanostructured PANI exhibits good electrochemical behavior in 0.1 M HCl electrolyte solution, indicating a potential application in sensors or electrochemical devices. In addition, the effect of OA concentration on the morphology of the tremella-like PANI was also investigated.Highlights► Tremella-like PANI was prepared in the presence of oxalic acid by a template-free method. ► Tremella-like PANI exhibits good electrochemical behavior. ► The obtained tremella-like PANI shows potential application in sensors or electrochemical devices.
Co-reporter:Haosen Fan, Ning Zhao, Hao Wang, Xiaofeng Li, Jian Xu
Materials Letters 2013 Volume 92() pp:157-160
Publication Date(Web):1 February 2013
DOI:10.1016/j.matlet.2012.10.048
Carpenterworm-like multidimensional architectures of polyaniline/multi-walled carbon nanotubes (PANI–MWNTs), with a diameter of about 2.5 μm and consisting of many interlaced PANI nanorods on the surface of MWNTs, were successfully synthesized in a mixture of ethanol and water. Chemical structure and composition of the prepared PANI–MWNTs nanocomposites were characterized by Fourier transform infrared (FTIR) spectroscopy, ultraviolet and visible spectroscopy (UV–vis), X-ray diffraction (XRD) and X-ray photoelectron spectroscopy (XPS). It has been found that the concentration of ethanol in the solution plays a critical role in controlling the morphology of the resultant nanocomposites. The obtained carpenterworm-like PANI–MWNTs nanocomposites exhibit enhanced electrochemical behavior in comparison with MWNTs and PANI, indicating a potential application in electrode material of supercapacitors or secondary batteries.Highlights► Carpenterworm-like PANI–MWNTs nanocomposites are prepared using a mixture of ethanol and H2O. ► PANI–MWNTs nanocomposites with different morphology are obtained by tuning the composition of the solvent. ► Carpenterworm-like PANI–MWNTs nanocomposites exhibits enhanced electrochemical behavior.
Co-reporter:Cai-zhen Zhu;Xiao-lan Yu;Xiao-fang Liu;Yun-zen Mao
Chinese Journal of Polymer Science 2013 Volume 31( Issue 5) pp:823-832
Publication Date(Web):2013 May
DOI:10.1007/s10118-013-1272-1
Structure of PAN fibers during pre-oxidation and carbonization was studied using two dimensional small angle X-ray scattering/wide angle X-ray diffraction (2D SAXS/WAXD). The SAXS results show that during pre-oxidation between 180 °C and 275 °C, the volume content of microvoids increases with the temperature increasing, which may be one of reasons for the decrease of tensile strength of pre-oxidized fibers. 253 °C was the critical transition temperature, the length, diameter, aspect ratio and orientation distribution of microvoids increased with temperature before this temperature and decreased after this temperature. After the high temperature carbonization, lots of spindly microvoids formed. WAXD patterns demonstrate that the crystallite size of PAN fibers first increased before 230 °C and then decreased with the increase of temperature during the pre-oxidation. The diffraction peak of PAN fibers at 2θ ≈ 17° almost disappeared at the end of preoxidation while the diffraction peak of aromatic structure at 2θ ≈ 25° appeared at 253 °C. During carbonization, the peak intensity at 2θ ≈ 25° increased apparently due to the formation of graphite structure. The results obtained give a deep understanding of the microstructure development in the PAN fibers during pre-oxidation and carbonization, which is important for the preparation of high performance carbon fibers.
Co-reporter:Hai-fan Xiang;Dong Wang;Hui-chao Liua 赵宁
Chinese Journal of Polymer Science 2013 Volume 31( Issue 3) pp:521-529
Publication Date(Web):2013 March
DOI:10.1007/s10118-013-1241-8
Sound absorption properties of natural kapok fibers have been investigated. Kapok fibrous assemblies with different bulk density, thickness, fiber length and orientation were manufactured, and their acoustical performances were evaluated by using an impedance tube instrument. Results show that the kapok fiber has excellent acoustical damping performance due to its natural hollow structure, and the sound absorption coefficients of kapok fibrous assemblies are significantly affected by the bulk density, thickness and arrangement of kapok fibers but less dependent on the fiber length. Compared with assemblies of commercial glass wool and degreasing cotton fibers, the kapok fiber assemblies with the same thickness but much smaller bulk density may have the similar sound absorption coefficients. Theoretical modelling of the acoustical damping performance of kapok fibers shows a good agreement with the experimental data. All the results demonstrate that kapok fiber is a promising light and environment-friendly sound absorption material.
Co-reporter:Xiao-fang Liu;Shuai-xia Tan;Xiao-li Zhang
Chinese Journal of Polymer Science 2013 Volume 31( Issue 7) pp:1022-1028
Publication Date(Web):2013 July
DOI:10.1007/s10118-013-1294-8
A full-field finite element method (FEM) analysis combined with electronic speckle pattern interferometry (ESPI) measurement was developed to investigate defect evolution in polymer films. Different from the previous reports, which only compare the ESPI experimental and FEM simulated results at several points or lines, herein the full-field FEM results were exported, subtracted with a continuous distribution. By choosing proper parameters and number of substeps, the simulated and experimental results showed excellent correspondence. Furthermore, the displacement fields vertical to the tensional direction were also presented, and the strain field was preliminarily evaluated. The current method of combination of ESPI and FEM allows for capturing the experimental fringe maps to validate and optimize FEM results simulated, and would give a higher security to structural and mechanical analysis of polymeric materials.
Co-reporter:Liang Zhang ; Junjie Wu ; Yongxin Wang ; Yuhua Long ; Ning Zhao ;Jian Xu
Journal of the American Chemical Society 2012 Volume 134(Issue 24) pp:9879-9881
Publication Date(Web):June 2, 2012
DOI:10.1021/ja303037j
We combine two amazing abilities found in nature: the superhydrophobic property of lotus leaf and the adhesive ability of mussel adhesive protein. The molecular structure mimic of the single units of adhesive proteins, dopamine, was polymerized in an alkaline aqueous solution to encapsulate microparticles. The as-formed thin polydopamine walls worked as reactive templates to generate silver nanoparticles on the capsuled particles. As a result, core/shell/satellite composite particles were generated with a hierarchical structure similar to the micromorphology of lotus leaf. The composite particles exhibited extremely water repellence after fluorination. Because dopamine can deposit and adhere to all kinds of materials, this method can be applied to diverse microparticles, from organic to inorganic. In addition, particles of different sizes and matters can be modified to superhydrophobic particles in one pot. Magnetic particles have also been prepared which could be used as oil-absorbent and magnetic controlled carriers. “Oil marbles” formed underwater were achieved for the first time.
Co-reporter:Xiaoli Yang, Ning Zhao, Qingzhu Zhou, Zhen Wang, Chunting Duan, Chao Cai, Xiaoli Zhang and Jian Xu
Journal of Materials Chemistry A 2012 vol. 22(Issue 34) pp:18010-18017
Publication Date(Web):10 Jul 2012
DOI:10.1039/C2JM33220E
A facile method was developed to fabricate hollow amino-functionalized organosilica microspheres based on the hydrolysis and condensation of 3-aminopropyltriethoxysilane (APTES) and tetraethoxysilane (TEOS) in an aqueous system without an additional template and catalyst. The hollow hybrid organosilica microspheres obtained have been characterized by scanning electron microscopy, transmission electron microscopy, and N2 adsorption–desorption measurements. The results of Fourier transform infrared spectroscopy, solid-state NMR spectroscopy, X-ray photoelectron spectroscopy and thermogravimetric analysis displayed the composition of the synthesized hollow microspheres and the presence of amino groups on the surface. A self-templated and self-catalyzed mechanism for the formation of the hollow microspheres is proposed: the protonated APTES acts as both a catalyst for the reaction and a stabilizer for the hydrophobic precursor droplets, while the droplets themselves act as soft templates, and the consumption of the precursors leads to the formation of a hollow structure. The morphology and the size distribution of the organosilica microspheres can be controlled by tuning the composition of the precursors, and the stirring speed, as well as the reaction temperature. The large cavity with an open hole on the shell and the reactive amino groups on the surface of the hybrid organosilica microspheres promise many potential applications. Examples of employing the microspheres as adsorbents and phase change microcapsules have been presented.
Co-reporter:Haosen Fan, Hao Wang, Ning Zhao, Xiaoli Zhang and Jian Xu
Journal of Materials Chemistry A 2012 vol. 22(Issue 6) pp:2774-2780
Publication Date(Web):15 Dec 2011
DOI:10.1039/C1JM14311E
A facile method was successfully developed for the preparation of a hierarchical nanocomposite of vertical polyaniline (PANI) nanorods aligned on the surface of functional multiwalled carbon nanotubes (FMWNTs) by in situ polymerization of PANI on the surface of FMWNTs. The formation mechanism was illustrated according to the morphological evolution of PANI-FMWNTs nanocomposite at different polymerization times. The hierarchical nanocomposite possessed higher special capacitance and better stability than each individual component as supercapacitor electrode materials due to the synergistic effect of both components, as well as to the special hierarchical structure, which not only increases the specific surface area of the nanocomposite but also facilitates the penetration of electrolyte ions. This research gives a better insight into the preparation of functional hybrid nanocomposites by combining different dimensional nanomaterials.
Co-reporter:Haosen Fan, Ning Zhao, Hao Wang, Yuhua Long, Xiaofeng Li and Jian Xu
RSC Advances 2012 vol. 2(Issue 31) pp:11887-11891
Publication Date(Web):08 Oct 2012
DOI:10.1039/C2RA21723F
Highly uniform core–shell structured polyaniline–multiwall carbon nanotube nanocomposites have been successfully prepared by noncovalent coating of a polyaniline shell on the wall of MWNTs with the assistance of 1-pyrenesulfonic acid. It is found that 1-pyrenesulfonic acid plays important roles in dispersing MWNTs and directing the polymerization of the polyaniline shell by the sulfonic groups. The obtained nanocomposites exhibit a higher specific capacitance. This research provides a new approach for designing core–shell hybrid materials with potential application in high-performance electrochemical supercapacitors.
Co-reporter:Haosen Fan, Ning Zhao, Hao Wang, Xiaofeng Li, Jian Xu
Materials Letters 2012 Volume 78() pp:42-45
Publication Date(Web):1 July 2012
DOI:10.1016/j.matlet.2012.03.053
Polyaniline with a leaf-like hierarchical structure of 3 μm in length, 2 μm in width, 100 nm in thickness and crisscrossed nanofibers decorated on the surface, was successfully prepared in one step polymerization of aniline in the presence of sodium heptafluorobutyrate. The synthesized polyaniline shows superhydrophobicity with a water contact angle of 151° due to the combination of the low surface tension of fluorinated chain and the rough micro/nanostructure. Chemical structure and composition of the resultant PANI were characterized by FTIR, UV–vis, XRD and XPS. The formation mechanism of the hierarchical structure was investigated by monitoring the morphology development with the polymerization time. This method is facile and applicable for the large scale fabrication. Many potential applications can be expected based on the superhydrophobic PANI micro/nanostructures.Highlights► Leaf-like PANI was prepared by using sodium heptafluorobutyrate. ► Leaf-like PANI exhibits good superhydrophobic property. ► The good superhydrophobicity of PANI is due to its hierarchical structure and the low surface tension.
Co-reporter:Haosen Fan, Hao Wang, Xiaolan Yu, Ning Zhao, Xiaoli Zhang, Jian Xu
Materials Letters 2012 Volume 71() pp:70-73
Publication Date(Web):15 March 2012
DOI:10.1016/j.matlet.2011.11.121
Different polyaniline (PANI) micro/nanostructures, such as hollow microdisks, nanospheres, and nanofibers, have been synthesized in the presence of polyvinylpyrrolidone (PVP) by changing the pH values of reaction system through chemical oxidation polymerization. The formation mechanism experiments indicated that the disk-shaped PANI originated from cycloidal nanoplates, which then self-assembled into disk-shaped PANI. And pH value has an important effect on the arranged state of PVP chains and further impacts the micro/nanostructures of obtained products. It is found that the obtained PANI micro/nanostructures exhibit better electrochemical behavior in HCl solution with the decrease of pH value of reaction system, indicating a potential application in biosensor.Highlights► Different PANI micro/nanostructures were synthesized by changing the pH values of reaction system. ► PANI micro/nanostructures exhibit good electrochemical behavior. ► PVP and pH values play significant roles in formation of PANI micro/nanostructures.
Co-reporter:Junjie Wu;Xiaoli Zhang;Jian Xu
Cellulose 2012 Volume 19( Issue 4) pp:1239-1249
Publication Date(Web):2012 August
DOI:10.1007/s10570-012-9731-3
Cellulose/silver nanoparticles (Ag NPs) composites were prepared and their catalytic performance was evaluated. Porous cellulose microspheres, fabricated from NaOH/thiourea aqueous solution by a sol–gel transition processing, were served as supports for Ag NPs synthesis by an eco-friendly hydrothermal method. The regenerated cellulose microspheres were designed as reducing reagent for hydrothermal reduction and also micro-reactors for controlling growth of Ag NPs. The structure and properties of obtained composite microspheres were characterized by Optical microscopy, UV–visible spectroscopy, WXRD, SEM, TEM and TG. The results indicated that Ag NPs were integrated successfully and dispersed uniformly in the cellulose matrix. Their size (8.3–18.6 nm), size distribution (3.4–7.7 nm), and content (1.1–4.9 wt%) were tunable by tailoring of the initial concentration of AgNO3. Moreover, the shape, integrity and thermal stability were firmly preserved for the obtained composite microspheres. The catalytic performance of the as-prepared cellulose/Ag composite microspheres was examined through a model reaction of 4-nitrophenol reduction in the presence of NaBH4. The composites microspheres exhibited good catalytic activity, which is much high than that of hydrogel/Ag NPs composites and comparable with polymer core–shell particles loading Ag NPs.
Co-reporter:Yongxin Wang, Xiaofang Liu, Xiaofeng Li, Junjie Wu, Yuhua Long, Ning Zhao, and Jian Xu
Langmuir 2012 Volume 28(Issue 31) pp:11276-11280
Publication Date(Web):July 24, 2012
DOI:10.1021/la301972r
The spreading of a miscible liquid with a low surface tension on a water surface generates the directional motion of submerged polymer hydrogels, which could be attributed to convective flows resulting from the gradient of surface tension along the surface (Marangoni effect). The direction and velocity of this motion can be well controlled by altering the driving conditions. Furthermore, a spherical hydrogel can smartly find the path to walk through a microfluidic maze when liquid mixing occurs near the maze exit. This convenient chemical driving approach to transporting submerged objects in a desired way may be useful in microfluidics, micromechanics, and other applications.
Co-reporter:Xiaofeng Li, Liang Zhang, Yongxin Wang, Xiaoli Yang, Ning Zhao, Xiaoli Zhang, and Jian Xu
Journal of the American Chemical Society 2011 Volume 133(Issue 11) pp:3736-3739
Publication Date(Web):February 24, 2011
DOI:10.1021/ja1106767
Patterned “bead in pore” composite film with hemispherical or mushroomlike TiO2 microparticles lying in the holes of a honeycomblike polystyrene matrix has been fabricated by a template-free bottom-up approach from a homogeneous solution of TiCl4/polystyrene/CHCl3 using the breath figures method. It is a very simple way to prepare hemispherical or mushroomlike TiO2 microparticles and to get the hexagonally nonclose-packed arrays of asymmetrical particles with or without polymer matrix, which have potential applications in photonics.
Co-reporter:Liang Zhang, Ning Zhao, Xiaofeng Li, Yuhua Long, Xiaoli Zhang and Jian Xu
Soft Matter 2011 vol. 7(Issue 8) pp:4050-4054
Publication Date(Web):03 Mar 2011
DOI:10.1039/C0SM01084G
Superhydrophobic surfaces, which have amazing abilities such as self-cleaning and drag reduction, have aroused great interest in both academic studies and industrial fields in the past decade. Although many methods and techniques to fabricate superhydrophobic surfaces have been investigated, most of the coatings have a lack of adherence which hinders the practical usage. Herein, we introduce a superhydrophobic coating developed from ethyl α-cyanoacrylate (ECA), which is a kind of widely used glue with tenacious adhesion to various substrates. A liquid film of ECA monomers was coated on a substrate and put in an environment of ammonia vapor and high humidity at room temperature. The polymerization concurrently started at the top of the film triggered by ammonia and at the bottom initiated by the substrate. A layer of PECA microfibers was formed at the surface first, and then vapor phase polymerization of the volatilized ECA monomers was conducted on the as-formed microfibers generating twisted and coiled micro/nanofibers. After the monomers were all consumed, a PECA coating with three layers were generated: one layer of micro/nanofibers on top, one layer of microfibers in the middle and one layer of bulk PECA at the bottom. The polymeric coating obtained a CA as high as 158° and SA of 4° due to the micro/nanofiber-structured surface and a good adhesion to the substrate.
Co-reporter:Haifan Xiang, Yuhua Long, Xiaolan Yu, Xiaoli Zhang, Ning Zhao and Jian Xu
CrystEngComm 2011 vol. 13(Issue 15) pp:4856-4860
Publication Date(Web):14 Mar 2011
DOI:10.1039/C0CE00980F
Here, we have introduced a novel and facile method to prepare porous hollow CuO nanofibers and Cu nanofibers via single-spinneret electrospinning of polyvinyl pyrrolidone (PVP)/copper acetate (Cu(CH3COO)2) solution followed by annealing and reduction. In this approach, the diameter and the shell thickness of the fibers can be simply adjusted by the concentration of PVP and the ratio of PVP to Cu(CH3COO)2. A possible mechanism is proposed to explain the formation of porous hollow CuO and Cu nanofiber. This method provides an new idea to prepare metal-oxide and metal fibers with a long continuous porous hollow morphology.
Co-reporter:Haifan Xiang, Liang Zhang, Zhen Wang, Xiaolan Yu, Yuhua Long, Xiaoli Zhang, Ning Zhao, Jian Xu
Journal of Colloid and Interface Science 2011 Volume 359(Issue 1) pp:296-303
Publication Date(Web):1 July 2011
DOI:10.1016/j.jcis.2011.03.076
Multifunctional superhydrophobic polymethylsilsesquioxane (PMSQ) surfaces with excellent solvent resistance, thermal stability and enhanced sound absorption property were manufactured by electrospinning. The surfaces with various hierarchical morphologies and hydrophobicity were obtained by electrospinning at the different stages of sol–gel transition of PMSQ prepolymer solution. At the stage with a proper viscosity the superhydrophobic PMSQ surface with a contact angle as high as 151° and a sliding angle as low as 8° was prepared. Due to the excellent thermal stability and solvent resistance properties of the cured PMSQ, the resultant surfaces remain superhydrophobicity after thermal treatment at 300 °C and immersion into many solvents. Additionally, an enhanced acoustical performance and ultra water repellency were obtained simultaneously when the traditional acoustical sponge was decorated with the electrospun PMSQ superhydrophobic surface. The robust superhydrophobic PMSQ surfaces may promise practical applications in many fields.Graphical abstractSuperhydrophobic PMSQ surfaces with excellent solvent resistance and thermal stability were prepared. Modifying sponge with PMSQ not only endows ultra water repellency, but also enhances acoustic performance by 12%.Highlights► Superhydrophobic PMSQ surfaces were prepared by electrospinning at sol–gel transition. ► Superhydrophobic PMSQ surfaces show excellent resistance to solvents. ► Superhydrophobic PMSQ surfaces show thermal stability as high as 300 °C. ► Superior acoustical performance was obtained when the sponge decorated with PMSQ.
Co-reporter:Xiaolan Yu, Haosen Fan, Hao Wang, Ning Zhao, Xiaoli Zhang, Jian Xu
Materials Letters 2011 Volume 65(17–18) pp:2812-2815
Publication Date(Web):September 2011
DOI:10.1016/j.matlet.2011.05.116
Flower-like polyaniline–polyvinyl alcohol (PANI/PVA) multidimensional architectures assembled from 2D petals were successfully synthesized in the dilute solution of PVA by the oxidation polymerization. PANI/PVA flowers have a diameter of about 2.5 μm and consist of many interlaced sheet petals. Chemical structure and composition of polymerized PANI/PVA were characterized by Fourier transform infrared (FTIR) spectroscopy, Ultraviolet and visible spectroscopy (UV–vis), X-ray diffraction (XRD) and X-ray photoelectron spectroscopy (XPS). In order to research the formation mechanism of the 3D flower-like PANI/PVA, their growth process was followed by measuring the morphological evolutions of products with the different polymerization times. The results showed that the flower-like PANI/PVA originated from sheet petals, which then self-assembled into flower-like microstructures. In addition, the effect of PVA concentration on the morphology of the 3D flower-like PANI/PVA was also investigated.
Co-reporter:Xiaolan Yu, Haosen Fan, Hao Wang, Ning Zhao, Xiaoli Zhang, Jian Xu
Materials Letters 2011 Volume 65(17–18) pp:2724-2727
Publication Date(Web):September 2011
DOI:10.1016/j.matlet.2011.05.051
A novel 2D leaf-like polyaniline with special hierarchical micro/nanostructures, a length of about 3 μm, width of about 2.3 μm and thickness of about 120 nm, has been successfully synthesized in the presence of poly (acrylic acid-co-maleic acid) sodium salt (PAA/MA-SS), which is self-assembled from 2D square nanoplate and 1D nanorods. Its surface consists of highly cross-linked nanorods of approximately 100 nm in length and 30 nm in diameter. In order to investigate the formation mechanism of such 2D leaf-like polyaniline, some micro/nanostructures of polyaniline are synthesized at different polymerization times and the results show that the polyaniline microleaves originate from square nanoplates, which then self-assemble into leaf-like micro/nanostructures with nanorods on the surface.
Co-reporter:Xiaoying Lu, Zhen Wang, Xiaoli Yang, Xun Xu, Liang Zhang, Ning Zhao, Jian Xu
Surface and Coatings Technology 2011 206(6) pp: 1490-1494
Publication Date(Web):
DOI:10.1016/j.surfcoat.2011.09.031
Co-reporter:Junjie Wu, Liang Zhang, Yongxin Wang, Yuhua Long, Huan Gao, Xiaoli Zhang, Ning Zhao, Yuanli Cai, and Jian Xu
Langmuir 2011 Volume 27(Issue 22) pp:13684-13691
Publication Date(Web):October 6, 2011
DOI:10.1021/la2027237
In this article, we report a bioinspired approach to preparing stable, functional multilayer films by the integration of mussel-inspired catechol oxidative chemistry into a layer-by-layer (LbL) assembly. A polyanion of poly(acrylic acid-g-dopamine) (PAA-dopamine) bearing catechol groups, a mussel adhesive protein-mimetic polymer, was synthesized as the building block for LbL assembly with poly(allylamine hydrochloride) (PAH). The oxidization of the incorporated catechol group under mild oxidative condition yields o-quinone, which exhibits high reactivity with amine and catechol, thus endowing the chemical covalence and retaining the assembled morphology of multilayer films. The cross-linked films showed excellent stability even in extremely acidic, basic, and highly concentrated aqueous salt solutions. The efficient chemical cross-linking allows for the production of intact free-standing films without using a sacrificial layer. Moreover, thiol-modified multilayer films with good stability were exploited by a combination of thiols-catechol addition and then oxidative cross-linking. The outstanding stability under harsh conditions and the facile functionalization of the PAA-dopamine/PAH multilayer films make them attractive for barriers, separation, and biomedical devices.
Co-reporter:Hongjun Dai, Xiaofeng Li, Yuhua Long, Junjie Wu, Songmiao Liang, Xiaoli Zhang, Ning Zhao and Jian Xu
Soft Matter 2009 vol. 5(Issue 10) pp:1987-1989
Publication Date(Web):06 Apr 2009
DOI:10.1039/B821363A
Multi-membrane hydrogels are newly promising carriers in biomedical fields. We fabricate alginate-based onion-like multi-membrane hydrogels starting from a template gel-core to shells through a dynamic self-assembly method, and investigate the influence of various factors on the formation of the complex system in detail. By precisely controlling the process of preparation, multi-layered hydrogels of different shapes either with or without defined internal space between separated layers can be prepared. And a pulse-like delivery of macromolecule has been achieved by this architecture.
Co-reporter:Haosen Fan, Hong Yu, Yufei Zhang, Jing Guo, Zhen Wang, Hao Wang, Xi Hao, Ning Zhao, Hongbo Geng, Zhengfei Dai, Qingyu Yan, Jian Xu
Nano Energy (March 2017) Volume 33() pp:
Publication Date(Web):March 2017
DOI:10.1016/j.nanoen.2017.01.043
•Hierarchical yolk shell structures assembled from ZnO@C nanocrystals were successfully prepared from zinc-cyanide hybrid coordination polymers.•The micro-nano secondary structure can both achieve high packing density and facilitate the Li+ ion diffusion.•The yolk-shell structure exhibit ultra-stable cycle life because it can further buffer the strain during repeated cycling to maintain the structural integrity.Uniform zinc-cyanide hybrid coordination polymer microspheres were successfully synthesized by a coprecipitation method. Then hierarchical yolk-shell structured and carbon coated ZnO microspheres (YC-ZnO) composed of ZnO@C nanocrystals were prepared by consecutive post annealing processes of these microspheres in argon and air atmosphere. Such micro-nano porous structures have the advantages of large specific surface area, good charge transport kinetics, and large cavity to accommodate the volume change and maintain the mechanical integrity of the electrode material. When evaluated as anode materials of lithium ion batteries, these ZnO yolk-shell spheres exhibited excellent battery performance with a high rate capacity and ultra-stable cycling stability.
Co-reporter:Xiaoli Yang, Ning Zhao, Qingzhu Zhou, Zhen Wang, Chunting Duan, Chao Cai, Xiaoli Zhang and Jian Xu
Journal of Materials Chemistry A 2012 - vol. 22(Issue 34) pp:
Publication Date(Web):
DOI:10.1039/C2JM33220E
Co-reporter:Heng Shen, Chunting Duan, Jing Guo, Ning Zhao and Jian Xu
Journal of Materials Chemistry A 2015 - vol. 3(Issue 32) pp:NaN16669-16669
Publication Date(Web):2015/07/09
DOI:10.1039/C5TA04188K
An environmentally friendly and facile approach was developed to synthesize boron nitride nanosheet/Ag nanoparticle hybrids (BNNS/Ag) in aqueous solution at room temperature without additional reductants. BNNSs were modified with a thin layer of tannic acid–ferric ion (TA–Fe) complex. Silver nanoparticles with a uniform diameter of approximately 7 nm were in situ formed on the surface of the modified BNNSs due to the strong reducibility of TA. The resultant nanohybrids showed excellent catalytic activity in reduction of 4-nitrophenol. BNNS/Au and BNNS/Pd nanohybrids can also be fabricated by this means, implying its extensive promise in catalytic, bio-medical and sensing fields.
Co-reporter:Dong Wang, Jing Guo, Huan Zhang, Beichen Cheng, Heng Shen, Ning Zhao and Jian Xu
Journal of Materials Chemistry A 2015 - vol. 3(Issue 24) pp:NaN12872-12872
Publication Date(Web):2015/05/11
DOI:10.1039/C5TA01915J
A strategy for combining covalent and non-covalent cross-links to construct multifunctional rubber materials with intelligent self-healing and shape memory ability is demonstrated. Rubbers were prepared by self-assembly of complementary polybutadiene oligomers bearing carboxylic acid and amine groups through reversible ionic hydrogen bonds via the acid–base reaction, and then further covalently cross-linked by tri-functional thiol via the thiol-ene reaction. The resulting polymers exhibit self-healing and shape memory functions owing to the reversible ionic hydrogen bonds. The covalent cross-linking density can be tuned to achieve tailorable mechanical and stimuli-responsive properties: a low covalent cross-linking density maintains the remarkable self-healing capability of rubber at ambient temperature without any external stimulus, while a high covalent cross-linking density improves the mechanical strength and induces shape memory behavior, but effective self-healing needs to be triggered at high temperature. This strategy might open a promising pathway to fabricate intelligent multifunctional polymers with versatile functions.
Co-reporter:Xiaoli Yang, Ning Zhao, Qingzhu Zhou, Chao Cai, Xiaoli Zhang and Jian Xu
Journal of Materials Chemistry A 2013 - vol. 1(Issue 20) pp:NaN3366-3366
Publication Date(Web):2013/03/26
DOI:10.1039/C3TC30324A
This paper describes a straightforward method to precisely prepare monodisperse ZrO2@SiO2 core–shell nanoparticles (CSNs) by sol–gel polymerization of TEOS in the presence of ZrO2 cores without additional capping agents. We studied the morphology and composition of CSNs by Scanning Electron Microscopy (SEM), Transmission Electron Microscopy (TEM) and X-ray Diffraction (XRD). It has been found that the citric acid groups adsorbed onto the ZrO2 surface during the preparation of ZrO2 as well as the slow hydrolysis and condensation of TEOS in isopropanol are crucial for the selective growth of silica on the surface of ZrO2 cores. The thickness of the silica shell can be facilely controlled from about 4 to 30 nm by varying the concentration of TEOS, with the refractive indices of the prepared CSNs tuned accordingly from about 1.2 to 1.9. The coated silica shell, which can be well dispersed in solvents such as methanol and ethanol, can improve the dispersibility of pure ZrO2 nanoparticles which can only be dispersed in water. Moreover, the formation of the silica shell improved the chemical reactivity of pure ZrO2 nanoparticles. After modifying with methyltriethoxysilane (MTES), the CSNs can be well dispersed in various organic solvents, such as dimethylbenzene, chloroform and isoamyl alcohol, which may find applications in optically transparent resins with controllable refractive index or organic silicon packaging materials with high refractive index for LED and so on. Additionally, other silane coupling agents can also be applied to modify the surface chemical properties of CSNs, which may provide more potential applications.
Co-reporter:Yi Hou, Zhen Wang, Jing Guo, Heng Shen, Huan Zhang, Ning Zhao, Yiping Zhao, Li Chen, Songmiao Liang, Yan Jin and Jian Xu
Journal of Materials Chemistry A 2015 - vol. 3(Issue 46) pp:NaN23260-23260
Publication Date(Web):2015/10/06
DOI:10.1039/C5TA05612H
Utilizing superhydrophobic porous materials in oil/water separation has attracted increasing research interest, however, most of these materials are usually complicated to fabricate or easily lose their functions in harsh circumstances. In this study, dispersion of poly[(3,3,3-trifluoropropyl)methylsiloxane] (PTFPMS) micro–nano aggregations in acetone/water was facially prepared via a simple phase separation method. The aggregations can be easily coated on the skeletons of various 2D and 3D porous substrates, endowing the porous materials with superhydrophobicity. The prepared superhydrophobic materials show excellent resistance to chemical erosion, mechanical abrasion, and high temperature (up to 400 °C). This robust superhydrophobicity promises application of the resultant porous materials in harsh environments, and examples of using these superhydrophobic porous materials to separate oil/water mixtures have been demonstrated. This simple and universal method is suitable for the large-scale preparation of porous materials with robust superhydrophobicity.
Co-reporter:Chao Cai, Xiaoli Yang, Zhen Wang, Haixia Dong, Hongwei Ma, Ning Zhao and Jian Xu
Journal of Materials Chemistry A 2015 - vol. 3(Issue 17) pp:NaN4259-4259
Publication Date(Web):2015/03/30
DOI:10.1039/C5TC00357A
This paper demonstrates a facile and effective improvement of abrasion resistance of silica nanoparticle (NP) based anti-reflective coatings via capillary condensation of 3-aminopropyl triethoxysilane (APTES). The quartz crystal microbalance (QCM) is used to test the abrasion resistance property. The versatility of this developed method is further illustrated by the successful application to the poor heat-resistant polymer substrates.
Co-reporter:Haosen Fan, Hao Wang, Ning Zhao, Xiaoli Zhang and Jian Xu
Journal of Materials Chemistry A 2012 - vol. 22(Issue 6) pp:NaN2780-2780
Publication Date(Web):2011/12/15
DOI:10.1039/C1JM14311E
A facile method was successfully developed for the preparation of a hierarchical nanocomposite of vertical polyaniline (PANI) nanorods aligned on the surface of functional multiwalled carbon nanotubes (FMWNTs) by in situ polymerization of PANI on the surface of FMWNTs. The formation mechanism was illustrated according to the morphological evolution of PANI-FMWNTs nanocomposite at different polymerization times. The hierarchical nanocomposite possessed higher special capacitance and better stability than each individual component as supercapacitor electrode materials due to the synergistic effect of both components, as well as to the special hierarchical structure, which not only increases the specific surface area of the nanocomposite but also facilitates the penetration of electrolyte ions. This research gives a better insight into the preparation of functional hybrid nanocomposites by combining different dimensional nanomaterials.