CaiFeng Wang

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Name: 王彩凤
Organization: Nanjing University of Technology , China
Department: State Key Laboratory of Materials-Oriented Chemical Engineering and College of Chemistry and Chemical Engineering
Title: Associate Professor(PhD)
Co-reporter:Chao Yu;Cai-Feng Wang;Su Chen
Advanced Functional Materials 2014 Volume 24( Issue 9) pp:1235-1242
Publication Date(Web):
DOI:10.1002/adfm.201302058

Given the increasing environmental and energy issues, materials with the ability to repair themselves following damage are highly desirable because this self-healing property can prolong the lifespan of materials and reduce replacement costs. Host–guest assemblies are a powerful approach to create supramolecular materials with versatile functions. Here, a new mode of radical polymerization is demonstrated which is achieved via magnetocaloric effect to fabricate novel host–guest supramolecular gels within 5 min. The resulting gels can repair themselves spontaneously when damaged, without the assistance of any external stimuli, and possess great mechanical strength. Moreover, the Fe3O4-doped supramolecular gels show accelerated self-healing (from 24 h to 3 h) under an applied magnetic field, which is attributed to the synergy between host–guest healing and a magnetocaloric effect. This strategy might open a promising avenue for accelerating the use of host–guest assemblies to rapidly build robust materials.

Co-reporter:Liangliang Zhu;Fuchun Shen;Jing Zhang;Cai-Feng Wang
Colloid and Polymer Science 2013 Volume 291( Issue 9) pp:2147-2154
Publication Date(Web):2013 September
DOI:10.1007/s00396-013-2953-6
We report herein a facile approach of fabricating fluorescent supraballs from CdTe nanocrystals (NCs)-loaded acrylosilane microemulsion by a simple microfluidic strategy. Initially, core–shell acrylosilane microemulsion with poly(methylmethacrylate-co-butylacrylate-co-vinyltri(isopropoxy)silane) (poly (MMA-co-BA-co-VPS)) as the core and poly(methylmethacrylate-co-butylacrylate-co-vinyltri(isopropoxy)silane-co-acrylamide) (poly(MMA-co-BA-co-VPS-co-AM)) as the shell were synthesized by differential microemulsion polymerization. Subsequently, CdTe NCs were assembled with these acrylosilane microemulsion particles in the presence of N′-(ethylcarbonimidoyl)-N, N-dimethylpropane-1, 3-diaminemonohydrochloride. Eventually, we fabricated uniformly distributed fluorescent supraballs using the as-prepared CdTe-loaded acrylosilane microemulsion as the discontinuous phase, and methylsilicone oil as the continuous phase by means of a microfluidic device. These fluorescent supraballs display unique colors and favorable fluorescence, which might be useful in optoelectronic applications, such as fluorescent switches, light-emitting diode displays, and illuminations.
Co-reporter:Nian Liu;Huan Shao;Cai-Feng Wang;Qiao-Ling Chen;Su Chen
Colloid and Polymer Science 2013 Volume 291( Issue 8) pp:1871-1879
Publication Date(Web):2013 August
DOI:10.1007/s00396-013-2924-y
We report the rapid synthesis of hydrogels with interpenetrating polymer networks (IPNs) by frontal polymerization (FP). Appropriate amounts of diacetone acrylamide (DAAM), N-methylolacrylamide (NMA), thermoplastic polyurethane (TPU), N,N′-methylenebisacrylamide (MBAA), and ammonium persulfate (APS)/N,N,N′,N′-tetramethylethylenediamine (TMEDA) were mixed together at ambient temperature. FP was initiated by transitorily heating the upper side of the reactants, and poly(DAAM-co-NMA)/TPU IPN hydrogels were obtained within minutes. The preparation parameters were thoroughly investigated. Moreover, we investigated the morphology, swelling capacity, chemical structure and the mechanical properties of poly(DAAM-co-NMA)/TPU IPN hydrogels, along with those of poly(DAAM-co-NMA) hydrogels without IPN structure for comparison. Interestingly, the mechanical strength of poly(DAAM-co-NMA)/TPU IPN hydrogels is notably improved in comparison with that of poly(DAAM-co-NMA) hydrogels. The results indicate that the IPN structure endows hydrogels with high mechanical strength, and FP can be applied as an alternative means for synthesis of IPN hydrogels with additional advantages of speed and efficiency.
Co-reporter:He-Yi Xie, Jian Yang, Sheng-Yang Yang, Cai-Feng Wang, Li Chen, Su Chen
Materials Letters 2011 Volume 65(Issue 11) pp:1669-1671
Publication Date(Web):15 June 2011
DOI:10.1016/j.matlet.2011.03.001
We report herein the facile synthesis of CdTe/montmorillonite (MMT) nanocomposite films via charge–charge interactions between the CdTe quantum dots (QDs) and MMT platelets. Firstly, negatively charged CdTe QDs were prepared with the use of thioglycolic acid (TGA) as ligand. Then hybrid of the as-prepared TGA-stabilized CdTe QDs with sodium montmorillonite (Na-MMT) and cetyltrimethylammonium-modified montmorillonite (CTA-MMT), respectively, afforded novel CdTe/MMT nanocomposite films. The structure and optical properties of CdTe/MMT nanocomposite films were thoroughly investigated by scanning electron microscope (SEM), ultraviolet transmittance reflection and photoluminescence (PL) measurements. Results showed that CdTe/(CTA-MMT) nanocomposite films exhibited highly enhanced PL intensity compared with CdTe/(Na-MMT) nanocomposite films. More importantly, CdTe QDs in CdTe/(CTA-MMT) nanocomposite films well maintained PL properties even after thermal annealing at 100 °C for 10 h.
Dodecylcarbamodithioic Acid
CADMIUM CHLORIDE DIHYDRATE
CARBAMODITHIOIC ACID, OCTYL-
Carbamodithioic acid, phenyl-
Carbamodithioic acid, cyclohexyl-
Carbamodithioic acid, propyl-