Bai Yang

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Name: 杨柏; Yang, Bai
Organization: Jilin University , China
Department: College of Chemistry
Title: (PhD)

TOPICS

Co-reporter:Jie Wu, Hao Zhang, Junhu Zhang, Tongjie Yao, Haizhu Sun, Bai Yang
Colloids and Surfaces A: Physicochemical and Engineering Aspects 2009 Volume 348(1–3) pp:240-247
Publication Date(Web):20 September 2009
DOI:10.1016/j.colsurfa.2009.07.031
In this study, the formation mechanism of the self-assembly structures of aqueous gold nanoparticles (NPs) was investigated through deliberately altering the species of ligands, solvent ratios, and especially solvent evaporation conditions. By analyzing UV–vis spectra, transmission electron microscope (TEM) images, and scanning electron microscope (SEM) images, it was found that the self-assembly process was dependent on both the equilibrium of various interparticle interactions in solution and the evaporation rate of solvents. The various interparticle interactions in solution generated an anisotropic interaction for one-dimension (1D) self-assembly, whereas the evaporation rate of solvents determined the specific of 1D derivative structures. Our results demonstrated an efficient protocol for spatial arrays of charged NPs with controllable morphologies.
Co-reporter:X. Gao;X. Yao;X. Yan;L. Xu;K. Zhang;J. Zhang;B. Yang;L. Jiang
Advanced Materials 2007 Volume 19(Issue 17) pp:2213-2217
Publication Date(Web):2 AUG 2007
DOI:10.1002/adma.200601946

The antifogging properties of mosquito compound eyes (see figure) result from their elaborate superhydrophobic surface structure, which consists of hexagonally non-close-packed nipples at the nanoscale and hexagonally close-packed hemispheres at the microscale. A soft-lithography approach is adopted to fabricate artificial compound eyes for exploring the effects of the hierarchical micro- and nanostructure on surface hydrophobicity.

Co-reporter:Xin Chen, Zhen-Tao Yu, Jie-Sheng Chen, Bai Yang
Materials Letters 2004 Volume 58(3–4) pp:384-386
Publication Date(Web):January 2004
DOI:10.1016/S0167-577X(03)00506-8
Employing the hydrothermal technique, CdS/polymer composite particles were prepared with the surfactant-free cadmium-containing polymer latexes synthesized via a surfactant-free emulsion copolymerization. The CdS/polymer composite particles have been characterized by FTIR spectroscopy, X-ray powder diffraction (XRD) and transmission electron microscopy (TEM).
Co-reporter:X. Chen;Z. Chen;N. Fu;G. Lu;B. Yang
Advanced Materials 2003 Volume 15(Issue 17) pp:
Publication Date(Web):1 SEP 2003
DOI:10.1002/adma.200305318
Co-reporter:H. Zhang;Z. Cui;Y. Wang;K. Zhang;X. Ji;C. Lü;B. Yang;M. Gao
Advanced Materials 2003 Volume 15(Issue 10) pp:
Publication Date(Web):16 MAY 2003
DOI:10.1002/adma.200304521
Co-reporter:Dongmei Wang, Junhu Zhang, Quan Lin, Lianshe Fu, Hongjie Zhang and Bai Yang  
Journal of Materials Chemistry A 2003 vol. 13(Issue 9) pp:2279-2284
Publication Date(Web):24 Jul 2003
DOI:10.1039/B305024F
Novel composite resins possessing good luminescent properties have been synthesized through a free radical copolymerization of styrene, α-methylacrylic acid and the binary or ternary complexes of lanthanide ions (Eu3+ and Tb3+). These polymer-based composite resins not only possess good transparency and mechanical performance but also exhibit an intense narrow band emission of lanthanide complexes under UV excitation. We characterized the molecular structure, physical and mechanical performance, and luminescent properties of the composite resins. Spectra investigations indicate that α-methyl-acrylic acid act as both solubilizer and ligand. Photoluminescence measurements indicate that the lanthanide complexes show superior emission lines and higher intensities in the resin matrix than in the corresponding pure complex powders, which can be attributed to the restriction of molecular motion of complexes by the polymer chain networks and the exclusion of water molecules from the complex. We also found that the luminescence intensity decreased with increasing content of α-methylacrylic acid in the copolymer system. The lifetime of the lanthanide complexes also lengthened when they were incorporated in the polymer matrix. In addition, we found that the relationships between emission intensity and Tb (Eu) content exhibit some extent of concentration quenching.
Co-reporter:Changli Lü, Zhanchen Cui, Yao Wang, Zuo Li, Cheng Guan, Bai Yang and Jiacong Shen  
Journal of Materials Chemistry A 2003 vol. 13(Issue 9) pp:2189-2195
Publication Date(Web):04 Aug 2003
DOI:10.1039/B304154A
Novel ZnS–poly(urethane-methacrylate macromer) (PUMM) nanocomposite films with high refractive index were prepared by incorporating thiophenol (PhSH)–4-thiomethyl styrene (TMSt)-capped ZnS nanoparticles into a urethane-methacrylate macromer (UMM), followed by spin-coating and ultraviolet radiation initiated free radical polymerization. PhSH–TMSt-capped colloidal ZnS solution was synthesized by reacting zinc acetate with H2S in N,N-dimethylformamide. UMM macromer was synthesized by reacting 2-hydroxyethyl methacrylate (HEMA) with isocyanate group terminated polythiourethane oligomer which was obtained from polyaddition of 2,2′-dimercaptoethyl sulfide (MES) with 2,4-tolylene diisocyanate (TDI). Thiol-capped ZnS nanoparticles were characterized and found to be 2.0–5.0 nm in diameter with a cubic phase structure. The chemical composition of these ZnS nanoparticles was determined to be Zn2+ ∶ S2− ∶ RS− = 1 ∶ 0.6 ∶ 0.6 using chemical analysis methods. The weight fraction of ZnS nanoparticles in the films was measured by TGA, and it accords well with that of theoretical calculation. FTIR and DSC studies show that ZnS nanoparticles were successfully immobilized into the polymer matrix and the resulting nanocomposite films have a good thermal stability. TEM images indicate that the ZnS nanoparticles were uniformly dispersed in the polymer matrix and the particles remained their original size (2–5 nm) before incorporation into the polymer matrix. The XPS depth profiling technique demonstrates that the ZnS nanoparticles were also dispersed homogeneously in the depth scales of the polymer matrix. The nanocomposite films show high optical transparency in the visible region (T > 95% at 550 nm) and high refractive index in the range of 1.645–1.796 at 632.8 nm as the content of thiol-capped ZnS nanoparticles linearly increased from 0 to 86 wt%.
Co-reporter:Hao Zhang, Zhen Zhou, Kun Liu, Ruibing Wang and Bai Yang  
Journal of Materials Chemistry A 2003 vol. 13(Issue 6) pp:1356-1361
Publication Date(Web):14 Apr 2003
DOI:10.1039/B212571D
We report the controlled deposition of carbazole-containing copolymers and fluorescent CdTe nanocrystals in layer-by-layer (LbL) assembled films. In this strategy, poly(acrylic acid) (PAA) acts as an important medium to enhance the interaction between nonionic copolymers and aqueous CdTe nanocrystals. PAA has a strong coordinative interaction with CdTe nanocrystals in the acidic pH range via interaction between the carboxyl in PAA and the cadmium on the surface of CdTe. Meanwhile, the strong H-bonding interaction between PAA and pyridine groups in copolymers makes it possible to fabricate deposited film. As characterized by optical spectroscopy, IR spectroscopy and TEM, our results show that CdTe nanocrystals can be embedded into carbazole-containing copolymers using a LbL assembly technique. Moreover, the photoluminescence of the resultant films can be tuned by using copolymers with different ratios of pyridine/carbazole and CdTe solutions with different PAA concentrations. Our method provides a useful approach for the assembly of aqueous semiconductor nanocrystals and nonionic polymers with an accurately controlled layer component.
Co-reporter:Changli Lü, Zhanchen Cui, Zuo Li, Bai Yang and Jiacong Shen  
Journal of Materials Chemistry A 2003 vol. 13(Issue 3) pp:526-530
Publication Date(Web):04 Feb 2003
DOI:10.1039/B208850A
High refractive index optical thin films of nano-ZnS/polythiourethane (PTU) composites have been prepared via immobilization of thiophenol (PhSH)/mercaptoethanol (ME)-capped ZnS nanoparticles into a PTU matrix. PhSH/ME-capped ZnS particles with a diameter of 2–6 nm were synthesized by reacting zinc acetate with H2S in N,N-dimethylformamide. The nanocomposite films with high refractive index were prepared by adding an isocyanate group terminated PTU oligomer, which was synthesized by polyaddition of 2,2′-dimercaptoethylsulfide (MES) and isophorone diisocyanate (IPDI), to a DMF solution containing colloidal ZnS particles, and followed by spin-coating and multi-step heat curing. FTIR studies show that the ZnS nanoparticles were successfully immobilized into the polymer matrix. TGA results indicates that the nanocomposite films have a good thermal stability and the weight fraction of ZnS particles in the films is well in accordance with that of theoretical calculations. TEM studies suggest that the ZnS nanoparticles with a diameter of 2–6 nm were well dispersed in the PTU matrix and maintained their original size before immobilization. The refractive index of the transparent ZnS/PTU nanocomposite films was in the range from 1.574 to 1.848 at 632.8 nm, which linearly increased with the content of PhSH/ME-capped ZnS from 0 to 97 wt%.
Co-reporter:Junhu Zhang, Litao Bai, Kai Zhang, Zhanchen Cui, Gang Zhang and Bai Yang  
Journal of Materials Chemistry A 2003 vol. 13(Issue 3) pp:514-517
Publication Date(Web):22 Jan 2003
DOI:10.1039/B211497F
A novel method for the assembly of metal nanoparticles is reported, in which polymer microspheres have been employed as both stabilizers and transport vehicles. We prepared sulfonated polystyrene microspheres and then introduced silver ions into the microspheres by ion exchange. Dispersal of the polymer microspheres in DMF led to the silver ions in them being reduced by the solvent; the resulting Ag nanoparticles were stabilized by the polymer network. In aqueous solution, the polymer microspheres are negatively charged and, by using layer-by-layer method, the prepared Ag nanoparticles can be self-assembled into films using the microspheres as transport vehicles.
Co-reporter:Gang Zhang, Yi Yu, Xin Chen, Yu Han, Yan Di, Bai Yang, Fengshou Xiao, Jiacong Shen
Journal of Colloid and Interface Science 2003 Volume 263(Issue 2) pp:467-472
Publication Date(Web):15 July 2003
DOI:10.1016/S0021-9797(03)00340-0
Nanosized hollow silica spheres with holes in the wall (denoted as silica nanobottles) have been successfully prepared by assembly of functional polymer nanospheres with tetraethoxysilane (TEOS) through hydrothermal methods, coupled with removal of the core by programmed calcination. The functional polymer nanospheres were obtained by emulsifier-free emulsion copolymerization of styrene and (ar-vinylbenzyl) trimethylammoium chloride. The silica nanobottle sample was characterized by thermogravimetric analysis (TG), differential thermal analysis (DTA), transmission electron microscopy (TEM), and nitrogen adsorption techniques. The above characterizations confirm that the silica nanobottles have holes of about 8 nm in the wall and this unique structural feature might be useful for their encapsulation. Furthermore, characterization by scanning electron microscopy (SEM), energy dispersive X-ray analysis (EDX), and UV–visible absorption (UV–vis) showed that the luminescent material Eu(TTA)3(TPPO)2 could be effectively encapsulated in silica nanobottles. This reveals that silica nanobottles have potential applications for nanotechniques.
Co-reporter:Kai Zhang;Xin Chen;Haitao Chen;Zhimin Chen;Zhanchen Cui
Macromolecular Materials and Engineering 2003 Volume 288(Issue 4) pp:380-385
Publication Date(Web):8 APR 2003
DOI:10.1002/mame.200390031

We describe a flexible method for preparing monodisperse silica-polystyrene core-shell microspheres. In this method, silica nanoparticles grafted with 3-(trimethoxysilyl)propyl methacrylate (MPS) were employed as seeds in an emulsion polymerization. The thickness of the shells could be changed through varying the amount of the monomer. The monodispersity and diameters of the core-shell microspheres were found to depend on the size of the grafted silica nanoparticles and the concentration of emulsifier. In addition, we investigated the formation mechanism of the core-shell microspheres.

Co-reporter:Changli Lü;Jingqi Guan;Cheng Guan;Zhanchen Cui;Jiacong Shen
Macromolecular Materials and Engineering 2003 Volume 288(Issue 9) pp:717-723
Publication Date(Web):22 AUG 2003
DOI:10.1002/mame.200300067

Hybrid optical films of TiO2-triethoxysilane-capped polythiourethane (TCPTU) with high refractive indices have been prepared via an in situ sol-gel method. The high refractive index triethoxysilane-capped polythiourethane (TCPTU) was synthesized by polyaddition of the triethoxysilane-modified trimercaptothioethylamine (TMTEA) and 2,2′-dimercaptoethylsulfide (MES) with 2,4-tolylene diisocyanate (TDI). The titania content in the hybrid films can be adjusted from 0 to 80 wt.-% by the feed ratio of titania precursor [Ti(OBu)4] to polymer (TCPTU). Both FTIR and DSC analyses indicate that there is chemical bonding between the titania domain and the polymer chain. TGA results suggest that the titania of high content was successfully incorporated into polymer matrices and this series of hybrid films have good thermal properties. AFM measurements indicate that in the hybrid films the titania domains are of nanosize scale and the domain size averagely decreases from 60–80 nm to 5–20 nm with increasing content of titania, and the variation of surface roughness for the hybrid films has the same trend. These may be relative to the content of TCPTU and the interaction between titania and polymer (TCPTU). The refractive indices of the hybrid films at 632.8 nm increased from 1 632 to 1 879 as the titania content varied from 0 to 80 wt.-%.

Co-reporter:Changli Lü;Zhanchen Cui;Yongxia Wang;Jiacong Shen
Journal of Applied Polymer Science 2003 Volume 89(Issue 9) pp:2426-2430
Publication Date(Web):12 JUN 2003
DOI:10.1002/app.12459

A series of novel high refractive index episulfide-type optical resins were prepared by ring-opening copolymerization of bis(β-epithiopropylthioethyl) sulfide (BEPTES) with episulfide derivative of diglydicyl ether of bisphenol A (ESDGEBA) and 2,4-tolylene diisocyanate (TDI), respectively, in the presence of triethylamine as a curing catalyst. The episulfide monomers, BEPTES and ESDGEBA, were synthesized from their corresponding epoxy compounds, respectively. The cured transparent resins exhibit high refractive index (nd > 1.63) and relatively low dispersion. The refractive index (nd) and Abbe's number (νd) of the BEPTES/ESDGEBA curing system increased linearly with the weight content of BEPTES monomer in the range from 1.633 and 34.0 for the copolymer with 10 wt % of BEPTES to 1.697 and 38.1 for the homopolymer of pure BEPTES. For the BEPTES/TDI curing system, the refractive index and Abbe's number varied linearly with the molar ratio of BEPTES to TDI from 1.652 and 28.7 to 1.669 and 34.6. High glass-transition temperatures (Tg > 130°C) of the cured BEPTES/TDI resins were observed, which indicate that the cured BEPTES/TDI resins possess a good heat resistance. The optical, physical, and thermal properties of the episulfide-type cured optical resins were also discussed in this study. © 2003 Wiley Periodicals, Inc. J Appl Polym Sci 89: 2426–2430, 2003

Co-reporter:Hao Zhang, Ruibing Wang, Gang Zhang, Bai Yang
Thin Solid Films 2003 Volume 429(1–2) pp:167-173
Publication Date(Web):1 April 2003
DOI:10.1016/S0040-6090(03)00059-2
Poly(methacrylic acid) (PMAA)-capped Fe3O4 nanoparticles were prepared by coprecipitation with PMAA in aqueous solution. Fe3O4 nanoparticles were further assembled with 2-nitro-N-methyl-4-diazonium-formaldehyde resin (NDR) to form a photosensitive precursor film, by virtue of the coulombic attraction between the negatively charged PMAA surface capping agent and the cationic polyelectrolyte of NDR. Covalent bonds were formed under ultraviolet irradiation. As a result of polymer capping of the nanoparticles and covalent linkage, a highly stable multilayer structure was formed. Transmission electron micrographs and selected area electron diffraction pattern revealed the Fe3O4 nanoparticles to be approximately 8 nm in diameter with a cubic phase structure. X-Ray photoelectron spectroscopy provided evidence for the presence of Fe3O4 nanoparticles and NDR within the ultrathin films. The UV-visible spectroscopy and atomic force microscopy measurements supported the improvement of the stability of the film, which became impervious to polar solvents when the linkages between the nanoparticles and polymer changed from ionic bonds to covalent bonds.
Co-reporter:Hao Zhang, Bai Yang
Thin Solid Films 2002 Volume 418(Issue 2) pp:169-174
Publication Date(Web):15 October 2002
DOI:10.1016/S0040-6090(02)00763-0
3-Mercaptopropionic acid-stabilized CdTe nanoparticles were prepared and assembled layer-by-layer with poly(diallyldimethylammonium chloride) (PDAC) to form a polymer-supported ultrathin film by virtue of the Coulombic interaction between negatively charged CdTe and positively charged PDAC. The composition of the CdTe nanoparticle multilayer films was analyzed by X-ray photoelectron spectroscopy (XPS) combined with optical absorbance and luminescence measurements. It was experimentally observed that Cd–thiol complexes on the surface of the CdTe nanoparticles provide the crucial chemical passivation responsible for the high photoluminescence (PL) efficiency of the CdTe particles. The high PL efficiency and high stability of CdTe particles corresponded to the particles with the high surface coverage with Cd–thiol complexes. Moreover, XPS data indicated the surface coverage with Cd–thiol complexes could be increased around the CdTe particle by either reflux or adjusting the pH of resulted CdTe colloidal suspension, which was consistent with the results from optical absorbance and luminescence spectra. It appeared that the popular method of constructing multilayer films could be used as a tool to characterize the surface composition of nanometer-sized particles.
1-(4-(4-Bromobutoxy)phenyl)-2-phenyldiazene
4-(4-(Phenyldiazenyl)phenoxy)butane-1-thiol
Diazene, 1-[4-[(6-bromohexyl)oxy]phenyl]-2-phenyl-