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RSC Advances · 2015 ·Vol. 5 ·期 91 ·74251-74255 · IF 3.84

Solvent-induced self-assembly synthesis of ultralong single crystalline organic NiOEP nanowires with high photoconductivity

Juan-Ye Wang,Hong-Dan Peng,Jia-Mei Yang,Jing-Hui Yan,Ge-Bo Pan

We develop a facile approach for the one-step growth of ultralong and high-quality NiOEP nanowires in a large area, through a solvent-induced self-assembly method without using any structure directing agents. The size of the nanowires can be controlled by changing the composites of solvent mixtures. Being assembled in visible-light sensors, these nanowires exhibit a fast, reversible, and stable response. The highest Ion/Ioff ratio and photoresponsivity of photodiodes could reach 681 and 10.1 mA W−1, respectively, which could be attributed to the perfect single crystal quality, large surface to volume ratio, and fewer recombination barriers within the nanostructures. The facile fabrication and good photoresponse make NiOEP nanowires promising in optoelectronic applications.

研究领域: 材料科学 · 纳米科技 · 光电子学 · 物理化学 · 功能材料
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INORGANIC CHEMISTRY COMMUNICATIONS · 2021 · IF 2.495

Self-assembly of MoS2 nanosheet on functionalized pomelo peel derived carbon and its electrochemical sensor behavior toward taxifolin

Xia Zhang,Qiumin Cao,Zhuohuan Guo,Meiyue Zhang,Meng Zhou,Zhenzhen Zhai,Yuandong Xu

MoS 2 nanosheet arrays grown on functional pomelo peel derived carbon (PPC) is constructed via in situ self-assembly method. The obtained MoS 2 /PPC composite is further used to fabricate electrochemical sensor for taxifolin detection. The current response of taxifolin on MoS 2 /PPC is significantly enhanced due to the synergistic effect between MoS 2 and PPC. It is found that the charge transfer impedance and the Ohmic resistance corresponding to MoS 2 /PPC are the lowest, indicating fast electron transfer rate and good conductivity. Further investigation reveals that the redox peak current is linearly related to the concentration of taxifolin in the range of 7 × 10 −8 –1 × 10 −5 mol·L −1 and the limit of detection is calculated to be 2.3 × 10 −8 mol·L −1 (S/N = 3). In addition, no obvious interfering phenomenonhas been observed in the detection process of taxifolin, demonstrating that MoS 2 /PPC presents good selectivity toward taxifolin determination.

研究领域: 材料科学 · 电化学 · 分析化学 · 纳米技术 · 生物传感器 · 环境监测
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CARBOHYDRATE POLYMERS · 2015 · IF 4.074

Antimicrobial and antioxidant surface modification of cellulose fibers using layer-by-layer deposition of chitosan and lignosulfonates

Hui Li,Lincai Peng

To confer cellulose fibers antimicrobial and antioxidant activities, chitosan (CS)/lignosulfonates (LS) multilayers were constructed on fibers surfaces through layer-by-layer deposition technique. The formation of CS/LS multilayers on cellulose fibers surfaces was verified by X-ray photoelectron spectroscopy (XPS) and zeta potential measurement. The surface morphologies of CS/LS multilayers on fibers surfaces were observed by atomic force microscopy (AFM). The results showed that characteristic element (i.e. N and S element) content increased with increasing bilayers number, the surface LS content increased linearly as a function of bilayers. Zeta potential of modified fibers was inversed after deposition of each layer. AFM phase images indicated that the cellulose microfibrils on fibers surfaces were gradually covered by granular LS aggregate. The antimicrobial testing results demonstrated that CS/LS multilayers modified fibers with CS in the outermost layer exhibited higher antimicrobial activity against Escherichia coli . The antioxidant testing results showed that antioxidant activity of CS/LS multilayers modified fibers was better than that of original fibers under the same oxidation conditions.

研究领域: 高分子材料 · 表面科学 · 生物医学工程 · 功能材料 · 纳米技术
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MACROMOLECULAR CHEMISTRY AND PHYSICS · 2012 ·Vol. 213 ·期 20 ·2192-2200 · IF 2.361

pH-Responsive Double-Hydrophilic Block Copolymers: Synthesis and Drug Delivery Application

Xiao-Hui Dai,Chun-Yan Hong,Cai-Yuan Pan

A novel double-hydrophilic block copolymer P(MEO 2 MA- co -OEGMA)- b -PAMA has been successfully synthesized by two-step RAFT polymerization. Then, the amino groups of PAMA blocks in the copolymers react with 1-pyrenecarboxaldehyde via a “Schiff-base” reaction, and the resulting copolymers are self-assembled to form spherical micelles in aqueous solution. Because the “Schiff-base” linkage is pH sensitive, the release rate of pyrene depends upon the pH of solution. Complete release is achieved at pH 1, and the control release is much faster at pH 5.5 than that at pH 7.4. With progress of pyrene release, the micelles are disassembled gradually and disappeared completely at last. This double-hydrophilic copolymer is a promising candidate of drug carrier for the aldehyde- containing hydrophobic drugs.

研究领域: 高分子化学 · 药剂学 · 纳米医学 · 生物材料 · 药物递送系统
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International Journal of Electrochemical Science · 2023 ·Vol. 13 ·期 2 ·1985-2000 · IF 1.5

Experimental and Theoretical Calculations on Corrosion Inhibition of Bronze in 0.5 M HCl by Some Schiff Bases

Zhe Zhang,Le Ruan,Weipeng Zhang,Yuzeng Lyu,Wei Shang,Yuqing Wen,Xiuying Li,Ling Wu,Yanni Jiao

The triazol-3-ylamine and three different kinds of Schiff base compounds are self-assembled on bronze surface. Electrochemical impedance spectroscopy and potentiodynamic polarization measurements show that the triazol-3-ylamine and Schiff base self-assembled films can protect bronze from corrosion in 0.5 M HCl solution. The corrosion efficiency increases with the self-assembly time increasing and reaches a stable value after 8 h. The highest corrosion efficiency of the bronze electrode modified with self-assembled films reaches 95.81% after immersing in 0.005 M 2,4-Dibromo-6-[(4H-[1,2,4]Triazol-3-ylimino)-methyl]-phenol Schiff base solution for 10 h. X-ray photoelectron spectroscopy and scanning electrochemical microscope are used to characterize the inhibitive ability of the self-assembled films. Quantum chemical calculations and dynamic simulations indicate that the triazol-3-ylamine and Schiff bases molecules can absorb on the copper surface via chemisorption. The adsorption energy increases with the number of aromatic rings.

研究领域: 材料腐蚀与防护 · 物理化学 · 表面科学 · 电化学 · 计算化学
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CHINESE JOURNAL OF CATALYSIS · 2019 ·Vol. 40 ·期 5 ·631-637 · IF 4.914

Ordered mesoporous Fe/TiO2 with light enhanced photo-Fenton activity

Zhenmin Xu,Ru Zheng,Yao Chen,Jian Zhu,Zhenfeng Bian

Ordered mesoporous Fe/TiO 2 was prepared by an evaporation-induced self-assembly method. The iron ions were in situ embedded in the pore wall of the TiO 2 framework. The catalyst has excellent light-assisted Fenton catalytic performance under UV and visible light irradiation. X-ray diffraction and transmission electron microscopy results showed that the TiO 2 samples have an ordered two-dimensional hexagonal pore structure and an anatase phase structure with high crystallinity . The ordered pore structure of the TiO 2 photocatalyst with a large specific surface area is beneficial to mass transfer and light harvesting. Furthermore, iron ions can be controlled by embedding them into the TiO 2 framework to prevent iron ion loss and inactivation. After five cycles, the reaction rate of the ordered mesoporous Fe/TiO 2 remained unchanged, indicating that the material has stable performance and broad application prospects for the purification of environmental pollutants .

研究领域: 材料科学 · 环境化学 · 催化化学 · 纳米科技 · 光化学
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COLLOIDS AND SURFACES A-PHYSICOCHEMICAL AND ENGINEERING ASPECTS · 2014 · IF 2.354

Controllable self-assembly of an amphiphilic drug with β-cyclodextrin and α-amylase

Shangyang Li,Pengyao Xing,Lin Zhang,Feifei Xin,Jinhui Nie,Hailu Wang,Mingfang Ma,Yurong Wu,Aiyou Hao

Herein, we report a novel responsive assembly system consisting of an amphiphilic drug fenspiride and β-cyclodextrin in host–guest approach. Fenspiride molecules can self-assembled into vesicles in aqueous solution. The obtained vesicles were characterized in detail by transmission electron microscopy (TEM), scanning electron microscopy (SEM) and atomic force microscopy (AFM). Furthermore, such a vesicular structure will be destroyed upon the addition of β-cyclodextrin due to the formation of inclusion complexes by host–guest interactions. In addition, amylase is a digestive enzyme which can catalyze the breakdown of starch into sugars. Adding α-amylase into the system could release fenspiride molecules, and trigger the self-assembly of fenspiride molecules again. It is anticipated that this research will provide widespread applications in the fields of responsive materials and biochemistry related to enzyme-responsive model system and host–guest chemistry.

研究领域: 药物化学 · 纳米医学 · 分子药剂学 · 生物材料 · 酶学 · 超分子化学
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MACROMOLECULAR CHEMISTRY AND PHYSICS · 2016 ·Vol. 217 ·期 9 ·1047-1056 · IF 2.495

Cross-Linked Nano-Objects Containing Aldehyde Groups: Synthesis via RAFT Dispersion Polymerization and Application

Liang Qiu,Chao-Ran Xu,Feng Zhong,Chun-Yan Hong,Cai-Yuan Pan

Pure cross-linked spherical micelles, nanowires, and vesicles are successfully fabricated from poly(2-hydroxypropyl methacrylate- b - p -(methacryloxyethoxy)benzaldehyde)s (PHPMA– b –PMAEBAs) through reversible addition-fragmentation chain transfer dispersion polymerization of MAEBA in methanol using PHPMA as a macro-CTA and subsequent cross-linking. The cross-linking reaction is conducted by stirring a mixture of 1,4-butanediamine and the resultant nano-objects in methanol at room temperature. For all polymerizations with feed molar ratios of MAEBA/PHPMA ranging from 75/1 to 240/1, the monomer MAEBA conversions are almost complete, and block copolymers with controlled molecular weight are obtained. The transmission electron microscopy, dynamic light scattering, and gel permeation chromatography results reveal that the following three factors significantly influence the morphology of the nano-objects: the feed molar ratio of MAEBA/PHPMA, the copolymer concentration, and the degree of polymerization of PHPMA. The cross-linked nano-objects are very stable in good solvents, the spheres and nanowires slightly decrease in size after cross-linking, whereas the vesicles slightly increase in size. The cross-linked nano-objects are stable in neutral solutions, but they dissociate in weekly acidic solutions. The loading of 1-pyrenemethylamine (PMA) into the vesicles and the unloading of PMA from the vesicles are studied.

研究领域: 高分子化学 · 纳米材料 · 药物递送 · 生物医学工程 · 胶体与界面科学
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Nanoscale · 2021 ·Vol. 13 ·期 23 ·10393-10401 · IF 7.79

Surfactant-mediated morphology evolution and self-assembly of cerium oxide nanocrystals for catalytic and supercapacitor applications

Xiaodong Hao,Shuai Zhang,Yang Xu,Liangyu Tang,Kazutoshi Inoue,Mitsuhiro Saito,Shufang Ma,Chunlin Chen,Bingshe Xu,Tadafumi Adschiri,Yuichi Ikuhara

Surfactant plays a remarkable role in determining the growth process (facet exposition) of colloidal nanocrystals (NCs) and the formation of self-assembled NC superstructures, the underlying mechanism of which, however, still requires elucidation. In this work, the mechanism of surfactant-mediated morphology evolution and self-assembly of CeO2 nanocrystals is elucidated by exploring the effect that surfactant modification has on the shape, size, exposed facets, and arrangement of the CeO2 NCs. It is directly proved that surfactant molecules determine the morphologies of the CeO2 NCs by preferentially bonding onto Ce-terminated {100} facets, changing from large truncated octahedra (mostly {111} and {100} exposed), to cubes (mostly {100} exposed) and small cuboctahedra (mostly {100} and {111} exposed) by increasing the amount of surfactant. The exposure degree of the {100} facets largely affects the concentration of Ce3+ in the CeO2 NCs, thus the cubic CeO2 NCs exhibit superior oxygen storage capacity and excellent supercapacitor performance due to a high fraction of exposed active {100} facets with great superstructure stability.

研究领域: 材料化学 · 纳米科学 · 催化化学 · 电化学 · 无机功能材料
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ELECTROCHIMICA ACTA · 2022 · IF 7.336

Facile preparation of electrodes of efficient electrolyte-supported solid oxide fuel cells using a direct assembly approach

Feihong Zhang,Qiaohang Weng,Yanxiang Zhang,Na Ai,San Ping Jiang,Chengzhi Guan,Yanqun Shao,Huihuang Fang,Yu Luo,Kongfa Chen

Solid oxide fuel cells (SOFCs) are the most efficient energy conversion technology to convert the chemical energy of fuels like hydrogen, natural gas, etc. to electricity. However, one of the limiting factors in the commercial viability of SOFCs technologies is the time-consuming and high-cost multiple cell fabrication processes. Here, we report the development of a facile procedure for the preparation of an electrolyte-supported cell with a Ni-Gd 0.1 Ce 0.9 O 1.95 composite anode and a La 0.6 Sr 0.4 Co 0.2 Fe 0.8 O 3-δ cathode, and the fabrication procedure of the electrodes decreases from four steps of screen-printing and sintering of conventional cell preparation processes to two steps of screen-printing using a direct assembly approach without the high-temperature sintering steps. The most important observation is the simultaneous formation of the electrode/electrolyte interfaces of both the anode and cathode by in situ passing a current through the directly assembled cells at 800 ℃. The power density of the directly assembled cell reaches 0.41 W cm −2 at a voltage of 0.7 V and 800 ℃, close to 0.46 W cm −2 of the sintered cell. The directly assembled cell shows comparable operational stability to the sintered cell at 800 ℃ for 100 h. This work sheds light on the facile fabrication of electrolyte-supported cells with substantially simplified preparation procedures and reduced costs.

研究领域: 材料科学 · 能源化学 · 电化学 · 燃料电池技术 · 无机功能材料
✓ 已验证 DOI 高影响因子
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APPLIED PHYSICS A-MATERIALS SCIENCE & PROCESSING · 2023 ·Vol. 129 ·期 10 ·682 · IF 2.7

MXene@CTAB@CMF three-dimensional elastic base for piezoresistive pressure sensors realized by electrostatic self-assembly

Yin Chunmei,Li Qinghua,Lu Zhiyi,Shi Yaochen,Lin Wei

A highly sensitive pressure-sensitive sensor based on MXene was developed using the electrostatic self-assembly method, with carbide sponges as the elastic substrate and a rational design. Specifically, CTAB was used to treat the carbide triamine sponge and conduct the electrostatic self-assembly with MXene to achieve a tightly combined conductive filler and substrate. The resulting pressure sensor showed excellent performance, with a high sensitivity of 15.05 kPa −1 under a range of 0–20 kPa, a response time of 0.1 s, and high durability under 2000 loading–unloading cycles. The minimum detection limit of the sensor was as low as 0.3 Pa, demonstrating excellent monitoring performance. Additionally, finite-element simulation analysis showed that MXene@CTAB@CMF had even better sensing performance at the same stress level. Moreover, the pressure sensor exhibited good sensing performance for various physiological signals and daily work monitoring of the human body, indicating its potential application value.

研究领域: 生物医学工程 · 纳米医学 · 柔性电子学 · 传感技术 · 材料科学
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Journal of Materials Chemistry A · 2012 ·Vol. 1 ·期 6 ·2278-2285 · IF 0

Assembling gold and platinum nanoparticles on resorcinarene modified graphene and their electrochemical applications

Jun Zhou,Ming Chen,Guowang Diao

An amphiphilic amino resorcinarene (T) was modified onto the surface of graphene oxide (GO) through covalent bond forces and non-covalent bond forces to prepare GO–T. The water-soluble graphene–T (GN–T) composite was prepared by the reduction of GO–T. Then, pre-prepared platinum nanoparticles (PtNPs) and different sized gold nanoparticles (AuNPs) could self-assemble onto the surface of GN–T through the plentiful amido groups of T to obtain GN–T–AuNPs and GN–T–PtNPs hybrid materials. It was verified that the AuNPs and PtNPs could be uniformly scattered on GN and the amount of AuNPs and PtNPs modified on GN could be adjusted by changing the weight ratio of T/GO. GN-T-PtNPs and GN-T-AuNPs composites showed the characteristics of being dispersible, stable and recyclable in water. Electrochemical results obviously revealed that GN–T–AuNPs and GN–T–PtNPs composites exhibited outstanding electrocatalytic properties.

研究领域: 纳米材料化学 · 电分析化学 · 功能复合材料 · 表面自组装 · 电催化
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