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ACS Applied Materials & Interfaces · 2016 · IF 7.145

Self-Assembly Fabrication of Coaxial Te@poly(3,4-ethylenedioxythiophene) Nanocables and Their Conversion to Pd@poly(3,4-ethylenedioxythiophene) Nanocables with a High Peroxidase-like Activity

Maoqiang Chi,Guangdi Nie,Yanzhou Jiang,Zezhou Yang,Zhen Zhang,Ce Wang,Xiaofeng Lu

Here, we report a simple one-step procedure to fabricate coaxial Te@poly(3,4-ethylenedioxythiophene) (PEDOT) nanocables via a self-assembly redox polymerization between 3,4-ethylenedioxythiophene monomer and the oxidant of sodium tellurite without the assistance of any templates and surfactants. The as-synthesized Te@PEDOT coaxial nanocables have diameters of center cores in the range of 5–10 nm, and the size of the outer shell from several nanometers to 15 nm. More interestingly, the as-prepared Te@PEDOT nanocables can be converted to Pd@PEDOT nanocables via a galvanic replacement reaction. The center core of the Pd nanowire exhibits a high crystallinity. The application of the synthesized Pd@PEDOT nanocables as peroxidase-like catalysts for the colorimetric detection of H2O2 is reported. The synergistic effect between the Pd nanowire and electrically conducting PEDOT enhances the catalytic activity toward the oxidation of the peroxidase substrate 3,3′,5,5′-tetramethylbenzidine in the presence of H2O2. A detection limit toward H2O2 is as low as 4.83 μM, and a linear range from 10 to 100 μM has been achieved. This work offers a potential versatile route for the fabrication of cable-like nanocomposites with conducting polymers and other active components, which display great promise in applications such as catalysis, nanoelectronic devices, and energy storage and conversion.

CAS / MDL: 13820-53-6
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CHEMICAL ENGINEERING JOURNAL · 2017 · IF 6.216

Ionic liquid-employed synthesis of Bi2E3 (E = S, Se, and Te) hierarchitectures: The case of Bi2S3 with superior visible-light-driven Cr(VI) photoreduction capacity

Runming Wang,Gang Cheng,Zan Dai,Jie Ding,Yunling Liu,Rong Chen

A general ionic-assisted microwave-ultrasonic combined synthetic strategy was developed to fabricate Bi 2 E 3 (E   =   S, Se, and Te) hierarchitectures. To understand the crystal phase transformation and morphological evolution of Bi 2 S 3 hierarchical nanostructures, the fabrication of Bi 2 S 3 hierarchitectures was investigated by varying sulfidation time and chlorination time. A topotactic transformation from BiOCl microsphere to Bi 2 S 3 hierarchitectures was proposed. It was found that the structure, size, and morphology of Bi 2 S 3 hierarchitectures could be delicately engineered by varying chlorination time, alkyl chain length, and concentration of ionic liquid. Moreover, the as-prepared Bi 2 S 3 hierarchitectures displayed superior capacity of Cr(VI) photoreduction to P25 and irregular Bi 2 S 3 nanostructures under visible light irradiation. Effects of morphology, pH value of reaction system, Cr(VI) concentration, and catalyst dosage on the Cr(VI) photoreduction capacity of Bi 2 S 3 hierarchitectures were also discussed. The enhancement of photoreduction capacity is not only attributed to the intrinsic good electron transfer ability of Bi 2 S 3 , but also to synergetic effects of special architectures, wide photoresponse range, high light photoadsorption, high BET surface area and good electron-hole separation performance. The systematic condition experiments and Cr(VI) photoreduction in electroplating and tannery wastewater experiments further demonstrated that the hierarchical Bi 2 S 3 nanospheres can be used in the actual Cr(VI)-containing wastewater treatment.

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Small · 2024 ·Vol. 20 ·期 48 ·2406179 · IF 13

Vacancy Manipulation by Ordered Mesoporous Induced Optimal Carrier Concentration and Low Lattice Thermal Conductivity in BixSb2−xTe3 Yielding Superior Thermoelectric Performance

Jiao Li,Wenlong Xu,Kangpeng Jin,Wanjia Zhang,Xiaoqing Lu,Guilong Pan,Tianyu Zhong,Xiyang Wang,Zhan Shi,Biao Xu,Yue Lou

For Bi x Sb 2− x Te 3 (BST) in thermoelectric field, the element ratio is easily influenced by the chemical environment, deviating from the stoichiometric ratio and giving rise to various intrinsic defects. In P-type polycrystalline BST, Sb Te and Bi Te are the primary forms of defects. Defect engineering is a crucial strategy for optimizing the electrical transport performance of Bi 2 Te 3 -based materials, but achieving synchronous improvement of thermal performance is challenging. In this study, mesoporous SiO 2 is utilized to successfully mitigate the adverse impacts of vacancy defects, resulting in an enhancement of the electrical transport performance and a pronounced reduction in thermal conductivity. Crystal and the microstructure of the continuous modulation contribute to the effective phonon–electronic decoupling. Ultimately, the peak zT of Bi 0.4 Sb 1.6 Te 3 /0.8 wt% SiO 2 (with a pore size of 4 nm) nanocomposites reaches as high as 1.5 at 348 K, and a thermoelectric conversion efficiency of 6.6% is achieved at Δ T = 222.7 K. These results present exciting possibilities for the realization of defect regulation in porous materials and hold reference significance for other material systems.

研究领域: 材料科学 · 热电学 · 纳米技术 · 固体物理学
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JOM · 2022 ·Vol. 75 ·期 5 ·1515-1529 · IF 2.597

Distribution Behaviors of As, Sb, Bi, Sn, Se, Te, Au and Ag Between Cu and Liquid Metal Phases in the Cu-Pb Binary System at 500–1080°C

Ge Yang,Liu Zhihong,Yu Zhiqian,Wang Huanwen,Lu Xingwu,Zhang Leru,Xia Longgong

The present study focused on the Cu-Pb system and investigating the distribution behaviors of various minor elements through the equilibration-quenching-EPMA analysis experimental technique. Obtained results showed that: (1) An intermetallic compound consisting mainly of Cu-Pb-Se-Te formed below 956°C. (2) As, Sb and Sn had similar distribution behaviors, which mainly entered the solid Cu phase at the temperature range of 500–900°C, but became concentrated in the liquid alloy phase at temperature range of 900–1060°C, and their distribution ratios increased along with increasing temperature. (3) Bi was mainly found in the liquid alloy phase, and its distribution ratio ranged from 6.8 to 836.5 at the experimental conditions. (4) Se and Te formed an intermetallic alloy phase under 900°C, and they enriched in the liquid alloy phase between 960°C and 1060°C. (5) Au was mainly found in the solid Cu phase at the temperature range of 500–900°C, and its distribution ratio was about 1.5 at 900–1060°C. The distribution ratio of Ag decreased from 8.7 to 2.3 when increasing the temperature from 500°C to 1060°C. Distribution behavior of As, Sb, Bi and Sn is consistent with their interfacial enthalpies with Cu and Pb.

CAS / MDL: 7440-50-8 7439-92-1
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