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首页> 外文期刊>Journal of Materials Chemistry, A. Materials for energy and sustainability >Surface reorganization engineering of the N-doped MoS2 heterostructures MoOx@N-doped MoS2-x by in situ electrochemical oxidation activation for efficient oxygen evolution reaction Electronic supplementary information (ESI) available. See DOI: 10.1039/c9ta01049a
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Surface reorganization engineering of the N-doped MoS2 heterostructures MoOx@N-doped MoS2-x by in situ electrochemical oxidation activation for efficient oxygen evolution reaction Electronic supplementary information (ESI) available. See DOI: 10.1039/c9ta01049a

机译:通过原位电化学氧化活化进行高效电化学氧化活化的N掺杂MOS2异质结构MOOX @ N-掺杂MOS2-X的表面重组工程。 见DOI:10.1039 / C9TA01049A

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摘要

Extensive experiments have demonstrated that molybdenum disulfide- based catalysts have excellent performance in hydrogen evolution; on the other hand, only few studies have been reported on the application of molybdenum disulfide- based catalysts in the oxygen evolution reaction. Herein, we report that surface reorganization engineering of nitrogen- doped MoS2 by in situ electrochemical oxidation successfully results in its significantly enhanced OER activity. In this study, the construction of the unique heterostructure MoOx@ N- doped MoS2x was performed in situ by electrochemical oxidation; based on the theoretical and experimental results, the electronic characteristics of the catalyst surface were adjusted, whereas the intrinsic properties of N- doped MoS2 were maintained. Due to the moderate amount of MoOx formed on the surface of N- doped MoS2, an optimized performance was achieved: excellent electrocatalytic activity with the very low overpotential of 270 mV at 10 mA cm2, the small Tafel slope of 61 mV dec1, and satisfactory stability. Our study provides a viable method to achieve efficient electrocatalysts via non- metal element doping and in situ electrochemical oxidation tuning, which result in the formation of the unique heterostructure of MoOx@ N- doped MoS2x in situ. This new type of core- shell heterostructure opens up a novel avenue for the rational design of high- performance OER electrocatalysts.
机译:广泛的实验表明,钼基型催化剂在氢进化方面具有优异的性能;另一方面,据报道,在氧气进化反应中的氧化钼基催化剂的应用中仅报道了少数研究。在此,我们报告了通过原位电化学氧化通过原位电化学氧化的表面重组工程成功导致其显着增强的OER活动。在该研究中,通过电化学氧化原位进行独特的异质结构MOOX @ N-掺杂MOS2X的结构;基于理论和实验结果,调节催化剂表面的电子特性,而N-掺杂MOS2的固有性质被保持。由于在N-掺杂MOS2的表面上形成的温度的MOOX,实现了优化的性能:优异的电催化活性,具有270mV的10 mA CM2,小Tafel斜率为61mV12120mV的极低的电催化活性,并且令人满意稳定。我们的研究提供了一种可通过非金属元素掺杂和原位电化学氧化调整来实现高效电催化剂的可行方法,从而形成MOOX @ N-掺杂MOS2x的独特异质结构。这种新型的核心壳异质结构为高性能Oer电催化剂的合理设计开辟了一个新颖的途径。

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    Yanshan Univ Coll Environm &

    Chem Engn Key Lab Appl Chem Qinhuangdao 066004 Hebei Peoples R China;

    Yanshan Univ Coll Environm &

    Chem Engn Key Lab Appl Chem Qinhuangdao 066004 Hebei Peoples R China;

    Yanshan Univ Coll Environm &

    Chem Engn Key Lab Appl Chem Qinhuangdao 066004 Hebei Peoples R China;

    Yanshan Univ Coll Environm &

    Chem Engn Key Lab Appl Chem Qinhuangdao 066004 Hebei Peoples R China;

    Yanshan Univ Coll Environm &

    Chem Engn Key Lab Appl Chem Qinhuangdao 066004 Hebei Peoples R China;

    Yanshan Univ Coll Environm &

    Chem Engn Key Lab Appl Chem Qinhuangdao 066004 Hebei Peoples R China;

    Yanshan Univ Coll Environm &

    Chem Engn Key Lab Appl Chem Qinhuangdao 066004 Hebei Peoples R China;

    Yanshan Univ Coll Environm &

    Chem Engn Key Lab Appl Chem Qinhuangdao 066004 Hebei Peoples R China;

    Yanshan Univ Coll Environm &

    Chem Engn Key Lab Appl Chem Qinhuangdao 066004 Hebei Peoples R China;

    Yanshan Univ Coll Environm &

    Chem Engn Key Lab Appl Chem Qinhuangdao 066004 Hebei Peoples R China;

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  • 正文语种 eng
  • 中图分类 工程材料学;
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