CoS2 nanowires supported graphdiyne for highly efficient hydrogen evolution reaction
Autor: | Min Liu, Kang Liu, Wangjing Xie, Zixiong Fan, Mingjian Yuan, Xiaojie Chen, Guodong Shi, Mei Wang, Xinliang Fu |
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Rok vydání: | 2021 |
Předmět: |
Tafel equation
Materials science Nanocomposite Nanowire Energy Engineering and Power Technology Heterojunction 02 engineering and technology Overpotential 010402 general chemistry 021001 nanoscience & nanotechnology 01 natural sciences 0104 chemical sciences Catalysis Electron transfer Fuel Technology Transition metal Chemical engineering Electrochemistry 0210 nano-technology Energy (miscellaneous) |
Zdroj: | Journal of Energy Chemistry. 60:272-278 |
ISSN: | 2095-4956 |
DOI: | 10.1016/j.jechem.2021.01.005 |
Popis: | Transition metal sulfides are an important category for hydrogen evolution reaction (HER). However, only few edge unsaturated sulfurs functionalize as catalytic sites, which has dramatically limited the catalytic activity and stability. In this work, planar unsaturated sulfurs in (211) plane of the CoS2 nanowires have been successfully activated through constructing Graphdiyne-CoS2 heterojunction nanocomposites. The corresponding electrons transfer energy barriers for these planar unsaturated sulfurs have been significantly diminished, which are induced by the synergetic effects of the sp1 hybridized carbons and unsaturated planar sulfurs. In addition, DFT simulations reveal the synergetic effects of the sp1 hybridized carbons and unsaturated planar sulfurs can promote electron transfer kinetics of the key step, Volmer-Heyrovsky step, of the reaction. As expected, the Graphdiyne-CoS2 heterojunction nanocomposites exhibit superior HER catalytic performance with low overpotential of 97 mV at 10 mA cm−2, and the Tafel slope of 56 mV dec−1. Furthermore, the heterojunction shows outstanding stability as well due to the protection of the Graphdiyne (GDY). The approach thus paves the way for the further efficient transition metal disulfides catalyst manufactures. |
Databáze: | OpenAIRE |
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