4.6 Article

Efficient hydrogen peroxide production enabled by exploring layered metal telluride as two electron oxygen reduction reaction electrocatalyst

期刊

JOURNAL OF ENERGY CHEMISTRY
卷 87, 期 -, 页码 247-255

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ELSEVIER
DOI: 10.1016/j.jechem.2023.08.027

关键词

Transition metal telluride; Oxygen reduction reaction; Charge polarization; Activity and selectivity; Hydrogen peroxide

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This study explores the use of layered nickel ditelluride as an electrocatalyst for the two-electron oxygen reduction reaction (2e- ORR), demonstrating high selectivity and activity in both alkaline and neutral media. In situ Raman spectra, theoretical calculations, and microstructural analysis reveal the underlying factors contributing to its excellent performance.
It is of great interest to develop the novel transition metal-based electrocatalysts with high selectivity and activity for two electron oxygen reduction reaction (2e- ORR). Herein, the nickel ditelluride (NiTe2) with layered structure was explored as the 2e- ORR electrocatalyst, which not only showed the highest 2e- selectivity more than 97%, but also delivered a slight activity decay after 5000 cycles in alkaline media. Moreover, when NiTe2 was assembled as the electrocatalyst in H-type electrolyzer, the on-site yield of H2O2 could reach up to 672 mmol h-1 g-1 under 0.45 V vs. RHE. Further in situ Raman spectra, theoretical calculation and post microstructural analysis synergistically unveiled that such a good 2e- ORR performance could be credited to the intrinsic layered crystal structure, the high compositional stability, as well as the electron modulation on the active site Ni atoms by neighboring Te atoms, leading to the exposure of active sites as well as the optimized adsorption free energy of Ni to -OOH. More inspiringly, such telluride electrocatalyst has also been demonstrated to exhibit high activity and selectivity towards 2e- ORR in neutral media.(c) 2023 Science Press and Dalian Institute of Chemical Physics, Chinese Academy of Sciences. Published by ELSEVIER B.V. and Science Press. All rights reserved.

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