In-situ engineered heterostructured nickel tellur-selenide nanosheets for robust overall water splitting

被引:49
作者
Wang, Jiajun [1 ]
Huang, Jun [2 ,3 ]
Chen, Guangliang [1 ]
Chen, Wei [2 ]
Li, Tongtong [1 ]
Meng, Aokai [2 ]
Ostrikov, Kostya [3 ]
机构
[1] Zhejiang Sci Tech Univ, Sch Mat Sci & Engn, Hangzhou 310018, Peoples R China
[2] Gannan Normal Univ, Sch Phys & Elect Informat, Ganzhou 341000, Jiangxi, Peoples R China
[3] Queensland Univ Technol QUT, Ctr Mat Sci, Ctr Clean Energy Technol & Pract, Ctr Waste free World, Brisbane, Qld 4000, Australia
基金
中国国家自然科学基金; 澳大利亚研究理事会;
关键词
Transition metal tellur-selenide; Electrocatalyst; In-situ engineering; Phase synergy; Overall water splitting; BIFUNCTIONAL ELECTROCATALYSTS; EFFICIENT; SURFACE; CONSTRUCTION; NANOWIRES; PHOSPHIDE;
D O I
10.1016/j.cej.2022.137297
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Due to the large Gibbs free energy of metal telluride for hydrogen generation, tellurium (Te) based materials are rarely reported as catalysts for overall water splitting. Herein, a facile hydrothermal method is used to engineer the stacked flower-like NiTe-NiSe nanosheets, thus nearing the application of transition metal telluride in clean and renewable energy field. Thanks to the hollow flower-shaped catalyst assembled with nanosheets, the active surface area of the optimized electrode material is 20 times larger than that of a single NiTe/NFF or NiSe/NFF, causing low overpotentials for delivering a current density of 10 mA cm-2 (j10) in the hydrogen (HER, 76 mV) and oxygen (OER, 164 mV) evolution processes. The OER activity of NiTe-NiSe/NFF exceeds that of benchmarked RuO2 even at moderate current densities above j115. Based on the results of experiments and DFT calculations, the unexpected high catalytic performance of NiTe-NiSe/NFF is attributed to the formed heterointerfaces and mismatched crystal lattice of NiTe, which effectively optimize the electronic structure through the phase synergy and cause a low adsorption free energy for the reactive intermediates.
引用
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页数:12
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