电化学
联轴节(管道)
材料科学
分解水
表面光电压
光电子学
纳米技术
化学
电极
物理
冶金
物理化学
生物化学
催化作用
光催化
量子力学
光谱学
作者
Huachuan Sun,Jue Yang,Jiangang Li,Zhishan Li,Xiang Ao,Yi Liu,Yi Zhang,Yi Li,Chundong Wang,Jiang Tang
标识
DOI:10.1016/j.apcatb.2020.118988
摘要
Abstract For hydrogen generation with water splitting, the sluggish reaction kinetics, the scarcity and costliness of the precious-metal catalysts make their practical applications being a big challenge. Herein, heterogeneous catalysts of NiTe@RuO2 and NiTe@NiFe-LDH are constructed by coupling ruthenium oxide (RuO2) and nickel-iron layered double hydroxide (NiFe-LDH) on T-shaped NiTe. The as-made NiTe@RuO2 and NiTe@NiFe-LDH catalysts exhibit outstanding hydrogen evolution reaction (HER) and oxygen evolution reaction (OER) activity, respectively. Theoretical calculation and experimental measurement show that the electron transfer at the interface favors the H* adsorption during HER process. We construct full electrochemical cells for overall water splitting using NiTe@RuO2 as the cathode and NiTe@NiFe-LDH as the anode, which delivers a current density of 200 mA cm−2 under a voltage of 1.63 V. When powdered by a solar cell with a voltage of 1.5 V, the full-cell worked well for continuous hydrogen/oxygen generation, showing its potential for sustainable green energy generation.
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