催化作用
电解质
化学工程
选择性
格式化
制氢
无机化学
氢
电化学
材料科学
氢燃料
碱金属
化学
电极
物理化学
有机化学
工程类
作者
Yao Hu,Yibo Wang,Yinan Zheng,Xin Yu,Junjie Ge,Yonghong Zhu,Xiaohui Guo
出处
期刊:Nano Research
[Springer Science+Business Media]
日期:2023-06-13
卷期号:16 (8): 10832-10839
被引量:38
标识
DOI:10.1007/s12274-023-5842-4
摘要
Glycerol oxidation reaction (GOR) coupled with hydrogen generation simultaneously is a promising strategy for developing sustainable energy conversion technologies, but the complexity of glycerol oxidation products and the high coupling hydrogen evolution potential limit its wide application. In this paper, a self-supported high-entropy selenide electrode can be fabricated via a simple hydrothermal process. Then, the prepared electrode as an advanced catalyst displays optimal catalytic activity (1.20 V at 10 mA·cm−2) and high selectivity for the formation of formate in GOR. The results show that the lattice distortion effect of high entropy materials composed of multiple elements is mainly responsible for the greatly improved catalytic activity and selectivity for GOR. Moreover, an advanced alkali-acid hybrid electrolytic cell was assembled that enables efficient energy-saving hydrogen generation and GOR simultaneously. Herein, the electrolyzer requires only 0.5 V applied voltage to reach 10 mA·cm−2 for hydrogen generation and maintains long-term operation stability.
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