High-entropy selenides: A new platform for highly selective oxidation of glycerol to formate and energy-saving hydrogen evolution in alkali-acid hybrid electrolytic cell

被引:16
|
作者
Yao, Hu [1 ]
Wang, Yibo [2 ]
Zheng, Yinan [1 ]
Yu, Xin [1 ]
Ge, Junjie [2 ]
Zhu, Yonghong [3 ]
Guo, Xiaohui [1 ]
机构
[1] Northwest Univ, Coll Chem & Mat Sci, Key Lab Synthet & Nat Funct Mol Chem, Minist Educ, Xian 710069, Peoples R China
[2] Changchun Inst Appl Chem, Changchun 130022, Peoples R China
[3] Northwest Univ, Sch Chem Engn, Xian, Peoples R China
关键词
high-entropy selenides; lattice distortion; glycerol oxidation reaction (GOR); formate; activity; LATTICE DISTORTION; FORMIC-ACID; ELECTROOXIDATION; CATALYST;
D O I
10.1007/s12274-023-5842-4
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
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 center dot 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 center dot cm(- 2) for hydrogen generation and maintains long-term operation stability.
引用
收藏
页码:10832 / 10839
页数:8
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