Eco-designed electrocatalysts for water splitting: A path toward carbon neutrality

被引:34
作者
Chen, Zhijie [1 ]
Wei, Wei [1 ]
Chen, Hong [2 ]
Ni, Bing-Jie [1 ]
机构
[1] Univ Technol Sydney, Ctr Technol Water & Wastewater, Sch Civil & Environm Engn, Ultimo, NSW 2007, Australia
[2] Southern Univ Sci & Technol, Sch Environm Sci & Engn, State Environm Protect Key Lab Integrated Surface, Shenzhen Key Lab Interfacial Sci & Engn Mat SKLISE, Shenzhen 518055, Peoples R China
基金
中国国家自然科学基金; 澳大利亚研究理事会;
关键词
Eco-designed catalysts; Waste -derived catalysts; Mineral electrocatalysts; Hydrogen evolution reaction; Oxygen evolution reaction; Hydrogen energy; HYDROGEN EVOLUTION REACTION; LITHIUM-ION BATTERIES; OXYGEN EVOLUTION; STAINLESS-STEEL; POROUS CARBON; HIGHLY EFFICIENT; DOPED CARBON; CATALYST; WASTE; BIOMASS;
D O I
10.1016/j.ijhydene.2022.03.046
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
Realizing sustainable hydrogen fuel production through water electrolysis is crucial to achieving carbon neutrality. However, the development of cost-effective electrocatalysts continues to be a challenge. Eco-designed electrocatalysts derived from wastes and naturally abundant materials have recently received increasing attention. The development of eco-designed electrocatalysts is of great environmental and economic significance and makes green hydrogen more accessible to the wider community. Here, recent advances in eco-designed electrocatalysts for water splitting are summarized. Eco-design strategies such as pyrolysis, ball milling, wet-chemical methods, and electrochemical treatment are first analyzed. Recent achievements in eco-designed electrocatalysts for hydrogen evolution reaction (HER), oxygen evolution reaction (OER), and overall water splitting (OWS) are then detailed, with an emphasis on analyzing the eco-design strategy-catalyst propertycatalytic performance correlation. Perspectives in this blooming field for a greener hydrogen economy are finally outlined.& COPY; 2022 Hydrogen Energy Publications LLC. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:6288 / 6307
页数:20
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