Defect-stabilized and oxygen-coordinated iron single-atom sites facilitate hydrogen peroxide electrosynthesis
Taotao GaoLu QiuMinghao XieZhaoyu JinPanpan LiGuihua Yu
Abstract
Oxygen-coordinated iron single-atom sites (Fe–O 4 ) modified with vacancy defects show high 2e − -ORR catalytic performance. The Fe–O 4 moiety is relevant to the selectivity and kinetic rate of the 2e − pathway while vacancy defects enhance the stability.
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