析氧
电催化剂
分解水
钴
电化学
无定形固体
贵金属
催化作用
材料科学
化学
氢
无机化学
化学工程
电极
物理化学
结晶学
有机化学
生物化学
光催化
工程类
作者
Yue Shi,Shuanglong Zhou,Jiaxin Liu,Xin Zhang,Jiao Yin,Tianrong Zhan,Yu Yang,Guangjiu Li,Jianping Lai,Lei Wang
标识
DOI:10.1016/j.apcatb.2023.123326
摘要
Developing integrated non-noble metal electrocatalysts with mass activity comparable to noble metal is a significant challenge for overall water splitting. Herein, we constructed an integrated amorphous cobalt phosphoselenide (a-CoPSe) electrode via amorphization and dual anion-mediated strategy, achieving a significant improvement in the electrochemical active surface area (ECSA) and turnover frequency (TOF). The a-CoPSe offers large ECSA (65.9 m2 g−1) and high TOF values of 35.7 s−1 for hydrogen evolution reaction (HER) and 31.9 s−1 for oxygen evolution reaction (OER) at 300 mV. The mass activities of a-CoPSe are 890.4 A g−1Co for HER at 300 mV and 677.4 A g−1Co for OER at 250 mV, which are comparable to commercial Pt/C (10014.6 A g−1) and RuO2 (232.6 A g−1). Theoretical calculation reveals amorphous cobalt with balanced charges regulated by phosphorus and selenium atoms simultaneously facilitate H2O* , H* , OH* and OOH* adsorption, which greatly promotes the HER and OER kinetics.
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