催化作用
析氧
海水
电解
电催化剂
电解水
化学工程
化学
电子转移
分解水
多金属氧酸盐
材料科学
无机化学
电化学
电极
光化学
物理化学
光催化
海洋学
地质学
工程类
电解质
生物化学
作者
Suyang Feng,Peng Rao,Yanhui Yu,Jing Li,Peilin Deng,Zhenye Kang,Shaolei Wang,Zhengpei Miao,Yijun Shen,Xinlong Tian,Zhifu Wu
标识
DOI:10.1016/j.electacta.2023.142870
摘要
The exploration of efficient, stable, and inexpensive oxygen evolution reaction (OER) catalysts is of great importance for the practical application of seawater electrolysis. In this work, CoSe2@CoO/CF catalysts are prepared by a simple and scalable one-step electrodeposition method, and the OER performance of the catalysts is investigated in depth. The CoSe2@CoO/CF catalyst (273 mV) shows significantly better activity than the IrO2 catalyst (435 mV). The catalyst can be steadily operated at high current densities (100 mA cm−2) for over 200 h in the 1.0 M KOH + seawater. Notably, the catalyst exhibits excellent selectivity with a Faraday efficiency of approximately 98% for OER, while the ClO− concentration is only 1.312×10−7 mol L−1 as measured by UV-visible characterization. Strong overlap between the Co 2p orbitals of monometallic bi-compound catalysts facilitates the rate of para-site electron transfer. In addition, the impressive performance is attributed to the urchin-like heterogeneous structure with abundant active centers.
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