过电位
析氧
催化作用
钴
格式化
钙钛矿(结构)
材料科学
甲醇
化学工程
化学
无机化学
氧气
物理化学
电化学
结晶学
电极
有机化学
工程类
作者
Haoqi Qiu,Bingen Yuan,Chuanxi Zhao,Jiaxin Dang,Chunfei Zhang,Qin Wang,Lan Xia,He Miao,Jinliang Yuan
标识
DOI:10.1016/j.ijhydene.2023.08.269
摘要
The cobalt (Co)-based perovskites as the promising oxygen evolution reaction (OER) catalysts have gained the significant attentions owing to their exceptional intrinsic catalytic activity. However, the major B-site element of Co in these perovskites is high cost and scarcity, which seriously limits their large-scale applications. In this work, we synthesize a high-entropy perovskite (HEP) with the low Co content and high OER catalytic activity. Also, the OER catalytic performances of the perovskites with the different B-site configurational entropies and compositions are systematically investigated. The optimized HEP with the composition of La0.7Sr0.3Co0.2Mn0.2Ni0.2Fe0.2Al0.2O3-x (L5) exhibits the outstanding OER activity with a low overpotential of 339 mV at 10 mA cm−2. Furthermore, no degradation of L5 is observed during long-term OER stability test for 100 h. Interestingly, L5 also shows the superior catalytic activity toward the methanol oxidation reaction (MOR). During the MOR catalytic process, a low overpotential of 219 mV can be achieved at 10 mA cm−2, and the value-added product of formate with the selectivity of ∼70% can be simultaneously obtained. The excellent OER and MOR performances of L5 can be related to the synergistic effects of the major B-site components and configuration entropy effect of HEPs. Our work proposes a promising high-entropy strategy to reduce the Co content in the Co-based perovskites as well as enhance their electrocatalytic activities.
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