A high-entropy and low-cobalt perovskite of La0.7Sr0.3Co0.2Mn0.2Ni0.2Fe0.2Al0.2O3-x for both oxygen evolution and methanol oxidation reactions

过电位 析氧 催化作用 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
出处
期刊:International Journal of Hydrogen Energy [Elsevier]
卷期号:51: 593-604 被引量:5
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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