催化作用
电催化剂
材料科学
氧化物
化学工程
无机化学
氧气
氧还原反应
磁滞
活化能
动力学
析氧
储能
氮气
氧化还原
开路电压
功率密度
电极
电流密度
化学
比表面积
燃料电池
作者
Seon Kyu Kim,Ramasamy Santhosh Kumar,Dilmurod Sayfiddinov,DONG JIN YOO
出处
期刊:Chemcatchem
[Wiley]
日期:2026-02-01
卷期号:18 (4)
被引量:2
标识
DOI:10.1002/cctc.202501872
摘要
ABSTRACT In recent years, zinc‐air batteries (ZABs) have attracted growing interest due to their low cost, high safety, eco‐friendliness, and high theoretical energy density. However, the slow kinetics of the oxygen reduction reaction (ORR) frequently limit the performance of ZABs. In this study, a carbon‐encircling trimetal catalyst was synthesized to obtain Pd@CrMnO/C. Characterization results show that the Pd@CrMnO/C catalyst exhibited a sheet‐like morphology, with more well‐defined crystalline domains on the surface. Nitrogen adsorption–desorption measurements reveal that Pd@CrMnO/C exhibits the H4‐type hysteresis loop with surface area of 7.06 m 2 /g and an average pore size of 9.0 nm. The prepared Pd@CrMnO/C catalyst exhibits a half‐wave potential of 0.74 V for ORR, indicating an exceptional ORR catalytic activity, because of its extremely stable structure and large number of active sites. Compared to CrMnO/C and MnO/C, the ZAB with Pd@CrMnO/C exhibits a higher power density of 210.7 mW/cm 2 and an open‐circuit voltage of 1.46 V. Furthermore, after 400 cycles (>65 h), the Pd@CrMnO/C‐based ZAB exhibits a small drop in efficiency (0.5%), indicating greater long‐term stability. These findings suggest that Pd@CrMnO/C is a promising catalyst for energy storage technologies.
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