钴
析氧
催化作用
电催化剂
电池(电)
硫代酰胺
化学
电积
耐久性
化学工程
材料科学
无机化学
电化学
电极
有机化学
电解质
复合材料
功率(物理)
物理
物理化学
量子力学
工程类
作者
S. Venkatesan,P. Ganesan
出处
期刊:Chemsuschem
[Wiley]
日期:2025-05-09
卷期号:18 (15): e202500739-e202500739
标识
DOI:10.1002/cssc.202500739
摘要
The critical process of fuel cells, metal‐air batteries, and electrolyzers are the oxygen evolution reaction (OER) and oxygen reduction reaction (ORR), which inherently have slow kinetics demand an electrocatalyst to enhance reaction rates, performance, and durability. Nonetheless, most nonprecious catalysts undergo heat treatment, involve multiple stages, and struggle with maintaining their active sites. Herein, the active sites is intended to maintain and the synthesis costs is lowered by eliminating the need for heat treatment, leading to the polymerization of cobalt thioamide linkages for a more efficient and durable cobalt thioamide polymer synthesized through a polycondensation. This coordination polymer catalyst is supported on Ketjen Black and exhibited superior OER ( E j10 = 1.57 V) and ORR ( E 1/2 = 0.71 V) performances. The potential efficiency during long‐term durability of this polymer is examined by performing continuous OER operation for 260 h and exhibiting only 5.1% performance decay. For ORR durability, only 39 mV is required after 30 000 cycles in accelerated durability tests compared with the initial cycle. This study highlights the potential of cobalt‐coordinated polymer on Ketjen Black as high‐performing and durable alternatives to benchmark catalysts for OER and ORR.
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