过电位
催化作用
材料科学
双功能
功率密度
化学工程
钴
析氧
密度泛函理论
电极
耐久性
拉曼光谱
纳米技术
双功能催化剂
电流密度
氧还原反应
瞬态(计算机编程)
电压
开路电压
氧还原
动力学
无机化学
降级(电信)
氧气
锂离子电池的纳米结构
燃料电池
作者
Manami Banerjee,Peng Ren,Greesh Kumar,Lucie M. Lindenbeck,Byoung Joon Park,Anna Rokicińska,Piotr Kuśtrowski,Adam Slabon,Francesco Ciucci,Ramendra Sundar Dey,Shoubhik Das
标识
DOI:10.1002/adfm.202519329
摘要
Abstract The development of cost‐effective catalysts for zinc–air batteries (ZABs) remain challenging due to the sluggish kinetics of oxygen reduction (ORR) and evolution (OER) at the cathode. In this context, a novel N‐doped graphitic shell‐encapsulated cobalt catalyst is presented as an air electrode with exceptional bifunctional activity, achieving an ORR half‐wave potential ( E 1/2 ) of 0.81 V and an OER overpotential of 349 mV in an alkaline medium. The catalyst demonstrated excellent cycling durability and delivered superior power density in both liquid and solid‐state ZABs. Furthermore, a quasi‐solid‐state ZAB is assembled with the catalyst, and it maintained a stable open‐circuit voltage (OCV) of 1.360 V for >10 000 s. The catalyst achieved a peak power density of 127 mW cm −2 —significantly outperforming the benchmark Pt/C + RuO 2 system (74 mW cm −2 ). When two tandem‐junction ZABs are connected in series, they achieved an OCV of 2.75 V and powering a “ZAB” LED strip and a mini fan. Furthermore, Density Functional Theory (DFT) calculations revealed that the enhanced performance resulted from optimized binding energies between the Co@N(py) active sites and reaction intermediates. An in situ Raman study is carried out to understand the catalytic mechanism through transient intermediate detection.
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