催化作用
材料科学
介孔材料
碳纤维
掺杂剂
贵金属
化学工程
锐钛矿
X射线吸收光谱法
密度泛函理论
纳米技术
无机化学
吸收光谱法
化学
复合材料
兴奋剂
有机化学
光电子学
计算化学
工程类
物理
复合数
光催化
量子力学
作者
Kailong Hu,Xudong Wang,Yixuan Hu,Haolin Hu,Xiaorong Lin,Xiaorong Lin,Kolan Madhav Reddy,Min Luo,Hua‐Jun Qiu,Xi Lin,Xi Lin
出处
期刊:ACS Nano
[American Chemical Society]
日期:2022-11-10
卷期号:16 (11): 19165-19173
被引量:69
标识
DOI:10.1021/acsnano.2c08332
摘要
Mesoporous carbon supported non-noble metals, as promising catalysts for boosting the oxygen reduction reaction (ORR) in metal-air batteries, usually face challenges of low activity and performance degradation caused by the catalyst detachment from carbon substrates. Herein, a one-stone-two-birds strategy is reported to simultaneously improve the ORR activity and anchor nanosized MnS catalysts on a mesoporous carbon framework via nitrogen (N) and sulfur (S) dopants (MnS/NS-C). Synchrotron-based X-ray absorption spectroscopy (XAS) confirms the existence of Mn–N and Mn–S bonds, which firmly anchor active MnS nanoparticles. Density functional theory (DFT) calculations reveal that the N, S codoping lowers the d-band center of Mn and optimizes ORR intermediate adsorption. An excellent ORR performance (the onset and half-wave potential of 1.07 and 0.91 V) and long-term durability are achieved for MnS/NS-C in alkaline media. The flexible Al-air battery, using MnS/NS-C as the cathode catalyst, shows a power density of 134.6 mW cm–2 in comparison to the Pt/C-based counterpart of 106.2 mW cm–2. This study constructs a stable interaction with non-noble catalysts and carbon substrates for enhancing catalytic activity and durability in metal-air batteries.
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