增强氧气减少的 p 块抗原子位点的轴向工程
Yanmin Hu1,2, Shuwen Niu1,3, Zedong Zhang4
1Key Laboratory of Carbon Materials of Zhejiang Province, College of Chemistry and Materials Engineering, Wenzhou University, Wenzhou, Zhejiang 325035, China.
Journal of the American Chemical Society
|June 9, 2025
概括
主组金属在氧降解反应 (ORR) 中通常是惰性的. 这项研究引入了SbN4-Cl催化剂,证明了高ORR效率和耐久性,优于传统的催化剂,并显示出Zn-空气电池的前景.
科学领域:
- 电化学
- 材料科学
- 催化剂
背景情况:
- 关闭d外的主要组金属通常被认为是氧降解反应 (ORR) 的催化无效.
- 优化金属站点的协调环境对于开发活性ORR电催化剂至关重要.
研究的目的:
- 为ORR设计和合成高效和耐用的电催化剂.
- 研究原子分散的 (Sb) 位点的催化机制.
主要方法:
- 在化碳 (NC) 上合成具有SbN4-Cl配置的原子分散的Sb位点催化剂.
- 密度函数理论 (DFT) 计算以阐明电子结构和反应机制.
- 电化学描述ORR活动和耐用性.
- 在气电池中进行测试.
主要成果:
- SbN4Cl/NC催化剂具有优异的ORR活性,半波电位 (E1/2) 为0.921V.
- 轴性Cl连接体调节Sb活性中心的电子结构,降低ORR能量屏障.
- 与3D过渡金属单原子催化剂和商业Pt/C相比,这些催化剂具有更高的耐用性.
- 在Zn空气电池应用中观察到出色的放电性能和长期耐用性.
结论:
- 原子分散的SbN4-Cl催化剂对ORR非常有效.
- 通过Cl联体进行电子调制是增强催化活性的关键.
- 这些催化剂对储能和转换装置,特别是气电池具有很大的潜力.
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