Boric Acid‐Assisted Pyrolysis for High‐Loading Single‐Atom Catalysts to Boost Oxygen Reduction Reaction in Zn‐Air Batteries

硼酸 热解 催化作用 碳化 碳纤维 氧气 化学工程 氧化钴 材料科学 化学 无机化学 纳米技术 冶金 有机化学 工程类 复合材料 复合数 扫描电子显微镜
作者
Chenxi Xu,Jiexing Wu,Liang Chen,Yi Gong,Boyang Mao,Jincan Zhang,Jinhai Deng,Mingxuan Mao,Yan Shi,Zhaohui Hou,Mengxue Cao,Huanxin Li,Haihui Zhou,Zhongyuan Huang,Yafei Kuang
出处
期刊:Energy & environmental materials [Wiley]
被引量:16
标识
DOI:10.1002/eem2.12569
摘要

The emerging of single‐atom catalysts (SACs) offers a great opportunity for the development of advanced energy storage and conversion devices due to their excellent activity and durability, but the actual mass production of high‐loading SACs is still challenging. Herein, a facile and green boron acid (H 3 BO 3 )‐assisted pyrolysis strategy is put forward to synthesize SACs by only using chitosan, cobalt salt and H 3 BO 3 as precursor, and the effect of H 3 BO 3 is deeply investigated. The results show that molten boron oxide derived from H 3 BO 3 as ideal high‐temperature carbonization media and blocking media play important role in the synthesis process. As a result, the acquired Co/N/B tri‐doped porous carbon framework (Co–N–B–C) not only presents hierarchical porous structure, large specific surface area and abundant carbon edges but also possesses high‐loading single Co atom (4.2 wt. %), thus giving rise to outstanding oxygen catalytic performance. When employed as a catalyst for air cathode in Zn‐air batteries, the resultant Co–N–B–C catalyst shows remarkable power density and long‐term stability. Clearly, our work gains deep insight into the role of H 3 BO 3 and provides a new avenue to synthesis of high‐performance SACs.
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