双功能
电催化剂
催化作用
析氧
甲醇
电池(电)
材料科学
化学
金属
色散(光学)
无机化学
化学工程
纳米技术
电极
物理化学
有机化学
冶金
电化学
功率(物理)
工程类
物理
量子力学
光学
作者
Zhonghuan Zhu,Bo Yu,Weiwei Sun,Shuangqiang Chen,Yong Wang,Xiaopeng Li,Li‐Ping Lv
标识
DOI:10.1016/j.jpowsour.2022.231583
摘要
Owing to their adjustable local structure and coordination environment, Fe single-metal site electrocatalysts become superior alternatives to the precious metal-based systems for oxygen reduction reactions (ORR) and oxygen evolution reactions (OER). However, they often suffer from complicated preparation methods. The optimized conditions hide in a narrow window and require a large amount of screening work. Moreover, the porous support may collapse during high temperature, resulting in dead volume and low atomic usage efficiency. Herein we report a facile build-up of atomically dispersed Fe single metal site (Fe–N–C) derived from Fe-doped thermalized covalent triazine frameworks (TTF) towards bifunctional ORR/OER catalysts. The TTF-derived carbon provides a platform for the formation and uniform dispersion of single-atom Fe–N catalytic centers. A high electrocatalytic behavior towards ORR (E1/2 = 0.891 V) and OER (Ej = 10 = 1.543 V) in alkaline medium is achieved with excellent stability and anti-methanol poisoning activity. Impressively, its metal mass activity is 62 times higher than commercial 20 wt% Pt/C. The Zn-air battery (ZAB) based on the catalyst achieves a high capacity of 783.2 mAh g−1, a low voltage gap of 0.55 V and an outstanding rechargeability of 1650 cycles (∼550 h), placing it as one of the best-performing ZABs.
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