Ding Kuixing, Ye Yu, Hu Jiugang, Zhao Liming, Jin Wei, Luo Jia, Cai Shan, Weng Baicheng, Zou Guoqiang, Hou Hongshuai, Ji Xiaobo
College of Chemistry and Chemical Engineering, Central South University, Changsha, 410083, People's Republic of China.
College of Standardization, China Jiliang University, Hangzhou, 310018, People's Republic of China.
Nanomicro Lett. 2023 Jan 3;15(1):28. doi: 10.1007/s40820-022-00994-3.
Efficient bifunctional catalysts for oxygen reduction reaction (ORR) and oxygen evolution reaction (OER) are vital for rechargeable Zn-air batteries (ZABs). Herein, an oxygen-respirable sponge-like Co@C-O-Cs catalyst with oxygen-rich active sites was designed and constructed for both ORR and OER by a facile carbon dot-assisted strategy. The aerophilic triphase interface of Co@C-O-Cs cathode efficiently boosts oxygen diffusion and transfer. The theoretical calculations and experimental studies revealed that the Co-C-COC active sites can redistribute the local charge density and lower the reaction energy barrier. The Co@C-O-Cs catalyst displays superior bifunctional catalytic activities with a half-wave potential of 0.82 V for ORR and an ultralow overpotential of 294 mV at 10 mA cm for OER. Moreover, it can drive the liquid ZABs with high peak power density (106.4 mW cm), specific capacity (720.7 mAh g), outstanding long-term cycle stability (over 750 cycles at 10 mA cm), and exhibits excellent feasibility in flexible all-solid-state ZABs. These findings provide new insights into the rational design of efficient bifunctional oxygen catalysts in rechargeable metal-air batteries.
用于氧还原反应(ORR)和析氧反应(OER)的高效双功能催化剂对于可充电锌空气电池(ZABs)至关重要。在此,通过一种简便的碳点辅助策略,设计并构建了一种具有富氧活性位点的可吸氧海绵状Co@C-O-Cs催化剂用于ORR和OER。Co@C-O-Cs阴极的亲气三相界面有效地促进了氧的扩散和转移。理论计算和实验研究表明,Co-C-COC活性位点可以重新分布局部电荷密度并降低反应能垒。Co@C-O-Cs催化剂表现出优异的双功能催化活性,ORR的半波电位为0.82 V,OER在10 mA cm时的过电位超低,为294 mV。此外,它可以驱动液体ZABs,具有高峰值功率密度(106.4 mW cm)、比容量(720.7 mAh g)、出色的长期循环稳定性(在10 mA cm下超过750次循环),并且在柔性全固态ZABs中表现出优异的可行性。这些发现为可充电金属空气电池中高效双功能氧催化剂的合理设计提供了新的见解。