Tang Wenhao, Teng Kewei, Guo Wengai, Gu Fan, Li Boya, Qi Ruiyu, Liu Ruiping, Lin Yuyin, Wu Miaomiao, Chen Yihuang
School of Chemical & Environmental Engineering, China University of Mining and Technology (Beijing), Beijing, 100083, P. R. China.
Department of Materials Science and Engineering, China University of Mining and Technology (Beijing), Beijing, 100083, P. R. China.
Small. 2022 Jul;18(27):e2202194. doi: 10.1002/smll.202202194. Epub 2022 Jun 3.
The ability to craft high-efficiency and non-precious bifunctional oxygen catalysts opens an enticing avenue for the real-world implementation of metal-air batteries (MABs). Herein, Co O encapsulated within nitrogen defect-rich g-C N (denoted Co O @ND-CN) as a bifunctional oxygen catalyst for MABs is prepared by graphitizing the zeolitic imidazolate framework (ZIF)-67@ND-CN. Co O @ND-CN possesses superb bifunctional catalytic performance, which facilitates the construction of high-performance MABs. Concretely, the rechargeable zinc-air battery based on Co O @ND-CN shows a superior round-trip efficiency of ≈60% with long-term durability (over 340 cycles), exceeding the battery with the state-of-the-art noble metals. The corresponding lithium-oxygen battery using Co O @ND-CN exhibits an excellent maximum discharge/charge capacity (9838.8/9657.6 mAh g ), an impressive discharge/charge overpotential (1.14 V/0.18 V), and outstanding cycling stability. Such compelling electrocatalytic processes and device performances of Co O @ND-CN originate from concurrent compositional (i.e., defect-engineering) and structural (i.e., wrinkled morphology with abundant porosity) elaboration as well as the well-defined synergy between Co O and ND-CN, which produce an advantageous surface electronic environment corroborated by theoretical modeling. By extension, a rich diversity of other metal oxides@ND-CN with adjustable defects, architecture, and enhanced activities may be rationally designed and crafted for both scientific research on catalytic properties and technological development in renewable energy conversion and storage systems.
制备高效且非贵金属的双功能氧催化剂的能力为金属空气电池(MABs)的实际应用开辟了一条诱人的途径。在此,通过对沸石咪唑酯骨架(ZIF)-67@ND-CN进行石墨化制备了封装在富含氮缺陷的g-CN中的CoO(表示为CoO@ND-CN)作为MABs的双功能氧催化剂。CoO@ND-CN具有卓越的双功能催化性能,这有助于构建高性能的MABs。具体而言,基于CoO@ND-CN的可充电锌空气电池显示出约60%的卓越往返效率以及长期耐久性(超过340次循环),超过了使用最先进贵金属的电池。使用CoO@ND-CN的相应锂氧电池表现出优异的最大放电/充电容量(9838.8/9657.6 mAh g)、令人印象深刻的放电/充电过电位(1.14 V/0.18 V)以及出色的循环稳定性。CoO@ND-CN如此引人注目的电催化过程和器件性能源于同时进行的成分(即缺陷工程)和结构(即具有丰富孔隙率的皱纹形态)优化以及CoO与ND-CN之间明确的协同作用,理论建模证实这产生了有利的表面电子环境。通过扩展,可以合理设计和制备出具有可调缺陷、结构和增强活性的多种其他金属氧化物@ND-CN,用于催化性能的科学研究以及可再生能源转换和存储系统的技术开发。