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源自钴基金属有机框架纳米片的三维多孔结构钴和氮掺杂碳纳米管电催化剂用于高性能锌空气电池

Three-dimensional porous structured cobalt- and nitrogen-doped carbon nanotube electrocatalyst derived from cobalt-based zeolitic imidazolate framework nanoleaves for high performance zinc-air battery.

作者信息

Zhu Qingying, Du Ziping, Zhang Lei, Zhang Qianling, Ren Xiangzhong, Li Yongliang

机构信息

College of Chemistry and Environmental Engineering, Shenzhen University, Shenzhen, Guangdong 518060, PR China.

College of Chemistry and Environmental Engineering, Shenzhen University, Shenzhen, Guangdong 518060, PR China; Guangdong Flexible Wearable Energy and Tools Engineering Technology Research Centre, Shenzhen University, Shenzhen 518060, PR China.

出版信息

J Colloid Interface Sci. 2024 Dec 15;676:1068-1078. doi: 10.1016/j.jcis.2024.07.143. Epub 2024 Jul 19.

Abstract

The development of efficient and cost-effective electrocatalysts to overcome the intrinsic sluggish kinetics of the oxygen reduction reaction (ORR) in zinc-air batteries is crucial. In this study, we introduce a strategy that integrates a template-assisted synthesis with subsequent thermal treatment to fabricate an active and stable cobalt-based nitrogen-doped carbon electrocatalyst, denoted as Co-N-CNT. The strategy adjusts the disordered architecture of the zeolitic imidazolate framework (ZIF) through the synergistic effect of bimetallic species, restricted the growth of zeolitic imidazolate framework nanoleaves (ZIF-L) using salt templates, and directed the transformation from a two-dimensional blade-like morphology to a three-dimensional multi-tiered composite structure. Notably, the Co-N-CNT-800 sample, synthesized at an optimized pyrolysis temperature of 800 °C, exhibits a half-wave potential of 0.89 V and demonstrates stability with sustained cycling over 21 h, which is comparable to the performance of commercial Pt/C electrocatalysts. Moreover, when employed as the cathode in zinc-air batteries, Co-N-CNT-800 not only surpasses Pt/C in terms of power density but also exhibits long-term charge/discharge stability. This findings offer a viable pathway for the design of active and cost-effective ORR electrocatalysts, holding promise for applications in the electrochemical energy storage and conversion systems.

摘要

开发高效且经济高效的电催化剂以克服锌空气电池中氧还原反应(ORR)固有的缓慢动力学至关重要。在本研究中,我们引入了一种将模板辅助合成与后续热处理相结合的策略,以制备一种活性和稳定的钴基氮掺杂碳电催化剂,记为Co-N-CNT。该策略通过双金属物种的协同作用调整沸石咪唑酯骨架(ZIF)的无序结构,使用盐模板限制沸石咪唑酯骨架纳米片(ZIF-L)的生长,并引导从二维叶片状形态转变为三维多层复合结构。值得注意的是,在800℃的优化热解温度下合成的Co-N-CNT-800样品表现出0.89V的半波电位,并在21小时以上的持续循环中表现出稳定性,这与商业Pt/C电催化剂的性能相当。此外,当用作锌空气电池的阴极时,Co-N-CNT-800不仅在功率密度方面超过Pt/C,而且还表现出长期的充放电稳定性。这些发现为设计活性和经济高效的ORR电催化剂提供了一条可行的途径,有望应用于电化学储能和转换系统。

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