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具有 Ni-Bis(dithiolene) 和 Co-porphyrin 单元的共价有机框架作为 Li-O 电池的双功能催化剂。

Covalent organic frameworks with Ni-Bis(dithiolene) and Co-porphyrin units as bifunctional catalysts for Li-O batteries.

机构信息

State Key Laboratory of Coordination Chemistry, Key Laboratory of Mesoscopic Chemistry of MOE, School of Chemistry and Chemical Engineering, Nanjing University, Nanjing 210023, P. R. China.

Center of Energy Storage Materials & Technology, College of Engineering and Applied Sciences, Jiangsu Key Laboratory of Artificial Functional Materials, National Laboratory of Solid State Microstructures, and Collaborative Innovation Center of Advanced Microstructures, Nanjing University, Nanjing 210023, P. R. China.

出版信息

Sci Adv. 2023 Feb 3;9(5):eadf2398. doi: 10.1126/sciadv.adf2398. Epub 2023 Feb 1.

Abstract

The rational design of efficient and stable catalysts for the oxygen reduction reaction and oxygen evolution reaction (ORR/OER) is the key to improving Li-O battery performance. Here, we report the construction of ORR/OER bifunctional cathode catalysts in a covalent organic framework (COF) platform by simultaneously incorporating Ni-bis(dithiolene) and Co-porphyrin units. The resulting bimetallic Ni/Co-COF exhibits high surface area, fairly good electrical conductivity, and excellent chemical stability. Li-O batteries with the Ni/Co-COF-based cathode show a low discharge/charge potential gap (1.0 V) and stable cycling (200 cycles) at a current density of 500 mA g, rivaling that of PtAu nanocrystals. Density functional theory computations and control experiments using nonmetal or single metal-based isostructural COFs reveal the critical role of Ni and Co sites in reducing the discharge/charge overpotentials and regulating the LiO deposition. This work highlights the advantage of bimetallic COFs in the rational design of efficient and stable Li-O batteries.

摘要

高效稳定的氧还原反应和氧析出反应(ORR/OER)催化剂的合理设计是提高锂电池性能的关键。在此,我们通过同时引入镍双(二硫烯)和钴卟啉单元,在共价有机框架(COF)平台上构建了 ORR/OER 双功能阴极催化剂。所得到的双金属 Ni/Co-COF 具有高比表面积、相当好的导电性和优异的化学稳定性。以 Ni/Co-COF 为基础的阴极的锂-氧电池在 500 mA g 的电流密度下具有低放电/充电电位间隙(1.0 V)和稳定的循环(200 次循环),可与 PtAu 纳米晶体相媲美。使用非金属或单金属基等结构 COF 的密度泛函理论计算和控制实验揭示了 Ni 和 Co 位点在降低放电/充电过电位和调节 LiO 沉积方面的关键作用。这项工作突出了双金属 COF 在合理设计高效稳定的锂-氧电池方面的优势。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c70e/9891699/99fe61b193cc/sciadv.adf2398-f1.jpg

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