Double spatial confinement on ruthenium nanoparticles inside carbon frameworks as durable catalysts for a quasi‐solid‐state Li–O2 battery
Meiling Wang,
Ying Yao,
Feiyang Yang,
Zhenwu Tang,
Jingjie Ren,
Cunzhong Zhang,
Feng Wu,
Xiangke Wang
Affiliations
Meiling Wang
Beijing Key Laboratory of Environmental Science and Engineering, School of Materials Science & Engineering Beijing Institute of Technology Beijing China
Ying Yao
Beijing Key Laboratory of Environmental Science and Engineering, School of Materials Science & Engineering Beijing Institute of Technology Beijing China
Feiyang Yang
Beijing Key Laboratory of Environmental Science and Engineering, School of Materials Science & Engineering Beijing Institute of Technology Beijing China
Zhenwu Tang
College of Life and Environmental Sciences Minzu University of China Beijing China
Jingjie Ren
Beijing Key Laboratory of Environmental Science and Engineering, School of Materials Science & Engineering Beijing Institute of Technology Beijing China
Cunzhong Zhang
Beijing Key Laboratory of Environmental Science and Engineering, School of Materials Science & Engineering Beijing Institute of Technology Beijing China
Feng Wu
Beijing Key Laboratory of Environmental Science and Engineering, School of Materials Science & Engineering Beijing Institute of Technology Beijing China
Xiangke Wang
College of Environmental Science and Engineering North China Electric Power University Beijing China
Abstract The rational design of large‐area exposure, nonagglomeration, and long‐range dispersion of metal nanoparticles (NPs) in the catalysts is critical for the development of energy storage and conversion systems. Little attention has been focused on modulating and developing catalyst interface contact engineering between a carbon substrate and dispersed metal. Here, a highly dispersed ultrafine ruthenium (Ru) NP strategy by double spatial confinement is proposed, that is, incorporating directed growth of metal–organic framework crystals into a bacterial cellulose templating substrate to integrate their respective merits as an excellent electrocatalytic cathode catalyst for a quasi‐solid‐state Li–O2 battery. The porous carbon matrix with highly dispersed ultrafine Ru NPs is well designed and used as cathode catalysts in a Li–O2 battery, demonstrating a high discharge areal capacity of 6.82 mAh cm–2 at 0.02 mA cm–2, a high‐rate capability of 4.93 mAh cm–2 at 0.2 mA cm–2, and stable discharge/charge cycling for up to 500 cycles (2000 h) with low overpotentials of ~1.4 V. This fundamental understanding of the structure–performance relationship demonstrates a new and promising approach to optimize highly efficient cathode catalysts for solid‐state Li–O2 batteries.
