Oxygen Vacancies Riched PrOx Polycrystalline Nanorods on Graphene Nanosheets as Advanced Oxygen Catalysts for Lithium‐Oxygen Batteries

Author:

Zhan Xingyi1,Zhang Yifan1,Su Liwei12ORCID,Zhang Lei1,Tong Zijin1,Wu Hao1,Wang Lianbang12,Wang Yuanhao3,Wang Xiaoxiang4ORCID

Affiliation:

1. State Key Laboratory Breeding Base of Green Chemistry-Synthesis Technology College of Chemical Engineering Zhejiang University of Technology Hangzhou 310014 P. R. China

2. Key Laboratory of the Ministry of Education for Advanced Catalysis Materials Zhejiang Normal University Jinhua 321004 China

3. Hoffmann Institute of Advanced Materials Shenzhen Polytechnic Shenzhen 518055 P. R. China

4. Anteotech Queensland 4113 Australia

Abstract

AbstractThe slow reaction kinetics of Li−O is currently the most pressing technical obstacle to the development of lithium‐oxygen batteries. The Li2O2′s growth/decomposition pathways dominate the battery performance and can be optimized by exploring efficient cathode catalysts. Herein, we prepare regular, polycrystalline, oxygen vacancy (VO)‐riched PrOx uniformly anchored on few‐layered graphene (FLG) nanosheets to boost the Li−O reactions. XRD, TGA, XPS, SEM, TEM, SEAD, and electrochemical test techniques are used to study their chemical composition, microstructure, battery performance, and the effect of FLG on the formation of polycrystalline and VO. It is confirmed that FLG provides a large specific surface area and good electron transport. Moreover, it works as an anchoring substrate to transform PrOx from single crystal to polycrystalline, which is beneficial for exposing catalytic sites and VO and improving the battery performance. This unique composition and structure offer efficient active sites, accelerate electron transport, and regulate the Li2O2′s nucleation to form nanofilms or nanosheets on the catalyst. With this cathode catalyst, the battery achieved an ultralow total overpotential of 0.618 V, with a discharge capacity of 11489 mAh g−1 in the ultimate‐capacity mode and a superior cyclability of 85 cycles under the limited capacity of 500 mAh g−1.

Funder

National Natural Science Foundation of China

Natural Science Foundation of Zhejiang Province

Zhejiang Normal University

Publisher

Wiley

Subject

Electrochemistry,Electrical and Electronic Engineering,Energy Engineering and Power Technology

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