摘要
Insertion host materials are considered as a candidate to replace metallic Zn anode. However, the high mass loading anode with good electrochemical performances is reported rarely. Herein, a few-atomic-layered Co-doped BiOBr nanosheet (Co-UTBiOBr) is prepared via one-step hydrothermal method and a free-standing flexible electrode consisting of Co-UTBiOBr and CNTs is designed. Ultrathin nanosheet (3 atomic layers) and CNTs accelerate Zn2+ and electron transfer respectively. The Co-doping is conducive to the reduced Zn2+ diffusion barrier, the improved volume expansion after Zn2+ intercalation, and the enhanced electronic conductivity of BiOBr, verified by experimental and theoretical studies. An insertion-conversion mechanism is proposed according to ex situ characterizations. Benefiting from many advantages, Co-UTBiOBr displays a high capacity of 150 mAh g(-1) at 0.1 A g(-1) and a long-term cyclic life with approximate to 100% capacity attention over 3000 cycles at 1 A g(-1). Remarkably, excellent electrochemical performances are maintained even at an ultrahigh mass loading of 15 mg cm(-2). Co-UTBiOBr//MnO2 "rocking chair" zinc-ion battery exhibits a stable capacity of approximate to 130 mAh g(-1) at 0.2 A g(-1) during cyclic test and its flexible quasi-solid-state battery shows outstanding stability under various bending states. This work provides a new idea for designing high mass loading anode.
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单位四川大学; 湘潭大学; 湖南农业大学