Few-Atomic-Layered Co-Doped BiOBr Nanosheet: Free-Standing Anode with Ultrahigh Mass Loading for “Rocking Chair” Zinc-Ion Battery

56Citations
Citations of this article
6Readers
Mendeley users who have this article in their library.

This article is free to access.

Abstract

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 ≈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 ≈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.

Cite

CITATION STYLE

APA

Long, B., Zhang, Q., Duan, T., Song, T., Pei, Y., Wang, X., … Wu, Y. (2022). Few-Atomic-Layered Co-Doped BiOBr Nanosheet: Free-Standing Anode with Ultrahigh Mass Loading for “Rocking Chair” Zinc-Ion Battery. Advanced Science, 9(32). https://doi.org/10.1002/advs.202204087

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free