Co-activation for enhanced K-ion storage in battery anodes

Author:

Feng Yanhong1,Lv Yawei1,Fu Hongwei1,Parekh Mihir2,Rao Apparao M2,Wang He3,Tai Xiaolin3,Yi Xianhui1,Lin Yue3,Zhou Jiang4ORCID,Lu Bingan15

Affiliation:

1. School of Physics and Electronics, Hunan University , Changsha 410082 , China

2. Department of Physics and Astronomy, Clemson Nanomaterials Institute, Clemson University , Clemson , SC 29643 , USA

3. Hefei National Research Center for Physical Sciences at the Microscale, University of Science and Technology of China , Hefei 230026 , China

4. School of Materials Science and Engineering, Central South University , Changsha 410083 , China

5. State Key Laboratory of Advanced Design and Manufacturing for Vehicle Body, Hunan University , Changsha 410082 , China

Abstract

ABSTRACT The relative natural abundance of potassium and potentially high energy density has established potassium-ion batteries as a promising technology for future large-scale global energy storage. However, the anodes’ low capacity and high discharge platform lead to low energy density, which impedes their rapid development. Herein, we present a possible co-activation mechanism between bismuth (Bi) and tin (Sn) that enhances K-ion storage in battery anodes. The co-activated Bi-Sn anode delivered a high capacity of 634 mAh g–1, with a discharge plateau as low as 0.35 V, and operated continuously for 500 cycles at a current density of 50 mA g–1, with a high Coulombic efficiency of 99.2%. This possible co-activation strategy for high potassium storage may be extended to other Na/Zn/Ca/Mg/Al ion battery technologies, thus providing insights into how to improve their energy storage ability.

Funder

National Natural Science Foundation of China

Youth Innovation Promotion Association of the Chinese Academy of Sciences

National Key Research and Development Program of China

Clemson University

Publisher

Oxford University Press (OUP)

Subject

Multidisciplinary

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