GeV4S8: a Novel Bimetallic Sulfide for Robust and Fast Potassium Storage

Author:

Chen Wen12,Hu Keyan2,Zheng Hongshun34,Pan Youtan2,Lv Zhuoran15,Tu Xueyang1,Zheng Chong6,He Tianwei4,Huang Fuqiang125ORCID,Dong Wujie15

Affiliation:

1. Shanghai, China State Key Laboratory of High Performance Ceramics and Superfine Microstructure Shanghai Institute of Ceramics Chinese Academy of Sciences Shanghai 200050 China

2. School of Mechanical and Electrical Engineering Jingdezhen Ceramic University Jingdezhen 333403 China

3. Southwest United Graduate School Kunming 650091 China

4. Yunnan Key Laboratory for Micro/Nano Materials & Technology National Center for International Research on Photoelectric and Energy Materials School of Materials and Energy Yunnan University Kunming 650091 China

5. State Key Lab of Metal Matrix Composites School of Materials Science and Engineering Shanghai Jiao Tong University Dongchuan Road 800 Shanghai 200240 China

6. Department of Chemistry and Biochemistry Northern Illinois University DeKalb IL 60115 USA

Abstract

AbstractPotassium‐ion batteries (PIBs) have attracted much attention due to their low production cost and abundant resources. Germanium is a promising alloying‐type anode with a high theoretical capacity for PIBs, yet suffering significant volume expansion and sluggish potassium‐ion transport kinetics. Herein, a rational strategy is formulated to disperse Ge atoms into transition metal V−S sulfide frameworks to form a loosely packed and metallic GeV4S8 medium. The theoretical prediction shows that GeV4S8 is conducive to the adsorption and diffusion of K+. The V−S frameworks provide fast ion/electron diffusion channels and also help to buffer the volume expansion during K+ insertion. In situ and ex situ characterizations manifest that KGe alloy clusters are constrained and dispersed by potassiated VS2 topological structure during discharging, and revert to the original GeV4S8 after charging. Consequently, as a novel anode for PIBs, GeV4S8 provides a high specific capacity of ≈400 mAh g−1 at 0.5 C, maintaining 160 mAh g−1 even at 12.5 C and ≈80% capacity after 1000 cycles at 5 C, superior to most of the state‐of‐the‐art anode materials. The proposed strategy of combining alloy and intercalation dual‐functional units is expected to open up a new way for high‐capacity and high‐rate anode for PIBs.

Funder

National Natural Science Foundation of China

Science and Technology Commission of Shanghai Municipality

Natural Science Foundation of Jiangxi Province

Publisher

Wiley

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