High sulfur-doped microporous carbon for high-rate potassium ion storage: Interspace design and solvent effect

被引:11
作者
Bo, Zheng [1 ]
Chen, Pengpeng [1 ]
Tian, Fei [1 ]
Huang, Yanzhong [1 ]
Zheng, Zhouwei [1 ]
Yan, Jianhua [1 ]
Cen, Kefa [1 ]
Yang, Huachao [1 ]
Ostrikov, Kostya [2 ,3 ]
机构
[1] Zhejiang Univ, Coll Energy Engn, State Key Lab Clean Energy Utilizat, Hangzhou 310027, Zhejiang Provin, Peoples R China
[2] Queensland Univ Technol QUT, Sch Chem & Phys, Brisbane, Qld 4000, Australia
[3] Queensland Univ Technol QUT, QUT Ctr Mat Sci, Brisbane, Qld 4000, Australia
基金
中国国家自然科学基金; 澳大利亚研究理事会;
关键词
Potassium ion batteries; Sulfur-doped carbon; Interspace design; Solvent effect; Rate performance; ANODES; ELECTROLYTE; GRAPHITE; NITROGEN; LITHIUM;
D O I
10.1016/j.carbon.2023.118261
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Carbon materials as promising anode for potassium ion batteries (PIBs) suffer from low rate performance, which is attributed to sluggish K+ transport stemming from limited carbon interspace and elusive solvent effect. Herein, interspace design and solvent effect are investigated to resolve this issue. Through an innovative salt template assisted molten sulfur method, large hollow pores, massive micropores and expanded interlayer spacing are integrated in a high sulfur-doped porous carbon (S-PC), showing obviously higher rate capability (351.5 and 122.3 mA h g-1 at 0.1 and 20 A g-1, respectively) than pristine porous carbon (PC). Furthermore, the S-PC exhibits significantly-higher rate performance in ester-based electrolyte (1 M KFSI/EC + DEC) than in ether one (1 M KFSI/DME). Kinetic study demonstrates advantage of interspace design and ester-based electrolyte on promoting faster K+ transport. The explicit solvent effect on S-PC is further examined by XPS and HRTEM analyses, revealing a desirable inorganic KF-salt-dominated, thin solid electrolyte interface (SEI) layer in ester based electrolyte. This work opens new avenues for precise design of advanced carbon materials for high-rate PIBs.
引用
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页数:12
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