Multi-heterostructured SnO2/SnSx embedded in carbon framework for high-performance sodium-ion storage

被引:9
|
作者
Bian, Haidong [1 ,2 ,3 ]
Li, Zebiao [4 ,5 ]
Pan, Jie [5 ]
Liao, Wenchao [2 ]
Li, Zhangjian [2 ]
Zhou, Binbin [5 ]
Zhang, Zheming [1 ,3 ]
Wu, Junwei [6 ]
Liu, Chen [2 ]
机构
[1] Beijing Inst Technol, Shenzhen Automot Res Inst, Shenzhen 518118, Guangdong, Peoples R China
[2] Shenzhen Univ, Coll Mat Sci & Engn, Shenzhen Key Lab Polymer Sci & Technol, Shenzhen 518055, Peoples R China
[3] Beijing Inst Technol, Natl Engn Lab Elect Vehicles, Beijing 100081, Peoples R China
[4] City Univ Hong Kong, Ctr Adv Struct Mat, Shenzhen Res Inst, 8 Yuexing 1st Rd,Shenzhen Hitech Ind Pk, Shenzhen 518055, Peoples R China
[5] City Univ Hong Kong, Dept Mat Sci & Engn, Kowloon, Tat Chee Ave 83, Hong Kong, Peoples R China
[6] Harbin Inst Technol Shenzhen, Dept Mat Sci & Engn, Shenzhen Key Lab Adv Mat, Shenzhen 518055, Peoples R China
基金
中国国家自然科学基金;
关键词
SnSx; SnO2; Carbon framework; Na-ion batteries; Multi-heterostructures; P-n junctions; CHARGE-TRANSFER; ANODE MATERIAL; LAYERED SNS; THIN-FILMS; IN-SITU; COMPOSITE; SN2S3; SNO2; HETEROJUNCTION; CONSTRUCTION;
D O I
10.1016/j.jcis.2022.08.011
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
Heterostructure materials, as newborn electrode materials for rechargeable batteries, are attracting increasing attention due to their robust architectures and superior electrochemical performances. It is widely believed that the inner electric field induced at the interface can improve the electric conductivity and ion diffusion kinetics, thus enhancing the long-term stability and high-rate performance of the batteries. Although much progress is made on heterostructure construction, the performance of the batteries is still far from satisfying the commercial applications. In this work, a new type of SnO2/SnSx (x = 1, 1.5) heterostructure embedded in carbon framework (C@SnO2/SnSx) is constructed via a facile sulfidation process. Compared to a single heterojunction, the multi-heterojunctions generated at SnO2/SnSx interface can induce an intensified built-in electric field, which promotes charge transportation and reaction kinetics of the electrode for Na-ions storage. Upon the sodiation process, the induced intensified electric field drives Na ions from Sn(2)S(3 )or SnO2 to SnS, while an inverse transportation of Na ions are accelerated upon the desodation process. As a result, C@SnO2/SnSx exhibits an outstanding reversible capacity of 510 mA h g(-1 )after 300 cycles at 200 mA g(-1). (C) 2022 Elsevier Inc. All rights reserved.
引用
收藏
页码:642 / 651
页数:10
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