Interfacial space charge design with desired electron density to enhance sodium storage of MoS2@Nb2O5 anode

被引:4
|
作者
Xu, Xin [1 ]
Robertson, Stuart Jacob [2 ]
Yang, Tao [1 ]
Chen, Fuzhou [1 ]
Geng, Xinhua [1 ]
Wang, Yanjun [3 ]
Ji, Feng [4 ]
Sun, Changlong [1 ]
Chen, Shengzhou [1 ]
Shao, Minhua [2 ,5 ,6 ]
Wang, Jiahai [1 ]
机构
[1] Guangzhou Univ, Sch Chem & Chem Engn, Guangzhou 510006, Guangdong, Peoples R China
[2] Hong Kong Univ Sci & Technol, Dept Chem & Biol Engn, Kowloon, Clear Water Bay, Hong Kong, Peoples R China
[3] Guangzhou Hengyun Enterprises Holdings Ltd, Guangzhou 510246, Guangdong, Peoples R China
[4] Guangzhou High Tech Zone Inst Energy Technol, Guangzhou 513019, Guangdong, Peoples R China
[5] Hong Kong Univ Sci & Technol, CIAC HK Joint Lab Hydrogen Energy, Kowloon, Clear Watery Bay, Hong Kong, Peoples R China
[6] Hong Kong Univ Sci & Technol, Fok Ying Tung Res Inst, Guangzhou Key Lab Electrochem Energy Storage Techn, Guangzhou 511458, Peoples R China
基金
美国国家科学基金会; 中国国家自然科学基金; 中国博士后科学基金;
关键词
Interfacial effect; Sodium-ion battery; Electrochemical reaction kinetics; DFT; OXIDE-ASSISTED SYNTHESIS; GRAPHENE-OXIDE; LITHIUM; NANOSHEETS; MOS2; HETEROSTRUCTURE;
D O I
10.1016/j.nanoen.2024.109739
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
The interfacial effect is crucial for achieving superior sodium-ion storage performance in MoS2-based anodes. In this study, we constructed an interfacial effect by hydrothermally synthesizing Nb2O5 nanoparticles on MoS2 nanosheets (MoS2@Nb2O5). XPS analysis confirms a significant chemical interaction between MoS2 and Nb2O5 through interfacial covalent bonding (Mo-S/Nb-O) which enhances interatomic electron migration. Electrochemical kinetic analysis indicates an increased pseudocapacitance contribution. The galvanostatic intermittent titration technique (GITT) analysis shows improved charge transfer kinetics. Ex-situ XPS results reveal the reversible intercalation/deintercalation and oxidation/reduction mechanisms of the MoS2@Nb2O5 anode. Density functional theory (DFT) results show that strong interfacial bonding significantly enhances electrochemical reaction kinetics. The discharge capacity of the MoS2@Nb2O5 anode reaches up to 414.5 mA h g- 1 at 0.1 A g- 1 after 200 cycles, and the capacity retention is approximately 97.5 % at 2.0 A g- 1 after 1000 cycles, demonstrating good rate capability and capacity retention. This in-situ interfacial construction strategy presents an effective approach to designing MoS2-based anodes with improved electrochemical performance.
引用
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页数:11
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