A dual heterostructure enables the stabilization of 1T-rich MoSe2 for enhanced storage of sodium ions

被引:7
|
作者
Chao, Yunfeng [1 ]
Jia, Shenghui [1 ]
Li, Jinzhao [1 ]
Chen, Guohui [1 ]
Liu, Lu [1 ]
Tang, Fei [1 ]
Zhu, Jianhua [1 ]
Wang, Caiyun [2 ]
Cui, Xinwei [1 ]
机构
[1] Zhengzhou Univ, Henan Inst Adv Technol, Zhengzhou 450052, Peoples R China
[2] Univ Wollongong, Intelligent Polymer Res Inst, Fac Engn & Informat Sci, Innovat Campus, N Wollongong, NSW 2500, Australia
基金
中国国家自然科学基金; 中国博士后科学基金;
关键词
NANOSHEETS; ANODE;
D O I
10.1039/d4sc02400a
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Electron injection effectively induces the formation of a 1T-rich phase to address the low conductivity of MoSe2. Nevertheless, overcoming the inherent metastability of the 1T phase (particularly during the conversion reactions that entail the decomposition-reconstruction of MoSe2 and volume expansion) remains a challenge. Guided by DFT results, we designed a composite with bimetal selenides-based heterostructures anchored on reduced graphene oxide (rGO) nanosheets (G-Cu2Se@MoSe2) to obtain stabilized 1T-rich MoSe2 and enhanced ion transfer. The construction of 1T-rich MoSe2 and built-in electric fields (BiEF) through electron transfer at the heterointerfaces were realized. Moreover, the rGO-metal selenides heterostructures with in situ-formed interfacial bonds could facilitate the reconstruction of the 1T-rich MoSe2-involved heterostructure and interfacial BiEF. Such a dual heterostructure endowed G-Cu2Se@MoSe2 with an excellent rate capability with a capacity of 288 mA h g(-1) at 50 A g(-1) and superior cycling stability with a capacity retention ratio of 89.6% (291 mA h g(-1)) after 15 000 cycles at 10 A g(-1). Insights into the functional mechanism and structural evolution of the 1T MoSe2-involved dual heterostructure from this work may provide guidelines for the development of MoSe2 and phase-engineering strategies for other polymorphistic materials.
引用
收藏
页码:11134 / 11144
页数:11
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