Interfacial‐Confined Isochronous Conversion to Biphasic Selenide Heterostructure with Enhanced Adsorption Behaviors for Robust High‐Rate Na‐Ion Storage

Author:

Cao Jun‐Ming1ORCID,Ma Ming‐Yang1,Liu Han‐Hao2,Yang Jia‐Lin1,Liu Yue1,Zhang Kai‐Yang1,Butt Faaz A.3,Gu Zhen‐Yi1,Li Kai1,Wu Xing‐Long12ORCID

Affiliation:

1. MOE Key Laboratory for UV Light‐Emitting Materials and Technology Northeast Normal University Changchun Jilin 130024 P. R. China

2. Department of Chemistry Northeast Normal University Changchun Jilin 130024 P. R. China

3. Materials Engineering Department NED University of Engineering and Technology Karachi 75300 Pakistan

Abstract

AbstractSodium‐ion batteries (SIBs) have gradually become one of the most promising energy storage techniques in the current era of post‐lithium‐ion batteries. For anodes, transitional metal selenides (TMSe) based materials are welcomed choices , owing to relatively higher specific capacities and enriched redox active sites. Nevertheless, current bottlenecks are blamed for their poor intrinsic electronic conductivities, and uncontrollable volume expansion during redox reactions. Given that, an interfacial‐confined isochronous conversion strategy is proposed, to prepare orthorhombic/cubic biphasic TMSe heterostructure, namely CuSe/Cu3VSe4, through using MXene as the precursor, followed by Cu/Se dual anchorage. As‐designed biphasic TMSe heterostructure endows unique hierarchical structure, which contains adequate insertion sites and diffusion spacing for Na ions, besides, the surficial pseudocapacitive storage behaviors can be also proceeded like 2D MXene. By further investigation on electronic structure, the theoretical calculations indicate that biphasic CuSe/Cu3VSe4 anode exhibits well‐enhanced properties, with smaller bandgap and thus greatly improves intrinsic poor conductivities. In addition, the dual redox centers can enhance the electrochemical Na ions storage abilities. As a result, the as‐designed biphasic TMSe anode can deliver a reversible specific capacity of 576.8 mAh g−1 at 0.1 A g−1, favorable Na affinity, and reduced diffusion barriers. This work discloses a synchronous solution toward demerits in conductivities and lifespan, which is inspiring for TMSe‐based anode development in SIBs systems.

Funder

National Key Research and Development Program of China

National Natural Science Foundation of China

China Postdoctoral Science Foundation

Fundamental Research Funds for the Central Universities

Jilin Provincial Scientific and Technological Development Program

Publisher

Wiley

Subject

Biomaterials,Biotechnology,General Materials Science,General Chemistry

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