4.8 Article

In Situ Fabrication of Cuprous Selenide Electrode via Selenization of Copper Current Collector for High-Efficiency Potassium-Ion and Sodium-Ion Storage

期刊

ADVANCED SCIENCE
卷 9, 期 5, 页码 -

出版社

WILEY
DOI: 10.1002/advs.202104630

关键词

cuprous selenides; electrode materials; potassium-ion battery; sodium-ion battery

资金

  1. National Natural Science Foundation of China [51972142]
  2. Department of Science and Technology of Jilin Province [20190701020GH]
  3. Fundamental Research Funds for the Central Universities
  4. National Postdoctoral Program for Innovative Talents [BX20180119]
  5. China Postdoctoral Science Foundation [2019M651194]

向作者/读者索取更多资源

A facile in situ fabrication method was developed to prepare an integrated cuprous selenide electrode for potassium-ion and sodium-ion storage. The electrode exhibited high performance due to its unique thin-film-like nanosheet morphology and robust structural stability, which effectively restrained volume change and loss of selenide species. This strategy opens up a new direction for designing and preparing high-performance electrodes.
Selenium-based materials are considered as desirable candidates for potassium-ion and sodium-ion storage. Herein, an in situ fabrication method is developed to prepare an integrated cuprous selenide electrode by means of directly chemical selenization of the copper current collector with commercial selenium powder. Interestingly, only the electrolyte of 1 m potassium hexafluorophosphate dissolved in 1,2-dimethoxyethane with higher highest occupied molecular orbital energy and lower desolvation energy facilitates the formation of polyselenide intermediates and the further selenization of the copper current collector. Benefiting from the unique thin-film-like nanosheet morphology and the robust structural stability of the integrated electrode, the volume change and the loss of selenide species could be effectively restrained. Therefore, high performance is achieved in both potassium-ion batteries (462 mA h g(-1) at 2 A g(-1) for 300 cycles) and sodium-ion batteries (775 mA h g(-1) at 2 A g(-1) for 4000 cycles). The facile fabrication strategy paves a new direction for the design and preparation of high-performance electrodes.

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