4.8 Article

Orthorhombic Cobalt Ditelluride with Te Vacancy Defects Anchoring on Elastic MXene Enables Efficient Potassium-Ion Storage

Journal

ADVANCED MATERIALS
Volume 33, Issue 31, Pages -

Publisher

WILEY-V C H VERLAG GMBH
DOI: 10.1002/adma.202100272

Keywords

cobalt ditelluride; MXenes; P doping; potassium-ion batteries; Te vacancies

Funding

  1. National Natural Science Foundation of China [22005223, 21975187]
  2. Guangdong Basic and Applied Basic Research Foundation [2019A1515012161]
  3. Special Innovational Project of Department of Education of Guangdong Province [2019KTSCX186, 2017KCXTD031]
  4. Science Foundation for Young Teachers of Wuyi University [2019td01]
  5. Science Foundation for High-Level Talents of Wuyi University [2018RC50, 2017RC23]
  6. Wuyi University-Hong Kong-Macao Joint Research Project [2019WGALH10]
  7. Innovative Leading Talents of Jiangmen [Jiangren (2019) 7]
  8. Science and Technology Projects of Jiangmen [2017) 307, (2017) 149, (2018) 352]
  9. Key Laboratory of Optoelectronic Materials and Applications in Guangdong Higher Education [2017KSYS011]
  10. Newton Advanced Fellowships [NAF/R2/180603]
  11. College Student Innovation and Entrepreneurship Training Program Project [2019CX27, 2019CX32, 2019CX41]

Ask authors/readers for more resources

A P-doping-induced orthorhombic CoTe2 nanowires with Te vacancy defects supported on MXene superstructure has been designed and prepared, demonstrating high potassium-storage performance in terms of reversible capacity, rate capability, and long-term cyclability. Kinetics analysis and first-principles calculations reveal superior pseudocapacitive property, high electronic conductivity, and favorable K+ ion adsorption and diffusion capability for fast K+ ion storage.
The fast and reversible potassiation/depotassiation of anode materials remains an elusive yet intriguing goal. Herein, a class of the P-doping-induced orthorhombic CoTe2 nanowires with Te vacancy defects supported on MXene (o-P-CoTe2/MXene) is designed and prepared, taking advantage of the synergistic effects of the conductive o-P-CoTe2 arrays with rich Te vacancy defects and the elastic MXene sheets with self-autoadjustable function. Consequently, the o-P-CoTe2/MXene superstructure exhibits boosted potassium-storage performance, in terms of high reversible capacity (373.7 mAh g(-1) at 0.2 A g(-1) after 200 cycles), remarkable rate capability (168.2 mAh g(-1) at 20 A g(-1)), and outstanding long-term cyclability (0.011% capacity decay per cycle over 2000 cycles at 2 A g(-1)), representing the best performance in transition-metal-dichalcogenides-based anodes to date. Impressively, the flexible full battery with o-P-CoTe2/MXene anode achieves a satisfying energy density of 275 Wh kg(-1) and high bending stability. The kinetics analysis and first-principles calculations reveal superior pseudocapacitive property, high electronic conductivity, and favorable K+ ion adsorption and diffusion capability, corroborating fast K+ ion storage. Especially, ex situ characterizations confirm o-P-CoTe2/MXene undergoes reversible evolutions of initially proceeding with the K+ ion insertion, followed by the conversion reaction mechanism.

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