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Non-negligible Influence of Oxygen in Hard Carbon as an Anode Material for Potassium-Ion Batteries.
Liu, Zhengyang; Wu, Shijie; Song, Yan; Yang, Tao; Ma, Zihui; Tian, Xiaodong; Liu, Zhanjun.
Afiliación
  • Liu Z; Key Laboratory of Carbon Materials, Institute of Coal Chemistry, Chinese Academy of Sciences, Taiyuan030001, China.
  • Wu S; Center of Materials Science and Optoelectronics Engineering, University of Chinese Academy of Sciences, Beijing100049, China.
  • Song Y; Key Laboratory of Carbon Materials, Institute of Coal Chemistry, Chinese Academy of Sciences, Taiyuan030001, China.
  • Yang T; Center of Materials Science and Optoelectronics Engineering, University of Chinese Academy of Sciences, Beijing100049, China.
  • Ma Z; Key Laboratory of Carbon Materials, Institute of Coal Chemistry, Chinese Academy of Sciences, Taiyuan030001, China.
  • Tian X; Center of Materials Science and Optoelectronics Engineering, University of Chinese Academy of Sciences, Beijing100049, China.
  • Liu Z; Key Laboratory of Carbon Materials, Institute of Coal Chemistry, Chinese Academy of Sciences, Taiyuan030001, China.
ACS Appl Mater Interfaces ; 14(42): 47674-47684, 2022 Oct 26.
Article en En | MEDLINE | ID: mdl-36223510
ABSTRACT
The development of potassium-ion batteries (PIBs) has been impeded by the lack of an appropriate carbon anode material that could accommodate K+ with a large ionic radius. Hard carbon with low cost and larger interlayer spacing is a promising anode material for PIBs. However, the impact of oxygen-containing functional groups in hard carbon (HC) is less reported. Herein, a hypercrosslinked polymer (HCLP) is prepared and used for the synthesis of microporous hard carbons with superior structural stability and abundant oxygen-containing functional groups and defects, in which the crosslinking agent provided copious oxygen atoms. It is found that a large number of C═O groups and micropores provide more storage sites for K+. The surface-controlled process is dominated by the reversible reaction of C═O + K+ + e- ↔ C-O-K, which directly increases the capacity contribution. The HCs obtained at 600 °C exhibit good cycling and rate performance with an initial specific capacity of about 254.3 mAh g-1 and the capacity retention of 83.2% after 200 cycles at 50 mA g-1. The capacity reached up to 121 mAh g-1 at 2 A g-1. A possible capacitive-adsorption mechanism is proposed by kinetic analysis. The redox reaction mechanism between C═O and K+ at the HC is clearly also revealed.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: ACS Appl Mater Interfaces Asunto de la revista: BIOTECNOLOGIA / ENGENHARIA BIOMEDICA Año: 2022 Tipo del documento: Article País de afiliación: China

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: ACS Appl Mater Interfaces Asunto de la revista: BIOTECNOLOGIA / ENGENHARIA BIOMEDICA Año: 2022 Tipo del documento: Article País de afiliación: China