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Heteroatoms-Doped Mesoporous Carbon Nanosheets with Dual Diffusion Pathways for Highly Efficient Potassium Ion Storage.
Wang, Haibing; Ding, Hao; Wang, Zhenzhu; Zhu, Yanyan; Chen, Zhonghui; Song, Bo.
Affiliation
  • Wang H; National Key Laboratory of Science and Technology on Advanced Composites in Special Environments, Harbin Institute of Technology, Harbin, 150001, China.
  • Ding H; Advanced Optoelectronic Technology Research Institute, Zhengzhou Research Institute, Harbin Institute of Technology, Zhengzhou, 450052, China.
  • Wang Z; College of Mathematics and Physics, Shanghai University of Electric Power, Shanghai, 200090, China.
  • Zhu Y; College of Mathematics and Physics, Shanghai University of Electric Power, Shanghai, 200090, China.
  • Chen Z; National Key Laboratory of Science and Technology on Advanced Composites in Special Environments, Harbin Institute of Technology, Harbin, 150001, China.
  • Song B; Advanced Optoelectronic Technology Research Institute, Zhengzhou Research Institute, Harbin Institute of Technology, Zhengzhou, 450052, China.
Small ; 20(27): e2310908, 2024 Jul.
Article in En | MEDLINE | ID: mdl-38279585
ABSTRACT
The high potassization/depotassization energy barriers and lack of efficient ion diffusion pathways are two serious obstacles for carbon-based materials to achieve satisfactory potassium ion storage performance. Herein, a facile and controllable one-step exfoliation-doping-etching strategy is proposed to construct heteroatoms (N, O, and S)-doped mesoporous few-layer carbon nanosheets (NOS-C). The mixed molten salts of KCl/K2SO4 are innovatively used as the exfoliators, dopants, and etching agents, which enable NOS-C with expanded interlayer spacing and uniformly distributed mesopores with the adjusted electronic structure of surrounding carbon atoms, contributing efficient dual (vertical and horizontal) K-ion diffusion pathways, low potassization/depotassization energy barriers and abundant active sites. Thus, the NOS anodes achieve a high reversible capacity of 516.8 mAh g-1 at 0.05 A g-1, superior rate capability of 202.8 mAh g-1 at 5 A g-1 and excellent long-term cyclic stability, and their practical application potential is demonstrated by the assembled potassium-ion full batteries. Moreover, a surface-interlayer synergetic K+ storage mechanism is revealed by a combined theoretical and experimental approach including in situ EIS, in situ Raman, ex situ XPS, and SEM analysis. The proposed K+ storage mechanism and unique structural engineering provide a new pathway for potassium-ion storage devices and even beyond.
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Small Journal subject: ENGENHARIA BIOMEDICA Year: 2024 Type: Article Affiliation country: China

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Small Journal subject: ENGENHARIA BIOMEDICA Year: 2024 Type: Article Affiliation country: China