| Literature DB >> 35266638 |
Qianli Cai1, Xinglong Li1, Ertao Hu1, Zhongyue Wang1, Peng Lv1, Jiajin Zheng1, Kehan Yu1,2, Wei Wei1,2, Kostya Ken Ostrikov3,4.
Abstract
Anatase TiO2 is a promising anode material for lithium-ion batteries (LIBs) and sodium-ion batteries (SIBs) due to its high specific capacity, low cost, and excellent cycle stability. However, low electrical conductivity and poor Na+ ion transport in TiO2 limit its practical applications. Here, substantially boosted Na+ ion transport and charge transfer kinetics are demonstrated by constructing a near-ideal non-rectifying titanium carbonitride/nitrogen-doped TiO2 (TiCx N1- x /N-TiO2 ) heterostructure. Owing to the fast plasma effects and metastable hybrid phases, the TiCx N1- x is epitaxially grown on TiO2 . Energy band engineering at the interface induces high electron densities and a strong built-in electric field, which lowers the Na+ diffusion barrier by a factor of 1.7. As a result, the TiCx N1- x /N-TiO2 electrode exhibits excellent electrochemical performance. The reversible specific capacities at rates of 0.1 and 10 C reach 312.3 and 173.7 mAh g-1 , respectively. After 600 cycles of charge and discharge at 10 C, the capacity retention rate is 98.7%. This work discovers an effective non-equilibrium plasma-enabled process to construct heterointerfaces that can enhance Na+ ion transport and provides generic guidelines for the design of heterostructures for a broader range of energy storage, separation, and other devices that rely on controlled ionic transport.Entities:
Keywords: diffusion barriers; heterostructures; plasma; sodium-ion batteries; titanium carbonitride; titanium dioxide
Year: 2022 PMID: 35266638 DOI: 10.1002/smll.202200694
Source DB: PubMed Journal: Small ISSN: 1613-6810 Impact factor: 13.281