材料科学
电导率
阳极
介孔材料
离子电导率
离子
扩散
多孔性
光电子学
锂(药物)
兴奋剂
空位缺陷
氧气
纳米技术
化学工程
电极
复合材料
物理化学
结晶学
催化作用
有机化学
化学
热力学
内分泌学
工程类
物理
医学
电解质
作者
Kangdong Tian,Zhongxiao Wang,Haoxiang Di,Haoyu Wang,Zhiwei Zhang,Shoubao Zhang,Rutao Wang,Luyuan Zhang,Chengxiang Wang,Longwei Yin
标识
DOI:10.1021/acsami.1c24909
摘要
TiNb 2 O 7 (TNO) is a competitive candidate of a fast-charging anode due to its high specific capacity. However, the insulator nature seriously hinders its rate performance. Herein, the La 3+ -doped mesoporous TiNb 2 O 7 materials (La–M–TNO) were first synthesized via a facile one-step solvothermal method with the assistance of polyvinyl pyrrolidone (PVP). The synergic effect of La 3+ doping and the mesoporous structure enables a dual improvement on the electronic conductivity and ionic diffusion coefficient, which delivers an impressive specific capacity of 213 mAh g –1 at 30 C. The capacity retention (@30C/@1C) increases from 33 to 53 and 74% for TNO, M–TNO, and La–M–TNO (0.03), respectively, demonstrating a step-by-step improvement of rate performance by making porous structures and intrinsic conductivity enhancement. DFT calculations verify that the enhancement in electronic conductivity due to La 3+ doping and oxygen vacancy, which induce localized energy levels via slight hybridization of O 2p, Ti 3d, and Nb 4d orbits. Meanwhile, the GITT result indicates that PVP-induced self-assembly of TNO accelerates the lithium ion diffusion rate by shortening the Li + diffusion path. This work verifies the effectiveness of the porous structure and highlights the significance of electronic conductivity to rate performance, especially at >30C. It provides a general approach to low-conductivity electrode materials for fast Li-ion storage.
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