兴奋剂
电化学
插层(化学)
材料科学
阴极
离子
钙钛矿(结构)
密度泛函理论
化学工程
扩散
相(物质)
无机化学
电极
纳米技术
化学物理
化学
物理化学
计算化学
光电子学
热力学
有机化学
工程类
物理
作者
Yong Li,Qinhao Shi,Xuan Yu,Fanghua Ning,Guoliang Liu,Xuan Wang,Juan Wang,Yunhua Xu,Yufeng Zhao
出处
期刊:Small
[Wiley]
日期:2024-02-15
卷期号:20 (27)
被引量:4
标识
DOI:10.1002/smll.202310756
摘要
Abstract P2‐phase layered cathodes play a pivotal role in sodium‐ion batteries due to their efficient Na + intercalation chemistry. However, limited by crystal disintegration and interfacial instability, bulk and interfacial failure plague their electrochemical performance. To address these challenges, a structural enhancement combined with surface modification is achieved through trace Y doping. Based on a synergistic combination of experimental results and density functional theory (DFT) calculations, the introduction of partial Y ions at the Na site (2d) acts as a stabilizing pillar, mitigating the electrostatic repulsions between adjacent TMO 2 slabs and thereby relieving internal structural stress. Furthermore, the presence of Y effectively optimizes the Ni 3d‐O 2p hybridization, resulting in enhanced electronic conductivity and a notable rapid charging ability, with a capacity of 77.3 mA h g −1 at 40 C. Concurrently, the introduction of Y also induces the formation of perovskite nano‐islands, which serve to minimize side reactions and modulate interfacial diffusion. As a result, the refined P2‐Na 0.65 Y 0.025 [Ni 0.33 Mn 0.67 ]O 2 cathode material exhibits an exceptionally low volume variation (≈1.99%), an impressive capacity retention of 83.3% even at −40 °C after1500 cycles at 1 C.
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