材料科学
阳极
储能
化学工程
钠
氧化还原
离子
法拉第效率
透射电子显微镜
纳米技术
电极
物理化学
冶金
热力学
化学
工程类
功率(物理)
物理
量子力学
作者
Baixin Peng,Zhuoran Lv,Shumao Xu,Jun Pan,Wei Zhao,Chenlong Dong,Fuqiang Huang
标识
DOI:10.1002/adma.202200863
摘要
Controllably tailoring alloying anode materials to achieve fast charging and enhanced structural stability is crucial for sodium-ion batteries with high rate and high capacity performance, yet remains a significant challenge owing to the huge volume change and sluggish sodiation kinetics. Here, a chemical tailoring tool is proposed and developed by atomically dispersing high-capacity Ge metal into the rigid and conductive sulfide framework for controllable reconstruction of GeS bonds to synergistically realize high capacity and high rate performance for sodium storage. The integrated GeTiS3 material with stable Ti-S framework and weak GeS bonding delivers high specific capacities of 678 mA h g-1 at 0.3 C over 100 cycles and 209 mA h g-1 at 32 C over 10 000 cycles, outperforming most of the reported alloying type anode materials for sodium storage. Interestingly, in situ Raman, X-ray diffraction (XRD), and ex situ transmission electron microscopy (TEM) characterizations reveal the formation of well-dispersed Nax Ge confined in the rigid Ti-S matrix with suppressed volume change after discharge. The synergistically coupled alloying-conversion and surface-dominated redox reactions with enhanced capacitive contribution and high reaction reversibility by a binding-energy-driven atomic scissors method would break new ground on designing a high-rate and high-capacity sodium-ion batteries.
科研通智能强力驱动
Strongly Powered by AbleSci AI