材料科学
兴奋剂
相(物质)
空位缺陷
结晶度
相变
储能
化学工程
纳米花
硒化物
化学物理
等离子体
纳米技术
光电子学
复合材料
凝聚态物理
冶金
热力学
纳米结构
硒
物理
工程类
量子力学
功率(物理)
有机化学
化学
作者
Hanna He,Zhang Hehe,Dan Huang,Wei Kuang,Xiaolong Li,Junnan Hao,Zhanhu Guo,Chuhong Zhang
标识
DOI:10.1002/adma.202200397
摘要
Metallic-phase selenide molybdenum (1T-MoSe2 ) has become a rising star for sodium storage in comparison with its semiconductor phase (2H-MoSe2 ) owing to the intrinsic metallic electronic conductivity and unimpeded Na+ diffusion structure. However, the thermodynamically unstable nature of 1T phase renders it an unprecedented challenge to realize its phase control and stabilization. Herein, a plasma-assisted P-doping-triggered phase-transition engineering is proposed to synthesize stabilized P-doped 1T phase MoSe2 nanoflower composites (P-1T-MoSe2 NFs). Mechanism analysis reveals significantly decreased phase-transition energy barriers of the plasma-induced Se-vacancy-rich MoSe2 from 2H to 1T owing to its low crystallinity and reduced structure stability. The vacancy-rich structure promotes highly concentrated P doping, which manipulates the electronic structure of the MoSe2 and urges its phase transition, acquiring a high transition efficiency of 91% accompanied with ultrahigh phase stability. As a result, the P-1T-MoSe2 NFs deliver an exceptional high reversible capacity of 510.8 mAh g-1 at 50 mA g-1 with no capacity fading over 1000 cycles at 5000 mA g-1 for sodium storage. The underlying mechanism of this phase-transition engineering verified by profound analysis provides informative guide for designing advanced materials for next-generation energy-storage systems.
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