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.
Keywords: mechanism analysis; metallic phase MoSe 2; phase-transition engineering; plasma-assisted P-doping; sodium-ion batteries.
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