TY - JOUR
T1 - Harnessing Plasma-Assisted Doping Engineering to Stabilize Metallic Phase MoSe2 for Fast and Durable Sodium-Ion Storage
AU - He, Hanna
AU - Zhang, Hehe
AU - Huang, Dan
AU - Kuang, Wei
AU - Li, Xiaolong
AU - Hao, Junnan
AU - Guo, Zaiping
AU - Zhang, Chuhong
PY - 2022/4/14
Y1 - 2022/4/14
N2 - 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. © 2022 Wiley-VCH GmbH.
AB - 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. © 2022 Wiley-VCH GmbH.
KW - mechanism analysis
KW - metallic phase MoSe 2
KW - phase-transition engineering
KW - plasma-assisted P-doping
KW - sodium-ion batteries
UR - http://www.scopus.com/inward/record.url?scp=85125341924&partnerID=8YFLogxK
UR - https://www.scopus.com/record/pubmetrics.uri?eid=2-s2.0-85125341924&origin=recordpage
U2 - 10.1002/adma.202200397
DO - 10.1002/adma.202200397
M3 - RGC 21 - Publication in refereed journal
C2 - 35137451
SN - 0935-9648
VL - 34
JO - Advanced Materials
JF - Advanced Materials
IS - 15
M1 - 2200397
ER -