TY - JOUR
T1 - Li+, Na+ co-stabilized vanadium oxide nanobelts with a bilayer structure for boosted zinc-ion storage performance
AU - Wang, Jinjin
AU - Zhao, Xiangyuan
AU - Kang, Jinzhao
AU - Wang, Xiaomei
AU - Yu, Hong
AU - Du, Cheng Feng
AU - Yan, Qingyu
N1 - Publisher Copyright:
© 2022 The Royal Society of Chemistry.
PY - 2022/9/8
Y1 - 2022/9/8
N2 - Addressing the structural instability and torpid kinetic limitation has been a pressing while challenging issue for vanadium oxide cathode materials to realize their outstanding performance in rechargeable aqueous zinc-ion batteries (ZIBs). Herein, vanadium oxide nanobelts with a bilayer structure (LiV3O8@NaV3O8, LVO@NVO) have been prepared successfully via a quick one-pot eutectic oxidation process. When evaluated as a cathode for ZIBs, the LVO@NVO shows an amazing capacity of 476 mA h g−1 at 0.05 A g−1, superior rate properties (236 mA h g−1 @ 5 A g−1), and excellent cycling capability over 2000 cycles with a capacity-retention of 93.4%. Owing to the pre-intercalated Li+ and Na+ cations and the resulting bilayer structure, higher pseudocapacitance, faster charge-transfer/ion-diffusion kinetics, and a robust architecture have been achieved in the LVO@NVO cathode, which are responsible for the superior zinc-ion storage performance. Furthermore, the energy storage mechanism based on Zn2+ and H+ co-intercalation/extraction has been proved.
AB - Addressing the structural instability and torpid kinetic limitation has been a pressing while challenging issue for vanadium oxide cathode materials to realize their outstanding performance in rechargeable aqueous zinc-ion batteries (ZIBs). Herein, vanadium oxide nanobelts with a bilayer structure (LiV3O8@NaV3O8, LVO@NVO) have been prepared successfully via a quick one-pot eutectic oxidation process. When evaluated as a cathode for ZIBs, the LVO@NVO shows an amazing capacity of 476 mA h g−1 at 0.05 A g−1, superior rate properties (236 mA h g−1 @ 5 A g−1), and excellent cycling capability over 2000 cycles with a capacity-retention of 93.4%. Owing to the pre-intercalated Li+ and Na+ cations and the resulting bilayer structure, higher pseudocapacitance, faster charge-transfer/ion-diffusion kinetics, and a robust architecture have been achieved in the LVO@NVO cathode, which are responsible for the superior zinc-ion storage performance. Furthermore, the energy storage mechanism based on Zn2+ and H+ co-intercalation/extraction has been proved.
UR - http://www.scopus.com/inward/record.url?scp=85140247091&partnerID=8YFLogxK
U2 - 10.1039/d2ta05803k
DO - 10.1039/d2ta05803k
M3 - 文章
AN - SCOPUS:85140247091
SN - 2050-7488
VL - 10
SP - 21531
EP - 21539
JO - Journal of Materials Chemistry A
JF - Journal of Materials Chemistry A
IS - 40
ER -