TY - JOUR
T1 - In-situ encapsulation of Ni3S2 nanoparticles into N-doped interconnected carbon networks for efficient lithium storage
AU - Li, Jiabao
AU - Li, Jinliang
AU - Ding, Zibiao
AU - Zhang, Xinlu
AU - Li, Yuquan
AU - Lu, Ting
AU - Yao, Yefeng
AU - Mai, Wenjie
AU - Pan, Likun
N1 - Publisher Copyright:
© 2019 Elsevier B.V.
PY - 2019/12/15
Y1 - 2019/12/15
N2 - Due to the conversion reaction induced high specific capacity, low cost and rich types, the interest on transition metal sulfides for efficient lithium storage has grown. Unfortunately, the intrinsically poor electrical conductivity and structure instability restrict their practical applications. Herein, an in-situ encapsulation strategy is developed to prepare the Ni3S2 nanoparticles encapsulated in interconnected N-doped porous carbon (Ni3S2@NC) through a facile freeze-drying approach and subsequent in-situ conversion. When evaluated as anode material for lithium-ion batteries (LIBs), the as-prepared Ni3S2@NC exhibits a remarkable lithium storage performance, including high reversible capacity (1335.4 mAh g−1 after 100 cycles at 0.1 A g−1), superior rate capability (507.7 mAh g−1 at 4 A g−1) and excellent long-term cycling stability (961.4 mAh g−1 after 600 cycles at 0.5 A g−1 and 862.8 mAh g−1 after 600 cycles at 1 A g−1), displaying one of the best lithium storage performances among the Ni3S2-based electrodes reported by now. Such an excellent lithium storage performance should be attributed to the unique structure advantages of Ni3S2@NC inherited from the in-situ encapsulation strategy, such as tight combination, increased electrical conductivity, shortened ion diffusion distance and buffering matrix provided by N-doped porous carbon networks. Importantly, the facile design and engineering strategy should also be applied to explore other nanoarchitectures to boost their lithium storage performances.
AB - Due to the conversion reaction induced high specific capacity, low cost and rich types, the interest on transition metal sulfides for efficient lithium storage has grown. Unfortunately, the intrinsically poor electrical conductivity and structure instability restrict their practical applications. Herein, an in-situ encapsulation strategy is developed to prepare the Ni3S2 nanoparticles encapsulated in interconnected N-doped porous carbon (Ni3S2@NC) through a facile freeze-drying approach and subsequent in-situ conversion. When evaluated as anode material for lithium-ion batteries (LIBs), the as-prepared Ni3S2@NC exhibits a remarkable lithium storage performance, including high reversible capacity (1335.4 mAh g−1 after 100 cycles at 0.1 A g−1), superior rate capability (507.7 mAh g−1 at 4 A g−1) and excellent long-term cycling stability (961.4 mAh g−1 after 600 cycles at 0.5 A g−1 and 862.8 mAh g−1 after 600 cycles at 1 A g−1), displaying one of the best lithium storage performances among the Ni3S2-based electrodes reported by now. Such an excellent lithium storage performance should be attributed to the unique structure advantages of Ni3S2@NC inherited from the in-situ encapsulation strategy, such as tight combination, increased electrical conductivity, shortened ion diffusion distance and buffering matrix provided by N-doped porous carbon networks. Importantly, the facile design and engineering strategy should also be applied to explore other nanoarchitectures to boost their lithium storage performances.
KW - Anode material
KW - Encapsulation
KW - In-situ fabrication
KW - Lithium-ion batteries
KW - NiS
UR - https://www.scopus.com/pages/publications/85068168340
U2 - 10.1016/j.cej.2019.122108
DO - 10.1016/j.cej.2019.122108
M3 - 文章
AN - SCOPUS:85068168340
SN - 1385-8947
VL - 378
JO - Chemical Engineering Journal
JF - Chemical Engineering Journal
M1 - 122108
ER -