TY - JOUR
T1 - Fabrication of S,N-doped carbon-coated SnS2/SnS heterostructures supported by hollow carbon microspheres for sodium-ion storage
AU - Gao, Suning
AU - Liu, Zaichun
AU - Yang, Liangtao
AU - Shao, Jie
AU - Qu, Qunting
AU - Wu, Yuping
AU - Adelhelm, Philipp
AU - Holze, Rudolf
N1 - Publisher Copyright:
© 2021 Electrochemical Society Inc.. All rights reserved.
PY - 2021/5
Y1 - 2021/5
N2 - Developing novel anode materials containing electroactive heterostructures which boost ion and charge transfer kinetics in a carbon matrix is still a great challenge. Here we report on a new smartly designed material: SnS2/SnS p-n heterostructures embedded in S,N-doped carbon layer supported by hollow carbon spheres (C@SnSx@C) by a facile method and applied as negative electrode material in sodium ion batteries. The C@SnSx@C2 (at optimized carbon ratio) negative electrode can deliver an initial reversible capacity of 636.5 mAh·g−1 at 0.1 A·g−1, superior rate capability (265.1 mAh·g−1 at rate of 10.0 A·g−1) and long cycle life (capacity retention of 96.3 % at 1.0 A·g−1 after 150 cycles). The SnS2/SnS p-n heterojunctions provide a lower sodium ion diffusion energy barrier (0.38 eV), higher Na+ adsorption energy (−4.66 eV) and higher electronic conductivity due to an internal electric field according to density functional theory calculations compared to plain SnS. Moreover, S,N-doped carbon facilitates electronic conductivity and buffers the volume changes during the conversion reaction-based SnSx upon sodium insertion and extraction process. Porous hollow carbon spheres contribute to prevent the agglomeration of SnS2/SnS nanosheets and keep the structural integrity. Our findings on this unique material might be extended to other ion battery technologies.
AB - Developing novel anode materials containing electroactive heterostructures which boost ion and charge transfer kinetics in a carbon matrix is still a great challenge. Here we report on a new smartly designed material: SnS2/SnS p-n heterostructures embedded in S,N-doped carbon layer supported by hollow carbon spheres (C@SnSx@C) by a facile method and applied as negative electrode material in sodium ion batteries. The C@SnSx@C2 (at optimized carbon ratio) negative electrode can deliver an initial reversible capacity of 636.5 mAh·g−1 at 0.1 A·g−1, superior rate capability (265.1 mAh·g−1 at rate of 10.0 A·g−1) and long cycle life (capacity retention of 96.3 % at 1.0 A·g−1 after 150 cycles). The SnS2/SnS p-n heterojunctions provide a lower sodium ion diffusion energy barrier (0.38 eV), higher Na+ adsorption energy (−4.66 eV) and higher electronic conductivity due to an internal electric field according to density functional theory calculations compared to plain SnS. Moreover, S,N-doped carbon facilitates electronic conductivity and buffers the volume changes during the conversion reaction-based SnSx upon sodium insertion and extraction process. Porous hollow carbon spheres contribute to prevent the agglomeration of SnS2/SnS nanosheets and keep the structural integrity. Our findings on this unique material might be extended to other ion battery technologies.
UR - http://www.scopus.com/inward/record.url?scp=85107566054&partnerID=8YFLogxK
U2 - 10.1149/1945-7111/abf5f6
DO - 10.1149/1945-7111/abf5f6
M3 - 文章
AN - SCOPUS:85107566054
SN - 0013-4651
VL - 168
JO - Journal of the Electrochemical Society
JF - Journal of the Electrochemical Society
IS - 5
M1 - 050527
ER -