TY - JOUR
T1 - An Inorganic-Rich Solid Electrolyte Interphase for Advanced Lithium-Metal Batteries in Carbonate Electrolytes
AU - Liu, Sufu
AU - Ji, Xiao
AU - Piao, Nan
AU - Chen, Ji
AU - Eidson, Nico
AU - Xu, Jijian
AU - Wang, Pengfei
AU - Chen, Long
AU - Zhang, Jiaxun
AU - Deng, Tao
AU - Hou, Singyuk
AU - Jin, Ting
AU - Wan, Hongli
AU - Li, Jingru
AU - Tu, Jiangping
AU - Wang, Chunsheng
N1 - Publisher Copyright:
© 2020 Wiley-VCH GmbH
PY - 2021/2/15
Y1 - 2021/2/15
N2 - In carbonate electrolytes, the organic–inorganic solid electrolyte interphase (SEI) formed on the Li-metal anode surface is strongly bonded to Li and experiences the same volume change as Li, thus it undergoes continuous cracking/reformation during plating/stripping cycles. Here, an inorganic-rich SEI is designed on a Li-metal surface to reduce its bonding energy with Li metal by dissolving 4m concentrated LiNO3 in dimethyl sulfoxide (DMSO) as an additive for a fluoroethylene-carbonate (FEC)-based electrolyte. Due to the aggregate structure of NO3− ions and their participation in the primary Li+ solvation sheath, abundant Li2O, Li3N, and LiNxOy grains are formed in the resulting SEI, in addition to the uniform LiF distribution from the reduction of PF6− ions. The weak bonding of the SEI (high interface energy) to Li can effectively promote Li diffusion along the SEI/Li interface and prevent Li dendrite penetration into the SEI. As a result, our designed carbonate electrolyte enables a Li anode to achieve a high Li plating/stripping Coulombic efficiency of 99.55 % (1 mA cm−2, 1.0 mAh cm−2) and the electrolyte also enables a Li||LiNi0.8Co0.1Mn0.1O2 (NMC811) full cell (2.5 mAh cm−2) to retain 75 % of its initial capacity after 200 cycles with an outstanding CE of 99.83 %.
AB - In carbonate electrolytes, the organic–inorganic solid electrolyte interphase (SEI) formed on the Li-metal anode surface is strongly bonded to Li and experiences the same volume change as Li, thus it undergoes continuous cracking/reformation during plating/stripping cycles. Here, an inorganic-rich SEI is designed on a Li-metal surface to reduce its bonding energy with Li metal by dissolving 4m concentrated LiNO3 in dimethyl sulfoxide (DMSO) as an additive for a fluoroethylene-carbonate (FEC)-based electrolyte. Due to the aggregate structure of NO3− ions and their participation in the primary Li+ solvation sheath, abundant Li2O, Li3N, and LiNxOy grains are formed in the resulting SEI, in addition to the uniform LiF distribution from the reduction of PF6− ions. The weak bonding of the SEI (high interface energy) to Li can effectively promote Li diffusion along the SEI/Li interface and prevent Li dendrite penetration into the SEI. As a result, our designed carbonate electrolyte enables a Li anode to achieve a high Li plating/stripping Coulombic efficiency of 99.55 % (1 mA cm−2, 1.0 mAh cm−2) and the electrolyte also enables a Li||LiNi0.8Co0.1Mn0.1O2 (NMC811) full cell (2.5 mAh cm−2) to retain 75 % of its initial capacity after 200 cycles with an outstanding CE of 99.83 %.
KW - carbonate electrolytes
KW - dendrite-free structures
KW - electrode interphases
KW - lithium nitrate
KW - lithium-metal batteries
UR - http://www.scopus.com/inward/record.url?scp=85097562425&partnerID=8YFLogxK
U2 - 10.1002/anie.202012005
DO - 10.1002/anie.202012005
M3 - 文章
C2 - 33166432
AN - SCOPUS:85097562425
SN - 1433-7851
VL - 60
SP - 3661
EP - 3671
JO - Angewandte Chemie - International Edition
JF - Angewandte Chemie - International Edition
IS - 7
ER -