TY - JOUR
T1 - Artificial Interphases for Highly Stable Lithium Metal Anode
AU - Xu, Rui
AU - Cheng, Xin Bing
AU - Yan, Chong
AU - Zhang, Xue Qiang
AU - Xiao, Ye
AU - Zhao, Chen Zi
AU - Huang, Jia Qi
AU - Zhang, Qiang
N1 - Publisher Copyright:
© 2019 Elsevier Inc.
PY - 2019/8/7
Y1 - 2019/8/7
N2 - Lithium (Li) metal anode is highly pursed as the “Holy Grail” electrode because of its extremely high theoretical capacity (3,860 mAh g−1, 10-fold higher than that of commercial graphite anode), low gravimetric density (0.534 g cm−3), and the most negative equilibrium potential (−3.045 V versus standard hydrogen electrode). During practical operation, however, the aforementioned merits are largely hidden by the highly unstable electrode-electrolyte interface originating from the intrinsic high reactivity of metallic Li, which directly dictates a low Coulombic efficiency and a widely observed lithium dendrite formation. Designing an artificial interface with various in situ and ex situ methods is employed as an emerging strategy to greatly alter the surface chemistry of Li metal anode, hence intuitively enhancing the interfacial compatibility toward the electrolyte and enabling a highly stable Li anode in working batteries. In this review, the recent efforts on strengthening the Li metal and liquid/solid-electrolyte interfaces with artificial films are comprehensively summarized and discussed, the significance of interface-related science and engineering in both liquid-state and solid-state Li metal batteries is highlighted, and the future research directions in this field are prospected.
AB - Lithium (Li) metal anode is highly pursed as the “Holy Grail” electrode because of its extremely high theoretical capacity (3,860 mAh g−1, 10-fold higher than that of commercial graphite anode), low gravimetric density (0.534 g cm−3), and the most negative equilibrium potential (−3.045 V versus standard hydrogen electrode). During practical operation, however, the aforementioned merits are largely hidden by the highly unstable electrode-electrolyte interface originating from the intrinsic high reactivity of metallic Li, which directly dictates a low Coulombic efficiency and a widely observed lithium dendrite formation. Designing an artificial interface with various in situ and ex situ methods is employed as an emerging strategy to greatly alter the surface chemistry of Li metal anode, hence intuitively enhancing the interfacial compatibility toward the electrolyte and enabling a highly stable Li anode in working batteries. In this review, the recent efforts on strengthening the Li metal and liquid/solid-electrolyte interfaces with artificial films are comprehensively summarized and discussed, the significance of interface-related science and engineering in both liquid-state and solid-state Li metal batteries is highlighted, and the future research directions in this field are prospected.
KW - artificial solid-electrolyte interphase
KW - dendrites
KW - energy materials
KW - lithium metal anode
KW - non-aqueous electrolyte
KW - rechargeable batteries
KW - solid-state electrolyte
UR - http://www.scopus.com/inward/record.url?scp=85074173280&partnerID=8YFLogxK
U2 - 10.1016/j.matt.2019.05.016
DO - 10.1016/j.matt.2019.05.016
M3 - Review article
AN - SCOPUS:85074173280
SN - 2590-2393
VL - 1
SP - 317
EP - 344
JO - Matter
JF - Matter
IS - 2
ER -