材料科学
集电器
阳极
电解质
法拉第效率
阴极
成核
润湿
化学工程
电池(电)
电极
铜
合金
复合材料
冶金
化学
工程类
物理
物理化学
功率(物理)
有机化学
量子力学
作者
Yixian Wang,Yijie Liu,Mai Nguyen,Jae‐Young Cho,Naman Katyal,Bairav S. Vishnugopi,Hongchang Hao,Ruyi Fang,Nan Wu,Pengcheng Liu,Partha P. Mukherjee,Jagjit Nanda,Graeme Henkelman,John Watt,David Mitlin
标识
DOI:10.1002/adma.202206762
摘要
A stable anode-free all-solid-state battery (AF-ASSB) with sulfide-based solid-electrolyte (SE) (argyrodite Li6 PS5 Cl) is achieved by tuning wetting of lithium metal on "empty" copper current-collector. Lithiophilic 1 µm Li2 Te is synthesized by exposing the collector to tellurium vapor, followed by in situ Li activation during the first charge. The Li2 Te significantly reduces the electrodeposition/electrodissolution overpotentials and improves Coulombic efficiency (CE). During continuous electrodeposition experiments using half-cells (1 mA cm-2 ), the accumulated thickness of electrodeposited Li on Li2 Te-Cu is more than 70 µm, which is the thickness of the Li foil counter-electrode. Full AF-ASSB with NMC811 cathode delivers an initial CE of 83% at 0.2C, with a cycling CE above 99%. Cryogenic focused ion beam (Cryo-FIB) sectioning demonstrates uniform electrodeposited metal microstructure, with no signs of voids or dendrites at the collector-SE interface. Electrodissolution is uniform and complete, with Li2 Te remaining structurally stable and adherent. By contrast, an unmodified Cu current-collector promotes inhomogeneous Li electrodeposition/electrodissolution, electrochemically inactive "dead metal," dendrites that extend into SE, and thick non-uniform solid electrolyte interphase (SEI) interspersed with pores. Density functional theory (DFT) and mesoscale calculations provide complementary insight regarding nucleation-growth behavior. Unlike conventional liquid-electrolyte metal batteries, the role of current collector/support lithiophilicity has not been explored for emerging AF-ASSBs.
科研通智能强力驱动
Strongly Powered by AbleSci AI