Evolution of Interfacial Phenomena Induced by Electrolyte Formulation and Hot Cycling of Anode-Free Li-Metal Batteries

电解质 阳极 成核 材料科学 X射线光电子能谱 扫描电子显微镜 法拉第效率 锂(药物) 分析化学(期刊) 化学工程 电极 化学 色谱法 工程类 有机化学 复合材料 医学 内分泌学 物理化学
作者
Kassie Nigus Shitaw,Chen‐Jui Huang,Sheng‐Chiang Yang,Yosef Nikodimos,Nigusu Tiruneh Temesgen,Semaw Kebede Merso,Shi‐Kai Jiang,Chia‐Hsin Wang,She–Huang Wu,Wei‐Nien Su,Bing‐Joe Hwang
出处
期刊:ACS applied energy materials [American Chemical Society]
卷期号:5 (6): 7770-7783 被引量:15
标识
DOI:10.1021/acsaem.2c01245
摘要

Even though the anode-free lithium metal battery (AFLMB) is the next promising energy-storage device because of its high energy density, the irreversible interfacial phenomena at the Cu/electrolyte interface are the key failure mechanisms of the AFLMBs. To the best of our knowledge, the interfacial phenomena associated with the capacity fading of AFLMBs are not reported yet. Herein, hot cycling combined with electrolyte formulation using 1% tris(trimethylsilyl) phosphite (TMSP) additive has been used as a protocol to systematically investigate the Cu/electrolyte interfacial phenomena of Li nucleation, compactness of deposited Li, inactive Li ("dead Li" and Li for solid–electrolyte interphase (SEI) formation "SEI-Li"), electrolyte decomposition, and SEI layer formation using a scanning electron microscope, scanning electron microscope-focused ion beam, titration gas chromatography, in situ gas chromatography–mass spectroscopy, and X-ray photoelectron spectroscopy, respectively. The synergy of hot cycling and the TMSP additive lowers the nucleation barrier in Li/Cu from 76.2 to 21.7 mV and increases the compactness of deposited Li from 32.3 to 43.8% and decreases "dead Li" from 45.18 to 10.86% and SEI-Li from 31.04 to 12.49% of anode-free Cu/NMC111. Because of the synergy effects, the Cu/NMC111 cell provides over 100 cycles with an average coulombic efficiency (avg. CE) of 98.6% for the first 60 cycles and a capacity retention (CR) of 60.4% at the end of the 60th cycle at 0.2/0.5 mA cm–2 charger/discharge current density, while the cell with 1 M LiPF6 EC/DEC at 25 °C offers only an avg. CE of 92.8% for the first 15 cycles with a CR of 40.4% at the 15th cycle. The results suggest that the synergy of hot cycling and electrolyte formulation decreases the surface area of deposited Li and stabilizes the interface that suppresses inventory Li loss. This work probes the Cu/electrolyte interfacial phenomena, attributed to the failure mechanisms of AFLMBs. It also sheds light on suitable strategies to stabilize the Cu interface for stable cycling of AFLMBs.
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