Turrell Stephen J, Liang Yi, Cai Tiancheng, Jagger Ben, Pasta Mauro
Department of Materials, University of Oxford, Parks Road, Oxford OX1 3PH, U.K.
The Faraday Institution, Quad One, Becquerel Avenue, Harwell Campus, Didcot OX11 0RA, U.K.
Chem Mater. 2025 Apr 25;37(9):3504-3518. doi: 10.1021/acs.chemmater.5c00483. eCollection 2025 May 13.
Lithium phosphorus oxynitride (LiPON) is one of the few solid electrolytes that form a truly passivating solid electrolyte interphase (SEI) when in contact with metallic lithium. Investigations into the origin of this stability may provide the insights needed to replicate it in the SEIs of alternative solid electrolyte materials. In this study, we used in situ lithium plating X-ray photoelectron spectroscopy (XPS) to investigate the formation and evolution of the Li-LiPON SEI. We show that the SEI is chemically and structurally inhomogeneous, with the fully reduced compounds identified in previous studies (LiO, LiN, and LiP) concentrated near the lithium metal side and partially lithiated species, including Li P, predominant closer to the LiPON side. LiP and Li P have recently been suggested as enablers of continuous SEI growth in thiophosphate solid electrolytes. We suggest that the stability of the Li-LiPON SEI is derived from a combination of the LiPON reduction potential (0.68 V vs Li/Li), which is below the oxidation potentials of the fully reduced SEI compounds, and the graded structure of the SEI, which ensures that the most reduced species are not in physical or electrical contact with the LiPON layer.
氮氧化锂磷(LiPON)是少数几种在与金属锂接触时能形成真正钝化固态电解质界面(SEI)的固态电解质之一。对这种稳定性来源的研究可能会为在其他固态电解质材料的SEI中复制这种稳定性提供所需的见解。在本研究中,我们使用原位锂电镀X射线光电子能谱(XPS)来研究Li-LiPON SEI的形成和演变。我们表明,SEI在化学和结构上是不均匀的,先前研究中确定的完全还原化合物(LiO、LiN和LiP)集中在锂金属一侧,而部分锂化物种,包括LiP,在更靠近LiPON一侧占主导地位。最近有人提出LiP和LiP是硫代磷酸盐固态电解质中SEI持续生长的促成因素。我们认为,Li-LiPON SEI的稳定性源于LiPON还原电位(相对于Li/Li为0.68 V),该电位低于完全还原的SEI化合物的氧化电位,以及SEI的梯度结构,这确保了还原程度最高的物种不会与LiPON层发生物理或电接触。