Muller-Bouvet D, Emery N, Tassali N, Panabière E, Bach S, Crosnier O, Brousse T, Cénac-Morthe C, Michalowicz A, Pereira-Ramos J P
Institut de Chimie et des Matériaux Paris Est, GESMAT, UMR CNRS UPEC 7182, 2 rue Henri Dunant, 94320 Thiais, France.
Phys Chem Chem Phys. 2017 Oct 18;19(40):27204-27211. doi: 10.1039/c7cp05207c.
A large data set of XAS (X-ray Absorption Spectroscopy) Manganese K-edge spectra has been collected operando and studied upon the electrochemical oxidation of the promising Li-ion battery anode material LiMnN. Using chemometric tools such as PCA (Principal Component Analysis) and MCR-ALS (Multivariate Curve resolution - Alternating Least Squares), three independent environment spectra were insulated. Based on the faradaic yield and well-chosen comparison of absorption spectrum energies within the frame of the coordination charge model, these environments were ascribed to unusual oxidation states allowed by nitride chemistry at a low potential (∼1.2 V vs. Li/Li), i.e. Mn (3d), Mn (3d) and Mn (3d). Also, their relative amounts are discussed with regard to the long-range structural variation which can be simply described by two successive biphasic domains followed by a solid-solution behaviour. Gathering this long-range and local structure information provides a complete picture of the redox mechanisms occurring in LiMnN.
通过对有前景的锂离子电池负极材料LiMnN进行电化学氧化,原位收集了大量X射线吸收光谱(XAS)锰K边光谱数据集并进行了研究。使用主成分分析(PCA)和多元曲线分辨-交替最小二乘法(MCR-ALS)等化学计量工具,分离出了三个独立的环境光谱。基于法拉第产率以及在配位电荷模型框架内对吸收光谱能量进行的精心选择的比较,这些环境归因于氮化物化学在低电位(相对于Li/Li约为1.2 V)下允许的异常氧化态,即Mn(3d)、Mn(3d)和Mn(3d)。此外,还针对可以简单地由两个连续的双相域随后是固溶体行为描述的长程结构变化,讨论了它们的相对含量。收集这些长程和局部结构信息,提供了LiMnN中发生的氧化还原机制的完整图景。