Liu Xiaosong, Wang Yung Jui, Barbiellini Bernardo, Hafiz Hasnain, Basak Susmita, Liu Jun, Richardson Thomas, Shu Guojiun, Chou Fangcheng, Weng Tsu-Chien, Nordlund Dennis, Sokaras Dimosthenis, Moritz Brian, Devereaux Thomas P, Qiao Ruimin, Chuang Yi-De, Bansil Arun, Hussain Zahid, Yang Wanli
Advance Light Source, Lawrence Berkeley National Laboratory, Berkeley, CA 94720, USA.
Phys Chem Chem Phys. 2015 Oct 21;17(39):26369-77. doi: 10.1039/c5cp04739k. Epub 2015 Sep 21.
LiFePO4 is a battery cathode material with high safety standards due to its unique electronic structure. We performed systematic experimental and theoretical studies based on soft X-ray emission, absorption, and hard X-ray Raman spectroscopy of LixFePO4 nanoparticles and single crystals. The results clearly show a non-rigid electron-state reconfiguration of both the occupied and unoccupied Fe-3d and O-2p states during the (de)lithiation process. We focus on the energy configurations of the occupied states of LiFePO4 and the unoccupied states of FePO4, which are the critical states where electrons are removed and injected during the charge and discharge process, respectively. In LiFePO4, the soft X-ray emission spectroscopy shows that, due to the Coulomb repulsion effect, the occupied Fe-3d states with the minority spin sit close to the Fermi level. In FePO4, the soft X-ray absorption and hard X-ray Raman spectroscopy show that the unoccupied Fe-3d states again sit close to the Fermi level. These critical 3d electron state configurations are consistent with the calculations based on modified Becke and Johnson potentials GGA+U (MBJGGA+U) framework, which improves the overall lineshape prediction compared with the conventionally used GGA+U method. The combined experimental and theoretical studies show that the non-rigid electron state reshuffling guarantees the stability of oxygen during the redox reaction throughout the charge and discharge process of LiFePO4 electrodes, leading to the intrinsic safe performance of the electrodes.
磷酸铁锂是一种因其独特电子结构而具有高安全标准的电池正极材料。我们基于磷酸铁锂纳米颗粒和单晶的软X射线发射、吸收以及硬X射线拉曼光谱进行了系统的实验和理论研究。结果清楚地表明,在(脱)锂过程中,占据态和未占据态的铁3d和氧2p态都发生了非刚性电子态重新配置。我们关注磷酸铁锂占据态和磷酸铁未占据态的能量配置,它们分别是充电和放电过程中电子被移除和注入的关键态。在磷酸铁锂中,软X射线发射光谱表明,由于库仑排斥效应,少数自旋的占据态铁3d态靠近费米能级。在磷酸铁中,软X射线吸收和硬X射线拉曼光谱表明,未占据态铁3d态同样靠近费米能级。这些关键的3d电子态配置与基于改进的贝克和约翰逊势GGA+U(MBJGGA+U)框架的计算结果一致,与传统使用的GGA+U方法相比,该框架改进了整体线形预测。实验和理论相结合的研究表明,非刚性电子态重新排列保证了在磷酸铁锂电极充放电过程的氧化还原反应中氧的稳定性,从而导致电极具有本质安全性能。