钒
氧化还原
X射线光电子能谱
锂(药物)
过渡金属
电化学
相变
化学
X射线吸收光谱法
电极
金属
结晶学
吸收光谱法
材料科学
无机化学
物理化学
化学工程
物理
工程类
内分泌学
医学
催化作用
量子力学
有机化学
生物化学
作者
Molleigh B. Preefer,Muna Saber,Qiulong Wei,Nicholas H. Bashian,Joshua D. Bocarsly,Wei Zhang,Glenn Lee,JoAnna Milam-Guerrero,Erica S. Howard,Rebecca C. Vincent,Brent C. Melot,Anton Van der Ven,Ram Seshadri,Bruce Dunn
标识
DOI:10.1021/acs.chemmater.0c00560
摘要
PNb9O25, a Wadsley–Roth compound whose structure is obtained by appropriate crystallographic shear of the ReO3 structure, is a high-power electrode material that can reach 85% of the equilibrium capacity in 30 min and 67% in 6 min. Here we show that multielectron redox, as observed through X-ray absorption spectroscopy and X-ray photoelectron spectroscopy, and an insulator-to-metal transition upon lithium insertion, as suggested by a number of complementary techniques, contribute to the impressive performance. Chemically tuning the tetrahedral site between phosphorus and vanadium leads to significant changes in the electrochemistry and kinetics of lithium insertion in the structure, pointing to larger implications for the use of crystallographic shear phases as fast-charging electrode materials.
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