摘要：Harvesting the promising high energy density of advanced electrode materials in lithium-ion batteries is critically dependent on a mechanistic understanding on how the materials function and degrade along with the battery ***,we tracked phase transformations during(de)lithiation of Sb_(2)Se_(3) single crystals using in situ high-resolution transmission electron microscopy(HRTEM)technique,and revealed electro-chemo-mechanical evolution at the reaction *** effect of this electro-chemo-mechanical coupling has a complicated interplay on the lithiation kinetics and causes various types of defects at the reaction front,including dislocation dipoles,antiphase boundaries,and *** return,the formed cracks and related defects build a path for fast diffusion of lithium ions and trigger a highly anisotropic lithiation at the twisted reaction front,giving rise to the formation of presumably "dead" Sb_(2)Se_(3) nanodomains in amorphous Li_(x)Sb_(2)Se_(3).The detailed mechanistic understanding may facilitate the rational design of high-capacity electrode materials for battery applications.

摘要：量子自旋霍尔绝缘体拥有具有带隙的体态和无能隙的一维拓扑边缘态.然而,由于拓扑边缘态局域在纳米尺度,所以很难用光学手段直接观测并区分体态和边缘态,这就限制了对拓扑边缘态独特的光学特性和光电响应等方面的研究和应用.Bi_(4)Br_(4)体材料的台阶存在一维非平庸的边缘态,多个台阶累加的效应使得通过较为宏观的光学和光电分析手段来研究一维边缘态成为可能.该工作利用中远红外显微吸收光谱和泵浦探测光谱,对比研究了Bi_(4)Br_(4)体和边缘的光学响应行为.研究发现Bi_(4)Br_(4)的边缘在小于带隙(约0.22 eV)的波段存在明显的强于体内的红外吸收,且该吸收呈现较强的各向异性.室温下的红外泵浦探测首次观察到边缘处载流子激发态超长的弛豫时间(1.5 ns),该激发态载流子寿命要比体内载流子寿命长两个量级.该工作证实体态和拓扑边缘态具有明显不同的光学和光电响应行为,为未来设计新型红外探测器提供了材料和物理基础.