首页> 美国卫生研究院文献>Nature Communications >Visualization of electrochemically driven solid-state phase transformations using operando hard X-ray spectro-imaging
【2h】

Visualization of electrochemically driven solid-state phase transformations using operando hard X-ray spectro-imaging

机译:使用操作性硬X射线光谱成像可视化电化学驱动的固态相变

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

In situ techniques with high temporal, spatial and chemical resolution are key to understand ubiquitous solid-state phase transformations, which are crucial to many technological applications. Hard X-ray spectro-imaging can visualize electrochemically driven phase transformations but demands considerably large samples with strong absorption signal so far. Here we show a conceptually new data analysis method to enable operando visualization of mechanistically relevant weakly absorbing samples at the nanoscale and study electrochemical reaction dynamics of iron fluoride, a promising high-capacity conversion cathode material. In two specially designed samples with distinctive microstructure and porosity, we observe homogeneous phase transformations during both discharge and charge, faster and more complete Li-storage occurring in porous polycrystalline iron fluoride, and further, incomplete charge reaction following a pathway different from conventional belief. These mechanistic insights provide guidelines for designing better conversion cathode materials to realize the promise of high-capacity lithium-ion batteries.
机译:具有高时间,空间和化学分辨率的原位技术是理解普遍存在的固态相变的关键,这对于许多技术应用而言都是至关重要的。硬X射线光谱成像可以观察到电化学驱动的相变,但到目前为止需要具有强大吸收信号的相当大的样品。在这里,我们展示了一种概念上新颖的数据分析方法,可在纳米级对机械相关的弱吸收样品进行操作可视化,并研究氟化铁(一种有前途的高容量转化正极材料)的电化学反应动力学。在两个具有独特的微观结构和孔隙率的经过特殊设计的样品中,我们观察到在放电和充电过程中均相变化,在多孔多晶氟化铁中发生更快,更完全的锂存储,以及沿着不同于常规观念的途径进行不完全充电反应。这些机理见解为设计更好的转换阴极材料提供了指导,以实现大容量锂离子电池的前景。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号