...
首页> 外文期刊>ACS nano >Decoupling electrochemical reaction and diffusion processes in ionically-conductive solids on the nanometer scale
【24h】

Decoupling electrochemical reaction and diffusion processes in ionically-conductive solids on the nanometer scale

机译:纳米级离子导电固体中的解耦电化学反应和扩散过程

获取原文
获取原文并翻译 | 示例
           

摘要

We have developed a scanning probe microscopy approach to explore voltage-controlled ion dynamics in ionically conductive solids and decouple transport and local electrochemical reactivity on the nanometer scale. Electrochemical strain microscopy allows detection of bias-induced ionic motion through the dynamic (0.1-1 MHz) local strain. Spectroscopic modes based on low-frequency (~1 Hz) voltage sweeps allow local ion dynamics to be probed locally. The bias dependence of the hysteretic strain response accessed through first-order reversal curve (FORC) measurements demonstrates that the process is activated at a certain critical voltage and is linear above this voltage everywhere on the surface. This suggests that FORC spectroscopic ESM data separates local electrochemical reaction and transport processes. The relevant parameters such as critical voltage and effective mobility can be extracted for each location and correlated with the microstructure. The evolution of these behaviors with the charging of the amorphous Si anode in a thin-film Li-ion battery is explored. A broad applicability of this method to other ionically conductive systems is predicted.
机译:我们已经开发了一种扫描探针显微镜方法,以探索离子导电固体中电压控制的离子动力学,并在纳米尺度上解耦传输和局部电化学反应性。电化学应变显微镜可以检测通过动态(0.1-1 MHz)局部应变产生的偏向离子运动。基于低频(〜1 Hz)电压扫描的光谱模式可以对局部离子动力学进行局部探测。通过一阶反向曲线(FORC)测量获得的磁滞应变响应的偏置依赖性证明,该过程在某个临界电压下被激活,并且在表面上的任何地方都高于该电压呈线性关系。这表明FORC光谱ESM数据将局部电化学反应和传输过程分开。可以为每个位置提取诸如临界电压和有效迁移率之类的相关参数,并将其与微结构相关联。探索了随着薄膜锂离子电池中非晶硅阳极的充电,这些行为的演变。预计该方法在其他离子导电系统中的广泛应用。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

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