基于同步加速器的Operando XRD和Operando扫描x射线显微镜研究了高c速率动态锂(de)插入途径

Bonho Koo, Jinkyu Chung, Juwon Kim, Hyejeong Hyun, Dimitrios Fraggedakis, Jian Wang, Namdong Kim, Markus Weigand, Tae Joo Shin, Daan Hein Alsem, Norman Salmon, Martin Z. Bazant, Jongwoo Lim
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摘要

锂离子插入动力学从根本上取决于(不)充电过程中的相变行为,了解速率相关动力学对大功率电池的发展至关重要。在高碳率下,动力学滞后被放大,相演化变得不均匀和不可预测。具体来说,包括LiNi x Mn y Co z o2 (NMC)和lifepo4 (LFP)在内的大多数电池电极的放电比充电更缓慢。在这里,我们开发了一种operando软x射线显微镜,在宽循环速率(0.01 - 10℃)范围内同时观察facet控制的单个电池颗粒中的表面电荷转移和大块锂扩散。我们的研究结果明确地表明,快速充电和快速放电之间的动态不对称分别源于自抑制富锂和自催化贫锂表面结构域。此外,我们开发了基于同步加速器的operando快速XRD来跟踪快速循环过程中的相演化。我们直接观察到,在高Li含量下,缓慢的Li扩散在充放电过程中引起了不同的相变,在充放电过程中分别发生了强烈的相分离和均匀的相变。此外,通过电化学控制NCM颗粒内锂离子浓度分布,即使在7c -速率下,相分离途径也可以重定向到固溶动力学。我们的工作为开发高功率应用和超快充电协议奠定了基础(图1)
本文章由计算机程序翻译,如有差异,请以英文原文为准。
High C-Rate Dynamic Lithium (de)Insertion Pathway Investigated via Synchrotron-Based Operando XRD and Operando Scanning x-Ray Microscopy
Lithium-ion insertion kinetics fundamentally hinges upon phase transformation behavior during (dis)charging and understanding the rate-dependent kinetics is crucial for the development of high-power batteries. At high c-rates, kinetic hysteresis is amplified and phase evolution becomes heterogeneous and unpredictable. Specifically, discharge becomes more sluggish than charging of most battery electrodes including LiNi x Mn y Co z O 2 (NMC) and LiFePO 4 (LFP). Here, we developed an operando soft x-ray microscopy to simultaneously observe surface charge transfer and bulk lithium diffusion in facet-controlled individual battery particles over a wide range of cycling rates (0.01 – 10C). Our result unambiguously reveals that dynamic asymmetry between fast charging and discharging originates from auto-inhibitory Li-rich and autocatalytic Li-poor surface domains, respectively. In addition, we developed synchrotron-based operando fast XRD to track phase evolution during fast cycling. We directly observed that sluggish Li diffusion at high Li content induces different phase transformations during charging and discharging, with strong phase separation and homogeneous phase transformation during charging and discharging, respectively. Moreover, by electrochemically manipulating the lithium-ion concentration distribution within NCM particles, phase separation pathway could be redirected to solid-solution kinetics even at 7 C-rate. Our work lays the groundwork for developing high-power applications and ultrafast charging protocols Figure 1
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