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电池电极表面附近金属溶解与再沉积动力学的原位表征与调控

Operando characterization and regulation of metal dissolution and redeposition dynamics near battery electrode surface.

作者信息

Zhang Yuxin, Hu Anyang, Xia Dawei, Hwang Sooyeon, Sainio Sami, Nordlund Dennis, Michel F Marc, Moore Robert B, Li Luxi, Lin Feng

机构信息

Department of Chemistry, Virginia Tech, Blacksburg, VA, USA.

Center for Functional Nanomaterials, Brookhaven National Laboratory, Upton, NY, USA.

出版信息

Nat Nanotechnol. 2023 Jul;18(7):790-797. doi: 10.1038/s41565-023-01367-6. Epub 2023 Apr 20.

DOI:10.1038/s41565-023-01367-6
PMID:37081082
Abstract

Mn dissolution has been a long-standing, ubiquitous issue that negatively impacts the performance of Mn-based battery materials. Mn dissolution involves complex chemical and structural transformations at the electrode-electrolyte interface. The continuously evolving electrode-electrolyte interface has posed great challenges for characterizing the dynamic interfacial process and quantitatively establishing the correlation with battery performance. In this study, we visualize and quantify the temporally and spatially resolved Mn dissolution/redeposition (D/R) dynamics of electrochemically operating Mn-containing cathodes. The particle-level and electrode-level analyses reveal that the D/R dynamics is associated with distinct interfacial degradation mechanisms at different states of charge. Our results statistically differentiate the contributions of surface reconstruction and Jahn-Teller distortion to the Mn dissolution at different operating voltages. Introducing sulfonated polymers (Nafion) into composite electrodes can modulate the D/R dynamics by trapping the dissolved Mn species and rapidly establishing local Mn D/R equilibrium. This work represents an inaugural effort to pinpoint the chemical and structural transformations responsible for Mn dissolution via an operando synchrotron study and develops an effective method to regulate Mn interfacial dynamics for improving battery performance.

摘要

锰溶解一直是一个长期存在的普遍问题,对锰基电池材料的性能产生负面影响。锰溶解涉及电极-电解质界面处复杂的化学和结构转变。不断演变的电极-电解质界面给表征动态界面过程以及定量建立与电池性能的相关性带来了巨大挑战。在本研究中,我们可视化并量化了电化学操作的含锰阴极在时间和空间上分辨的锰溶解/再沉积(D/R)动力学。颗粒级和电极级分析表明,D/R动力学与不同充电状态下不同的界面降解机制相关。我们的结果从统计学上区分了表面重构和 Jahn-Teller 畸变在不同工作电压下对锰溶解的贡献。将磺化聚合物(Nafion)引入复合电极可以通过捕获溶解的锰物种并快速建立局部锰 D/R 平衡来调节 D/R 动力学。这项工作是首次通过原位同步加速器研究来确定导致锰溶解的化学和结构转变,并开发一种有效方法来调节锰界面动力学以改善电池性能。

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