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液体环境下透射电子显微镜中荷电固-液界面的原子动力学

Atomic dynamics of electrified solid-liquid interfaces in liquid-cell TEM.

机构信息

Materials Sciences Division, Lawrence Berkeley National Laboratory, Berkeley, CA, USA.

Harvard John A. Paulson School of Engineering and Applied Sciences, Harvard University, Cambridge, MA, USA.

出版信息

Nature. 2024 Jun;630(8017):643-647. doi: 10.1038/s41586-024-07479-w. Epub 2024 Jun 19.

Abstract

Electrified solid-liquid interfaces (ESLIs) play a key role in various electrochemical processes relevant to energy, biology and geochemistry. The electron and mass transport at the electrified interfaces may result in structural modifications that markedly influence the reaction pathways. For example, electrocatalyst surface restructuring during reactions can substantially affect the catalysis mechanisms and reaction products. Despite its importance, direct probing the atomic dynamics of solid-liquid interfaces under electric biasing is challenging owing to the nature of being buried in liquid electrolytes and the limited spatial resolution of current techniques for in situ imaging through liquids. Here, with our development of advanced polymer electrochemical liquid cells for transmission electron microscopy (TEM), we are able to directly monitor the atomic dynamics of ESLIs during copper (Cu)-catalysed CO electroreduction reactions (COERs). Our observation reveals a fluctuating liquid-like amorphous interphase. It undergoes reversible crystalline-amorphous structural transformations and flows along the electrified Cu surface, thus mediating the crystalline Cu surface restructuring and mass loss through the interphase layer. The combination of real-time observation and theoretical calculations unveils an amorphization-mediated restructuring mechanism resulting from charge-activated surface reactions with the electrolyte. Our results open many opportunities to explore the atomic dynamics and its impact in broad systems involving ESLIs by taking advantage of the in situ imaging capability.

摘要

电固液界面(ESLIs)在与能源、生物学和地球化学相关的各种电化学过程中起着关键作用。在带电界面处的电子和质量输运可能导致结构修饰,从而显著影响反应途径。例如,反应过程中电催化剂表面重构可以极大地影响催化机制和反应产物。尽管其重要性,但是由于处于液体电解质中,并且由于当前用于通过液体进行原位成像的技术的空间分辨率有限,因此直接探测电偏压下固液界面的原子动力学具有挑战性。在这里,通过我们开发的用于透射电子显微镜(TEM)的先进聚合物电化学液体池,我们能够直接监测铜(Cu)催化的 CO 电还原反应(COER)过程中 ESLIs 的原子动力学。我们的观察结果揭示了一种波动的液态无定形中间相。它经历了可逆的结晶-无定形结构转变,并沿着带电的 Cu 表面流动,从而通过中间相层介导结晶 Cu 表面重构和质量损失。实时观察和理论计算的结合揭示了一种由电解质中带电荷的表面反应激活的非晶化介导的重构机制。我们的结果通过利用原位成像能力,为探索广泛涉及 ESLIs 的系统中的原子动力学及其影响提供了许多机会。

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