原位观测单原子催化剂的结构演变:从合成到催化

Lei Wang , Shuyuan Lyu , Shuohao Li
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引用次数: 0

摘要

原子分散的单原子催化剂(SAC)具有很高的原子利用效率和特定选择性,因此在过去十年中得到了广泛的研究。尽管人们提出了许多策略来获得高密度和高稳定性的 SAC,但反应过程中发生的转化机制仍不清楚。本综述总结了 SAC 在制备过程中的结构演变,以及在环境条件下利用各种电子显微镜技术在原子尺度上进行的反应。目前有关 SACs 的最新环境电子显微镜研究主要集中在多孔碳、金属或金属氧化物以及一些特定的复合材料上。本研究还探讨了 SAC 在各种反应条件下的动态演化。最后,我们强调了当前研究面临的挑战和不足,并展望了未来探索 SACs 的环境策略。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

In-situ observation of structural evolution of single-atom catalysts: From synthesis to catalysis

In-situ observation of structural evolution of single-atom catalysts: From synthesis to catalysis

Atomically dispersed single-atom catalysts (SACs) have been extensively studied over the past decade because of their high atom utilization efficiencies and specific selectivities. Although numerous strategies have been proposed to obtain SACs with high densities and stabilities, the transformation mechanism that occurs during the reaction is still unclear. This review summarizes the structural evolution of SACs in the preparation process and reaction with various electron microscopy techniques at atomic scale under environmental conditions. Current state-of-the-art environmental electron microscopy studies on SACs mainly focus on porous carbons, metals or metal oxides, and some specific composite materials. The dynamic evolution of SACs under various reaction conditions is also investigated in this study. Finally, we highlight the challenges and drawbacks of the current studies and the prospects for the future exploration of SACs with environmental strategies.

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