Spatially and temporally understanding dynamic solid-electrolyte interfaces in carbon dioxide electroreduction
The ubiquity of solid-liquid interfaces in nature and the significant role of their atomic-scale structure in determining interfacial properties have led to intensive research. Particularly in electrocatalysis, however, a molecular-level picture that clearly describes the dynamic interfacial structu...
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Published in | Chemical Society reviews Vol. 52; no. 15; pp. 513 - 55 |
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Main Authors | , , , , , , , |
Format | Journal Article |
Language | English |
Published |
England
Royal Society of Chemistry
31.07.2023
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Subjects | |
Online Access | Get full text |
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Summary: | The ubiquity of solid-liquid interfaces in nature and the significant role of their atomic-scale structure in determining interfacial properties have led to intensive research. Particularly in electrocatalysis, however, a molecular-level picture that clearly describes the dynamic interfacial structures and organizations with their correlation to preferred reaction pathways in electrochemical reactions remains poorly understood. In this review, CO
2
electroreduction reaction (CO
2
RR) is spatially and temporally understood as a result of intricate interactions at the interface, in which the interfacial features are highly relevant. We start with the discussion of current understandings and model development associated with the charged electrochemical interface as well as its dynamic landscape. We further highlight the interactive dynamics from the interfacial field, catalyst surface charges and various gradients in electrolyte and interfacial water structures at interfaces under CO
2
RR working conditions, with emphasis on the interfacial-structure dependence of catalytic reactivity/selectivity. Significantly, a probing energy-dependent "
in situ
characterization map" for dynamic interfaces based on various complementary
in situ
/
operando
techniques is proposed, aiming to present a comprehensive picture of interfacial electrocatalysis and to provide a more unified research framework. Moreover, recent milestones in both experimental and theoretical aspects to establish the correct profile of electrochemical interfaces are stressed. Finally, we present key scientific challenges with related perspectives toward future opportunities for this exciting frontier.
A molecular-level picture clearly describing the dynamic interfacial interactions with their correlation to CO
2
RR properties is established, which enables us to spatially and temporally understand electrochemical reactions at the solid-liquid interface. |
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Bibliography: | Hui-Ying Tan received her master's degree in Chemistry from National Taiwan University in 2021. Currently, she continues as a research assistant in Hao Ming Chen's group. Her research focuses on the development of single atom materials for electrocatalysis. Yi-Jun Xu is a full professor working at Fuzhou University, P. R. China. He received his PhD degree from Cardiff University in 2006. From 2007 to 2009, he worked as a postdoctoral research fellow at the Fritz Haber Institute of the Max Planck Society. He is a Fellow of Royal Society of Chemistry (FRSC) and his current research interests primarily focus on heterogeneous photoredox catalysis, mainly focusing on the design of composite-based catalysts, the fundamental studies of catalyst structures and catalytic reaction mechanisms, and exploring their versatile redox catalytic applications in heterogeneous photocatalysis. Jiali Wang obtained her PhD degree in Materials Science from Northwestern Polytechnical University in 2019. After this, she joined Hao Ming Chen's group as a postdoctoral fellow at National Taiwan University. Her current research interest focuses on the development of metal-based/single-atom nanomaterials and in situ methodologies for electrochemical energy conversion and storage. Prof. Hao Ming Chen received his BSc, MSc and PhD in Chemistry from National Taiwan University, and then worked as a postdoctoral fellow in National Taiwan University. He then did his postdoctoral research at the University of California, Berkeley, and joined the Department of Chemistry, National Taiwan University, as an assistant professor in the summer of 2013 and was promoted to full professor in 2021. His current research interests include the development of in situ/operando methodology toward the liquid/solid interfacial study and the synthesis of nanomaterials for energy conversion. Ming-Yu Qi is now pursuing his PhD degree under the supervision of Prof. Yi-Jun Xu at the College of Chemistry, State Key Laboratory of Photocatalysis on Energy and Environment, Fuzhou University, P. R. China. His main research interests focus on the fabrication of semiconductor quantum dot-based composite materials for functional applications in photoredox coupled catalysis systems. Jing-Yu Li is now pursuing her PhD degree under the supervision of Prof. Yi-Jun Xu at the College of Chemistry, State Key Laboratory of Photocatalysis on Energy and Environment, Fuzhou University, P. R. China. Her current research interests focus on the synthesis and application of composite-based catalysts in synergistic dual function coupling photocatalysis. ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 14 ObjectType-Review-3 content type line 23 |
ISSN: | 0306-0012 1460-4744 1460-4744 |
DOI: | 10.1039/d2cs00441k |