Current Opinion in Electrochemistry最新文献

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In-situ spectroelectrochemical analysis for understanding photophysical properties of halide perovskite nanocrystals 了解卤化物钙钛矿纳米晶体光物理性质的原位光谱电化学分析
IF 7.9 2区 化学
Current Opinion in Electrochemistry Pub Date : 2025-02-27 DOI: 10.1016/j.coelec.2025.101676
Byeongsung Kim , Bárbara Vallejos-Díaz , Andrés F. Gualdrón-Reyes , Seog Joon Yoon , Donghoon Han
{"title":"In-situ spectroelectrochemical analysis for understanding photophysical properties of halide perovskite nanocrystals","authors":"Byeongsung Kim ,&nbsp;Bárbara Vallejos-Díaz ,&nbsp;Andrés F. Gualdrón-Reyes ,&nbsp;Seog Joon Yoon ,&nbsp;Donghoon Han","doi":"10.1016/j.coelec.2025.101676","DOIUrl":"10.1016/j.coelec.2025.101676","url":null,"abstract":"<div><div>Halide perovskite nanocrystals (PNCs) are promising materials for optoelectronic devices and photocatalysts in solar photoelectrochemical (PEC) reactions due to their redox properties. These systems rely on effective charge separation, recombination, and transport under electrochemical bias or light irradiation within charge-transporting environments. However, the stability of PNCs is significantly influenced by the solvents and electrolytes used, often leading to irreversible structural transformations and loss of intrinsic properties. This review emphasizes the importance of electrochemical and <em>in-situ</em> spectroelectrochemical techniques for characterizing PNCs’ redox properties, band structure, and halide defect sites that drive redox reactions and structural deformation. The discussion provides insights into modifying PNCs for use in optoelectronic devices or PEC cells and introduces innovative strategies to enhance their structural stability and improve device performance. This comprehensive analysis aims to bridge material stability and functional optimization in PNC-based applications.</div></div>","PeriodicalId":11028,"journal":{"name":"Current Opinion in Electrochemistry","volume":"51 ","pages":"Article 101676"},"PeriodicalIF":7.9,"publicationDate":"2025-02-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143636289","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Intricacies in the electrochemical interface due to the surface structure and surface electronics states and their probing 由于表面结构和表面电子状态及其探测而导致的电化学界面的复杂性
IF 7.9 2区 化学
Current Opinion in Electrochemistry Pub Date : 2025-02-27 DOI: 10.1016/j.coelec.2025.101675
Ashis Kumar Satpati , Sudipa Manna
{"title":"Intricacies in the electrochemical interface due to the surface structure and surface electronics states and their probing","authors":"Ashis Kumar Satpati ,&nbsp;Sudipa Manna","doi":"10.1016/j.coelec.2025.101675","DOIUrl":"10.1016/j.coelec.2025.101675","url":null,"abstract":"<div><div>Electrochemical interface is complex, which has led to significant research interest in the field of analytical chemistry, biochemistry, and materials science. The present article provides a brief overview of the surface structure, surface electronic states, and their electrochemical aspects that are having implications in the energy harvesting and storage and also in the development of sensor. Discussions have been extended to the surface states in layer materials, single atom catalysis (SAC), and dual atom catalysis (DAC) along with their brief synthesis protocols. A few important characterization tools, along with examples, are discussed in this short review.</div></div>","PeriodicalId":11028,"journal":{"name":"Current Opinion in Electrochemistry","volume":"51 ","pages":"Article 101675"},"PeriodicalIF":7.9,"publicationDate":"2025-02-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143683072","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Throwing light on synthetic molecular photoelectrocatalysis (part I): Coupling both techniques and results interpretation 揭示合成分子光电催化(第一部分):耦合技术和结果解释
IF 7.9 2区 化学
Current Opinion in Electrochemistry Pub Date : 2025-02-25 DOI: 10.1016/j.coelec.2025.101673
Erick Steven Patiño-Alonzo , José Manuel Ramos-Villaseñor , Julio Romero-Ibañez , Bernardo A. Frontana-Uribe
{"title":"Throwing light on synthetic molecular photoelectrocatalysis (part I): Coupling both techniques and results interpretation","authors":"Erick Steven Patiño-Alonzo ,&nbsp;José Manuel Ramos-Villaseñor ,&nbsp;Julio Romero-Ibañez ,&nbsp;Bernardo A. Frontana-Uribe","doi":"10.1016/j.coelec.2025.101673","DOIUrl":"10.1016/j.coelec.2025.101673","url":null,"abstract":"<div><div>The conjunction of organic electrosynthesis (OES) and photoredox catalysis (PRC), coined as molecular photoelectrocatalysis (M-PEC), allows the generation of highly reducing/oxidizing species. Albeit short-lived, these species activate molecules to construct synthetically valuable intermediates with an energy requirement that would normally be out of the reach of PRC or OES alone. Nevertheless, it is not easy to do so efficiently, as PRC and OES have their own experimental challenges, and coupling both techniques adds even more complexity. Several authors have enthusiastically accepted the challenge of maneuvering through that complexity in the laboratory. This first part discusses the experiments used in fundamental studies on M-PEC, focusing on how valuable information is obtained through analytical techniques, and its use to favor the M-PEC reaction performance. This data lead to a better understanding of these reactions and increase the probability of success in synthetic applications.</div></div>","PeriodicalId":11028,"journal":{"name":"Current Opinion in Electrochemistry","volume":"51 ","pages":"Article 101673"},"PeriodicalIF":7.9,"publicationDate":"2025-02-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143683068","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Throwing Light on Synthetic Molecular Photoelectrocatalysis (Part II): selected recent transformations of organic compounds and a future perspective in organic synthesis 揭示合成分子光电催化(第二部分):有机化合物的最新转化和有机合成的未来展望
IF 7.9 2区 化学
Current Opinion in Electrochemistry Pub Date : 2025-02-25 DOI: 10.1016/j.coelec.2025.101674
Erick Steven Patiño-Alonzo , José Manuel Ramos-Villaseñor , Julio Romero-Ibañez , Bernardo A. Frontana-Uribe
{"title":"Throwing Light on Synthetic Molecular Photoelectrocatalysis (Part II): selected recent transformations of organic compounds and a future perspective in organic synthesis","authors":"Erick Steven Patiño-Alonzo ,&nbsp;José Manuel Ramos-Villaseñor ,&nbsp;Julio Romero-Ibañez ,&nbsp;Bernardo A. Frontana-Uribe","doi":"10.1016/j.coelec.2025.101674","DOIUrl":"10.1016/j.coelec.2025.101674","url":null,"abstract":"<div><div>Photoredox catalysis (PRC) and organic electrosynthesis (OES) have demonstrated their value in activating molecules and achieving important chemical transformations that would be impossible by other conventional strategies. Although there are specific situations where these techniques have yet to be effective alone, their combination, molecular photoelectrocatalysis (M-PEC), has made it possible to achieve transformations of molecules with otherwise unattainable redox potentials. In this current opinion, we analyze how M-PEC has enhanced or unlocked some selected transformations. Particularly, M-PEC variants of olefination, imine reduction, oxygenation of C(sp3)-H bonds, C(sp<sup>2</sup>)-H trifluoromethylation, C(sp<sup>2</sup>)-F functionalization, C(sp<sup>3</sup>)-X borylation will be revised and compared to their PRC and OES counterparts to highlight the importance of adapting (or combining) both techniques in constructing molecules. Also, a section related to asymmetric M-PEC is reviewed.</div></div>","PeriodicalId":11028,"journal":{"name":"Current Opinion in Electrochemistry","volume":"51 ","pages":"Article 101674"},"PeriodicalIF":7.9,"publicationDate":"2025-02-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143636288","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Advances in electro-optical methods for monitoring confined spaces 监测密闭空间的光电方法研究进展
IF 7.9 2区 化学
Current Opinion in Electrochemistry Pub Date : 2025-02-20 DOI: 10.1016/j.coelec.2025.101672
Dong Liu , Siyuan Wang , Shuda Liu , Yi-Lun Ying , Yi-Tao Long
{"title":"Advances in electro-optical methods for monitoring confined spaces","authors":"Dong Liu ,&nbsp;Siyuan Wang ,&nbsp;Shuda Liu ,&nbsp;Yi-Lun Ying ,&nbsp;Yi-Tao Long","doi":"10.1016/j.coelec.2025.101672","DOIUrl":"10.1016/j.coelec.2025.101672","url":null,"abstract":"<div><div>Understanding the interfacial behaviors of electroactive materials at the electrode is critically important for advancing electrochemical sensing and catalysis. Coupling electrochemistry with optical methods is emerging as a powerful tool for single-entity analysis, favoring in-depth insights into electrochemical processes. This review focuses on recent advances in electro-optical methods for monitoring confined spaces. The effects from light irradiation on the regulation of electrochemical behaviors of probes at nano/microelectrode are discussed, as revealed through collision electrochemistry-based strategies for single-entity analysis. Advances in the coupling of electrochemistry with fluorescence for the detection of single molecules and single cells are summarized. Finally, we highlight the achievements in electrochemical surface-enhanced Raman spectroscopy for interpreting redox reaction mechanisms at metal confinement.</div></div>","PeriodicalId":11028,"journal":{"name":"Current Opinion in Electrochemistry","volume":"51 ","pages":"Article 101672"},"PeriodicalIF":7.9,"publicationDate":"2025-02-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143580147","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Atomistic simulations of heterogeneous electrocatalysis at the center of sustainable carbon feedstocks 多相电催化在可持续碳原料中心的原子模拟
IF 7.9 2区 化学
Current Opinion in Electrochemistry Pub Date : 2025-02-14 DOI: 10.1016/j.coelec.2025.101671
Stefan Ringe , Gabriele Raabe
{"title":"Atomistic simulations of heterogeneous electrocatalysis at the center of sustainable carbon feedstocks","authors":"Stefan Ringe ,&nbsp;Gabriele Raabe","doi":"10.1016/j.coelec.2025.101671","DOIUrl":"10.1016/j.coelec.2025.101671","url":null,"abstract":"<div><div>In the face of global warming, the electrochemical valorization of sustainable carbon feedstocks has a high potential to advance green chemistry and promote environmentally friendly practices. Computational simulations have become indispensable in shedding light on specific aspects of electrocatalytic processes. Modern techniques incorporate the effects of the electric double layer, enhancing their ability to model realistic systems. This review provides an overview and critical discussion of the latest developments. Density functional theory remains the preferred method for studying electrode reactions and interfacial effects on stationary or short-time scales. In contrast, force field-based methods excel at providing a full statistical sampling of solid–liquid interfaces. Machine learning techniques represent a critical step toward desirable multi-purpose, multi-scale methods that deliver high accuracy and coupling across multiple time and length scales.</div></div>","PeriodicalId":11028,"journal":{"name":"Current Opinion in Electrochemistry","volume":"51 ","pages":"Article 101671"},"PeriodicalIF":7.9,"publicationDate":"2025-02-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143644151","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Prospects of using high entropy oxides as catalysts for the oxygen evolution reaction 高熵氧化物作为析氧反应催化剂的展望
IF 7.9 2区 化学
Current Opinion in Electrochemistry Pub Date : 2025-02-13 DOI: 10.1016/j.coelec.2025.101670
Katrine Louise Svane
{"title":"Prospects of using high entropy oxides as catalysts for the oxygen evolution reaction","authors":"Katrine Louise Svane","doi":"10.1016/j.coelec.2025.101670","DOIUrl":"10.1016/j.coelec.2025.101670","url":null,"abstract":"<div><div>High entropy oxides (HEOs), containing five or more different metal atoms in addition to oxygen, present a large composition space with rich opportunity to optimise the material properties towards specific applications. Here, the potential of HEOs as electrocatalysts for the oxygen evolution reaction is reviewed. Using rutile oxides as an example, it is demonstrated how the balance between different reaction pathways can be modified by alloying, affecting both activity and stability. Furthermore, alloying leads to changes in the electronic structure, including changes in conductivity and charge transfer between elements. For rutile oxides, the charge transfer improves the activity of the less active elements; however, it correlates with a favourable enthalpy of mixing that may hamper the formation of a randomly ordered crystal. Although these insights may be used to narrow the field of candidate materials, the complementary development of experimental and theoretical models capable of identifying relevant compositions remains important.</div></div>","PeriodicalId":11028,"journal":{"name":"Current Opinion in Electrochemistry","volume":"51 ","pages":"Article 101670"},"PeriodicalIF":7.9,"publicationDate":"2025-02-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143547825","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Grand canonical view on electrochemical energetics at applied potential in a nutshell 应用电位下电化学能量学的大规范观点概述
IF 7.9 2区 化学
Current Opinion in Electrochemistry Pub Date : 2025-02-07 DOI: 10.1016/j.coelec.2025.101656
Nicolas G. Hörmann
{"title":"Grand canonical view on electrochemical energetics at applied potential in a nutshell","authors":"Nicolas G. Hörmann","doi":"10.1016/j.coelec.2025.101656","DOIUrl":"10.1016/j.coelec.2025.101656","url":null,"abstract":"<div><div>In this review, I summarize the foundations and motivation of modern grand canonical descriptions of electrified interfaces, which represent a thermodynamically consistent framework for assessing electronically adiabatic energetics and kinetics as a function of the applied electrode potential. The discussion will center around the ubiquitous coupled proton-electron transfer process at electrified metal-water interfaces and highlight the conceptual differences to the classical understanding and viewpoint. Finally, I present a range of important recent insights about the energetics of protons along their (adiabatic) adsorption path.</div></div>","PeriodicalId":11028,"journal":{"name":"Current Opinion in Electrochemistry","volume":"51 ","pages":"Article 101656"},"PeriodicalIF":7.9,"publicationDate":"2025-02-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143512587","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Mass transport and heterogeneous electron transfer in high-concentration electrolytes: From conventional to two-dimensional material electrodes 高浓度电解质中的质量传递和非均质电子转移:从常规到二维材料电极
IF 7.9 2区 化学
Current Opinion in Electrochemistry Pub Date : 2025-02-07 DOI: 10.1016/j.coelec.2025.101667
Shuai Liu , Guilhem Pignol , Corinne Lagrost , Bingwei Mao , Philippe Hapiot , Jiawei Yan
{"title":"Mass transport and heterogeneous electron transfer in high-concentration electrolytes: From conventional to two-dimensional material electrodes","authors":"Shuai Liu ,&nbsp;Guilhem Pignol ,&nbsp;Corinne Lagrost ,&nbsp;Bingwei Mao ,&nbsp;Philippe Hapiot ,&nbsp;Jiawei Yan","doi":"10.1016/j.coelec.2025.101667","DOIUrl":"10.1016/j.coelec.2025.101667","url":null,"abstract":"<div><div>Two-dimensional materials in high-concentration electrolytes have emerged as promising candidates for studying heterogeneous electron transfer kinetics due to their diverse applications in energy storage and conversion. However, the existing theoretical frameworks and experimental techniques often fall short in accurately describing these complex systems. A comprehensive understanding of electron transfer processes at the electrode–electrolyte interface in high-concentration electrolytes is crucial for advancing our knowledge of interfacial electrochemical phenomena and refining theoretical models. This review summarizes recent efforts focusing on the heterogeneous electron transfer at the electrode–high-concentration electrolyte interfaces, particularly ionic liquids and deep eutectic solvents, and we briefly assess the limitations of existing kinetic studies and outline potential avenues with emphasizing the strengthen of scanning electrochemical microscopy in future research in this field.</div></div>","PeriodicalId":11028,"journal":{"name":"Current Opinion in Electrochemistry","volume":"51 ","pages":"Article 101667"},"PeriodicalIF":7.9,"publicationDate":"2025-02-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143488445","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Advances in CO2 reduction on bulk and two-dimensional electrocatalysts: From first principles to experimental outcomes 体积和二维电催化剂上CO2还原的进展:从第一原理到实验结果
IF 7.9 2区 化学
Current Opinion in Electrochemistry Pub Date : 2025-02-06 DOI: 10.1016/j.coelec.2025.101668
Raghavendra Rajagopalan , Shivam Chaturvedi , Neeru Chaudhary , Abhijit Gogoi , Tej S. Choksi , Ananth Govind Rajan
{"title":"Advances in CO2 reduction on bulk and two-dimensional electrocatalysts: From first principles to experimental outcomes","authors":"Raghavendra Rajagopalan ,&nbsp;Shivam Chaturvedi ,&nbsp;Neeru Chaudhary ,&nbsp;Abhijit Gogoi ,&nbsp;Tej S. Choksi ,&nbsp;Ananth Govind Rajan","doi":"10.1016/j.coelec.2025.101668","DOIUrl":"10.1016/j.coelec.2025.101668","url":null,"abstract":"<div><div>Designing catalyst materials for the electrochemical carbon dioxide reduction reaction (CO<sub>2</sub>RR) requires an understanding of the underlying thermodynamics and kinetics. In this review, we discuss the characteristics of two-dimensional (2D) and bulk materials, which distinguish their catalytic properties. We map catalyst performance in the faradaic efficiency–applied potential space for various hydrocarbons and oxygenates on these catalyst classes. We explain different approaches for modeling catalytic CO<sub>2</sub>RR, such as the computational hydrogen electrode, grand canonical (GC) potential kinetics, and GC density functional theory, with the lattermost accurately capturing potential-dependent kinetics. We review recent attempts made to break scaling relationships between intermediate adsorption energies and describe unique features found in 2D materials. Finally, we compare kinetics on both material classes using microkinetic modeling. We conclude that future studies should focus on realistic simulations of the electrode–electrolyte interface and combining the favorable properties of 2D and bulk materials to engineer high-performance CO<sub>2</sub>RR catalysts.</div></div>","PeriodicalId":11028,"journal":{"name":"Current Opinion in Electrochemistry","volume":"51 ","pages":"Article 101668"},"PeriodicalIF":7.9,"publicationDate":"2025-02-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143562950","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
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