Current Opinion in Electrochemistry最新文献

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Measuring the flatband potential in 2D semiconductors: Pitfalls and a possible SECCM solution 测量二维半导体中的平带电位:陷阱和可能的SECCM解决方案
IF 7.9 2区 化学
Current Opinion in Electrochemistry Pub Date : 2025-04-28 DOI: 10.1016/j.coelec.2025.101703
Ava R. Chard, Justin B. Sambur
{"title":"Measuring the flatband potential in 2D semiconductors: Pitfalls and a possible SECCM solution","authors":"Ava R. Chard,&nbsp;Justin B. Sambur","doi":"10.1016/j.coelec.2025.101703","DOIUrl":"10.1016/j.coelec.2025.101703","url":null,"abstract":"<div><div>The flatband potential (<em>V</em><sub>fb</sub>) is a critical parameter in semiconductor electrochemistry, defining the potential at which no excess charge exists at the semiconductor/electrolyte interface. It serves as a key reference for interpreting charge transfer kinetics and current–voltage behavior. However, conventional methods like Mott–Schottky analysis fail for atomically thin 2D materials due to the breakdown of the depletion approximation. This perspective examines the limitations of traditional <em>V</em><sub>fb</sub> measurements for 2D semiconductors and the experimental challenges that arise. To address these issues, we propose using scanning electrochemical cell microscopy (SECCM) to spatially resolve the potential of zero charge (<em>V</em><sub>pzc</sub>), equivalent to <em>V</em><sub>fb</sub>. This approach mitigates sample heterogeneity issues, such as pinholes or multilayer defects, and offers a pathway to more accurate electrochemical characterization. Ultimately, this method will enhance understanding of current–potential behavior in 2D materials, supporting the design of advanced systems for photoelectrocatalysis, energy conversion, and sensing.</div></div>","PeriodicalId":11028,"journal":{"name":"Current Opinion in Electrochemistry","volume":"52 ","pages":"Article 101703"},"PeriodicalIF":7.9,"publicationDate":"2025-04-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144083872","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
Operando methods for the elucidation of electrolyte effects in electrocatalysis 阐明电催化中电解质效应的操作方法
IF 7.9 2区 化学
Current Opinion in Electrochemistry Pub Date : 2025-04-17 DOI: 10.1016/j.coelec.2025.101700
Kees E. Kolmeijer, Rik V. Mom
{"title":"Operando methods for the elucidation of electrolyte effects in electrocatalysis","authors":"Kees E. Kolmeijer,&nbsp;Rik V. Mom","doi":"10.1016/j.coelec.2025.101700","DOIUrl":"10.1016/j.coelec.2025.101700","url":null,"abstract":"<div><div>The electrolyte pH, ion composition, and solvent are important design parameters in electrocatalytic systems, which directly impact the system’s catalytic activity, selectivity and stability. However, the relationship between the electrolyte composition and electrocatalytic performance is complex, and at present difficult to predict. To elucidate the underlying principles that govern electrolyte effects in electrocatalysis, <em>operando</em> techniques capable of resolving the active site structures at the electrode–electrolyte interface play a crucial role. Here, we review the current capabilities of these <em>operando</em> techniques and analyze how they can be used to find the rules of the game for electrolyte engineering.</div></div>","PeriodicalId":11028,"journal":{"name":"Current Opinion in Electrochemistry","volume":"51 ","pages":"Article 101700"},"PeriodicalIF":7.9,"publicationDate":"2025-04-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143931798","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
Effects of electrolyte cations on the oxygen evolution reaction 电解质阳离子对析氧反应的影响
IF 7.9 2区 化学
Current Opinion in Electrochemistry Pub Date : 2025-04-16 DOI: 10.1016/j.coelec.2025.101697
Boqiang Chen, Dunwei Wang, Matthias M. Waegele
{"title":"Effects of electrolyte cations on the oxygen evolution reaction","authors":"Boqiang Chen,&nbsp;Dunwei Wang,&nbsp;Matthias M. Waegele","doi":"10.1016/j.coelec.2025.101697","DOIUrl":"10.1016/j.coelec.2025.101697","url":null,"abstract":"<div><div>The oxidation of water to molecular oxygen, referred to as the oxygen evolution reaction (OER), is often the kinetic bottleneck in the formation of renewable fuels. The rate of the OER is strongly dependent on electrolyte properties, such as pH, ionic strength, and the identities of anions and cations. To advance OER catalysis, it is essential to understand the mechanisms by which the electrolyte influences the rate of the OER. In this article, we discuss recent work concerned with the effects of electrolyte cations on the OER. We examine how cations modulate apparent Arrhenius parameters, their effects on the interfacial water structure, their direct interactions with intermediates, and how they alter the rate through non-kinetic effects. The survey reveals that cations can influence the OER through a diversity of mechanisms and that their effects strongly depend on catalyst composition and reaction conditions.</div></div>","PeriodicalId":11028,"journal":{"name":"Current Opinion in Electrochemistry","volume":"51 ","pages":"Article 101697"},"PeriodicalIF":7.9,"publicationDate":"2025-04-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143911477","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
3D-printed thermoplastic sensors for electrochemical biosensing 用于电化学生物传感的3d打印热塑性传感器
IF 7.9 2区 化学
Current Opinion in Electrochemistry Pub Date : 2025-04-15 DOI: 10.1016/j.coelec.2025.101699
Christos Kokkinos
{"title":"3D-printed thermoplastic sensors for electrochemical biosensing","authors":"Christos Kokkinos","doi":"10.1016/j.coelec.2025.101699","DOIUrl":"10.1016/j.coelec.2025.101699","url":null,"abstract":"<div><div>While the importance of electrochemical sensors in diagnostics is well established—offering rapid and selective biomarker determinations in complex matrices—there is a continuous request for simpler, more cost-effective and sustainable sensor fabrication procedures. 3D-printing technologies, particularly fused deposition modeling (FDM), allow for the digital, rapid, and labor-free fabrication of disposable (bio)sensors, while also enabling the printing of fully integrated, miniaturized plastic devices within points-of-need settings. This review highlights recent trends in the development of 3D-printed thermoplastic (bio)sensors and mini devices that utilize bioelements and artificial biomimetic materials for biomolecules monitoring. Additionally, it provides an overview of the synthesis of tailor-made 3D printable conductive filaments incorporating biofunctional materials, from which ready-to-use sensors are fabricated for direct biosensing.</div></div>","PeriodicalId":11028,"journal":{"name":"Current Opinion in Electrochemistry","volume":"51 ","pages":"Article 101699"},"PeriodicalIF":7.9,"publicationDate":"2025-04-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143906727","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
Cation effects in electrochemical CO2 reduction 电化学CO2还原中的阳离子效应
IF 7.9 2区 化学
Current Opinion in Electrochemistry Pub Date : 2025-04-14 DOI: 10.1016/j.coelec.2025.101698
Adnan Ozden , Yanwei Lum
{"title":"Cation effects in electrochemical CO2 reduction","authors":"Adnan Ozden ,&nbsp;Yanwei Lum","doi":"10.1016/j.coelec.2025.101698","DOIUrl":"10.1016/j.coelec.2025.101698","url":null,"abstract":"<div><div>Electrochemical CO<sub>2</sub> reduction (CO<sub>2</sub>R) provides a pathway toward the sustainable production of chemicals. Recent catalyst- and system-level innovations have enabled electrosynthesis of multi-carbon products at practical productivities (&gt;200 mA cm<sup>−2</sup>) and single-pass CO<sub>2</sub> conversion efficiencies (&gt;80 %). However, practical CO<sub>2</sub>R requires high single product selectivity (&gt;85 %) without compromising readily-achieved metrics. Coupling these metrics in a single system warrants clear understanding of the electrical double layer at the catalyst–electrolyte interface. Combining selective catalysts with cation effects can effectively tune CO<sub>2</sub>R kinetics at the catalyst–electrolyte interface. Here we overview recent progress and current understanding on the sophisticated nature of the cation effects and underscore critical parameters that influence cation distributions in the electrical double layer. We highlight the emerging characterization and computational approaches to elucidate cation effects on CO<sub>2</sub>R. Finally, we emphasize research directions through which cation effects could be coupled with other micro-reaction environment tuning strategies for further selectivity and efficiency improvements.</div></div>","PeriodicalId":11028,"journal":{"name":"Current Opinion in Electrochemistry","volume":"51 ","pages":"Article 101698"},"PeriodicalIF":7.9,"publicationDate":"2025-04-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143886949","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
Nanoconfined constructs for electrochemical aptamer-based in vivo biosensing 基于电化学适体体的体内生物传感纳米结构
IF 7.9 2区 化学
Current Opinion in Electrochemistry Pub Date : 2025-04-11 DOI: 10.1016/j.coelec.2025.101695
Grayson F. Huldin , Junming Huang , Kaiyu X. Fu
{"title":"Nanoconfined constructs for electrochemical aptamer-based in vivo biosensing","authors":"Grayson F. Huldin ,&nbsp;Junming Huang ,&nbsp;Kaiyu X. Fu","doi":"10.1016/j.coelec.2025.101695","DOIUrl":"10.1016/j.coelec.2025.101695","url":null,"abstract":"<div><div>In the last two decades, electrochemical aptamer-based (EAB) sensors have grown rapidly due to their high sensitivity, good selectivity, excellent biocompatibility, and flexible architectures among the wide range of biosensing platforms. Yet, achieving continuous, long-term, and <em>in vivo</em> monitoring remains challenging due to obstacles like device miniaturization, signal amplification, and sensor stability. To tackle these hurdles, researchers are leveraging nanostructured electrodes, leading to new EAB designs with improved <em>in vivo</em> biosensing performance. This opinion provides a brief overview of the development and latest progress in nanoconfined constructs for EAB <em>in vivo</em> biosensing. We illustrate fundamental sensing principles, the various nanostructures being explored, and their respective advantages. These nanostructured EABs hold promise for applications spanning disease diagnostics, environmental surveillance, and food safety management. Finally, we address the persistent challenges EABs face and discuss potential future directions, offering insights into how these sensors can continue to evolve and foster more effective healthcare technologies.</div></div>","PeriodicalId":11028,"journal":{"name":"Current Opinion in Electrochemistry","volume":"51 ","pages":"Article 101695"},"PeriodicalIF":7.9,"publicationDate":"2025-04-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143895850","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
Expanding our view on active sites in electrocatalysis 拓展了我们对电催化活性位点的认识
IF 7.9 2区 化学
Current Opinion in Electrochemistry Pub Date : 2025-04-11 DOI: 10.1016/j.coelec.2025.101692
Ana M. Gómez–Marín , Katrin F. Domke
{"title":"Expanding our view on active sites in electrocatalysis","authors":"Ana M. Gómez–Marín ,&nbsp;Katrin F. Domke","doi":"10.1016/j.coelec.2025.101692","DOIUrl":"10.1016/j.coelec.2025.101692","url":null,"abstract":"<div><div>At the heart of electrocatalyst design and development lies the concept of active sites that are usually identified as those sites for adsorption where the conversion of interest occurs. However, electrochemical interfaces are complex systems where the exact structure and dynamics of interfacial species during a reaction greatly depend on the local reactive microenvironment, including co-adsorbates and solvent molecules, that may include structural transformations upon adsorption, the charge-transfer dynamics, and/or the <em>x,y</em> charge-induced electric field distribution. We review the concept of active sites in electrocatalysis within these lines in light of recent studies that point out the necessity to expand the still widely spread idea of quasi-static atomic-scale sites toward the picture of a dynamically reactive microenvironment: the active site can extend over several tens on nanometers due to surface structural transformations during the reaction, includes interdependent components such as electrode and electrolyte as well as target reactant geometric and electronic structures, and often spontaneously rearranges <em>during</em> the electrocatalytic reaction. Thus, to define optimal reactions conditions, the reactive microenvironment as a whole needs to be considered.</div></div>","PeriodicalId":11028,"journal":{"name":"Current Opinion in Electrochemistry","volume":"51 ","pages":"Article 101692"},"PeriodicalIF":7.9,"publicationDate":"2025-04-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143906726","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
Recent advancements related to silver-based electrocatalysts for carbon dioxide reduction reaction to carbon monoxide 银基电催化剂在二氧化碳还原成一氧化碳反应中的最新进展
IF 7.9 2区 化学
Current Opinion in Electrochemistry Pub Date : 2025-04-11 DOI: 10.1016/j.coelec.2025.101696
Cristina Tricella, Mohsin Muhyuddin, Roberto Nisticò, Sergio Tosoni, Carlo Santoro
{"title":"Recent advancements related to silver-based electrocatalysts for carbon dioxide reduction reaction to carbon monoxide","authors":"Cristina Tricella,&nbsp;Mohsin Muhyuddin,&nbsp;Roberto Nisticò,&nbsp;Sergio Tosoni,&nbsp;Carlo Santoro","doi":"10.1016/j.coelec.2025.101696","DOIUrl":"10.1016/j.coelec.2025.101696","url":null,"abstract":"<div><div>Electrochemical CO<sub>2</sub> reduction reaction (CO<sub>2</sub>RR) is a progressive step toward the reduction of planetary carbon footprint. In this way, CO<sub>2</sub> can be valorized into valuable products, and particularly, CO<sub>2</sub> can be reduced to gaseous products (e.g. CO or methane) or into liquid products (i.e. C<sub>1</sub>, C<sub>2</sub>, C<sub>3</sub>, etc.). Interestingly, CO<sub>2</sub>RR and hydrogen reduction reaction (HER) are competitive reactions; therefore, syngas (CO + H<sub>2</sub>) can also be produced at different H<sub>2</sub>:CO ratios. Depending on the transition metal used as an electrocatalyst for the CO<sub>2</sub>RR, the selectivity toward a specific product can be properly tuned. In this opinion, the attention is focused on the reduction of CO<sub>2</sub> to CO using Ag-based electrocatalysts. Reaction mechanisms to produce H<sub>2</sub>, CO, and formate are described and highlighted. The effect of the morphology is described, and the performance of Ag-based electrocatalysts toward CO<sub>2</sub>-to-CO and syngas production is presented, focusing on the recent available literature.</div></div>","PeriodicalId":11028,"journal":{"name":"Current Opinion in Electrochemistry","volume":"51 ","pages":"Article 101696"},"PeriodicalIF":7.9,"publicationDate":"2025-04-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143922936","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
Unlocking emerging catalytic applications of single-entity collision electrochemistry 解锁单一实体碰撞电化学的新兴催化应用
IF 7.9 2区 化学
Current Opinion in Electrochemistry Pub Date : 2025-04-08 DOI: 10.1016/j.coelec.2025.101694
Yixiao Wang, Wei Ma
{"title":"Unlocking emerging catalytic applications of single-entity collision electrochemistry","authors":"Yixiao Wang,&nbsp;Wei Ma","doi":"10.1016/j.coelec.2025.101694","DOIUrl":"10.1016/j.coelec.2025.101694","url":null,"abstract":"<div><div>Establishing the link between catalytic activity and the structure of individual entities in an ensemble system can be challenging, as the presented data are often averaged in bulk system. Single-entity collision electrochemistry (SECE) stands out as a powerful tool for investigating the intrinsic catalytic activities of single entities with high sensitivity, high throughput, and fast response. Recent advancements in SECE technology have demonstrated significant potential in various emerging applications, particularly in the rapid screening of catalysts and supports, in situ identification of catalytic activity and assembly structure, and real-time monitoring of dynamic catalytic behaviors. This review summarizes the recent research results, pioneering studies, and future trends in this field. It also discusses the challenges faced by SECE in exploring new application scenarios.</div></div>","PeriodicalId":11028,"journal":{"name":"Current Opinion in Electrochemistry","volume":"51 ","pages":"Article 101694"},"PeriodicalIF":7.9,"publicationDate":"2025-04-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143891670","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
Overcoming dichotomy between surface and bulk of electrode: Conducting polymers 克服电极表面和体积之间的二分法:导电聚合物
IF 7.9 2区 化学
Current Opinion in Electrochemistry Pub Date : 2025-04-04 DOI: 10.1016/j.coelec.2025.101691
Viktor Gueskine , Penghui Ding , Reverant Crispin , Mikhail Vagin
{"title":"Overcoming dichotomy between surface and bulk of electrode: Conducting polymers","authors":"Viktor Gueskine ,&nbsp;Penghui Ding ,&nbsp;Reverant Crispin ,&nbsp;Mikhail Vagin","doi":"10.1016/j.coelec.2025.101691","DOIUrl":"10.1016/j.coelec.2025.101691","url":null,"abstract":"<div><div>The surface of the solid-state electrodes constructed from atomic crystals is inherently uncertain due to its chemical unsaturation as its atoms lack the surrounding by the atoms of the same type as in the bulk and its exposure to a different phase. This complicates the evaluation of properties for the high surface area electrodes achieved by porosity. Conducting polymers (CP) are intrinsically conductive molecular solids built from polymeric conjugated molecules without covalent bounds between them. The molecular character of CP implies the translation of identical state from the bulk to the surface of the film without additional surface-induced defects. The absence of covalent bonds between backbones enables the access of external electrolyte to individual chain of CP forming the electrical double layer at the molecular scale. Here we discuss the combination of molecular porosity of CP with its inherent selectivity of ion transport as a special case of porous electrode. We also discuss how the Gibbs phase rule can help in understanding CP electrochemistry.</div></div>","PeriodicalId":11028,"journal":{"name":"Current Opinion in Electrochemistry","volume":"51 ","pages":"Article 101691"},"PeriodicalIF":7.9,"publicationDate":"2025-04-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143863972","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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