• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

铂电极和玻碳电极上深共熔溶剂微分电容的直接测量

Direct Measurement of the Differential Capacitance of Deep Eutectic Solvents on Platinum and Glassy Carbon Electrodes.

作者信息

Jitvisate Monchai

机构信息

School of Physics, Institute of Science, Suranaree University of Technology, Nakhon Ratchasima, 30000, Thailand.

出版信息

J Phys Chem Lett. 2024 Sep 26;15(38):9637-9643. doi: 10.1021/acs.jpclett.4c02428. Epub 2024 Sep 16.

DOI:10.1021/acs.jpclett.4c02428
PMID:39282944
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11440589/
Abstract

Differential capacitance is a crucial parameter that connects the experimental observation of electrical double-layer behavior with theoretical models. However, the current number of reported differential capacitance values for deep eutectic solvents remains limited, making it challenging to verify or refute existing models. In this study, we systematically investigate the differential capacitance in deep eutectic solvents using chronoamperometry. By comparing metal and glassy carbon electrodes across various liquid combinations and ion concentrations, we observed a range of distinct capacitance characteristics. While some findings align with the existing mean-field model for ionic liquids, others clearly reflect the influence of electrode materials, with certain cases resisting full explanation by current theoretical models. These results underscore the importance of selecting appropriate electrode materials in experimental studies of such electrolytes and highlight the need for further theoretical advancements in understanding this complex liquid system.

摘要

微分电容是一个关键参数,它将双电层行为的实验观测与理论模型联系起来。然而,目前报道的深共熔溶剂的微分电容值数量仍然有限,这使得验证或反驳现有模型具有挑战性。在本研究中,我们使用计时电流法系统地研究了深共熔溶剂中的微分电容。通过比较各种液体组合和离子浓度下的金属电极和玻碳电极,我们观察到了一系列不同的电容特性。虽然一些发现与现有的离子液体平均场模型一致,但其他发现清楚地反映了电极材料的影响,某些情况目前的理论模型无法完全解释。这些结果强调了在这类电解质的实验研究中选择合适电极材料的重要性,并突出了在理解这个复杂液体系统方面进一步理论进展的必要性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6631/11440589/a4b24f107ef8/jz4c02428_0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6631/11440589/bebbb044308d/jz4c02428_0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6631/11440589/e64b097f5859/jz4c02428_0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6631/11440589/c3fd12aa55bc/jz4c02428_0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6631/11440589/a4b24f107ef8/jz4c02428_0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6631/11440589/bebbb044308d/jz4c02428_0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6631/11440589/e64b097f5859/jz4c02428_0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6631/11440589/c3fd12aa55bc/jz4c02428_0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6631/11440589/a4b24f107ef8/jz4c02428_0004.jpg

相似文献

1
Direct Measurement of the Differential Capacitance of Deep Eutectic Solvents on Platinum and Glassy Carbon Electrodes.铂电极和玻碳电极上深共熔溶剂微分电容的直接测量
J Phys Chem Lett. 2024 Sep 26;15(38):9637-9643. doi: 10.1021/acs.jpclett.4c02428. Epub 2024 Sep 16.
2
Direct Measurement of the Differential Capacitance of Solvent-Free and Dilute Ionic Liquids.无溶剂和稀离子液体微分电容的直接测量
J Phys Chem Lett. 2018 Jan 4;9(1):126-131. doi: 10.1021/acs.jpclett.7b02946. Epub 2017 Dec 20.
3
Differential capacitance of the double layer at the electrode/ionic liquids interface.电极/离子液体界面双层的微分电容。
Phys Chem Chem Phys. 2010 Oct 21;12(39):12499-512. doi: 10.1039/c0cp00170h. Epub 2010 Aug 19.
4
Computational and Experimental Study of Li-Doped Ionic Liquids at Electrified Interfaces.锂掺杂离子液体在带电界面的计算与实验研究
J Phys Chem C Nanomater Interfaces. 2016 Jun 9;120(22):11993-12011. doi: 10.1021/acs.jpcc.6b02449. Epub 2016 May 24.
5
Influence of surface nanostructure-induced innermost ion structuring on capacitance of carbon/ionic liquid double layers.表面纳米结构诱导的最内层离子结构对碳/离子液体双层电容的影响。
Phys Chem Chem Phys. 2024 Feb 14;26(7):5932-5946. doi: 10.1039/d3cp05617a.
6
Understanding the bulk and interfacial structures of ternary and binary deep eutectic solvents with a constant potential method: a molecular dynamics study.用恒定电位法理解三元和二元深层共熔溶剂的本体和界面结构:一项分子动力学研究
Phys Chem Chem Phys. 2022 May 11;24(18):10962-10973. doi: 10.1039/d2cp01014c.
7
Double layer effects on metal nucleation in deep eutectic solvents.双层效应对深共晶溶剂中金属成核的影响。
Phys Chem Chem Phys. 2011 Jun 7;13(21):10224-31. doi: 10.1039/c0cp02244f. Epub 2011 Apr 26.
8
A "counter-charge layer in generalized solvents" framework for electrical double layers in neat and hybrid ionic liquid electrolytes.在纯净和混合离子液体电解质中双电层的“广义溶剂中反电荷层”框架。
Phys Chem Chem Phys. 2011 Aug 28;13(32):14723-34. doi: 10.1039/c1cp21428d. Epub 2011 Jul 13.
9
Anomalous Capacitance Maximum of the Glassy Carbon-Ionic Liquid Interface through Dilution with Organic Solvents.
J Phys Chem Lett. 2015 Jul 2;6(13):2644-8. doi: 10.1021/acs.jpclett.5b00899. Epub 2015 Jun 23.
10
Ionic liquid near a charged wall: structure and capacitance of electrical double layer.带电壁附近的离子液体:双电层的结构与电容
J Phys Chem B. 2008 Sep 25;112(38):11868-72. doi: 10.1021/jp803440q. Epub 2008 Aug 26.

本文引用的文献

1
Hydrogen Bond Donors Dictate the Frictional Response in Deep Eutectic Solvents.氢键供体决定了深层共熔溶剂中的摩擦响应。
Langmuir. 2024 Mar 19;40(11):5695-5700. doi: 10.1021/acs.langmuir.3c03303. Epub 2024 Mar 5.
2
Understanding the Electrode-Electrolyte Interfaces of Ionic Liquids and Deep Eutectic Solvents.理解离子液体和深共熔溶剂的电极-电解质界面
Langmuir. 2024 Feb 20;40(7):3283-3300. doi: 10.1021/acs.langmuir.3c03397. Epub 2024 Feb 11.
3
Understanding the Electric Double-Layer Structure, Capacitance, and Charging Dynamics.
了解双电层结构、电容和充电动力学。
Chem Rev. 2022 Jun 22;122(12):10821-10859. doi: 10.1021/acs.chemrev.2c00097. Epub 2022 May 20.
4
Understanding the bulk and interfacial structures of ternary and binary deep eutectic solvents with a constant potential method: a molecular dynamics study.用恒定电位法理解三元和二元深层共熔溶剂的本体和界面结构:一项分子动力学研究
Phys Chem Chem Phys. 2022 May 11;24(18):10962-10973. doi: 10.1039/d2cp01014c.
5
Deep Eutectic Solvents: A Review of Fundamentals and Applications.深共熔溶剂:基础与应用综述。
Chem Rev. 2021 Feb 10;121(3):1232-1285. doi: 10.1021/acs.chemrev.0c00385. Epub 2020 Dec 14.
6
Nanolubrication in deep eutectic solvents.
Phys Chem Chem Phys. 2020 Sep 23;22(36):20253-20264. doi: 10.1039/d0cp03787g.
7
Atomistic Insight into the Electrochemical Double Layer of Choline Chloride-Urea Deep Eutectic Solvents: Clustered Interfacial Structuring.氯化胆碱-尿素低共熔溶剂双电层的原子尺度洞察:簇状界面结构
J Phys Chem Lett. 2018 Nov 1;9(21):6296-6304. doi: 10.1021/acs.jpclett.8b01718. Epub 2018 Oct 22.
8
Direct Measurement of the Differential Capacitance of Solvent-Free and Dilute Ionic Liquids.无溶剂和稀离子液体微分电容的直接测量
J Phys Chem Lett. 2018 Jan 4;9(1):126-131. doi: 10.1021/acs.jpclett.7b02946. Epub 2017 Dec 20.
9
Reevaluation of Performance of Electric Double-layer Capacitors from Constant-current Charge/Discharge and Cyclic Voltammetry.恒流充放电和循环伏安法对双电层电容器性能的重新评估。
Sci Rep. 2016 Dec 9;6:38568. doi: 10.1038/srep38568.
10
In situ PM-IRRAS of a glassy carbon electrode/deep eutectic solvent interface.玻碳电极/深共熔溶剂界面的原位偏振调制红外反射吸收光谱法
Phys Chem Chem Phys. 2015 May 21;17(19):12870-80. doi: 10.1039/c5cp00070j.