The physical electrochemistry of the carbon/ionic liquids interface underpins the processes occurring in a vast range of applications spanning electrochemical energy storage, iontronic devices, and lubrication. Elucidating the charge storage mechanisms at the carbon/electrolyte interface will lead to a better understanding of the operational principles of such systems. Herein, we probe the charge stored at the electrochemical double layer formed between model carbon systems, ranging from single-layer graphene to graphite and the ionic liquid 1-ethyl-3-methylimidazolium bis(trifluoromethylsulfonyl)imide (EMIM-TFSI). The effect of the number of graphene layers on the overall capacitance of the interface is investigated. We demonstrate that in pure EMIM-TFSI and at moderate potential biases, the electronic properties of graphene and graphite govern the overall capacitance of the interface, while the electrolyte contribution to the latter is less significant. In mixtures of EMIM-TFSI with solvents of varying relative permittivity, the complex interplay between electrolyte ions and solvent molecules is shown to influence the charge stored at the interface, which under certain conditions overcomes the effects of relative permittivity. This work provides additional experimental insights into the continuously advancing topic of electrochemical double-layer structure at the interface between room temperature ionic liquids and carbon materials.
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http://dx.doi.org/10.1021/acs.jpcc.3c08269 | DOI Listing |
ACS Appl Mater Interfaces
December 2024
School of Mechanical Engineering, Hangzhou Dianzi University, Hangzhou 310018, China.
Flexible sensors are increasingly significant in applications such as smart wearables and human-computer interactions. However, typical flexible sensors are spatially limited and can generally detect only one deformation mode. This study presents a novel multimodal flexible sensor that combines three sensing units: optoelectronics, ionic liquids, and conductive fabrics.
View Article and Find Full Text PDFChemSusChem
December 2024
Technical University of Denmark: Danmarks Tekniske Universitet, Department of Energy Conversion and Storage, Anker Engelunds Vej 1, 2800, Kongens Lyngby, DENMARK.
Deep eutectic solvents (DESs) are an emerging class of ionic liquids with high tunability and promise for battery applications. In this study, we investigated acetamide-based DESs for Zn batteries, focusing on a synergistic mixture of two known acetamide (Ace)-based DESs: Ace4ZnCl2 and Ace4ZnTFSI2. By combining these two DESs in various ratios, we aimed to enhance ionic conductivity and optimize electrochemical performance while addressing corrosion concerns.
View Article and Find Full Text PDFEnviron Health (Wash)
December 2024
Institute of Environmental Research at Greater Bay Area, Key Laboratory for Water Quality and Conservation of the Pearl River Delta, Ministry of Education, Guangzhou University, Guangzhou 510006, China.
The rational design of molecules with the desired functionality presents a significant challenge in chemistry. Moreover, it is worth noting that making chemicals safe and sustainable is crucial to bringing them to the market. To address this, we propose a novel deep learning framework developed explicitly for inverse design of molecules with both functionality and biocompatibility.
View Article and Find Full Text PDFJ Colloid Interface Sci
December 2024
College of Chemistry and Materials Engineering, Bohai University, Jinzhou 121013, China. Electronic address:
The unique structure and strong interaction of multiphase hybrid materials have garnered significant attention as prospective candidates for electrode materials in the realm of energy storage. The present study presents a rational design of a functional NiSe-CoSe/N, B double-doped carbon hybrid composite (NCS/C), resulting in the emergence of various novel cooperative regulatory mechanisms involving: (i) the heterogeneous structure of NiSe and CoSe generates built-in electric fields to increase electron mobility; (ii) the incorporation of polyatomic double-doped carbon (N, and B) expedites electron transfer rate; intriguingly, (iii) ionic liquids not only serve as polyatomic dopants in the reaction system but also influence the microstructure of the composite. Benefiting from these synergistic effects, the NCS/C hybrid exhibits remarkable charge storage capacity and rapid electrochemical kinetics, driven by its multi-fold hollow structure and multicomponent cooperative modulation.
View Article and Find Full Text PDFSpectrochim Acta A Mol Biomol Spectrosc
December 2024
Department of Chemistry, Presidency University, Kolkata 700073, India. Electronic address:
Pyrene fluorescence in aqueous solutions of two surface active ionic liquids, namely, 1-decyl-3-methylimidazolium chloride, and 1-hexadecyl-3-methylimidazolium chloride was investigated in presence of a biopolymer sodium alginate. The principal objective of this study was to explore the influence of the length of the hydrocarbon tails of these surface active ionic liquids on the possible location of the probe (pyrene) molecules in presence of the additive. While an abrupt decrease in the values of the ratio of the intensity of the first vibronic band to that of the third band of pyrene emission spectrum with concentration was observed for 1-hexadecyl-3-methylimidazolium chloride in presence of sodium alginate like the polymer-free case reported earlier, there was a peculiar reversal for 1-decyl-3-methylimidazolium chloride + sodium alginate.
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