The in situ molecular characterization of reaction intermediates and products at electrode-electrolyte interfaces is central to mechanistic studies of complex electrochemical processes, yet a great challenge. The coupling of electrochemistry (EC) and mass spectrometry (MS) has seen rapid development and found broad applicability in tackling challenges in analytical and bioanalytical chemistry. However, few truly in situ and real-time EC-MS studies have been reported at electrode-electrolyte interfaces. An innovative EC-MS coupling method named in situ liquid secondary ion mass spectrometry (SIMS) was recently developed by combining SIMS with a vacuum compatible microfluidic electrochemical device. Using this novel capability, we report the first in situ elucidation of the electro-oxidation mechanism of a biologically significant organic compound, ascorbic acid (AA), at the electrode-electrolyte interface. The short-lived radical intermediate was successfully captured, which had not been detected directly before. Moreover, we demonstrated the power of this new technique in real-time monitoring of the formation and dynamic evolution of electrical double layers at the electrode-electrolyte interface. This work suggests further promising applications of in situ liquid SIMS in studying more complex chemical and biological events at the electrode-electrolyte interface.
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http://dx.doi.org/10.1021/acs.analchem.6b04189 | DOI Listing |
Materials (Basel)
January 2025
College of Safety Science and Engineering, Nanjing Tech University, Nanjing 211816, China.
An experimental investigation is conducted to identify the optimal blend of fluoroethylene carbonate (FEC), 3,3,3-trifluoropropylene carbonate (TFEC), and various fluorinated ethers, including 1,1,2,2-tetrafluoroethyl-2,2,2-trifluoroethyl ether (HFE), 1,1,2,2-tetrafluoroethyl-2,2,3,3-tetrafluoropropyl ether (TTE), and bis(2,2,2-trifluoroethyl) ether (BTE), to enhance the performances of lithium-ion cells at high voltage. The cell incorporating TTE exhibits a significantly superior capacity for retention after long-term cycling at 4.5 V, which might be attributed to the improved kinetics of lithium ions and the generation of a thin, reliable, and inorganic-rich electrode-electrolyte interface.
View Article and Find Full Text PDFFood Chem
January 2025
Materials Research Institute and Department of Ecosystem Science and Management, 204 Energy and the Environment Laboratory, The Pennsylvania State University, University Park, PA 16802, USA. Electronic address:
This work presents a convenient and easy-to-operate method for synthesizing the functionally integrated nanocomposite of nitrogen-doped multi walled carbon nanotube networks (N-CNTs) and cobalt 2-methylimidazole (ZIF-67) nanoparticles. The N-CNTs@ZIF-67 nanocomposite was utilized to design a novel electrochemical sensing platform for detecting gallic acid (GA). The N-CNTs@ZIF-67 modified glass carbon electrode (GCE) demonstrated high sensitivity for GA electrochemical detection (LOD: 10.
View Article and Find Full Text PDFLangmuir
January 2025
College of Materials Science and Engineering, Sichuan University, Chengdu 610064, China.
Metallic Zn is a promising anode for high-safety, low-cost, and large-scale energy storage systems. However, it is strongly hindered by unstable electrode/electrolyte interface issues, including zinc dendrite, corrosion, passivation, and hydrogen evolution reactions. In this work, an in situ interface protection strategy is established by turning the corrosion/passivation byproducts (zinc hydroxide sulfates, ZHSs) into a stable hybrid protection layer.
View Article and Find Full Text PDFChem Commun (Camb)
January 2025
Department of Applied Chemistry, Ritsumeikan University, 1-1-1 Nojihigashi, Kusatsu, Shiga, 525-8577, Japan.
Acetonitrile is a low-viscosity solvent that can enhance charge transfer kinetics at the electrode/electrolyte interface, although its cathodic instability limits its demonstration. This study employed a dual-compartment cell separated by a solid electrolyte to demonstrate that an acetonitrile-based electrolyte enhanced the interfacial charge transfer kinetics compared to those of carbonate-based electrolytes.
View Article and Find Full Text PDFNatl Sci Rev
January 2025
State Key Laboratory of Advanced Chemical Power Sources, Engineering Research Center of High-efficiency Energy Storage (Ministry of Education), College of Chemistry, Nankai University, Tianjin 300071, China.
Aqueous zinc batteries offer promising prospects for large-scale energy storage, yet their application is limited by undesired side reactions at the electrode/electrolyte interface. Here, we report a universal approach for the building of an electrode/electrolyte interphase (EEI) layer on both the cathode and the anode through the self-polymerization of electrolyte additives. In an exemplified Zn||VO·nHO cell, we reveal that the glutamate additive undergoes radical-initiated electro-polymerization on the cathode and polycondensation on the anode, yielding polyglutamic acid-dominated EEI layers on both electrodes.
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