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Journal of Electrochemistry

Journal

Electrochemical interface

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Full-Text Articles in Nanoscience and Nanotechnology

Rational Design Of Electrochemical Molecular Probes For Highly Selective And Long-Term Measurement In Vivo, Yue Wang, Li-Min Zhang, Yang Tian Mar 2022

Rational Design Of Electrochemical Molecular Probes For Highly Selective And Long-Term Measurement In Vivo, Yue Wang, Li-Min Zhang, Yang Tian

Journal of Electrochemistry

Designing electrochemical interfaces for in vivo analysis of neurochemicals with high selectivity and long-term stability is vital for monitoring dynamic variation and dissecting the complex mechanisms of pathogenesis in living animals. This review focuses on the development of electrochemical interfaces based on rational design of molecular probes for in vivo measurement with high selectivity and high stability from three aspects: (1) Specific recognition probes were rationally designed and created to remarkably improve the selectivity of in vivo analysis in a complicated brain environment. (2) The Au-C≡C functionalized surface was developed to remarkably enhance the stability of molecular assembly, and employed …


An Investigation On The Structure Of Au(111)/Imidazolium-Based Ionic Liquid Interface: Effect Of Alkyl Side Chain Length, Li Chen, Shuai Liu, Mian-Gang Li, Jian-Jia Su, Jia-Wei Yan, Bing-Wei Mao Oct 2018

An Investigation On The Structure Of Au(111)/Imidazolium-Based Ionic Liquid Interface: Effect Of Alkyl Side Chain Length, Li Chen, Shuai Liu, Mian-Gang Li, Jian-Jia Su, Jia-Wei Yan, Bing-Wei Mao

Journal of Electrochemistry

In this work, we comparatively investigated the interfacial structures at Au(111) electrode surfaces in two ionic liquids (ILs) with different alkyl chain lengths by combining AFM force curve technique and electrochemical methods. The number and stability of the layering structures, and their potential-dependency were analyzed. The experimental results indicated that the tendencies of force-potential curves in the two ILs behave the same way. At potentials close to PZC, the ions arrange loosely, which lowers the stability of the layering structure. As the potential shifting away from PZC, more ions attach to electrode surface, which increases the stability of layering structure, …


An Stm Study On The Structure Of Pt(100)/Ionic Liquid Omipf6 Interface, Jin Peng, Mian-Gang Li, Li-Qiang Xie, Jia-Wei Yan, Bing-Wei Mao Dec 2016

An Stm Study On The Structure Of Pt(100)/Ionic Liquid Omipf6 Interface, Jin Peng, Mian-Gang Li, Li-Qiang Xie, Jia-Wei Yan, Bing-Wei Mao

Journal of Electrochemistry

Potential-dependent structures of Pt(100)/ionic liquid 1-methyl-3-octylimidazolium hexafluorophosphate (OMIPF6) interface have been studied by electrochemical scanning tunneling microscopy (ECSTM). The cation OMI+ forms ordered structure on Pt(100) surface, which exists in a potential region of about 1.2 V. When the potential is more negative than -0.6 V, it can be seen that the ordered structure transforms to disordered structure. When the potential shifts positively to +0.6 V, the desorption of cations OMI+ occurs, which indicates that strong electrostatic repulsion is needed to overcome chemical interaction between OMIPF6 and Pt(100) surface, leading to the desorption. The above results …


Density Functional Theory Studies Of Surface-Enhanced Raman Spectroscopy In Electrochemical Interfaces, Liu-Bin Zhao, De-Yin Wu, Bin Ren, Zhong-Qun Tian Aug 2010

Density Functional Theory Studies Of Surface-Enhanced Raman Spectroscopy In Electrochemical Interfaces, Liu-Bin Zhao, De-Yin Wu, Bin Ren, Zhong-Qun Tian

Journal of Electrochemistry

Quantum chemical density functional theory and Raman scattering theory were used to study the bonding mechanism and surface-enhanced Raman spectroscopy of pyridine adsorbed on transition metals (Ⅷ group) and coinage metals (IB group) . SERS studies of pyridine-metal systems have been reviewed. Chemical bonding mechanism as well as photo-driven charge transfer mechanism was considered to investigate the vibrational frequency shift and the enhancement of SERS intensity in electrochemical interfaces. Our theoretical results can be used to interpret the SERS phenomena dependent on metals,excitation wavelengths,and applied potentials.


Confocal Microprobe Raman Spectroscopy For Investigating The Electrochemical Interface, Bin Ren, Feng Ming Liu, Xufeng Lin, Zhong-Qun Tian Feb 2001

Confocal Microprobe Raman Spectroscopy For Investigating The Electrochemical Interface, Bin Ren, Feng Ming Liu, Xufeng Lin, Zhong-Qun Tian

Journal of Electrochemistry

The invention of the surface enhanced Raman spectroscopy (SERS) in the mid of 1970s, opened an entirely new and very promising area. However, it was found that SERS of practical application in electrochemistry can only be found on noble metal surfaces, such as Ag, Au and Cu that exhibit huge surface enhancement [1] . This greatly limits the application of SERS in electrochemistry. In electrocatalysis, corrosion inhibition, sensor, and power source, the most widely used materials are Pt, Fe and Ni and their alloys as well as Si. Thus, it is of great significance to extend surface Raman study to …