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Relevant bibliographies by topics / Electrochemical interface

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Academic literature on the topic 'Electrochemical interface'

Author: Grafiati

Published: 4 June 2021

Last updated: 2 February 2022

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Journal articles on the topic "Electrochemical interface"

1

Bond, AlanM. "Electrochemical Interfaces: Modern Techniques for In-Situ Interface Characterization." Analytica Chimica Acta 258, no. 2 (March 1992): 349–50. http://dx.doi.org/10.1016/0003-2670(92)85118-p.

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Holze, Rudolf. "Electrochemical Interfaces: Modern Techniques for In-Situ Interface Characterisation." Electrochimica Acta 37, no. 8 (June 1992): 1461. http://dx.doi.org/10.1016/0013-4686(92)87023-s.

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Vitt, Joseph E. "Books: Studying the Electrochemical Interface." Analytical Chemistry 68, no. 9 (May 1996): 320A—321A. http://dx.doi.org/10.1021/ac961919x.

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Chung, Taek Dong, Seok Hee Han, Joohee Jeon, Sung Il Kim, Min-Ah Oh, Wonkyung Cho, Sun-heui Yoon, Ji Yong Kim, and Chang Il Shin. "Electrochemical Neural Interface and Iontronics." ECS Meeting Abstracts MA2020-02, no. 44 (November 23, 2020): 2792. http://dx.doi.org/10.1149/ma2020-02442792mtgabs.

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Avila, Edith Ariza, and L. A. Rocha. "Evaluation of Corrosion Resistance of Multi-Layered Ti/Glass-Ceramic Interfaces by Electrochemical Impedance Spectroscopy." Materials Science Forum 492-493 (August 2005): 189–94. http://dx.doi.org/10.4028/www.scientific.net/msf.492-493.189.

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Practical applications of metal/ceramic joints can be found in the biomedical field regarding the encapsulation of implantable telemetric devices, the fabrication of crowns and bridges for dental restoration, or in the production of drug delivery systems, biomedical sensors and electrodes. Most of metal/ceramic joints are produced by the active metal brazing technique, which originates a multi-layered interface which should be able of accommodating the abrupt electronic, crystallographic, chemical, mechanical and thermo-mechanical discontinuity that characterize these systems. Additionally, when considering biomedical applications, corrosion resistance becomes of prime importance. In this work, the corrosion resistance of Ti/glass-ceramic interfaces obtained by active metal brazing was evaluated by electrochemical impedance spectroscopy (EIS) tests. The electrochemical behaviour of the interface was monitored, as a function of time, in a simulated physiological solution at room temperature. In order to evaluate the contribution of each layer and galvanic interactions between them, to the degradation mechanism of the interface, individual samples, representative of reaction layers present at the interface, were fabricated and electrochemically tested. Results show that the corrosion behaviour, of the whole interface was strongly influenced by the chemical composition of its constitutive layers. Thus, layers containing high contents of both titanium and silver showed a polarisation resistance increase with the immersion time, as a result of the formation of a thermodynamically stable passive film. On the other hand, the copper rich layer, appears to be the main responsible for the interface degradation. In fact, for high immersion times, an instable passive film is formed and, as a consequence, large amounts of copper are released. Galvanic interactions between the copper and the silver rich layers where also identified.

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Bagger, Alexander, Logi Arnarson, Martin H. Hansen, Eckhard Spohr, and Jan Rossmeisl. "Electrochemical CO Reduction: A Property of the Electrochemical Interface." Journal of the American Chemical Society 141, no. 4 (January 8, 2019): 1506–14. http://dx.doi.org/10.1021/jacs.8b08839.

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You, Hoydoo, and Zoltán Nagy. "Applications of Synchrotron Surface X-Ray Scattering Studies of Electrochemical Interfaces." MRS Bulletin 24, no. 1 (January 1999): 36–40. http://dx.doi.org/10.1557/s088376940005171x.

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Aqueous-solution/solid interfaces are ubiquitous in modern manufacturing environments as well as in our living environment, and studies of such interfaces are an active area of science and engineering research. An important area is the study of liquid/solid interfaces under active electrochemical control, which has many immediate technological implications, for example, corrosion/passivation of metals and energy storage in batteries and ultracapacitors. The central phenomenon of electrochemistry is the charge transfer at the interface, and the region of interest is usually wider than a single atomic layer, ranging from a monolayer to thousands of angstroms, extending into both phases.Despite the technological and environmental importance of liquid/solid interfaces, the atomic level understanding of such interfaces had been very much hampered by the absence of nondestructive, in situ experimental techniques. The situation has changed somewhat in recent decades with the development of the largely ex situ ultrahigh vacuum (UHV) surface science, modern spectroscopic techniques, and modern surface microscopy.However in situ experiments of electrochemical interfaces are difficult, stemming from the special nature of these interfaces. These are so-called buried interfaces in which the solid electrode surface is covered by a relatively thick liquid layer. For this reason, the probe we use in the structural investigation must satisfy simultaneously two conditions: (1) the technique must be surface/interface sensitive, and (2) absorption of the probe in the liquid phase must be sufficiently small for penetration to and from the interface of interest without significant intensity loss.

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Power, Aoife C., Brian Gorey, Shaneel Chandra, and James Chapman. "Carbon nanomaterials and their application to electrochemical sensors: a review." Nanotechnology Reviews 7, no. 1 (February 23, 2018): 19–41. http://dx.doi.org/10.1515/ntrev-2017-0160.

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AbstractCarbon has long been applied as an electrochemical sensing interface owing to its unique electrochemical properties. Moreover, recent advances in material design and synthesis, particularly nanomaterials, has produced robust electrochemical sensing systems that display superior analytical performance. Carbon nanotubes (CNTs) are one of the most extensively studied nanostructures because of their unique properties. In terms of electroanalysis, the ability of CNTs to augment the electrochemical reactivity of important biomolecules and promote electron transfer reactions of proteins is of particular interest. The remarkable sensitivity of CNTs to changes in surface conductivity due to the presence of adsorbates permits their application as highly sensitive nanoscale sensors. CNT-modified electrodes have also demonstrated their utility as anchors for biomolecules such as nucleic acids, and their ability to diminish surface fouling effects. Consequently, CNTs are highly attractive to researchers as a basis for many electrochemical sensors. Similarly, synthetic diamonds electrochemical properties, such as superior chemical inertness and biocompatibility, make it desirable both for (bio) chemical sensing and as the electrochemical interface for biological systems. This is highlighted by the recent development of multiple electrochemical diamond-based biosensors and bio interfaces.

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Yang, Fan, PeiLin Deng, Qingyong Wang, Jiexin Zhu, Ya Yan, Liang Zhou, Kai Qi, Hongfang Liu, Ho Seok Park, and Bao Yu Xia. "Metal–organic framework-derived cupric oxide polycrystalline nanowires for selective carbon dioxide electroreduction to C2 valuables." Journal of Materials Chemistry A 8, no. 25 (2020): 12418–23. http://dx.doi.org/10.1039/d0ta03565c.

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Enriching the interface: metal–organic framework-derived copper oxide nanowires with abundant crystalline interfaces contribute to the efficient electrochemical CO₂ reduction towards fast hydrocarbon generation.

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Ouyang, Yixin, Yehui Zhang, Peter S. Rice, Li Shi, Jinlan Wang, and P. Hu. "Electrochemical CO2 reduction: water/catalyst interface versus polymer/catalyst interface." Journal of Materials Chemistry A 9, no. 32 (2021): 17474–80. http://dx.doi.org/10.1039/d1ta04867h.

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Alkaline polymer electrolyte electrolytic cells (APEECs) have the potential to replace aqueous-phase CO2 electrolyzer. Full reaction kinetics at polymer/copper interface is obtained to present a fundamental understanding of the superiority of APEECs.

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Dissertations / Theses on the topic "Electrochemical interface"

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Bohm, Sivasambu. "Optical and electrochemical studies of the silicon/electrolyte interface." Thesis, University of Bath, 1997. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.362286.

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Harlow, G. S. "Surface X-ray diffraction studies of the electrochemical interface." Thesis, University of Liverpool, 2016. http://livrepository.liverpool.ac.uk/3003643/.

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This thesis describes the application of in-situ surface X-ray diffraction (SXRD) experiments to the study of electrochemical interfaces. Measurements performed at synchrotron radiation facilities are used to provide in-sight into the surface structure of electrodes and the electrochemical double layer. The impact of structural changes on electrochemical reactivity, and likewise the impact of electrochemical processes on electrode structure are discussed. Measurements of the Au (111) reconstruction in alkaline solution indicate that the presence of CO causes the partial lifting of the reconstruction; it is suggested that this leads to an increase in defects and this is the underlying reason for CO promoted gold catalysis. In-situ SXRD measurements with a non-aqueous electrolyte are presented, representing a technological advance in the study of electrochemical interfaces. Crystal truncation rods (CTRs) measured at the Pt (111) / non-aqueous acetonitrile interface are used to determine the structure of both the electrode surface and the electrolyte close to the interface. The results indicate that acetonitrile undergoes a potential dependant reorientation but, in the presence of molecular oxygen, the acetonitrile molecules close to the electrode are dissociated and therefore cannot reorient. Measurements of CTRs at the Pt (111) / electrolyte interface for several aqueous electrolytes are combined with CTRs measured in non-aqueous acetonitrile to explore the dependence of surface relaxation on adsorption. Fits to CTRs are also used to determine the double layer structure at aqueous Pt (111) / acetonitrile interfaces and how it varies with acetonitrile concentration. The results indicate that the acetonitrile adsorption increases with concentration and that the double layer region compresses.

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Wilson, Natalie Elizabeth. "In-situ and model infrared studies of the electrochemical interface." Thesis, University of Southampton, 1999. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.313195.

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Yamada, Yuki. "Studies on Electrochemical Reactions at Interface between Graphite and Solution." 京都大学 (Kyoto University), 2010. http://hdl.handle.net/2433/126811.

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Guymon, Clint. "MPSA effects on copper electrodeposition : understanding molecular behavior at the electrochemical interface /." Diss., CLICK HERE for online access, 2006. http://contentdm.lib.byu.edu/ETD/image/etd1112.pdf.

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Abel, Julia Catherine. "Investigation of the electrode/electrolyte interface using ultra fast electrochemical ellipsometry." Thesis, University of Newcastle Upon Tyne, 2001. http://hdl.handle.net/10443/799.

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Electrochemical ellipsometry is employed to determine the real and imaginary parts of the refractive index and the thickness of thin films as functions of the potential applied to the electrode upon which the film is grown. The relatively recent advent of an analyser with no moving parts, the Stokesmeter, has removed previous time restraints and allows microsecond resolution. The Newcastle system is extremely novel, using a Stokesmeter, and thus being capable of 325 gs resolution, and also being electrochemically interfaced. The ellipsometric studies have concentrated on the growth and behaviour of a series of electroactive polymers derived from salicylaldehydes (Salens). [Ni(SaltMe)] and [Ni(SaIdMe)] were found to yield stable homogeneous films upon polymerisation, however while the behaviour during film growth was similar, marked differences were observed during potential cycling, poly[Ni(SaIdMe)] showing a marked decrease in thickness near the anodic limit not observed for poly[Ni(Saltme)], indicating that even minor changes to ligand structure well away from the site of polymerisation may have significant effects on the resulting film. The behaviour of poly[Ni(OMeSaltMe)] during polymerisation is more complicated; initially a homogeneous film is produced, however about half way through the growth process the film becomes inhomogeneous, and remains so during subsequent potential cycling. This behaviour was also observed for poly[Pd(OMeSalen)], indicating electron donating groups around the phenyl rings of the ligand have a profound effect on the nature of the polymer films, possibly far more so than the identity of the central metal.

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Zhao, Meng. "Understanding Electrochemical Interface Properties by Comprehensive Self-Consistent Density Functional Theory." Case Western Reserve University School of Graduate Studies / OhioLINK, 2017. http://rave.ohiolink.edu/etdc/view?acc_num=case1491315734773944.

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Nolan, Melissa A. "Microfabricated iridium arrays : failure mechanisms, investigation of the Hg-Ir interface and their use in Cu or Hg determination /." Thesis, Connect to Dissertations & Theses @ Tufts University, 1999.

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Thesis (Ph.D.)--Tufts University, 1999.
Adviser: Samuel P. Kaunaves. Submitted to the Dept. of Chemistry. Includes bibliographical references (leaves 190). Access restricted to members of the Tufts University community. Also available via the World Wide Web;

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Janek, Jürgen, and Björn Luerßen. "Study of electrochemical interface processes by locally resolving photoelectron spectroscopy and microscopy." Universitätsbibliothek Leipzig, 2015. http://nbn-resolving.de/urn:nbn:de:bsz:15-qucosa-186682.

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Guymon, Clint Gordon. "MPSA Effects on Copper Electrodeposition: Understanding Molecular Behavior at the Electrochemical Interface." BYU ScholarsArchive, 2005. https://scholarsarchive.byu.edu/etd/333.

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In this work the structure of the electrochemical metal-liquid interface is determined through use of quantum mechanics, molecular simulation, and experiment. Herein are profiled the molecular dynamics details and results of solid-liquid interfaces at flat non-specific solid surfaces and copper metal electrodes. Ab initio quantum-mechanical calculations are reported and define the interatomic potentials in the simulations. Some of the quantum-mechanical calculations involve small copper clusters interacting with 3-mercaptopropanesulfonic acid (MPSA), sodium, chloride, bisulfate and cuprous ions. In connection with these I develop the electrode charge dynamics (ECD) routine to treat the charge mobility in a metal. ECD bridges the gap between small-scale metal-cluster ab initio calculations and large-scale simulations of metal surfaces of arbitrary geometry. As water is the most abundant surface species in aqueous systems, water determines much of the interfacial dynamics. In contrast to prior simulation work, simulations in this work show the presence of a dense 2D ice-like rhombus structure of water on the surface that is relatively impervious to perturbation by typical electrode charges. I also find that chloride ions are adsorbed at both positive and negative electrode potentials, in agreement with experimental findings. Including internal modes of vibration in the water model enhances the ion contact adsorption at the solid surface. In superconformal filling of copper chip interconnects, organic additives are used to bottom-up fill high-aspect ratio trenches or vias. I use molecular dynamics and rotating-disk-electrode experiments to provide insight into the function of MPSA, one such additive. It is concluded that the thiol head group of MPSA inhibits copper deposition by preferentially occupying the active surface sites. The sulfonate head group participates in binding the copper ions and facilitating their transfer to the surface. Chloride ions reduce the work function of the copper electrode, reduce the binding energy of MPSA to the copper surface, and attenuate the binding of copper ions to the sulfonate head group of MPSA.

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Books on the topic "Electrochemical interface"

1

1951-, Yafyasov Adil M., and Bogevolnov Vladislav B. 1954-, eds. Field-effect in semiconductor-electrolyte interface: Application to investigations of electronic properties of the semiconductor surfaces. Princeton, NJ: Princeton, 2006.

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2

Kazarinov, Vladimir E., ed. The Interface Structure and Electrochemical Processes at the Boundary Between Two Immiscible Liquids. Berlin, Heidelberg: Springer Berlin Heidelberg, 1987. http://dx.doi.org/10.1007/978-3-642-71881-6.

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Jerkiewicz, Gregory, Manuel P. Soriaga, Kohei Uosaki, and Andrzej Wieckowski, eds. Solid-Liquid Electrochemical Interfaces. Washington, DC: American Chemical Society, 1997. http://dx.doi.org/10.1021/bk-1997-0656.

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O, Andriyko Yuriy, Nauer Gerhard E, and SpringerLink (Online service), eds. Many-electron Electrochemical Processes: Reactions in Molten Salts, Room-Temperature Ionic Liquids and Ionic Solutions. Berlin, Heidelberg: Springer Berlin Heidelberg, 2013.

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5

D, Abruña Héctor, ed. Electrochemical interfaces: Modern techniques for in-situ interface characterization. New York: VCH Pub., 1991.

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Abruna, Hector D. Electrochemical Interfaces: Modern Techniques for In-Situ Interface Characterization. Vch Pub, 1991.

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7

Boyette, Stacey E. Investigations of the electrode-solution interface in microheterogeneous solutions involving surfactants. 1991.

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The Interface Structure and Electrochemical Processes at the Boundary Between Two Immiscible Liquids. Springer, 2011.

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9

E, Kazarinov V., and Boguslavskiĭ L. I, eds. The Interface structure and electrochemical processes at the boundary between two immiscible liquids. Berlin: Springer-Verlag, 1987.

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Müller, A., S. E. C. Dale, and M. A. Engbarth. Micromagnetic Measurements on Electrochemically Grown Mesoscopic Superconductors. Edited by A. V. Narlikar. Oxford University Press, 2017. http://dx.doi.org/10.1093/oxfordhb/9780198738169.013.10.

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This article examines the behavior of superconductivity in mesoscopic type-I superconductors based on micromagnetic measurements on two electrochemically grown mesoscopic superconductors, namely lead and tin. It first provides an overview of the basic properties of mesoscopic superconductivity and the interface between two different superconductors that are in close contact with one another. It then describes the electrochemical preparation of β-tin samples in a variety of shapes and sizes in the mesoscopic regime. It also presents the results of micromagnetic measurements, carried out using micro-Hall probes, including observations of the vortex states in mesoscopic tin and lead triangles and of proximity effects in lead/tin core–shell structures.

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Book chapters on the topic "Electrochemical interface"

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Ye, Shen. "Electrochemical Infrared Spectroscopy." In Compendium of Surface and Interface Analysis, 79–85. Singapore: Springer Singapore, 2018. http://dx.doi.org/10.1007/978-981-10-6156-1_14.

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Takahashi, Yasufumi. "Scanning Electrochemical Microscopy." In Compendium of Surface and Interface Analysis, 551–56. Singapore: Springer Singapore, 2018. http://dx.doi.org/10.1007/978-981-10-6156-1_89.

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Utsunomiya, Toru, Yasuyuki Yokota, and Ken-ichi Fukui. "Electrochemical Atomic Force Microscopy." In Compendium of Surface and Interface Analysis, 73–78. Singapore: Springer Singapore, 2018. http://dx.doi.org/10.1007/978-981-10-6156-1_13.

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Nishino, Tomoaki. "Electrochemical Scanning Tunneling Microscopy." In Compendium of Surface and Interface Analysis, 87–90. Singapore: Springer Singapore, 2018. http://dx.doi.org/10.1007/978-981-10-6156-1_15.

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Yagi, Ichizo. "Electrochemical Second Harmonic Generation." In Compendium of Surface and Interface Analysis, 91–95. Singapore: Springer Singapore, 2018. http://dx.doi.org/10.1007/978-981-10-6156-1_16.

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Noguchi, Hidenori. "Electrochemical Sum Frequency Generation." In Compendium of Surface and Interface Analysis, 97–101. Singapore: Springer Singapore, 2018. http://dx.doi.org/10.1007/978-981-10-6156-1_17.

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Oshima, Yoshifumi. "Electrochemical Transmission Electron Microscopy." In Compendium of Surface and Interface Analysis, 109–12. Singapore: Springer Singapore, 2018. http://dx.doi.org/10.1007/978-981-10-6156-1_19.

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Kondo, Toshihiro. "Electrochemical Surface X-Ray Scattering." In Compendium of Surface and Interface Analysis, 103–8. Singapore: Springer Singapore, 2018. http://dx.doi.org/10.1007/978-981-10-6156-1_18.

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Masuda, Takuya. "Electrochemical X-Ray Photoelectron Spectroscopy." In Compendium of Surface and Interface Analysis, 119–25. Singapore: Springer Singapore, 2018. http://dx.doi.org/10.1007/978-981-10-6156-1_21.

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Lindsay, S. M., T. W. Jing, J. Pan, D. Lampner, A. Vaught, J. P. Lewis, and O. F. Sankey. "Electron Tunneling in Electrochemical STM." In Nanoscale Probes of the Solid/Liquid Interface, 25–43. Dordrecht: Springer Netherlands, 1995. http://dx.doi.org/10.1007/978-94-015-8435-7_3.

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Conference papers on the topic "Electrochemical interface"

1

Lombardo, L., S. Generelli, N. Tscharner, D. Migliorelli, and N. Donato. "A compact electronic interface for electrochemical sensors." In 2016 IEEE Sensors Applications Symposium (SAS). IEEE, 2016. http://dx.doi.org/10.1109/sas.2016.7479885.

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Peterson, Andrew. "Constant-potential reactions at the electrochemical interface." In International Conference on Electrocatalysis for Energy Applications and Sustainable Chemicals. València: Fundació Scito, 2020. http://dx.doi.org/10.29363/nanoge.ecocat.2020.029.

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Ghoreishizadeh, Sara, Cristina Boero, Antonio Pullini, Camilla Baj-Rossi, Sandro Carrara, and Giovanni De Micheli. "Sub-mW reconfigurable interface IC for electrochemical sensing." In 2014 IEEE Biomedical Circuits and Systems Conference (BioCAS). IEEE, 2014. http://dx.doi.org/10.1109/biocas.2014.6981705.

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Liao, Yu-Te. "A CMOS Multimodality Electrochemical Sensing Interface IC for Healthcare." In 2021 International Symposium on VLSI Design, Automation and Test (VLSI-DAT). IEEE, 2021. http://dx.doi.org/10.1109/vlsi-dat52063.2021.9427335.

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Cherenkov, Ivan, Eugeny Kharanzhevskiy, Ajsylu Safiullina, Aliya Gimazdinova, and Ravil' Davlyatshin. "DEVELOPMENT OF ELECTROCHEMICAL INTERFACE ELEMENTS FOR CELL-ON-CHIP SYSTEMS." In XVI International interdisciplinary congress "Neuroscience for Medicine and Psychology". LLC MAKS Press, 2020. http://dx.doi.org/10.29003/m1326.sudak.ns2020-16/506-507.

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Jog, Aakash, Yahav Avigal, Assaf Avital, Jayteerth Amble, Aviv Peled, and Yosi Shacham-Diamand. "An Integrated Electronic Interface for Bio-electrochemical Plant-based Sensors." In 2020 IEEE SENSORS. IEEE, 2020. http://dx.doi.org/10.1109/sensors47125.2020.9278777.

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Khan, Sharif, Shafaat A. Bazaz, Dean M. Aslam, and H. Y. Chan. "Electrochemical interface characterization of MEMS based brain implantable all-diamond microelectrodes probe." In 2013 18th International Conference on Digital Signal Processing (DSP). IEEE, 2013. http://dx.doi.org/10.1109/siecpc.2013.6550984.

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Khor, Sook Mei, Guozhen Liu, Jason B. Harper, Sridhar G. Iyengar, and J. Justin Gooding. "Strategies for fabricating a biorecognition interface for a label free electrochemical immunosensor." In 2010 International Conference on Nanoscience and Nanotechnology (ICONN). IEEE, 2010. http://dx.doi.org/10.1109/iconn.2010.6045168.

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Kar, Debashis, and David M. Saylor. "A Diffuse Interface Model to Simulate Electrochemical Response of Medical Implant Materials." In ASME 2013 Conference on Frontiers in Medical Devices: Applications of Computer Modeling and Simulation. American Society of Mechanical Engineers, 2013. http://dx.doi.org/10.1115/fmd2013-16020.

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The purpose of the present work is to model corrosion of implant materials (such as nitinol or stainless steel) in simulated environments both under static and dynamic conditions. The present model seeks to imitate the potentiodynamic testing protocol defined as in ASTM F2129, which is used to evaluate the corrosion susceptibility of small implant devices. The model is currently limited to one dimension and hence the effect of physical features, such as defects and crevices, on corrosion is not the focus of this study.

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Chen, Yi-Chia, Shao-Yung Lu, Jui-Hsiang Tsai, and Yu-Te Liao. "A Power-Efficient, Bi-Directional Readout Interface Circuit for Cyclic-Voltammetry Electrochemical Sensors." In 2019 International Symposium on VLSI Design, Automation and Test (VLSI-DAT). IEEE, 2019. http://dx.doi.org/10.1109/vlsi-dat.2019.8741529.

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Reports on the topic "Electrochemical interface"

1

Go, David B., David M. Bartels, R. M. Sankaran, and Rohan Akolkar. Probing Electrochemical Reactions at a Plasma-Liquid Interface. Fort Belvoir, VA: Defense Technical Information Center, February 2015. http://dx.doi.org/10.21236/ada625639.

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Nookala, Munichandraiah. Electrochemical Investigations of the Interface at Li/Li+ Ion Conducting Channel. Fort Belvoir, VA: Defense Technical Information Center, October 2006. http://dx.doi.org/10.21236/ada466535.

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Fernandez-Serra, Maria Victoria. First principles modeling of the metal-electrolyte interface: A novel approach to the study of the electrochemical interface. Office of Scientific and Technical Information (OSTI), September 2016. http://dx.doi.org/10.2172/1323901.

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Nookala, Munichandraiah. Electrochemical Investigations of the Interface at Li/Li+ Ion Conducting Channel (Supplemental). Fort Belvoir, VA: Defense Technical Information Center, November 2007. http://dx.doi.org/10.21236/ada476088.

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C Taylor, R Kelly, and M Neurock. Phase Transitions Involving Dissociated States of Water at the Electrochemical Ni(111)/H2O Interface. Office of Scientific and Technical Information (OSTI), April 2006. http://dx.doi.org/10.2172/882552.

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Yahnke, Mark S. The application of solid-state NMR spectroscopy to electrochemical systems: CO adsorption on Pt electrocatalysts at the aqueous-electrode interface. Office of Scientific and Technical Information (OSTI), December 1996. http://dx.doi.org/10.2172/451231.

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Rudnicki, James D., Frank R. McLarnon, and Elton J. Cairns. Application of photothermal deflection spectroscopy to electrochemical interfaces. Office of Scientific and Technical Information (OSTI), March 1992. http://dx.doi.org/10.2172/10145628.

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Rudnicki, J. D., F. R. McLarnon, and E. J. Cairns. Application of photothermal deflection spectroscopy to electrochemical interfaces. Office of Scientific and Technical Information (OSTI), March 1992. http://dx.doi.org/10.2172/5280798.

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Hayden, Carl C., and Roger L. Farrow. Molecular-scale measurements of electric fields at electrochemical interfaces. Office of Scientific and Technical Information (OSTI), January 2011. http://dx.doi.org/10.2172/1010418.

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Morgan, Dane. Enhancement of SOFC Cathode Electrochemical Performance Using Multi-Phase Interfaces. Office of Scientific and Technical Information (OSTI), September 2015. http://dx.doi.org/10.2172/1253141.

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