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1

Yasuda, Kouji, and Toshiyuki Nohira. "Electrochemical production of silicon." High Temperature Materials and Processes 41, no. 1 (January 1, 2022): 247–78. http://dx.doi.org/10.1515/htmp-2022-0033.

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Abstract Silicon solar cells are crucial devices for generating renewable energy to promote the energy and environmental fields. Presently, high-purity silicon, which is employed in solar cells, is manufactured commercially via the Siemens process. This process is based on hydrogen reduction and/or the thermal decomposition of trichlorosilane gas. The electrochemical process of producing silicon has attracted enormous attention as an alternative to the existing Siemens process. Thus, this article reviews different scientific investigations of the electrochemical production of silicon by classifying them based on the employed principles (electrorefining, electrowinning, and solid-state reduction) and electrolytes (molten oxides, fluorides, chlorides, fluorides–chlorides, ionic liquids [ILs], and organic solvents). The features of the electrolytic production of silicon in each electrolyte, as well as the prospects, are discussed.
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2

LIN, G., R. KAINTHLA, N. PACKHAM, O. VELEV, and J. BOCKRIS. "On electrochemical tritium production." International Journal of Hydrogen Energy 15, no. 8 (1990): 537–50. http://dx.doi.org/10.1016/0360-3199(80)90001-4.

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3

Tseung, A. C. C. "Electrochemical hydrogen technologies. Electrochemical production and combustion of hydrogen." Journal of Electroanalytical Chemistry and Interfacial Electrochemistry 317, no. 1-2 (November 1991): 303–5. http://dx.doi.org/10.1016/0022-0728(91)85024-j.

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4

Hine, F., M. Yasuda, Y. Ogata, T. Kojima, and Yang Weiyi. "Electrochemical Production of Potassium Carbonate." Journal of The Electrochemical Society 132, no. 10 (October 1, 1985): 2336–40. http://dx.doi.org/10.1149/1.2113574.

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5

Eisazadeh, H., G. Spinks, and G. G. Wallace. "Electrochemical production of polypyrrole colloids." Polymer 35, no. 17 (August 1994): 3801–3. http://dx.doi.org/10.1016/0032-3861(94)90569-x.

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6

Moratalla, Ángela, Mayra K. S. Monteiro, Cristina Sáez, Elisama V. Dos Santos, and Manuel A. Rodrigo. "Full and Sustainable Electrochemical Production of Chlorine Dioxide." Catalysts 12, no. 3 (March 9, 2022): 315. http://dx.doi.org/10.3390/catal12030315.

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With the final purpose of manufacturing electrochemically-based devices that produce chloride dioxide efficiently, this paper focuses on the production of chlorates and hydrogen peroxide in two different electrochemical cells, in which operation conditions are selected to obtain high efficiencies, and in the subsequent combination of both electrochemically manufactured solutions to produce chlorine dioxide. Results demonstrate that suitable reagents can be produced by electrolyzing 20 g L−1 sodium chloride solutions at 50 mA cm−2 and 50 °C, and 3000 mg L−1 NaClO4 solutions at 5.0 mA cm−2 and 15 °C with current efficiencies of 30.9% and 48.0%, respectively. Different tests performed with these electrolyzed solutions, and also with commercial hydrogen peroxide and chlorate solutions, demonstrate that the ratio between both reagents plays a very important role in the efficiency in the production of chlorine dioxide. Results clearly showed that, surplus chlorate should be contained in the reagent media to prevent further reduction of chlorine dioxide by hydrogen peroxide and consequently, loses of efficiency in the process. During the reaction, a gas with a high oxidation capacity and consisting mainly in chloride dioxide is produced. The results contributed to the maximum conversion reached being 89.65% using electrolyzed solutions as precursors of ClO2, confirming that this technology can be promising to manufacture portable ClO2 devices.
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7

Salverda, Michael, Antony Raj Thiruppathi, Farnood Pakravan, Peter C. Wood, and Aicheng Chen. "Electrochemical Exfoliation of Graphite to Graphene-Based Nanomaterials." Molecules 27, no. 24 (December 7, 2022): 8643. http://dx.doi.org/10.3390/molecules27248643.

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Here, we report on a new automated electrochemical process for the production of graphene oxide (GO) from graphite though electrochemical exfoliation. The effects of the electrolyte and applied voltage were investigated and optimized. The morphology, structure and composition of the electrochemically exfoliated GO (EGO) were probed by scanning electron microscopy (SEM), transmission electron microscopy (TEM), X-ray diffraction (XRD), energy dispersive X-ray (EDX) spectroscopy, X-ray photoelectron spectroscopy (XPS), FTIR spectroscopy and Raman spectroscopy. Important metrics such as the oxygen content (25.3 at.%), defect density (ID/IG = 0.85) and number of layers of the formed EGO were determined. The EGO was also compared with the GO prepared using the traditional chemical method, demonstrating the effectiveness of the automated electrochemical process. The electrochemical properties of the EGO, CGO and other carbon-based materials were further investigated and compared. The automated electrochemical exfoliation of natural graphite powder demonstrated in the present study does not require any binders; it is facile, cost-effective and easy to scale up for a large-scale production of graphene-based nanomaterials for various applications.
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8

Kishimoto, Naoyuki, Saki Ito, Masaaki Kato, and Hideo Otsu. "Efficacy of an electrochemical flow cell introduced into the electrochemical Fenton-type process using a Cu(I)/HOCl system." Water Science and Technology 80, no. 1 (July 1, 2019): 184–90. http://dx.doi.org/10.2166/wst.2019.267.

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Abstract An electrochemical flow cell was introduced into the electrochemical Fenton-type process using a Cu(I)/HOCl system. The effects of the current density and the initial cupric ion (Cu2+) concentration on the process performance were discussed. The current efficiency of the process improved from 6.1% for an electrolytic tank system to 33% for the electrochemical flow cell system at a current density of 5.0 mA/cm2 and an initial Cu2+ concentration of 1.0 mM. The current efficiency increased to 58% for Cu2+ concentrations of 2.0 mM and beyond. The cathodic reduction of Cu2+ to the cuprous ion (Cu+) emerged as the rate-determining step in comparison to the anodic production of free chlorine. The introduction of the electrochemical flow cell enhanced the cathodic production of Cu+ by reinforcing the mass transfer of the Cu2+ to the cathode, and the detachment of micro bubbles generated electrochemically at the cathode surface. A decrease in the current density and an increase in the initial Cu2+ concentration also improved the current efficiency by promoting the cathodic production of Cu+. This involved the prevention of the cathodic reduction of protons to hydrogen gas and the elevation of the electrode potential of the cathodic reaction from Cu2+ to Cu+.
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9

Popczyk, Magdalena, Julian Kubisztal, Bożena Łosiewicz, and A. Budniok. "Production and Electrochemical Characterization of Nickel Based Composite Coatings Containing Chromium Group Metal and Silicon Powders." Solid State Phenomena 228 (March 2015): 219–24. http://dx.doi.org/10.4028/www.scientific.net/ssp.228.219.

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The Ni+Cr+Si, Ni+Mo+Si and Ni+W+Si composite coatings were obtained by electrodeposition of crystalline nickel from an electrolyte containing suspension of suitable metallic and non-metallic components (Cr, Mo, W and Si). These coatings were obtained galvanostatically at the current density of jdep = -0.100 A cm-2 and at the temperature of 338 K. Chemical composition of the coatings was determined by energy dispersive spectroscopy (EDS). The electrochemical activity of these electrocatalysts was studied in the process of hydrogen evolution reaction (HER) in 5 M KOH solution using steady-state polarization and electrochemical impedance spectroscopy (EIS) methods. The kinetic parameters of the HER on particular electrode materials were determined. It was found that Ni+Mo+Si composite coatings are characterized by enhanced electrochemical activity towards the HER as compared with Ni+W+Si and Ni+Cr+Si coatings due to the presence of Mo and increase in electrochemically active surface area.
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10

Pak, Daewon, and Santha Chakrovortty. "Hydroxyl radical production in electrochemical reactor." International Journal of Environment and Pollution 27, no. 1/2/3 (2006): 195. http://dx.doi.org/10.1504/ijep.2006.010462.

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11

Garcia, Amanda C., Carlos Sánchez-Martínez, Ivan Bakker, and Earl Goetheer. "Sustainable Electrochemical Production of Tartaric Acid." ACS Sustainable Chemistry & Engineering 8, no. 28 (June 22, 2020): 10454–60. http://dx.doi.org/10.1021/acssuschemeng.0c02493.

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12

Sharp, Duncan, Stephen Forsythe, and James Davis. "Electrochemical Monitoring of Singlet Oxygen Production." Electroanalysis 21, no. 21 (November 2009): 2293–96. http://dx.doi.org/10.1002/elan.200904682.

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13

Eisazadeh, H., K. J. Gilmore, A. J. Hodgson, G. Spinks, and G. G. Wallace. "Electrochemical production of conducting polymer colloids." Colloids and Surfaces A: Physicochemical and Engineering Aspects 103, no. 3 (October 1995): 281–88. http://dx.doi.org/10.1016/0927-7757(95)03297-q.

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14

Goodridge, F., S. Harrison, and R. E. Plimley. "The electrochemical production of propylene oxide." Journal of Electroanalytical Chemistry and Interfacial Electrochemistry 214, no. 1-2 (December 1986): 283–93. http://dx.doi.org/10.1016/0022-0728(86)80103-6.

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15

Gouws, S., B. Barton, P. L. R. Loyson, and B. Zeelie. "Electrochemical production of alkoxy-substituted phenols." Electrochimica Acta 53, no. 13 (May 2008): 4544–49. http://dx.doi.org/10.1016/j.electacta.2008.01.047.

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16

Okada, Fumio, Shunya Tanaka, Shinya Tanaka, and Kazunari Naya. "Electrochemical Production of 70wtppm Ozone Water." Electrochimica Acta 153 (January 2015): 210–16. http://dx.doi.org/10.1016/j.electacta.2014.12.010.

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17

Yakar Elbeyli, İffet, Abdullah Zahid Turan, and İ. Ersan Kalafatoğlu. "The electrochemical production of boric acid." Journal of Chemical Technology & Biotechnology 90, no. 10 (August 19, 2014): 1855–60. http://dx.doi.org/10.1002/jctb.4496.

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18

Koleva, Ralitza, Toma Stankulov, Reneta Boukoureshtlieva, Huseyin Yemendzhiev, Anton Momchilov, and Valentin Nenov. "Alternative Biological Process for Livestock Manure Utilization and Energy Production Using Microbial Fuel Cells." Journal of The Electrochemical Society 169, no. 3 (March 1, 2022): 034521. http://dx.doi.org/10.1149/1945-7111/ac5853.

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Carbon-based porous materials are most widely used for Microbial Fuel Cells (MFC) based on their unique properties facilitating and allowing the development of high surface area electrode. The electrochemically active layer of the electrode was prepared using two types of catalysts: activated carbon (Norit NK) and activated carbon promoted with CoTMPP (AC/CoTMPP). Mobilization of phosphate ions in the liquid phase was observed during the process of livestock manure treatment. From 20 mg l−1 initially, the concentration of dissolved phosphates reached 100 mg l−1 after 96 h. Increased concentration of ammonium ions in the medium was also observed, indicating ongoing anaerobic mineralization of the organic matter. The processes taking place in the bio electrochemical reactor used result in recovery of nutrients and production of energy. A maximum current density of 140 μА cm−2 was reached during the MFC operation. The chemical oxygen demand (COD) removal rates were relatively high (above 2 g O2/L/h) for both differently catalyzed cathode configurations. As widely reported elsewhere, the electrochemical results confirm that a gas-diffusion electrode using activated carbon catalyst is very well suited as a positive electrode for use in bio electrochemical systems.
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19

Egorov, V. G., M. A. Vasechkin, O. Yu Davydov, A. V. Pribytkov, and E. D. Chertov. "Electrochemical water treatment plant for food production." IOP Conference Series: Earth and Environmental Science 640, no. 7 (February 1, 2021): 072038. http://dx.doi.org/10.1088/1755-1315/640/7/072038.

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20

Onoda, Mitsuyoshi, Shigenao Namba, Masaki Fujimoto, and Hiroshi Nakayama. "Production of polypyrrole fiber by electrochemical polymerization." IEEJ Transactions on Fundamentals and Materials 114, no. 11 (1994): 835–36. http://dx.doi.org/10.1541/ieejfms1990.114.11_835.

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21

Demeev, B., V. Dzekunov, and M. Nauryzbaev. "Electrochemical production of ultrafine powders of copper." Chemical Bulletin of Kazakh National University, no. 4 (December 1, 2011): 218. http://dx.doi.org/10.15328/chemb_2011_4218-226.

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22

Abakumov, Maxim Vasilyevich, Artem Vladimirovich Kolesnikov, Maxim Konstantinovich Isaev, Chan Moe Nyein, and Akhmetov Ildar Akhmetov. "PRODUCTION OF PEROXODISULFURIC ACID BY ELECTROCHEMICAL METHOD." Chemical Industry Today, no. 4 (2022): 36–43. http://dx.doi.org/10.53884/27132854_2022_4_36.

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23

Yang, Hong Bin, and Bin Liu. "Electrochemical looping hydrogen production at room temperature." Chem Catalysis 1, no. 7 (December 2021): 1365–66. http://dx.doi.org/10.1016/j.checat.2021.11.012.

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24

Xie, Kaiyu, and Ali Reza Kamali. "Electrochemical production of hydrogen in molten salt." Energy Conversion and Management 251 (January 2022): 114980. http://dx.doi.org/10.1016/j.enconman.2021.114980.

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25

Perego, Andrea, Devashish Kulkarni, Hung-Ming Chang, Xinbo Wang, Jianlei Wei, Mo Li, and Iryna V. Zenyuk. "Electrochemical Flow Reactor for Cement Clinker Production." ECS Meeting Abstracts MA2021-02, no. 27 (October 19, 2021): 840. http://dx.doi.org/10.1149/ma2021-0227840mtgabs.

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26

Howalt, J. G., and T. Vegge. "Electrochemical ammonia production on molybdenum nitride nanoclusters." Physical Chemistry Chemical Physics 15, no. 48 (2013): 20957. http://dx.doi.org/10.1039/c3cp53160k.

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27

Eranskaya, T. Yu, and V. S. Rimkevich. "Electrochemical production of aluminum hydroxide from kaolins." Theoretical Foundations of Chemical Engineering 50, no. 5 (September 2016): 806–11. http://dx.doi.org/10.1134/s0040579516050055.

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28

Baranov, I. L., L. S. Stanovaya, L. V. Tabulina, and T. G. Rusal'skaya. "Electrochemical Production of Ultrathin Silicon Dioxide Films." Russian Journal of Electrochemistry 40, no. 2 (February 2004): 200–202. http://dx.doi.org/10.1023/b:ruel.0000016335.48491.6a.

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29

Murashkina, A. A., D. A. Medvedev, V. S. Sergeeva, and A. K. Demin. "Hydrogen production by electrochemical reforming of ethanol." Petroleum Chemistry 53, no. 7 (November 13, 2013): 489–93. http://dx.doi.org/10.1134/s0965544113070128.

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30

Hsu, W. K., J. Li, H. Terrones, M. Terrones, N. Grobert, Y. Q. Zhu, S. Trasobares, et al. "Electrochemical production of low-melting metal nanowires." Chemical Physics Letters 301, no. 1-2 (February 1999): 159–66. http://dx.doi.org/10.1016/s0009-2614(99)00003-2.

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31

Barisci, J. N., A. J. Hodgson, L. Liu, G. G. Wallace, and G. Harper. "Electrochemical production of protein-containing polypyrrole colloids." Reactive and Functional Polymers 39, no. 3 (March 1999): 269–75. http://dx.doi.org/10.1016/s1381-5148(98)00005-4.

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32

Yu, Pei, Zhiming Tian, Sean E. Lowe, Jingchao Song, Zhirui Ma, Xin Wang, Zhao Jun Han, et al. "Mechanically-Assisted Electrochemical Production of Graphene Oxide." Chemistry of Materials 28, no. 22 (November 11, 2016): 8429–38. http://dx.doi.org/10.1021/acs.chemmater.6b04415.

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33

DANDAPANI, B., and J. BOCKRIS. "Electrochemical recycling of iron for hydrogen production." International Journal of Hydrogen Energy 11, no. 2 (1986): 101–5. http://dx.doi.org/10.1016/0360-3199(86)90047-9.

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34

Kjos, Ole Sigmund, Geir Martin Haarberg, and Ana Maria Martinez. "Electrochemical Production of Titanium from Oxycarbide Anodes." Key Engineering Materials 436 (May 2010): 93–101. http://dx.doi.org/10.4028/www.scientific.net/kem.436.93.

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The aim of this work was to improve the quality of the produced titanium at the cathode in electrolysis experiments using a titanium oxycarbide anode, which is made of a solid solution of TiC and TiO. Two different approaches were tested: solid titanium deposition from a NaCl-Na3AlF6 electrolyte, and a standard NaCl-KCl electrolyte with a liquid metal cathode producing a titanium alloy.
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35

Raja, M. "Production of copper nanoparticles by electrochemical process." Powder Metallurgy and Metal Ceramics 47, no. 7-8 (July 2008): 402–5. http://dx.doi.org/10.1007/s11106-008-9034-2.

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36

Dimitrov, Aleksandar T., Ana Tomova, Anita Grozdanov, Orce Popovski, and Perica Paunović. "Electrochemical production, characterization, and application of MWCNTs." Journal of Solid State Electrochemistry 17, no. 2 (October 13, 2012): 399–407. http://dx.doi.org/10.1007/s10008-012-1896-z.

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37

Osarinmwian, C., I. M. Mellor, and E. P. L. Roberts. "Titanium production in rotationally symmetric electrochemical reactors." Electrochimica Acta 164 (May 2015): 48–54. http://dx.doi.org/10.1016/j.electacta.2015.02.146.

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38

Thirumal, Vediyappan, T. V. M. Sreekanth, Kisoo Yoo, and Jinho Kim. "Facile Preparations of Electrochemically Exfoliated N-Doped Graphene Nanosheets from Spent Zn-Carbon Primary Batteries Recycled for Supercapacitors Using Natural Sea Water Electrolytes." Energies 15, no. 22 (November 18, 2022): 8650. http://dx.doi.org/10.3390/en15228650.

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A single production of nitrogen-doped graphene nanosheets was developed in this present work from a spent Zn-C primary battery. The electrochemically exfoliated nitrogen-doped graphene nanosheets (EC-N-GNS) was applied in supercapacitor symmetric devices. As-prepared EC-N-GNS was utilized for a symmetric supercapacitor with natural seawater multivalent ion electrolyte. The recycling of graphite into nitrogen-doped graphene was characterized by X-ray diffraction and RAMAN spectroscopy. The few-layered morphological structures of EC-N-GNS were analyzed by field emission scanning electron microscope and field emission transmission electron microscope. The electrochemical analysis of the cyclic voltammetry curves observed an electrochemical double-layer capacitor (EDLC) behavior with a potential window of −0.8 V to +0.5 V. The electrochemical galvanostatic charge—discharge study was obtained to be maximum specific capacitance (Csp)—67.69 F/g and 43.07 F/g at a current density of 1 A/g. We promising the facile single-step electrochemically exfoliated EC-N-GNS was obtained from a waste zinc-carbon primary battery to recycle the graphite electrodes. The superior electrochemical performance comparatively bulk graphite and EC-N-GNS for potential energy storage supercapacitor applications.
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39

Feng, Gaomin, Beibei Liu, Jinghang Li, Tianlei Cheng, Zhanglong Huang, Xianhua Wang, and Heping (Peace) Cheng. "Mitoflash biogenesis and its role in the autoregulation of mitochondrial proton electrochemical potential." Journal of General Physiology 151, no. 6 (March 15, 2019): 727–37. http://dx.doi.org/10.1085/jgp.201812176.

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Respiring mitochondria undergo an intermittent electrical and chemical excitation called mitochondrial flash (mitoflash), which transiently uncouples mitochondrial respiration from ATP production. How a mitoflash is generated and what specific role it plays in bioenergetics remain incompletely understood. Here, we investigate mitoflash biogenesis in isolated cardiac mitochondria by varying the respiratory states and substrate supply and by dissecting the involvement of different electron transfer chain (ETC) complexes. We find that robust mitoflash activity occurs once mitochondria are electrochemically charged by state II/IV respiration (i.e., no ATP synthesis at Complex V), regardless of the substrate entry site (Complex I, Complex II, or Complex IV). Inhibiting forward electron transfer abolishes, while blocking reverse electron transfer generally augments, mitoflash production. Switching from state II/IV to state III respiration, to allow for ATP synthesis at Complex V, markedly diminishes mitoflash activity. Intriguingly, when mitochondria are electrochemically charged by the ATPase activity of Complex V, mitoflashes are generated independently of ETC activity. These findings suggest that mitoflash biogenesis is mechanistically linked to the build up of mitochondrial electrochemical potential rather than ETC activity alone, and may functionally counteract overcharging of the mitochondria and hence serve as an autoregulator of mitochondrial proton electrochemical potential.
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40

Li, Qiang, Wei Ying Liu, Guo Yin Sun, and Juan Fang Shang. "Research Progress of Combined Application of Sol-Gel and Electrochemistry." Key Engineering Materials 768 (April 2018): 119–28. http://dx.doi.org/10.4028/www.scientific.net/kem.768.119.

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There were many advantages for functional materials production using Sol-gel method, such as low operating temperature and easy doping. So, it was widely used in materials preparation, such as nano powders, films, functional glass, nanoceramic and modified electrode. The sol-gel modified electrode has extensive application in electrochemical analysis and electrochemical sensors. In addition, the film by electrodeposition can be tightly assembled on electrode substrate and its structure and shape can be easily regulated. So, The two methods are combined to make better use of their respective advantages. Up to now, the film materials using electrochemically induced sol-gel had been used in electrochemistry analysis and functional films preparation. In this paper, it was summarized that the progress of combined application of sol-gel and electrochemistry. Mainly including sol-gel materials, modified electrodes, electrochemical analysis and sensors, and electrochemical induction sol-gel method for the preparation of thin film materials.
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41

Choi, Hyeonggeun, Suok Lee, Min-Cheol Kim, Yeonsu Park, A.-Rang Jang, Wook Ahn, Jung Inn Sohn, Jong Bae Park, John Hong, and Young-Woo Lee. "Hierarchically Ordinated Two-Dimensional MoS2 Nanosheets on Three-Dimensional Reduced Graphene Oxide Aerogels as Highly Active and Stable Catalysts for Hydrogen Evolution Reaction." Catalysts 11, no. 2 (January 30, 2021): 182. http://dx.doi.org/10.3390/catal11020182.

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Анотація:
Hydrogen gas (H2) is being intensively proposed as a next-generation clean energy owing to the depletion of fossil fuels. Electrochemical water splitting is one of the most promising processes for hydrogen production. Furthermore, many efforts focusing on electrochemical water splitting have been made to develop low-cost, electrochemically active, and stable catalysts for efficient hydrogen production. MoS2 has emerged as an attractive material for developing catalysts for the hydrogen evolution reaction (HER). Hence, in this study, we design hierarchically ordinated two-dimensional (2D) MoS2 nanosheets on three-dimensional (3D) reduced graphene oxide (rGO) (H-2D/3D-MoS2-rGO) aerogel structures as a new class of electrocatalysts for the HER. We use the one-pot hydrothermal synthesis route for developing high-performance electroactive materials for the HER. The as-prepared H-2D/3D-MoS2-rGO contains a unique 3D hierarchical structure providing large surface areas owing to the 3D porous networks of rGO and more active sites owing to the many edge sites in the MoS2 nanosheets. In addition, the H-2D/3D-MoS2-rGO structure exhibits remarkable electrochemical properties during the HER. It shows a lower overpotential than pure MoS2 and excellent electrochemical stability owing to the large number of active sites (highly exposed edge sites) and high electrical conductivity from the rGO structure.
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42

Jo, Seunghwan, Young-Woo Lee, John Hong, and Jung Inn Sohn. "Simple and Facile Fabrication of Anion-Vacancy-Induced MoO3−X Catalysts for Enhanced Hydrogen Evolution Activity." Catalysts 10, no. 10 (October 14, 2020): 1180. http://dx.doi.org/10.3390/catal10101180.

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Advanced catalysts for clean hydrogen generation and storage offer an attractive possibility for developing a sustainable and ecofriendly future energy system. Transition metal oxides (TMO) are appealing candidates to be largely considered as electrode catalysts. However, for practical applications, there are still challenges—the intrinsic catalytic properties of TMOs should be further improved and TMOs should be synthesized by practical routes for cost-effective and scalable production of catalysts. Therefore, finding promising ways to fabricate highly active TMOs with outstanding electrochemical hydrogen evolution performance is required. Here, we present a direct and facile synthetic approach to successfully provide highly efficient MoO3−X catalysts with electrochemically active oxygen vacancies through a one-step thermal activation process on a Mo metal mesh. Variations in the oxidation states of molybdenum oxides can significantly increase the active sites of the catalysts and improve the electrochemical activity, making these oxide compounds suitable for hydrogen evolution reaction (HER). Compared to the bare Mo mesh and fully oxidized Mo (MoO3) electrodes, the fabricated MoO3−X electrode exhibits better electrochemical performance in terms of overpotentials and Tafel slope, as well as the electrochemical 1000 cycling stability, confirming the improved HER performance of MoO3−X. This provides new insight into the simple procedure suitable for the large-production supply.
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43

Hung, Yi-Fang, Chia Cheng, Chun-Kai Huang, and Chii-Rong Yang. "A Facile Method for Batch Preparation of Electrochemically Reduced Graphene Oxide." Nanomaterials 9, no. 3 (March 5, 2019): 376. http://dx.doi.org/10.3390/nano9030376.

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The electrochemical reduction of graphene oxide (GO) is an environmentally friendly and energy-saving method for improving the characteristics of GO. However, GO films must be coated on the cathode electrode in advance when usingthis technique. Thus, the formed electrochemically reduced GO (ERGO) films can be used only as sensing or conductive materials in devices because mass production of the flakes is not possible. Therefore, this study proposes a facile electrochemical reduction technique. In this technique, GO flakes can be directly used as reduced materials, and no GO films are required in advance. A 0.1 M phosphate buffered saline solution was used as the electrolyte, which is a highly safe chemical agent. Experimental results revealed that the as-prepared GO flakes were electrochemically reduced to form ERGO flakes by using a −10 V bias for 8 h. The ratio of the D-band and G-band feature peaks was increased from 0.86 to 1.12, as revealed by Raman spectroscopy, the π-π stacking interaction operating between the ERGO and GO has been revealed by UV-Vis absorption spectroscopy, and the C–O ratio was increased from 2.02 to 2.56, as indicated by X-ray photoelectron spectroscopy. The electrical conductivity of the ERGO film (3.83 × 10−1 S·cm−1) was considerably better than that of the GO film (7.92 × 10−4 S·cm−1). These results demonstrate that the proposed electrochemical reduction technique can provide high-quality ERGO flakes and that it has potential for large-scale production.
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44

Shlosberg, Yaniv, Kimi C. Rubino, Nathan S. Nasseri, and Andrea S. Carlini. "Photocurrent Production from Cherries in a Bio-Electrochemical Cell." Electrochem 4, no. 1 (February 9, 2023): 47–55. http://dx.doi.org/10.3390/electrochem4010005.

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In recent years, clean energy technologies that meet ever-increasing energy demands without the risk of environmental contamination has been a major interest. One approach is the utilization of plant leaves, which release redox-active NADPH as a result of photosynthesis, to generate photocurrent. In this work, we show for the first time that photocurrent can be harvested directly from the fruit of a cherry tree when associated with a bio-electrochemical cell. Furthermore, we apply electrochemical and spectroscopic methods to show that NADH in the fruit plays a major role in electric current production.
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45

Guo, Jinyu, Elizabeth R. Corson, and William Abraham Tarpeh. "Characterization of Interfacial Properties in Electrochemical Nitrate Reduction to Optimize Ammonia Production." ECS Meeting Abstracts MA2022-01, no. 26 (July 7, 2022): 1236. http://dx.doi.org/10.1149/ma2022-01261236mtgabs.

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Nitrate pollution of wastewater from agricultural runoff and industrial waste streams is common around the globe. Nitrate negatively impacts the environment through harmful algal blooms and can be dangerous for human consumption. Rather than treat nitrate as a waste, we electrochemically reduce nitrate (NO3RR) to ammonia (NO3 - + 9H+ + 8e- → NH3 + 3H2O), a commonly used fertilizer and clean fuel. Electrochemical treatment can enable on-site, modular treatment powered by renewable energy. As an inner-sphere reaction involving multiple hydrogenation and electron-transfer steps, the activity and selectivity of electrochemical NO3RR to NH3 are strongly influenced by properties at the electrode–electrolyte interface. When potential is applied, the electric double layer (EDL) forms that comprises ordered molecular layers extending up to 10 Å from the surface. This EDL is the primary environment where the heterogeneous NO3RR occurs and can impact the reaction in several ways, including blocking catalytic sites and stabilizing reactants and reaction intermediates. To understand the molecular mechanisms of these impacts, the EDL structure is studied with x-ray reflectivity (XRR), which provides atomic-level resolution of the near-surface electron density profile and reveals the number of ordered layers, the distance of each layer from the surface, the ion surface coverage, and the degree of hydration of ions in each layer. We complement these investigations with operando attenuated total reflectance–surface-enhanced infrared absorption spectroscopy (ATR–SEIRAS) under similar reaction conditions to investigate the adsorbed reactants, intermediates, and local pH. Furthermore, composition and structure of the EDL can change with varying bulk electrolyte compositions and mass transport regimes, which also provide levers to control reaction activity and selectivity. We use a continuum model (generalized modified Poisson–Nernst–Planck, GMPNP) to develop the spatial profiles of the electric field, reactant nitrate concentration, cation concentrations, and pH outside the EDL and how they change as functions of applied potential, bulk electrolyte composition, and flow rate. Taken together, our results relate 1) bulk electrolyte properties with interfacial EDL properties and 2) interfacial properties with reaction activity and selectivity, informing the choice of operating parameters such as electrolyte composition and flow rate to optimize ammonia production in electrochemical NO3RR.
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46

Contigiani, Camila C., Juan P. Fornés, Omar González Pérez, and José M. Bisang. "Colloidal sulphur production by electrochemical oxidation of sulphide in a swirling flow reactor." Reaction Chemistry & Engineering 7, no. 2 (2022): 326–32. http://dx.doi.org/10.1039/d1re00395j.

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47

Walke, Witold, and Joanna Przondziono. "Electrochemical Behaviour of Stainless Steel Wire for Urology." Solid State Phenomena 165 (June 2010): 404–9. http://dx.doi.org/10.4028/www.scientific.net/ssp.165.404.

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The study presents results of pitting corrosion tests and analysis of chemical composition of X2CrNiMo 17-12-2 steel surface layer with diversified strain hardening and the method of surface preparation after 30-day exposure to artificial urine. Samples with electrochemically polished as well as with electrochemically polished and chemically passivated surface were selected for the tests. Electrochemical passivation was applied in order to obtain extremely smooth surface (Ra0.16 m). Pitting corrosion tests were performed by means of potentiodynamic method, where analysis of chemical composition of the layer formed on the steel surface was conducted using X-ray photoelectron spectroscopy (XPS). The tests were carried out in order to determine suitability of X2CrNiMo 17-12-2 steel with modified surface and diversified strain hardening for production of wire used in urology.
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48

Vasilescu, Alina, Pablo Fanjul-Bolado, Ana-Maria Titoiu, Roxana Porumb, and Petru Epure. "Progress in Electrochemical (Bio)Sensors for Monitoring Wine Production." Chemosensors 7, no. 4 (December 16, 2019): 66. http://dx.doi.org/10.3390/chemosensors7040066.

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Анотація:
Electrochemical sensors and biosensors have been proposed as fast and cost effective analytical tools, meeting the robustness and performance requirements for industrial process monitoring. In wine production, electrochemical biosensors have proven useful for monitoring critical parameters related to alcoholic fermentation (AF), malolactic fermentation (MLF), determining the impact of the various technological steps and treatments on wine quality, or assessing the differences due to wine age, grape variety, vineyard or geographical region. This review summarizes the current information on the voltamperometric biosensors developed for monitoring wine production with a focus on sensing concepts tested in industry-like settings and on the main quality parameters such as glucose, alcohol, malic and lactic acids, phenolic compounds and allergens. Recent progress featuring nanomaterial-enabled enhancement of sensor performance and applications based on screen-printed electrodes is emphasized. A case study presents the monitoring of alcoholic fermentation based on commercial biosensors adapted with minimal method development for the detection of glucose and phenolic compounds in wine and included in an automated monitoring system. The current challenges and perspectives for the wider application of electrochemical sensors in monitoring industrial processes such as wine production are discussed.
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49

Rodríguez-Peña, Mayra, José Antonio Barrios Pérez, Javier Llanos, Cristina Sáez, Manuel Andrés Rodrigo, and Carlos Eduardo Barrera-Díaz. "New insights about the electrochemical production of ozone." Current Opinion in Electrochemistry 27 (June 2021): 100697. http://dx.doi.org/10.1016/j.coelec.2021.100697.

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50

Yuan, Boyan, and Toru H. Okabe. "Production of Fine Tantalum Powder by Electrochemical Method." MATERIALS TRANSACTIONS 48, no. 10 (2007): 2687–94. http://dx.doi.org/10.2320/matertrans.m-mra2007876.

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