Effect of temperature on process and kinetic parameters of the hydrogen evolution reaction of X80 under CP

2021 ◽  
Vol ahead-of-print (ahead-of-print) ◽  
Author(s):  
Shixiong Wu ◽  
Zhiming Gao ◽  
Da-Hai Xia ◽  
Meijun Wu ◽  
Yingjie Liu ◽  
...  

Purpose This paper aims to study the effect of temperature on the process and kinetic parameters of the hydrogen evolution reaction of X80 under cathodic protection (CP) in 3.5% NaCl solution. Design/methodology/approach Potentiodynamic polarization combined with the hydrogen permeation test is used to analyze the hydrogen evolution reaction (HER) process and the rate-determining step for which is diagnosed through the electrochemical impedance spectrum method. Then, the influence of temperature on kinetic parameters of HER can be known from the results obtained by using the Iver-Pickering-Zamenzadeh model for data analysis. Findings The results show that the HER proceeds through Volmer–Tafel route with the Volmer reaction acting as the rate-controlling step; Increasing temperature gives a higher activity of the HER on X80, it also accelerates the hydrogen desorption and diffusion of hydrogen into the metal. Originality/value There exist few studies on the topic of how temperature affects the HER process. It is imperative to conduct a relevant study to give some instruction in cathodic protection system design and this paper fulfills this need.


2013 ◽  
Vol 772 ◽  
pp. 343-348
Author(s):  
Zhao Xiong Yan ◽  
Zhi Hua Xu ◽  
Li Hong Zhu

TiO2nanotube arrays (TNAs) modified by CuO (CuO-TNAs) catalysts were prepared by an impregnating-calcinating method using the electrochemically prepared TNAs and Cu (NO3)2as precursors and were characterized by scanning electron microscope, transmission electron microscopy, X-ray diffraction spectroscopy and UV-visible spectroscopy. The electrocatalytic properties of the CuO-TNAs samples for hydrogen evolution reaction (HER) were investigated by linear sweep curves, electrochemical impedance spectrum and current-time curves. The results showed that the electrocatalytic activity of TNAs for hydrogen evolution reaction (HER) was significantly enhanced by CuO modification, and the electrocatalytic activity of CuO-TNAs catalysts could be further promoted by visible-light illumination. The combination of visible-light irradiation with applying a controlled potential may provide new insight into enhancing the performances of the cathode for hydrogen evolution reaction.



2020 ◽  
Vol 67 (2) ◽  
pp. 197-204
Author(s):  
JiaYu Zhou ◽  
Zili Li ◽  
JianGuo Liu ◽  
Xiao Xing ◽  
Gan Cui ◽  
...  

Purpose The purpose of this paper is to quantify the influence of alternating current (AC) interference on hydrogen evolution reaction of X80 steel. Design/methodology/approach The hydrogen evolution potential was obtained by cathodic potentiodynamic polarization curve. The instantaneous potential under AC interference was obtained by high-frequency acquisition with three-electrode system. Electrochemical impedance spectroscopy and Tafel polarization curves were used to study the influence mechanism of AC interference on instantaneous potential. Findings It was concluded that the hydrogen evolution reaction could occur on X80 steel under AC interference. There were critical AC current densities of about 100 to 200 A/m2, beyond which the cathode reaction of X80 steel changed from oxygen absorption to hydrogen evolution. Besides the pH value, the initial polarization potential EZ and impedance module of the steel/electrolyte interface under AC interference were also the factors that affected the critical AC densities in different solutions. Originality/value This research quantified the hydrogen evolution capacity of X80 steel under AC interference, which could be applied to clear the effect of AC interference on hydrogen evolution reaction.



2021 ◽  
Vol ahead-of-print (ahead-of-print) ◽  
Author(s):  
Huizhong Zhang ◽  
Yu Zuo ◽  
Pengfei Ju ◽  
Jian Zhang ◽  
Xuhui Zhao ◽  
...  

Purpose The purpose of this paper is to study the variations of composition and properties of the passive film on 316 L stainless steel surface in 80°C, 0.5 mol L-1 H2SO4 + 2 mg L-1 NaF solution, is helpful to understand the mechanisms of corrosion resistancethe of plated Pd on 316 L ss. Design/methodology/approach The variations of composition and properties of the passive film on 316 L stainless steel surface in 80°C, 0.5 mol L-1 H2SO4 + 2 mg L-1 NaF solution after connected to Pd electrode were studied with methods of potential monitor, X-ray photoelectron spectroscopy analysis and electrochemical impedance spectrum (EIS) measurement. Findings By connecting to a Pd electrode, the potential of the SS sample increased from the active region to the passive region. By connecting to the Pd electrode, the contents of Cr, Cr(OH)3 and Fe3O4 in passive film increased obviously. With increased Pd/SS area ratio, the Cr(OH)3 content in passive film increased but the Fe3O4 content changed little. The results show that after connecting to Pd the corrosion resistance of the passive film on 316 L stainless steel increases obviously, which may be attributed to the more compact passive film because of higher Cr, Cr(OH)3 and Fe3O4 contents and less point defects in the film. Originality/value The effects and mechanism of Pd on passivation of SS was studied.



2019 ◽  
Vol 10 ◽  
pp. 62-70 ◽  
Author(s):  
Yong Li ◽  
Peng Yang ◽  
Bin Wang ◽  
Zhongqing Liu

Bimetallic phosphides have been attracting increasing attention due to their synergistic effect for improving the hydrogen evolution reaction as compared to monometallic phosphides. In this work, NiCoP modified hybrid electrodes were fabricated by a one-step electrodeposition process with TiO2 nanotube arrays (TNAs) as a carrier. X-ray diffraction, transmission electron microscopy, UV–vis diffuse reflection spectroscopy, X-ray photoelectron spectroscopy and scanning transmission electron microscopy/energy-dispersive X-ray spectroscopy were used to characterize the physiochemical properties of the samples. The electrochemical performance was investigated by cyclic voltammetry, linear sweep voltammetry, and electrochemical impedance spectroscopy. We show that after incorporating Co into Ni–P, the resulting Ni x Co y P/TNAs present enhanced electrocatalytic activity due to the improved electron transfer and increased electrochemically active surface area (ECSA). In 0.5 mol L−1 H2SO4 electrolyte, the Ni x Co y P/TNAs (x = 3.84, y = 0.78) demonstrated an ECSA value of 52.1 mF cm−2, which is 3.8 times that of Ni–P/TNAs (13.7 mF cm−2). In a two-electrode system with a Pt sheet as the anode, the Ni x Co y P/TNAs presented a bath voltage of 1.92 V at 100 mA cm−2, which is an improvment of 79% over that of 1.07 V at 10 mA cm−2.



2019 ◽  
Vol 2019 ◽  
pp. 1-4
Author(s):  
Zhihong Zhang ◽  
Baoying Wang ◽  
Yijing Zhang ◽  
Gehong Zhang ◽  
Yujing Wang

A novel heteropoly acid salt, Na6[Ni(Mo11ZrO39)]·20H2O, has been synthesized by the means of acidification and adding the reactants into the solution step by step. The heteropoly compound was characterized by elemental analysis, TGA/DSC, infrared spectrum, ultraviolet spectrum, X-ray diffraction, and SEM. Its protonic conduction was measured by the means of the electrochemical impedance spectrum. The results showed that it belongs to the Keggin type, and its conductivity value was 1.23 × 10–2 S/cm at 23°C when the relative humidity was 60%, and the conductivity enhanced with the elevated temperature. Its proton conduction mechanism was in accordance with vehicle mechanism, and the activation energy was 27.82 kJ/mol.



2013 ◽  
Vol 78 (4) ◽  
pp. 549-554 ◽  
Author(s):  
Uros Lacnjevac

Composite Ni-MoO2 coatings were prepared and characterized with respect to their possible application as electrocatalysts for the hydrogen evolution reaction (HER) in alkaline solution. The composites were electrodeposited onto Ni meshes from an ammonium chloride Ni solution with suspended MoO2 particles in simulated industrial conditions for production of commercial cathodes. The influence of the concentration of MoO2 particles in the solution and deposition current density on the morphology, chemical and phase composition of obtained coatings was investigated by scanning electron microscopy (SEM), energy dispersive X-ray spectroscopy (EDS) and X-ray diffraction (XRD). Catalytic activity for the HER of the coatings was examined by polarization measurements in a 32 wt. % NaOH solution at 90?C and compared to the activity of the commercial De Nora?s cathode (DN). It was shown that the most active Ni-MoO2 coating exhibits better polarization characteristics for the HER than the DN cathode. The mechanism of the HER on the specified Ni-MoO2 coating was investigated in 8 mol dm-3 NaOH at 30?C by means of steady-state polarization measurements and an electrochemical impedance spectroscopy (EIS) method. Based on the theoretical interpretation of the experimental data, rate constants of the three individual steps of the HER were determined and the source of catalytic activity of the coating was elucidated.



NANO ◽  
2020 ◽  
Vol 15 (07) ◽  
pp. 2050089
Author(s):  
Litong Niu ◽  
Shaoping Hu ◽  
Yali Ma ◽  
Mingming Wang ◽  
Bolin Lv ◽  
...  

Novel ZnIn2S4/FeUiO-66 (ZFeU) photocatalyst with different proportion of FeUiO-66 has been successfully prepared by a facile one-pot solvothermal reaction. The as-synthesized nanocomposites have been thoroughly characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), Fourier transform-infrared spectroscopy (FT-IR), UV-Vis diffuse reflectance spectroscopy (UV-Vis DRS), Brunauer–Emmett–Teller (BET) characterization, photoluminescence (PL) analysis and electrochemical impedance spectrum (EIS). The photocatalytic performance of ZFeU nanocomposites for the photodegradation of RhB under visible light irradiation was better than that of ZnIn2S4 and FeUiO-66 alone. The experiment results showed the 20% ZFeU nanocomposites had the best photocatalytic properties. At the same time, a probable mechanism was discussed and it was believed that introduction of FeUiO-66 on ZnIn2S4 would minimize the recombination of photogenerated electron-hole pairs, leading to the enhancement of the photocatalytic activity.



2019 ◽  
Vol 308 ◽  
pp. 328-336 ◽  
Author(s):  
Dominique Koster ◽  
Aleksandar R. Zeradjanin ◽  
Alberto Battistel ◽  
Fabio La Mantia


Crystals ◽  
2020 ◽  
Vol 10 (5) ◽  
pp. 356
Author(s):  
Kasimayan Uma ◽  
Elavarasan Muniranthinam ◽  
Siewhui Chong ◽  
Thomas C.-K Yang ◽  
Ja-Hon Lin

This report presents the synthesis of ZnO nanorod/α-Fe2O3 composites by the hydrothermal method with different weight percentages of α-Fe2O3 nanoparticles. The as-synthesized nanorod composites were characterized by different techniques, such as X-ray diffraction (XRD), Fourier transform-infrared (FT-IR), field emission scanning electron microscopy (FE-SEM), electrochemical impedance spectroscopy (EIS), and X-ray photoelectron spectroscopy (XPS). From our results, it was found that the ZnO/α-Fe2O3 (3 wt%) nanorod composites exhibit a higher hydrogen evolution reaction (HER) activity when compared to other composites. The synergetic effect between ZnO and (3 wt%) of α-Fe2O3 nanocomposites resulted in a low onset potential of −125 mV, which can effectively produce more H2 than pure ZnO. The H2 production rate over the composite of ZnO/α-Fe2O3 (3 wt%) clearly shows a significant improvement in the photocatalytic activity in the heterojunction of the ZnO nanorods and α-Fe2O3 nanoparticles on nickel foam.



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