The use of amorphous TiO (a-TiO), deposited by atomic layer deposition, is a common strategy to protect semiconductors from degradation when used in water-splitting photoelectrochemical (PEC) cells. Electrochemical impedance spectroscopy (EIS) is a suitable technique to study these PEC cells because it is capable of deconvoluting multiple processes occurring during operation, therefore providing information about mechanisms leading to the overall device performance. When biased under hydrogen evolution conditions, EIS shows that two simultaneous processes occur in a-TiO-protected photocathodes, which introduces an ambiguity in choosing the correct equivalent circuit to describe the operating device. In this report, a model p-Si|a-TiO|Pt photocathode system is used to show that the Maxwell circuit best describes the operating mechanism, as opposed to the more commonly used Voight and nested circuits. This indicates that, under hydrogen evolution conditions, both faradaic and nonfaradaic processes are occurring. Whereas the faradaic process corresponds to the hydrogen evolution reaction itself, the nonfaradaic process is traced to the p-Si|a-TiO interface.
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http://dx.doi.org/10.1021/acsami.4c07588 | DOI Listing |
Nano Lett
January 2025
Jiangxi Provincial Key Laboratory of Green Hydrogen and Advanced Catalysis, College of Physics, Communication and Electronics, Jiangxi Normal University, 99 Ziyang Avenue, Nanchang 330022, Jiangxi, China.
studies of the relationship between surface spin configurations and spin-related electrocatalytic reactions are crucial for understanding how magnetic catalysts enhance oxygen evolution reaction (OER) performance under magnetic fields. In this work, 2D FeSe nanosheets with rich surface spin configurations are synthesized via chemical vapor deposition. magnetic force microscopy and Raman spectroscopy reveal that a 200 mT magnetic field eliminates spin-disordered domain walls, forming a spin-ordered single-domain structure, which lowers the OER energy barrier, as confirmed by theoretical calculations.
View Article and Find Full Text PDFInorg Chem
January 2025
School of Chemistry and Chemical Engineering, School of Pharmacy, Jiangsu University, Zhenjiang 212013, P. R. China.
Electrochemical water splitting is a promising method for the generation of "green hydrogen", a renewable and sustainable energy source. However, the complex, multistep synthesis processes, often involving hazardous or expensive chemicals, limit its broader adoption. Herein, a nitrate (NO) anion-intercalated nickel-iron-cerium mixed-metal (oxy)hydroxide heterostructure electrocatalyst is fabricated on nickel foam (NiFeCeOH@NF) via a simple electrodeposition method followed by cyclic voltammetry activation to enhance its surface properties.
View Article and Find Full Text PDFJ Am Chem Soc
January 2025
Department of Chemistry, University of California, Berkeley, California 94720, United States.
Switchable selectivity achieved by altering reaction conditions within the same photocatalytic system offers great advantages for sustainable chemical transformations and renewable energy conversion. In this study, we investigate an efficient photocatalytic methanol dehydrogenation with controlled selectivity by varying the concentration of nickel cocatalyst, using zinc indium sulfide nanocrystals as a semiconductor photocatalyst, which enables the production of either formaldehyde or ethylene glycol with high selectivity. Control experiments revealed that formaldehyde is initially generated and can either serve as a terminal product or intermediate in producing ethylene glycol, depending on the nickel concentration in the solution.
View Article and Find Full Text PDFDalton Trans
January 2025
School of Material Science and Engineering, Hebei University of Technology, Tianjin 300130, P. R. China.
The design of acidic oxygen evolution reaction (OER) electrocatalysts with high activity and durability is the key to achieving efficient hydrogen production. Herein, we report a Cr-doped RuO (RuCrO) catalyst that exhibits good OER activity in acidic electrolytes. The doping of Cr increases the valence state of Ru, which enhances the activity of the catalyst, and a current density of 10 mA cm can be achieved at only 235 mV, which is superior to that of unmodified RuO of 299 mV.
View Article and Find Full Text PDFAcc Chem Res
January 2025
State Key Laboratory of Physical Chemistry of Solid Surfaces, Key Laboratory of Chemical Biology of Fujian Province, College of Chemistry and Chemical Engineering, and Discipline of Intelligent Instrument and Equipment, Xiamen University, Xiamen 361005, P. R. China.
ConspectusMolecular photoelectrocatalysis, which combines the merits of photocatalysis and organic electrosynthesis, including their green attributes and capacity to offer novel reactivity and selectivity, represents an emerging field in organic chemistry that addresses the growing demands for environmental sustainability and synthetic efficiency. This synergistic approach permits access to a wider range of redox potentials, facilitates redox transformations under gentler electrode potentials, and decreases the use of external harsh redox reagents. Despite these potential advantages, this area did not receive significant attention until 2019, when we and others reported the first examples of modern molecular photoelectrocatalysis.
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