Covalent functionalization of tungsten disulfide (WS ) with photo- and electro-active nickel-porphyrin (NiP) is reported. Exfoliated WS interfacing NiP moieties with 1,2-dithiolane linkages is assayed in the oxygen evolution reaction under both dark and illuminated conditions. The hybrid material presented, WS -NiP, is fully characterized with complementary spectroscopic, microscopic, and thermal techniques. Standard yet advanced electrochemical techniques, such as linear sweep voltammetry, electrochemical impedance spectroscopy, and calculation of the electrochemically active surface area, are used to delineate the catalytic profile of WS -NiP. In-depth study of thin films with transient photocurrent and photovoltage response assays uncovers photo-enhanced electrocatalytic behavior. The observed photo-enhanced electrocatalytic activity of WS -NiP is attributed to the presence of Ni centers coordinated and stabilized by the N motifs of tetrapyrrole rings at the tethered porphyrin derivative chains, which work as photoreceptors. This pioneering work opens wide routes for water oxidation, further contributing to the development of non-noble metal electrocatalysts.
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http://dx.doi.org/10.1002/cssc.202202322 | DOI Listing |
Front Chem
April 2024
Department of Chemistry, Missouri University of Science and Technology, Rolla, MO, United States.
The photo-enhanced electrocatalytic method of oxygen evolution reaction (OER) shows promise for enhancing the effectiveness of clear energy generation through water splitting by using renewable and sustainable source of energy. However, despite benefits of photoelectrocatalytic (PEC) water splitting, its uses are constrained by its low efficiency as a result of charge carrier recombination, a large overpotential, and sluggish reaction kinetics. Here, we illustrate that Nickel telluride (NiTe) synthesized by hydrothermal methods can function as an extremely effective photo-coupled electrochemical oxygen evolution reaction (POER) catalyst.
View Article and Find Full Text PDFJ Colloid Interface Sci
April 2024
School of Chemistry and Chemical Engineering/State Key Laboratory Incubation Base for Green Processing of Chemical Engineering, Shihezi University, Shihezi 832003, China. Electronic address:
NiMo-based electrocatalysts are widely regarded as promising electrocatalysts for overall water splitting (OWS). However, to solve the problem of slow reaction kinetics and serious deactivation at high current density, the reasonable design of NiMo-based electrocatalysts is still a great challenge. In this work, NiMo-based phosphorus/sulfide heterostructure electrocatalysts with different Ce doping ratios (5%/10%/15%Ce-NiMo-PS@NF) have been designed using the combination of cation doping and heterostructure engineering.
View Article and Find Full Text PDFSmall
March 2023
Department of Chemistry, Capital Normal University, Beijing, 100048, China.
Direct electrocatalytic reduction of N to NH under mild conditions is attracting considerable interests but still remains enormous challenges in terms of respect of intrinsic catalytic activity and limited electrocatalytic efficiency. Herein, a photo-enhanced strategy is developed to improve the NRR activity on Cu single atoms catalysts. The atomically dispersed Cu single atoms supported TiO nanosheets (Cu SAs/TiO ) achieve a Faradaic Efficiency (12.
View Article and Find Full Text PDFChemSusChem
April 2023
Theoretical and Physical Chemistry Institute, National Hellenic Research Foundation, 48 Vassileos Constantinou Avenue, 11635, Athens, Greece.
Chem Commun (Camb)
September 2021
Key Laboratory for Colloid and Interface Chemistry of State Education Ministry, School of Chemistry and Chemical Engineering, Shandong University, Jinan 250100, China.
A gold-ruthenium/zinc oxide nanorod composite was synthesized. The electrochemical catalytic efficiency of the noble metal-semiconductor nanostructure increased by nearly 30% under the irradiation of an external light source. It provides an efficient way of thinking for the design of electrocatalysts with a photoresponse.
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