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For decades, the sulfido molybdenum complexes like [MoS ] , [Mo S ] , [Mo S ] have gained great attention because of their chemical versatility as well as their structural similarity to the edge-plan of the molybdenum disulfide (MoS ) which shows promising catalytic ability for the H generation. In this work, we report on the investigation of the dinuclear complex [Mo S ] in both organic and aqueous solution. We demonstrate that [Mo S ] is not intact during the H evolution catalysis when it is assayed as a homogeneous catalyst in an electrolyte solution (e. g. in DMF or water solvent) nor when it is immobilized on an electrode surface (e. g. mesoporous carbon black). It transforms into the polymeric amorphous molybdenum sulfide [MoS] which subsequently acts as an actual catalyst. We discuss on the possible [Mo S ] to [MoS] transformation mechanism by employing an arsenal of electrochemical analysis, spectroscopic analyses and microscopic analyses. Effects of the electrochemical operating conditions to the [Mo S ] to [MoS] transformation as well as to the chemical nature and the catalytic performance of the [MoS] product are also emphasized.
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http://dx.doi.org/10.1002/asia.202300394 | DOI Listing |
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September 2025
Key Laboratory of Bio-Inspired Smart Interfacial Science and Technology of Ministry of Education, School of Chemistry, Beijing Advanced Innovation Center for Biomedical Engineering, Beihang University, Beijing, 100191, P. R. China.
In recent years, light-controlled ion transport systems have attracted widespread attention, however, the use of photoresponsive materials suffers from rapid carrier recombination, thermal field limitations, and narrow spectral response, which significantly restricts their performance enhancement in osmotic energy conversion. This study innovatively couples "blue energy" (osmotic energy) with "green energy" (solar energy), assembling graphene oxide/molybdenum disulfide/sulfonated cellulose nanocrystal (GO/ MoS/CNC) ion-channel membranes. Under solar irradiation, the energy level difference between MoS and GO effectively suppresses the recombination of photogenerated carriers, generating more active electrons and significantly enhancing the carrier density, thereby improving the current flux and ion selectivity.
View Article and Find Full Text PDFJ Colloid Interface Sci
September 2025
Department of Thermal Science and Energy Engineering, University of Science and Technology of China, 96 Jinzhai Road, Hefei 230026, PR China. Electronic address:
Heterojunctions have garnered significant attention in the field of photocatalysis due to their exceptional ability to facilitate the separation of photogenerated charge carriers and their high efficiency in hydrogen reaction. However, their overall photocatalytic performance is often constrained by electron transport rates and suboptimal hydrogen adsorption/desorption kinetics. To address these challenges, this study develops a g-CN/MoS@MoC dual-effect synergistic solid-state Z-type heterojunction, synthesized through the in-situ sulfurization of MoC combined with ultrasonic self-assembly technique.
View Article and Find Full Text PDFAnal Bioanal Chem
September 2025
Hebei Key Laboratory of Public Health Safety, Key Laboratory of Medicinal Chemistry and Molecular Diagnosis of Ministry of Education, College of Public Health, College of Chemistry and Materials Science, Hebei University, Baoding, 071002, China.
This work presents the development of a highly sensitive, selective, and efficient aptamer-based fluorescent sensor for detecting cortisol in human urine. Carbon quantum dots-nucleic acid aptamer (CQDs-Apt) synthesized with excellent photoluminescent properties and stability, were selected as the fluorescent probe. In the presence of MoS-NSs, CQDs-Apt adsorbed onto the surface of MoS-NSs via electrostatic and π-π interactions, leading to strong and rapid fluorescence quenching due to static quenching mechanism between them.
View Article and Find Full Text PDFAdv Sci (Weinh)
September 2025
Thin Film Materials Research Center, Korea Research Institute of Chemical Technology, Daejeon, 34114, Republic of Korea.
Molybdenum disulfide (MoS) has recently emerged as a promising material for the development of triboelectric nanogenerators (TENGs) owing to its inherently negative triboelectric properties when paired with polymeric layers, along with its notable transparency and mechanical flexibility. However, MoS-based TENGs operating in the contact-separation mode encounter critical limitations, including mechanical wear and limited triboelectric performance, particularly within the constraints of conventional 2D geometries. This paper reports the novel one-step laser-assisted synthesis of hemispherical MoS through the controlled nucleation and growth of MoS precursor seeds.
View Article and Find Full Text PDFSmall
September 2025
Department of Materials Science, Key Laboratory of Automobile Materials, MOE and State Key Laboratory of High Pressure and Superhard Materials, International Center of Future Science, Jilin University, Changchun, 130012, China.
Molybdenum disulfide (MoS) exhibits excellent lubrication capacity rooted in its layered structure, but it suffers significant structural and functional deterioration due to oxidation in ambient environments, limiting its applications. Concerted efforts are focused on enhancing the antioxidation ability of MoS, but challenges remain. This work conceptualizes and demonstrates a contrarian design of MoS-based film via metal incorporation and oxidation based on consideration of key fundamental principles of thermodynamics, chemistry, and physical mechanics.
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