Direct methanol fuel cells with high energy conversion efficiency and low hazard emissions have aroused great attention from both academic and industrial communities, but their large-scale commercial application has been blocked by high costs as well as short lifespan of the anode Pt catalysts. Here, we demonstrate a simple and scalable noncovalent strategy for the synthesis of quasi-one-dimensional (1D) Pt nanoworms grown on poly(diallyldimethyl-ammonium chloride) (PDDA)-functionalized TiCT nanosheets as anode catalysts for methanol electrooxidation. Interestingly, the introduction of PDDA on TiCT nanosheets can not only effectively adjust their surface charge property to strengthen the electrostatic interaction between metal and support but also induce the stereoassembly of worm-shaped Pt nanocrystals with abundant catalytically active grain boundaries, which enable the resulting hybrid to express high electrocatalytic activity, remarkable durability, and strong antipoisoning ability for methanol electrooxidation, which are better than those of the traditional Pt nanoparticle electrocatalysts loaded on carbon black, carbon nanotubes, reduced graphene oxide, and MXene matrixes. Theoretical simulations disclose that the more stable worm-shaped Pt configuration with an optimized electronic structure on the TiCT surface possesses a weaker CO adsorption ability than that of the Pt nanoclusters, thereby providing a dramatically enhanced and sustainable electrocatalytic performance.
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http://dx.doi.org/10.1021/acsami.0c02806 | DOI Listing |
Nat Commun
January 2025
WA School of Mines: Minerals, Energy and Chemical Engineering (WASM-MECE), Curtin University, Perth, WA, 6102, Australia.
Reducing green hydrogen production cost is critical for its widespread application. Proton-exchange-membrane water electrolyzers are among the most promising technologies, and significant research has been focused on developing more active, durable, and cost-effective catalysts to replace expensive iridium in the anode. Ruthenium oxide is a leading alternative while its stability is inadequate.
View Article and Find Full Text PDFJ Colloid Interface Sci
January 2025
College of Chemistry, Chemical Engineering and Materials Science, Shandong Normal University, Jinan 250014 Shandong, China; Center for High Altitude Medicine, West China Hospital, Sichuan University, Chengdu 610041 Sichuan, China. Electronic address:
Seawater splitting is increasingly recognized as a promising technique for hydrogen production, while the lack of good electrocatalysts and detrimental chlorine chemistry may hinder further development of this technology. Here, the interfacial engineering of manganese dioxide nanoparticles decorated on NiFe layered double hydroxide supported on nickel foam (MnO@NiFe LDH/NF) is reported, which works as a robust catalyst for alkaline seawater oxidation. Density functional theory calculations and experiment findings reveal that MnO@NiFe LDH/NF can selectively enrich OH and repel Cl in oxygen evolution reaction (OER).
View Article and Find Full Text PDFJ Colloid Interface Sci
January 2025
Alan G. MacDiarmid Institute, College of Chemistry, Jilin University, 2699 Qianjin Street, Changchun 130012, PR China. Electronic address:
Water electrolysis represents a green and efficient strategy for hydrogen (H) production. However, the four-electron transfer process involved in its anodic oxygen evolution reaction (OER) half-reaction restricts the H generation rate. Employing hydrazine oxidation reaction (HzOR) as a substitute for OER in H generation can dramatically reduce energy consumption.
View Article and Find Full Text PDFThis paper explores the process of forming arrays of vertically oriented carbon nanotubes (CNTs) localized on metal electrodes using thin porous anodic alumina (PAA) on a solid substrate. On a silicon substrate, a titanium film served as the electrode layer, and an aluminium film served as the base layer in the initial film structure. A PAA template was formed from the Al film using two-step electrochemical anodizing.
View Article and Find Full Text PDFACS Appl Mater Interfaces
January 2025
Department of Mechanical Engineering, Boston University, 110 Cummington Mall, Boston, Massachusetts 02215, United States.
Hydrogen bubble adhesion to the electrode presents a major obstacle for green hydrogen generation via the hydrogen evolution reaction (HER) as it would induce undesired overpotential and undermine the reaction efficiency by reducing reaction area, increasing transport resistance, and creating an undesired ion concentration gradient. While electrodes with aerophobic/hydrophilic surfaces have been developed to facilitate bubble detachment, they primarily rely on micro- and nanostructured catalyst surfaces to enhance buoyance-induced bubble departure. Here, we demonstrate that introducing nonreactive yet more hydrophilic surfaces can promote coalescence-induced bubble departure, thereby significantly reducing the transport overpotential and improving HER performance.
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