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Nanoporous thin films (NPTFs) of noble metals are known for their exceptional durability, biocompatibility, and enlarged yet modifiable surface in broad biosensing applications. However, it remains challenging to devise a viable NPTF fabrication method that is generally applicable to different types of noble metals and for generating micro/nanopatterns. Here, we present a liquid-metal-based approach for transforming noble metal thin films and their lithographically formed patterns into NPTFs with mesoscale pores. For this purpose, a gallium (Ga)-based process in the liquid state of the metal is implemented. During fabrication, the noble metal thin films are first converted into compact layers of Ga-containing intermetallic crystals, followed by selective removal of the less noble Ga to create mesoporous networks. Compared to their nonporous counterparts, the noble metal NPTFs exhibit increased electroactive surface area, enhanced current density, and improved antifouling performance, all to a substantial degree, in different biosensing settings. Notably, gold NPTFs demonstrate excellent sensitivity and selectivity toward dopamine in a human serum environment. Given that the fabrication can be carried out at near room temperature and avoids harsh conditions, we expect our method to expedite the use of noble metal NPTFs and patterns in developing high-performance biosensors and other noble metal surface-enabled applications.
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http://dx.doi.org/10.1021/acsnano.4c15552 | DOI Listing |
Nanoscale
September 2025
Fujian Key Laboratory of Drug Target Discovery and Structural and Functional Research, Higher Educational Key Laboratory for Nano Biomedical Technology of Fujian Province, The School of Pharmacy, Fujian Medical University, Fuzhou, Fujian 350122, People's Republic of China.
The rational design of non-precious metal catalysts as a replacement for Pd is of great importance for catalyzing various important chemical reactions. To realize this purpose, the palladium-like superatom NbN was doped into a defective graphene quantum dot (GQD) model with a double-vacancy site to design a novel single superatom catalyst, namely, NbN@GQD, based on density functional theory (DFT), and its catalytic activity for the Suzuki reaction was theoretically investigated. Our results reveal that this designed catalyst exhibits satisfactory activity with a small rate-limiting energy barrier of 25.
View Article and Find Full Text PDFOrg Biomol Chem
September 2025
Beijing National Laboratory for Molecular Sciences, CAS Key Laboratory of Molecular Recognition and Function, Center for Carbon Neutral Chemistry, Institute of Chemistry, Chinese Academy of Sciences, Beijing 100190, China.
Despite great advances in decarbonylation of aldehydes using noble metals, the reaction is largely limited to high reaction temperatures and displays poor functional group tolerance. Herein, we report photo-irradiated decarbonylation of aldehydes, promoted by -W(N)(dppe), at room temperature. A wide range of substrates with diverse functional groups underwent decarbonylation efficiently to give the corresponding arene and alkane products in moderate to high yields.
View Article and Find Full Text PDFACS Electrochem
September 2025
Department of Chemistry, University of Warwick, Coventry CV4 7AL, United Kingdom.
The surface structure of an electrocatalyst plays a crucial role in determining the activity. As a model system, gold has been widely investigated as an electro-oxidation catalyst, although there has been much less research on the oxygen evolution reaction (OER) in the potential region of gold oxidation. Here, we combine voltammetric scanning electrochemical cell microscopy (SECCM) and electron backscatter diffraction (EBSD), at different spatial and angular resolutions, respectively, to correlate the local crystallographic structure of polycrystalline goldfocusing on grains close to (113), (011), (114), and (111) orientationswith the electrocatalytic behavior for the OER.
View Article and Find Full Text PDFRSC Adv
September 2025
Department of Chemical Engineering and Green Technology, Institute of Chemical Technology (ICT) Mumbai Maharashtra 400019 India
The sustainable synthesis of bio-based monomers from renewable biomass intermediates is a central goal in green chemistry and biorefinery innovation. This study introduces a synergistic catalytic-enzymatic strategy for the efficient and eco-friendly oxidation of 5-hydroxymethylfurfural (5-HMF) into 2,5-furandicarboxylic acid (FDCA), a key monomer for next-generation biodegradable plastics. The catalytic phase employed non-noble metal catalysts, MnO and Co-Mn supported on activated carbon (Co-Mn/AC), under mild batch reaction conditions at 90 °C.
View Article and Find Full Text PDFJ Colloid Interface Sci
September 2025
Faculty of Chemical Engineering, Kunming University of Science and Technology, Kunming 650093, China.
Encapsulation of non-noble bimetallic nanoparticles within a zeolite framework can improve the stability and accessibility of active sites, but the single microporous structure and poor metal stability decreased the catalytic performance of the catalyst. Here, 3D hierarchical ZSM-5 zeolite encapsulated NiCo nanoparticles (NiCo@3DHZ5) were synthesized by Bottom-up confined steam-assisted crystallization (SAC) one-pot hydrothermal method and applied to the hydrodeoxygenation of vanillin. A series of characterizations showed that highly stable alloyed NiCo nanoparticles were encapsulated in a framework of 3DHZ5, the strong metal-zeolite interactions resulted in highly dispersed NiCo nano-alloys facilitated hydrogen adsorption and spillover of active hydrogen atoms, and the 3D hierarchical structure promoted oxygenated substrate diffusion, the synergy interaction between the alloy particles confined in the 3DHZ5 pores and the acidic sites on the zeolite surface promoted the selective conversion of vanillin.
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