The fabrication of hybrid active sites that synergistically contain nanoclusters and single atoms (SAs) is vital for electrocatalysts to achieve excellent activity and durability. Herein, we develop a ligand-assisted pyrolysis strategy using nanoclusters (AuPd(SCHPh)) with alloy cores and protected ligands to build AuPd cluster sites embraced by satellite Pd SAs. In the thermal drive control process, different thermodynamic properties of the alloy atoms and the confinement effects of organic ligands allow for the mild spillover of the single-component metal Pd, resulting in the formation of AuPd alloy nanoclusters tightly encompassed by isolated Pd atoms. Experiments and theoretical calculations indicated that the satellite Pd atoms can optimize the electronic structure of the AuPd nanoclusters and Au sites in the alloy to facilitate the adsorption and dissociation of HO, thus enhancing the hydrogen evolution reaction (HER) activity. The optimal AuPd/Pd-600 exhibits outstanding electrocatalytic activity toward HER, with overpotentials of 21 and 38 mV at 10 mA cm in acidic and alkaline media, respectively. Moreover, the mass activity and turnover frequency of AuPd/Pd-600 are one order of magnitude higher than those of commercial Pd/C and Pt/C catalysts. This facile strategy for constructing hybrid catalytic centers using ligand-protected nanoclusters provides efficient insights for the further design of nanocluster-based electrocatalysts synergized by SAs.
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http://dx.doi.org/10.1021/acsnano.4c11554 | DOI Listing |
J Mater Chem A Mater
December 2024
Materials Chemistry and Catalysis, Debye Institute for Nanomaterials Science, Utrecht University 3584 CG Utrecht The Netherlands
The catalytic and plasmonic properties of bimetallic gold-palladium (Au-Pd) nanoparticles (NPs) critically depend on the distribution of the Au and Pd atoms inside the nanoparticle bulk and at the surface. Under operating conditions, the atomic distribution is highly dynamic. Analyzing gas induced redistribution kinetics at operating temperatures is therefore key in designing and understanding the behavior of Au-Pd nanoparticles for applications in thermal and light-driven catalysis, but requires advanced characterization strategies.
View Article and Find Full Text PDFJ Am Chem Soc
December 2024
Department of Chemistry, University of Pittsburgh, 219 Parkman Avenue, Pittsburgh, Pennsylvania 15260, United States.
Simultaneously controlling both stoichiometry and atom arrangement during the synthesis of multimetallic nanoparticles is often challenging, especially when the desired metal precursors exhibit large differences in their intrinsic reduction kinetics. In such cases, traditional synthetic methods often lead to the formation of exclusively phase-segregated structures. In this study, we demonstrate that the relative reduction kinetics of the metal precursors can be manipulated independently of their intrinsic differences in reduction rates by modulating the instantaneous concentrations of the metal cation precursors.
View Article and Find Full Text PDFSmall
January 2025
Shanghai Key Laboratory of Molecular Catalysis and Innovative Materials, Department of Chemistry, Fudan University, Shanghai, 200433, P. R. China.
Developing and fabricating a heterogeneous catalyst for efficient formic acid (FA) dehydrogenation coupled with CO hydrogenation back to FA is a promising approach to constructing a complete CO-mediated hydrogen release-storage system, which remains challenging. Herein, a facile two-step strategy involving high-temperature pyrolysis and wet chemical reduction processes can synthesize efficient pyridinic-nitrogen-modified carbon-loaded gold-palladium alloy nanodots (AuPd alloy NDs). These NDs exhibit a prominent electron synergistic effect between Au and Pd components and tunable alloy-support interactions.
View Article and Find Full Text PDFACS Nano
November 2024
Henan Key Laboratory of Crystalline Molecular Functional Materials and College of Chemistry, Zhengzhou University, Zhengzhou 450001, China.
The fabrication of hybrid active sites that synergistically contain nanoclusters and single atoms (SAs) is vital for electrocatalysts to achieve excellent activity and durability. Herein, we develop a ligand-assisted pyrolysis strategy using nanoclusters (AuPd(SCHPh)) with alloy cores and protected ligands to build AuPd cluster sites embraced by satellite Pd SAs. In the thermal drive control process, different thermodynamic properties of the alloy atoms and the confinement effects of organic ligands allow for the mild spillover of the single-component metal Pd, resulting in the formation of AuPd alloy nanoclusters tightly encompassed by isolated Pd atoms.
View Article and Find Full Text PDFSmall
January 2025
Department of Chemistry, Zhejiang University, Hangzhou, 310058, China.
Altered redox homeostasis has long been observed in cancer cells, which can be exploited for therapeutic benefits. However, reactive oxygen species (ROS) pleiotropy coupling with reductive adaptation in cancer cells poses a formidable challenge for redox dyshomeostasis-based cancer therapy. Herein, a AuPd alloying nanozyme-glutathione (GSH) biosynthesis inhibitor co-delivery system (B-BMES) is developed using dendritic SiO as a matrix to target cancer redox homeostasis.
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