98%
921
2 minutes
20
Platinum is one of the best-performing catalysts for the hydrogen evolution reaction (HER). However, high cost and scarcity severely hinder the large-scale application of Pt electrocatalysts. Constructing highly dispersed ultrasmall Platinum entities is thereby a very effective strategy to increase Pt utilization and mass activities, and reduce costs. Herein, highly dispersed Pt entities composed of a mixture of Pt single atoms, clusters, and nanoparticles are synthesized on mesoporous N-doped carbon nanospheres. The presence of Pt single atoms, clusters, and nanoparticles is demonstrated by combining among others aberration-corrected annular dark-field scanning transmission electron microscopy, X-ray absorption spectroscopy, and electrochemical CO stripping. The best catalyst exhibits excellent geometric and Pt HER mass activity, respectively ≈4 and 26 times higher than that of a commercial Pt/C reference and a Pt catalyst supported on nonporous N-doped carbon nanofibers with similar Pt loadings. Noteworthily, after optimization of the geometrical Pt electrode loading, the best catalyst exhibits ultrahigh Pt and catalyst mass activities (56 ± 3 A mg and 11.7 ± 0.6 A mg at -50 mV vs. reversible hydrogen electrode), which are respectively ≈1.5 and 58 times higher than the highest Pt and catalyst mass activities for Pt single-atom and cluster-based catalysts reported so far.
Download full-text PDF |
Source |
---|---|
http://dx.doi.org/10.1002/smll.202205885 | DOI Listing |
Proc Natl Acad Sci U S A
September 2025
Geballe Laboratory for Advanced Materials, Stanford University, Stanford, CA 94305.
The iron-based high-[Formula: see text] superconductors (SCs) exhibit rich phase diagrams with intertwined phases, including magnetism, nematicity, and superconductivity. The superconducting [Formula: see text] in many of these materials is maximized in the regime of strong nematic fluctuations, making the role of nematicity in influencing the superconductivity a topic of intense research. Here, we use the AC elastocaloric effect (ECE) to map out the phase diagram of Ba(FeCo)As near optimal doping.
View Article and Find Full Text PDFACS Appl Mater Interfaces
September 2025
State Key Laboratory of Fluid Power and Mechatronic Systems, Zhejiang University, Hangzhou, Zhejiang 310058, China.
We report an electro-enhanced catalytic etching approach for direct atomic-level patterning of single-crystal 4H-SiC (0001) surfaces. The process utilizes platinum-coated probes under a negative sample bias, which enhances catalytic reactions and promotes etching of SiC without additional mechanical load. Unlike traditional etching approaches that rely on hazardous chemicals such as hydrofluoric acid, this approach operates under ambient conditions, offering improved safety and environmental compatibility.
View Article and Find Full Text PDFACS Nano
September 2025
School of Materials and Energy, Guangdong University of Technology, Guangzhou 510006, China.
Chemical C-N coupling from CO and N toward urea synthesis is an appealing approach for Bosch-Meiser urea production. However, this process faces significant challenges, including the difficulty of N activation, high energy barriers, and low selectivity. In this study, we theoretically designed a Ni triple-atom doped CuO catalyst, Ni TAC@CuO, which exhibits exceptional urea synthesis performance.
View Article and Find Full Text PDFInorg Chem
September 2025
College of Chemistry and Materials Science, The key Laboratory of Functional Molecular Solids, Ministry of Education, The Key Laboratory of Electrochemical Clean Energy of Anhui Higher Education Institutes, Anhui Provincial Engineering Laboratory for New-Energy Vehicle Battery Energy-Storage Materia
Conventional acid-catalyzed acetalization faces significant challenges in catalyst recovery and poses environmental concerns. Herein, we develop a CeO-supported Pd single-atom catalyst (Pd/CeO) that eliminates the reliance on liquid acids by creating a localized H-rich microenvironment through heterolytic H activation. X-ray absorption near-edge structure and extended X-ray absorption fine structure analyses confirm the atomic dispersion of Pd via Pd-O-Ce coordination, while density functional theory (DFT) calculations reveal strong metal-support interactions (SMSI) that facilitate electron transfer from CeO oxygen to Pd, downshifting the Pd d-band center and optimizing H activation.
View Article and Find Full Text PDFJ Am Chem Soc
September 2025
Nanochemistry Department, Max Planck Institute for Solid State Research, Heisenbergstraße 1, 70569 Stuttgart, Germany.
Covalent organic frameworks (COFs) have been emerging as versatile reticular materials due to their tunable structures and functionalities, enabled by precise molecular engineering at the atomic level. While the integration of multiple components into COFs has substantially expanded their structural complexity, the strategic engineering of diverse functionalities within a single framework the random distribution of linkers with varying lengths remains largely unexplored. Here, we report a series of highly crystalline mixed-length multivariate COFs synthesized using azobenzene and bipyridine as linkers, where tuning the ratio of linkers and incorporating palladium effectively modulates the balance between near-infrared (NIR) light absorption and catalytic sites for NIR-generation of hydrogen peroxide (HO).
View Article and Find Full Text PDF