High-melting point alloy catalysts have been reported to be effective for the structure-controlled growth of single-wall carbon nanotubes (SWCNTs). However, some fundamental issues remain unclear because of the complex catalytic growth environment. Here, we directly investigated the active catalytic phase of Co-W-C alloy catalyst, the growth kinetics of CNTs, and their interfacial dynamics using closed-cell environmental transmission electron microscopy at atmospheric pressure. The alloy catalyst was precisely identified as a cubic η-carbide phase that remained unchanged during the whole CNT growth process. Rotations of the catalyst nanoparticles during CNT growth were observed, implying a weak interfacial interaction and undefined orientation dependence for the solid catalyst. Theoretical calculations suggested that the growth kinetics are determined by the diffusion of carbon atoms on the surface of the η-carbide catalyst and through the interface of the catalyst-CNT wall.
Download full-text PDF |
Source |
---|---|
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9728978 | PMC |
http://dx.doi.org/10.1126/sciadv.abo5686 | DOI Listing |
ACS Appl Mater Interfaces
December 2024
Institute of Materials for Energy and Environment, College of Materials Science and Engineering, Qingdao University, Qingdao 266071, PR China.
Pd-based nanocatalysts hold significant promise for application in alkaline direct ethanol fuel cells (DEFCs). To address the challenges of low Pd atom utilization and poor reaction kinetics in conventional Pd-based catalysts, a self-etching strategy has been developed to synthesize PdPb nanoparticles (NPs) with tunable size and abundant tensile strain. The nanoparticles demonstrated a markedly enhanced electrocatalytic performance.
View Article and Find Full Text PDFACS Appl Mater Interfaces
January 2025
School of Chemistry and Chemical Engineering, Beijing Institute of Technology, Beijing 100081, China.
Carbon-supported Pt-based catalysts are the most effective catalysts for direct methanol fuel cells (DMFCs). However, challenges such as high Pt loading, cost, and susceptibility to CO poisoning severely hinder the development of DMFCs. In this paper, CoFeO@polymer@ZIF-67 is prepared successfully through sequential solution polymerization and in situ growth with modified CoFeO as the core.
View Article and Find Full Text PDFACS Appl Mater Interfaces
January 2025
Institute of Materials, China Academy of Engineering Physics, Jiangyou 621908, China.
Solar-driven dry reforming of methane (DRM) offers a milder, more cost-effective, and promising environmentally friendly pathway compared to traditional thermal catalytic DRM. Numerous studies have extensively investigated inexpensive Ni-based catalysts for application in solar-driven DRM. However, these catalysts often suffer from activity loss due to carbon accumulation.
View Article and Find Full Text PDFNat Commun
January 2025
School of Chemical Engineering, The University of Adelaide, Adelaide, SA, Australia.
High-entropy alloy nanoparticles (HEA-NPs) exhibit favorable properties in catalytic processes, as their multi-metallic sites ensure both high intrinsic activity and atomic efficiency. However, controlled synthesis of uniform multi-metallic ensembles at the atomic level remains challenging. This study successfully loads HEA-NPs onto a nitrogen-doped carbon carrier (HEAs) and pioneers the application in peroxymonosulfate (PMS) activation to drive Fenton-like oxidation.
View Article and Find Full Text PDFPhys Chem Chem Phys
January 2025
The Institute for Solid State Physics, The University of Tokyo, 5-1-5 Kashiwanoha, Kashiwa, Chiba 277-8581, Japan.
Formic acid (HCOOH) is one of the essential molecules for CO utilization including methanol synthesis and hydrogen carriers. In this study, we have investigated the chemical processes of hydrogen and HCOOH on a dilute-alloy Pd-Cu(111) surface using high-resolution X-ray photoelectron spectroscopy (HR-XPS) and density functional theory (DFT) calculations. The present Pd-Cu(111) surface was prepared at 500 K, and the observed core-level shifts of Pd 3d indicate that Pd atoms were located at the surface and subsurface sites: 335.
View Article and Find Full Text PDFEnter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!