98%
921
2 minutes
20
Individual cobalt atoms trapped within a bilayer of C have been produced by the deposition of Co atoms onto a C double layer supported on graphite. High-resolution scanning tunneling microscopy (STM) reveals two stable states of a single cobalt atom coordinated with three C molecules, which is denoted as (C)Co. The diffusion of the cobalt atoms within the C layers is highly limited, resulting in the effective capture of single cobalt atoms in the interstitial sites of the close-packed C layers. Density functional theory calculations show that the Co atom is located in the tetrahedral void between two close-packed C layers. The most stable configuration of (C)Co consists of two C molecules from the top layer with the third C from the bottom layer. A less stable configuration of (C)Co where all three C molecules are from the top layer was also observed at room temperature.
Download full-text PDF |
Source |
---|---|
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11923648 | PMC |
http://dx.doi.org/10.1021/acsomega.5c00176 | DOI Listing |
Bioelectrochemistry
September 2025
Radiation Microbiology Department, National Center for Radiation Research and Technology, Egyptian Atomic Energy Authority, 11371 Cairo, Egypt. Electronic address:
The rapid increase in population has driven the demand for fossil fuel energy, contributing to increased carbon emissions that ultimately accelerate global warming and climate change. Battery storage systems have many advantages over conventional energy sources. However, they face limitations such as energy storage, cost, and environmental hazards that come with the use of chemical binders.
View Article and Find Full Text PDFAdv Sci (Weinh)
September 2025
Hangzhou International Innovation Institute, Beihang University, Hangzhou, 311115, China.
The difference in hydroxyl adsorption between Ni and Fe sites in NiFeOOH limits the efficient dual-site synergistic mechanism (DSSM) during oxygen evolution reaction (OER). Here, a novel needle-array electrodeposition is reported for the scalable and efficient fabrication of Co and Y co-doped NiFeOOH catalyst. It achieves an ultralow overpotential of 270 mV at 1 A cm with a small Tafel slope of 30.
View Article and Find Full Text PDFACS Appl Mater Interfaces
September 2025
School of Materials and New Energy, South China Normal University, Shanwei 516600, China.
Nowadays, the continuous advancement of sodium-ion battery technology has made it an important choice in the new energy field and promoted the development of lithium-ion batteries. The cycling stability of cathode materials for sodium-ion batteries at high voltage (>4.0 V) is still a key challenge.
View Article and Find Full Text PDFACS Nano
September 2025
Institut National de la Recherche Scientifique (INRS), Center Énergie Matériaux Télécommunications, Varennes, Québec J3X 1P7, Canada.
Owing to its chemical stability and molecular-level structural tunability, the molecular electrocatalyst cobalt phthalocyanine (CoPc) demonstrates significant potential for the electrochemical reduction of CO (CORR). However, the specific catalytic reaction process of CORR and the dynamic structural evolution mechanisms of CoPc remain a contentious subject. Elucidating the reaction pathways of CO electroreduction to CO and tracking structural evolution pose substantial challenges.
View Article and Find Full Text PDFACS Nano
September 2025
Key Laboratory of Eco-chemical Engineering, International Science and Technology Cooperation Base of Eco-chemical Engineering and Green Manufacturing, College of Chemistry and Molecular Engineering, Qingdao University of Science and Technology, Qingdao 266042, P. R. China.
Development of aprotic lithium-oxygen (Li-O) batteries suffers from slow cathode reaction kinetics, numerous side reactions, and large polarization, which are intimately related to the discharge product of LiO. Here, we designed and prepared a modified CoO nanoparticle with atomic Ru substitution at octahedral Co sites supported by carbon nanocages (RuCoO@HCNs) as a cathode catalyst. The asymmetrical octahedral Ru-O-Co units trigger a strong electron coupling effect, leading to charge redistribution and optimization of the d-orbital energy levels, thus facilitating oxygen activation and conversion into superoxide anions during discharging.
View Article and Find Full Text PDF