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Triangulenes as neutral radicals are becoming promising candidates for future applications such as spintronics and quantum technologies. To extend the potential of the advanced materials, it is of importance to control their electronic and magnetic properties by multiple graphitic nitrogen doping. Here, we synthesize triaza[5]triangulene on Au(111) by cyclodehydrogenation, and its derivatives by cleaving C-N bonds. Bond-resolved scanning tunneling microscopy and scanning tunneling spectroscopy provided detailed structural information and evidence for open-shell singlet ground state. The antiferromagnetic arrangement of the spins in positively doped triaza[5]triangulene was further confirmed by density function theory calculations. The key aspect of triangulenes with multiple graphitic nitrogen is the extra p electrons composing the π orbitals, favoring charge transfer to the substrate and changing their low-energy excitations. Our findings pave the way for the exploration of exotic low-dimensional quantum phases of matter in heteroatom doped organic systems.
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http://dx.doi.org/10.1002/anie.202411893 | DOI Listing |
ACS Appl Mater Interfaces
September 2025
National Energy Metal Resources and New Materials Key Laboratory Engineering Research Center of the Ministry of Education for Advanced Battery Materials Hunan Provincial Key Laboratory of Nonferrous Value-Added Metallurgy School of Metallurgy and Environment, Central South University, Changsha 41008
Hard carbon (HC), recognized as the most promising anode material for sodium-ion batteries (SIBs), exhibits multiple forms of sodium storage (adsorption on graphitic layers, insertion between graphitic sheets, and filling in closed pores). Low initial coulombic efficiency (ICE) and low plateau region capacity are the main issues with HC, and it is necessary to understand the evolution laws of graphitic layers and closed pores. Here, we regulate the structure of graphitic layers by deliberately changing the oxygen content in HC materials and reveal the mechanism of formation of closed pores.
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September 2025
Liming Vocational University, Quanzhou, Fujian, China.
Synergistic reduction of graphene oxide (GO) using different reducing agents represents an effective approach for reduced graphene oxide (rGO) synthesis. In this study, the rGO (rGO-Vc+Urea) was prepared by combining vitamin C (Vc) and urea as co-reducing agents with the modified Hummer's method. Compared to samples reduced solely with Vc or urea, the co-reducing agents significantly reduced the required reaction time (to 2 hours) and temperature (to 120°C), while yielding material with superior electrical resistivity (1.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
August 2025
Key Laboratory of Industrial Ecology and Environmental Engineering (Ministry of Education, China), School of Environmental Science and Technology, Dalian University of Technology, Dalian, 116024, China.
The photocatalytic synthesis of urea from CO and N co-reduction presents a promising alternative to the conventional energy-intensive Haber-Bosch process. However, competitive adsorption on the catalyst surface often limits selectivity and yield. Here, we designed hollow graphitic carbon nitride (g-CN) spheres, which serve as a high surface area scaffold for precise anchoring of Fe─Cu diatomic sites.
View Article and Find Full Text PDFNanoscale
August 2025
Departamento de Física, Universidade Federal de Pernambuco, Av. Prof. Moraes Rego, 1235, Cidade Universitária, Recife, PE 50670-901, Brazil.
We demonstrate random laser (RL) emission from rhodamine 610 using graphitic carbon nitride (g-CN) nanosheets synthesized using a thermal polymerization method as scatterers in a liquid suspension to provide feedback for the RL emission. To characterize RL action and its threshold value, we observed replica symmetry breaking that leads to a transition from a photonic paramagnet to a photonic spin glass for four concentrations of g-CN. Additionally, we applied a fast Fourier transform to the RL spectra to gain insights into the photon optical path lengths, which aids in evaluating the feedback mechanism.
View Article and Find Full Text PDFEnviron Sci Technol
September 2025
State Key Laboratory of Hydraulics and Mountain River Engineering, College of Architecture and Environment, Sichuan University, Chengdu 610065, China.
To address the challenges of low hydrogen peroxide utilization efficiency and excessive iron sludge accumulation in conventional Fenton processes, metal-free carbon cocatalysts harness their cost-effectiveness, ecofriendliness, and modifiable surface to propel green and enhanced Fenton chemistry. Their cocatalytic efficacy stems from structural features (pore architecture, hybridization state, and dimension) and surface properties (defect, heteroatom, functional group, graphitic structure, and site distribution), resulting in carbon cocatalysts playing multifaceted roles in assisting Fenton systems. This overview provides mechanistic insights into carbon cocatalyzed Fenton reactions, focusing on electron sources for iron reduction, and categorizes mechanisms into three approaches (electron donors, carbon-Fe(III) complexes, and electron mediators).
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