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π electron configuration plays a pivotal role in metal-free carbon catalysts, and its delocalization degree overwhelmingly dominates catalytic activity. However, precise and targeted regulation of inherent π electrons still remain challenging. Here, one chemical-bond-targeted physical clipping strategy is proposed and effectively adopted in the cutting-edge carbon material system of graphdiyne (GDY) as a concept-of-proof. The delocalized electrons are expected to be periodically reformatted for substantially enhancing π electron delocalization. Via theoretical screening and well-designed experiments, periodical interruption of Csp-Csp bonds in GDY can render sp-C sites with decent activity, ultimately yielding top-ranking electrocatalytic performance without intentionally introducing external decoration. The as-proposed concept endows a universal prescription to push the limit of delocalization degree, thus shedding novel light on the rational design of decent metal-free catalysts.
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http://dx.doi.org/10.1002/anie.202211094 | DOI Listing |
J Phys Chem Lett
September 2025
Tianjin Key Laboratory of Film Electronic and Communication Devices, School of Integrated Circuit Science and Engineering, Tianjin University of Technology, Tianjin 300384, China.
Achieving UVA/B-selective, skin-inspired nociceptors with perception and blockade functions at the single-unit device level remains challenging. This is because the device necessitates distinct components for every performance metric, thereby leading to complex preparation processes and restricted performance, as well as the absence of deep UV (UVB and below)-selective semiconductors. Here, to address this, we develop a structure-simplification skin-inspired nociceptor using a reverse type-II CuAgSbI/MoS heterostructure.
View Article and Find Full Text PDFJ Colloid Interface Sci
December 2025
Department of Polymer Materials and Engineering, College of Materials & Metallurgy, Guizhou University, Huaxi District, Guiyang 550025, PR China. Electronic address:
Photocatalytic oxygen reduction to hydrogen peroxide (HO) via two-electron oxygen reduction reaction (2e-ORR) over g-CN-based photocatalysts offers a sustainable and environmentally friendly production route. However, the efficient utilization of photogenerated electrons remains a major challenge due to the inherent mismatch between rapid charge dynamics and sluggish surface redox kinetics. Here, thiophene rings were incorporated into the framework of crystalline carbon nitride (PCCN) containing cyanamide groups via symmetric imine (C=N) linkages, aiming to enhance electron delocalization and facilitate HO production.
View Article and Find Full Text PDFJ Chem Phys
July 2025
Institut für Physikalische und Theoretische Chemie, Universität Würzburg, Am Hubland, 97074 Würzburg, Germany.
Coupling molecular transition dipole moments to surface-plasmon polaritons (SPPs) results in the formation of new optical quasiparticles, i.e., plexcitons.
View Article and Find Full Text PDFJ Org Chem
August 2025
Department of Chemistry, University of California-Davis, Davis, California 95616, United States.
Analyses of nucleus-independent chemical shifts (NICS) and normalized multicentered bond orders (nMCBO) along reaction coordinates were used to quantify the degree of cyclic delocalization occurring during various reactions as a criterion for determining whether reactions are pericyclic. The magnitude of the -sampled average NICS, , and nMCBO near the transition structure were found to be good indicators of pericyclicity, but the topology of along the intrinsic reaction coordinate proved to be more informative.
View Article and Find Full Text PDFACS Nano
July 2025
Materials, Chemical and Computational Science Directorate, National Renewable Energy Laboratory, Golden, Colorado 80401, United States.
Graphene nanoribbons (GNRs) are quantum-confined π-conjugated monolayer semiconductors with attractive properties for optoelectronic applications. However, the ground- and excited-state properties of charge carriers in GNRs are still poorly understood, particularly with regards to the coupling between charges and the GNR lattice and the degree to which this coupling impacts local and macroscopic charge transport. To address this issue, we systematically correlate carrier density-dependent charge transport with spectroscopic modulations in chemically doped thin films of armchair graphene nanoribbons (9-aGNRs).
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