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Ammonia (NH) is vital in global production and energy cycles. Electrocatalytic nitrate reduction (e-NORR) offers a promising route for nitrogen (N) conversion and NH synthesis, yet it faces challenges like competing reactions and low catalyst activity. This study proposes a synergistic mechanism incorporating a proton donor to mediate O-end e-NORR, addressing these limitations. A novel method combining ultraviolet radiation reduction, confined synthesis, and microwave treatment was developed to create a model catalyst embedding Cu single atoms on La-based nanoparticles (p-CNCuLa-m). DFT analysis emphasizes the critical role of La-based clusters as proton donors in e-NORR, while in situ characterization reveals an O-end adsorption reduction mechanism. The catalyst achieves a remarkable Faraday efficiency (FE) of 97.7%, producing 10.6 mol g h of NH, surpassing most prior studies. In a flow cell, it demonstrated exceptional stability, with only a 9% decrease in current density after 111 hours and a NH production rate of 1.57 mg/h/cm. The proton donor mechanism's effectiveness highlights its potential for advancing electrocatalyst design. Beyond NH production, the O-end mechanism opens avenues for exploring molecular-oriented coupling reactions in e-NORR, paving the way for innovative electrochemical synthesis applications.
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http://dx.doi.org/10.1002/adma.202415632 | DOI Listing |
Acc Chem Res
September 2025
Department of Chemistry, FRQNT Centre for Green Chemistry and Catalysis, McGill University, 801 Sherbrooke Street W, Montréal, Québec H3A 0B8, Canada.
ConspectusMolecular photochemistry, by harnessing the excited states of organic molecules, provides a platform fundamentally distinct from thermochemistry for generating reactive open-shell or spin-active species under mild conditions. Among its diverse applications, the resurgence of the Minisci-type reaction, a transformation historically reliant on thermally initiated radical conditions, has been fueled by modern photochemical strategies with improved efficiency and selectivity. Consequently, the photochemical Minisci-type reaction ranks among the most enabling methods for C()-H functionalizations of heteroarenes, which are of particular significance in medicinal chemistry for the rapid diversification of bioactive scaffolds.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
September 2025
State Key Laboratory of Analytical Chemistry for Life Science, School of Chemistry and Chemical Engineering, Nanjing University, Nanjing, 210023, China.
Electrochemical synthesis of ammonia (NH) is a promising green alternative to the conventional Haber-Bosch process. Here, we report the synthesis of a heteroatomic metal-metal bonded dual atomic (DA) Mn-Cu catalytic site embedded within nitrogen-doped carbon (NC) matrix for high-performance electrochemical reduction of N to NH. The asymmetric electronic distribution localized at the dual atomic sites synergistically enhances the adsorption and activation of N, facilitating the complex proton-coupled electron transfer process.
View Article and Find Full Text PDFDalton Trans
September 2025
College of Chemistry, Beijing Normal University, No. 19, Xin-wai street, Beijing 100875, People's Republic of China.
The design of multidentate ligands incorporating both hard and soft donors is of fundamental interest and importance in coordination chemistry. Here, we report a novel class of tetradentate dianionic bisphenolate-bisphosphine (PO) ligands featuring hybrid hard (phenolate) and soft (phosphine) donor atoms. Titanium(IV) and titanium(III) chloride complexes of the PO ligands were synthesized and characterized by X-ray crystallography, NMR spectroscopy, solution magnetic susceptibility measurements (Evans method) and EPR spectroscopy, revealing distorted octahedral geometries and providing insight into coordination modes and spin states.
View Article and Find Full Text PDFJ Chem Phys
September 2025
Department of Chemistry, Princeton University, Princeton, New Jersey 08544, USA.
Proton-coupled electron transfer (PCET) is pervasive throughout chemistry, biology, and physics. Over the last few decades, we have developed a general theoretical formulation for PCET that includes the quantum mechanical effects of the electrons and transferring protons, including hydrogen tunneling, as well as the reorganization of the environment and the donor-acceptor fluctuations. Analytical rate constants have been derived in various well-defined regimes.
View Article and Find Full Text PDFRSC Adv
August 2025
ETSEAFiV, UdL Av. de l'Alcalde Rovira Roure, 191 25198 Lleida Spain
A key challenge in industrial processes is replacing fossil-based solvents with sustainable, renewable alternatives while minimizing industrial waste and enhancing sustainability. Deep eutectic solvents (DESs), with their exceptional properties, offer a promising solution. These solvents can be tailored from a wide variety of hydrogen bond donors (HBDs) and acceptors (HBAs), making them highly customizable, cost-effective, and versatile.
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