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The electrocatalytic aqueous ammonia oxidation (AO) represents a more sustainable alternative to accessing nitrite (NO) and nitrate (NO). We now report that Cu(pyalk) {pyalk = 2-(pyridin-2-yl)propan-2-oate}, previously employed as a homogeneous water oxidation (WO) catalyst, is also active for selective AO in aqueous environments. The traditional Griess analytical test for NO/NO was modified to permit the operation in the presence of the otherwise interfering Cu ion. Choosing the right pH is crucial for achieving high AO selectivity, with optimal formation of NO occurring at pH 9 (faradaic efficiency 62%). Electrochemical analysis reveals a monometallic reaction pathway and offers a plausible explanation for the chemoselectivity: at pH 9, AO is dominant, while at elevated pH 13, WO dominates.
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http://dx.doi.org/10.1021/jacs.4c11822 | DOI Listing |
Inorg Chem
September 2025
College of Chemistry, Chemical Engineering and Materials Science, Collaborative Innovation Center of Suzhou Nano Science and Technology, Soochow University, Suzhou, Jiangsu 215123, China.
The electrochemical reduction of CO into valuable C products presents a sustainable and efficient strategy for the utilization of CO and long-term renewable energy storage. Yet, enhancing the efficiency of the electrocatalytic CO reduction reaction (eCORR) in aqueous systems remains challenging due to the difficulty in activating both CO and HO molecules. In this study, we focus on water activation generating reactive hydrogen species (*H) to boost C product selectivity.
View Article and Find Full Text PDFLangmuir
September 2025
Advanced Polymer Laboratory, Department of Polymer Science and Technology, Government College of Engineering and Leather Technology (Post Graduate), Maulana Abul Kalam Azad University of Technology, Salt Lake City, Kolkata 700106, West Bengal, India.
This research provides a constructive approach for developing high-performance polymer nanohybrids toward enhancing optoelectronic properties, fluorogenic viscosity sensing, and metal-free electrocatalytic oxidation of glycerol to value-added organic(s). Herein, reduced graphene oxide (RGO) and mildly oxidized RGO (MRGO) are strategically combined with fluorescent electroactive polymers (FEPs) to develop a promising sustainable metal-free electrocatalytic system suitable for amplifying opto-electrochemical properties, multiplatform sensing capacity, and electrocatalytic efficiency. The optimized polymeric counterpart (FEP2) promotes dual-state emission in the supramolecular network of RGO-/MRGO-incorporated fluorescent electroactive hybrid polymers (RFEHPs/MFEHPs) through physicochemically confined atypical electron-rich -C(═O)NH-/-C(═O)O-/-SOH fluorophores of (hydroxyethyl)methacrylate and 2-acrylamido-2-methylpropane-1-sulfonic acid monomers.
View Article and Find Full Text PDFMolecules
August 2025
Grupo de Investigación de Farmacia y Medio Ambiente (FARQUIMA), Universidad Pedagógica y Tecnológica de Colombia, Avenida Central del Norte, vía Paipa, Tunja 150003, Boyacá, Colombia.
This review article describes the most recent studies carried out on the catalytic hydrodechlorination (HDC) of Diclofenac (DFC). In this context, the most commonly employed catalytic materials for the removal of DFC from aqueous matrices are reviewed, along with their main performance outcomes. Various strategies for the HDC of DFC are discussed, including conventional approaches that rely on molecular hydrogen as the electron donor, as well as emerging alternatives based on biocatalytic and electrocatalytic processes.
View Article and Find Full Text PDFChem Commun (Camb)
August 2025
Institute of Energy Supply Technology for High-end Equipment, Jiangsu Collaborative Innovation Center of Atmospheric Environment and Equipment Technology, Jiangsu Key Laboratory of Atmospheric Environment Monitoring and Pollution Control, School of Environmental Science and Engineering, Nanjing Univ
Lithium carbon dioxide (Li-CO) batteries have recently attracted extensive attention since they offer a great approach to simultaneously realize CO capture and conversion. However, the sluggish kinetics and complex reaction mechanism at the cathodic side significantly hinder the improvement in the performance of Li-CO batteries. Therefore, highly-efficient electrocatalysts are required to solve the problems encountered in Li-CO batteries.
View Article and Find Full Text PDFChemSusChem
August 2025
Key Laboratory of Applied Surface and Colloid Chemistry, Ministry of Education, School of Chemistry and Chemical Engineering, Shaanxi Normal University, Xi'an, 710119, China.
Electrocatalytic CO reduction reaction (CORR) is involved in new energy conversion scheme. Although many electrocatalysts for CORR have been developed, improving the activity and selectivity of molecular catalysts in aqueous solutions remains a challenge. Herein, the synthesis and electrocatalytic CORR features of doubly urea-bridged face-to-face dinuclear metalloporphyrins 1-M (M = Co, Fe) are reported.
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