Aug 2026· Advances in Materials· pp.
e74766
· 0 citations· 34 references
Medicine
Abstract
Cyclohexanol electrooxidation reaction (CHAOR) offers a sustainable route for producing adipic acid. However, achieving high ring-opening efficiency and stable long-term yield remains challenging due to limited understanding of active oxygen species and reaction pathway. In this study, Ru single atoms and oxygen vacancies are used to construct a synergistic interface for efficient CHAOR. Oxygen vacancies serve as structural promoters by creating Lewis acid sites that enhance organic species adsorption and mitigate the agglomeration of Ru atoms. Atomically dispersed Ru sites act as functional modulators by disrupting the interfacial hydrogen-bond network-as confirmed by in situ Raman-to lower the *OH formation barrier and facilitate the accessibility of organic molecules to the catalytic surface, as supported by quartz crystal microbalance experiments and density functional theory calculations. The tandem electrochemical-chemical mechanism is elucidated: *OH formation is the electrochemical step, while its reaction with organics is the chemical step. Benefiting from the synergy, Ru-NiOx achieves 100% conversion and 87% AA (adipic acid) yield at 1.45 VRHE. Furthermore, a photovoltaic-electrolysis system is developed to address solar intermittency and power fluctuations, in which Ru-NiOx exhibits excellent stability over 1000 h with a maximum productivity of 204.4 µmol cm-2 h-1. Scaling to eight electrolyzers demonstrates good scalability, indicating strong potential for practical application.
Ir-based anodes for proton exchange membrane water electrolysis (PEMWE) often degrade when lattice oxygen participates in acidic OER, accelerating Ir dissolution. Here, we engineer the interfacial water microenvironment by alloying Au with low-crystallinity Ir nanoclusters on TiO2 (IrAu0.12@TiO2). The Ir-Au work-func...
Meng-Qiu Dai, Qing Mao, Yang Chen et al.· ACS Catalysis· 0 citations
Stable and efficient non−precious electrocatalysts are crucial for the industrialization of anion exchange membrane water electrolysis as a green hydrogen production technology. Here, we show a synergistic dual-anion engineering combining Se doping and surface [B(OH)4]− modification to overcome the activity-stability t...
Highly active and durable anode electrocatalysts are crucial for acidic oxygen evolution reaction (OER) in proton exchange membrane water electrolyzers (PEMWE), yet IrO2-based catalysts often face a trade-off between activity and stability. In this study, a Cr-IrO2 catalyst is developed through partial substitution of...
Kai-Li Wang, Maojun Pei, Shu-Qi Deng et al.· Advances in Materials· 0 citations
In hydrogen production, electrocatalysts featuring edge sites as active centers, modulation of its edge site coordination environment could greatly improve the reaction kinetics by effectively reducing the energy barrier. Here, we report a novel catalyst formulation obtained by the electrochemical deposition of rutheni...
Jin-Song Zhou, Tsz-Kei Leung, Denis A. Kuznetsov et al.· Angewandte Chemie· 0 citations
Anion exchange membrane water electrolysis (AEMWE) is recognized as a promising technology for green hydrogen production. The development of high-performance non-noble-metal-based (NNM) electrocatalysts is crucial for its industrial-scale deployment. However, in alkaline media, they typically face a critical challenge...
Yu Zhang, Zi-Hao Chen, Xiao-Xiao Huang et al.· Advances in Materials· 0 citations
Electrochemically reducing CO2 holds promise for producing value-added chemicals. Achieving this requires electrocatalysts with high selectivity and energy efficiency. Nanopocket engineering enhances catalytic activity by modulating interfacial reactivity and stabilizing key intermediates, especially those involved i...
Asmita Jana, M. F. Guzman, F. Habibzadeh et al.· Journal of the American Chem...· 0 citations
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