Ag Cluster‐Modified K0.5Na0.5NbO3 Piezocatalyst for Enhanced Electrochemical Dinitrogen Reduction Reaction
Source abstract
Abstract
Efforts in finding alternatives to Haber–Bosch process for chemical synthesis of ammonia still struggle with efficient N2 activation. Piezoelectric materials are promising cocatalysts to enhance the chemical kinetics of dinitrogen (N2) reduction through, built‐in electric fields, upon mechanical activation, which can modulate the surface electrochemical potential. This work reports on the influence of piezoelectric potassium sodium niobate (K0.5Na0.5NbO3, KNN) as a lead‐free cocatalyst for the electrochemical nitrogen reduction reaction to ammonia (NH3) under mild conditions, on a silver (Ag) catalyst. For piezoactivation, modified H‐cell is engineered with the working electrode (Ag/KNN), enabling external mechanical actuating during electrochemical process. The results demonstrate that transient dipoles generated on the KNN surface through localized electric field improve threefold NH3 production (3.6 μg h−1 cm−2) and a Faradaic efficiency up to 75%. Piezoinfluence is investigated through actuation‐induced, linear sweep voltammetry, electrochemical impedance spectroscopy, chronoamperometry, and open‐circuit potential measurements.
Source: crossref · Quality: baseline
Research context
OpenAlex topics: Ammonia Synthesis and Nitrogen Reduction · Advanced Photocatalysis Techniques · Caching and Content Delivery
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Institute of Inorganic and Materials Chemistry University of Cologne 50939 Cologne Germany
Brazilian Nanotechnology National Laboratory (LNNano) Brazilian Center for Research in Energy and Materials (CNPEM) – Campinas São Paulo 13083‐100 Brazil
Institute of Chemistry State University of Campinas (UNICAMP) – Campinas São Paulo 13083‐100 Brazil
Clausius Institute for Physical and Theoretical Chemistry University Bonn 53121 Bonn Germany
Funding
Deutsche Forschungsgemeinschaft
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