Electrocatalytic upgrading of renewable biomass-derived glycerol represents a sustainable method to produce value-added chemicals, but the complex reaction network of key intermediates during the glycerol oxidation poses challenges to product selectivity. Herein, we report a nickel-doped tungsten oxide catalyst grown on nickel foam (Ni-WOx/NF) for the highly selective electrooxidation of glycerol to formic acid (FA). This optimized catalyst achieves an FA Faraday efficiency (FE) of 95.1% and operates stably for over 18 h, outperforming conventional non-precious metal catalysts. Mechanistic understanding revealed that nickel doping effectively modulates the valence states of tungsten, increasing the proportion of low-valent W4+ species. This promotes the desorption of FA from the catalytic interface, thereby inhibiting its over-oxidation and enhancing selectivity. Taking a step forward, an integrated electrocatalytic system coupling the anodic glycerol oxidation reaction (GOR) with the cathodic nitrate reduction reaction (NO3-RR) is constructed. This system enables the simultaneous coproduction of FA and ammonia (NH3), achieving a high FE for FA of 96.9% along with sustained stability over 12 h, demonstrating significant potential for practical applications. This work demonstrates a sustainable catalytic system for selective glycerol oxidation by precisely regulating the reaction pathways of key intermediates.
Transition-metal hydroxides are promising electrocatalysts for small-molecule oxidation, yet their poor conductivity severely limits charge-transfer kinetics. Herein, we report the nitridation-induced metallization of semi-insulating NiNi3(OH)x into highly conductive metallic nickel (Ni0) via a hydrothermal ammonia tre...
Obeylaw Moyo, Zhi-Wei Wei, Jia-Qiao Yang et al.· Applied Physics Letters· 0 citations
Pairing the carbon dioxide reduction process with the electrocatalytic oxidation of glycerol (GOR), instead of the typically applied oxygen evolution reaction, can substantially decrease the cell voltage while forming high-value products at both electrodes. In this contribution, glycerol oxidation was driven as the a...
A. Kormányos, Adrienn Szirmai, Yu-Han Chen et al.· ACS Catalysis· 0 citations
The anodic electro-oxidation of ethanol is central to energy conversion, electro-synthesis, and hydrogen-producing electrolyzers, yet the lack of inexpensive electro-catalysts combining high activity and selectivity toward acetic acid, along with durability, remains a critical challenge. Herein, we report the ambient...
Electrocatalytic glycerol oxidation to formic acid (FA) offers a sustainable route for biomass valorization, yet non-noble metal catalysts generally suffer from sluggish C-C bond cleavage and poor product selectivity. Here we report an amorphous nickel–cobalt oxyhydroxide bearing both metal and oxygen vacancies (D-NiCo...
Zepan Sun, Yan-Zheng Feng, Guanjie Li et al.· Catalysts· 0 citations
An effective strategy to lower the operating voltage and system cost of water electrolysis for green hydrogen production is to couple the hydrogen evolution reaction with a kinetically facile oxidation reaction instead of the oxygen evolution reaction. Formaldehyde oxidation reaction (FOR) is ideal for this, as it ge...
Aniruddha Bhide, Nainesh Patel, Sahil Thorawade et al.· Energy & Fuels· 0 citations
Replacing the sluggish anodic oxygen evolution reaction (OER) with value‐added processes like the ethanol oxidation reaction (EOR) enhances the economic viability of water electrolysis. However, the rational design of low‐cost, durable electrocatalysts that selectively drive partial oxidation pathways under harsh a...
Ashish Gaur, Seung-Ho Yu, Mingi Kim et al.· Carbon Energy· 0 citations
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