Related Experiment Video
Updated: Jan 15, 2026

Solar-Driven Electrochemical Green Fuel Production from CO2 and Water Using Ti3C2Tx MXene-Supported CuZn and NiCo Catalysts
Published on: November 7, 2025
Bifunctional Fe─Ru─VC Catalyst for Energy Efficient Tandem Alkaline Electrolysis of Hydrazine and 4-nitrophenol
Ali Mohammadi1, Hanseung Kim2, Mohammad Javad Arshia3
1Department of Energy and Materials Engineering, Dongguk University-Seoul, Seoul, 100-715, Republic of Korea.
Abstract:
Alternate electrocatalytic reactions can turn pollutants into green fuels, offering an energy-efficient approach. Coupling hydrazine oxidation reaction (HzOR), with 4-nitrophenol hydrogenation (4-NPHR) is especially promising. Here, we report a bifunctional electrocatalyst composed of defect-rich Fe-Ru alloy clusters uniformly anchored on vanadium carbide (Fe─Ru─VC), synthesized via scalable ball milling and thermal annealing. Fe─Ru─VC exhibits excellent electrocatalytic activity toward both HzOR and 4-NPHR, requiring a low overpotential of 145 mV at 10 mA cm-2 and a favorable Tafel slope of 68.9 mV dec-1 for HzOR, with stability exceeding 90 h in 1M KOH. For 1 mM 4-NPHR, superior Fe-Ru-VC performance is achieved -7.2 mA cm-2 at 100 mV, highlighting its high efficiency. Furthermore, a paired H-cell electrolyzer (HzOR||4-NPHR) operates at only 200 mV to deliver 40 mA cm-2, underscoring its low energy demand. In situ Raman spectroscopy confirms the formation of Fe─Ru(OOH) as active sites, UV-Vis analysis confirms rapid 4-NP degradation, and DFT calculations demonstrate enhanced electronic interactions at the Ru─Fe junction, consistent with experimental observations. The outstanding activity is attributed to synergistic Fe-Ru interactions, the presence of zigzag edge defects, and the excellent conductivity of the VC support.
More Related Videos
09:21Tuning the Acidity of Pt/ CNTs Catalysts for Hydrodeoxygenation of Diphenyl Ether
Published on: August 17, 2019
10:10Application of Elemental Lanthanides in the Selective C-F Activation of Trifluoromethylated Benzofulvenes Providing Access to Various Difluoroalkenes
Published on: July 28, 2018
Related Concept Videos
Reduction of Alkenes: Asymmetric Catalytic Hydrogenation
The metal catalyst used can be either heterogeneous or homogeneous. When hydrogenation of an alkene generates a chiral center, a pair of enantiomeric products is expected to form. However, an enantiomeric excess of one of the products can be facilitated using an enantioselective reaction or an...
Nitriles to Amines: LiAlH4 Reduction
As shown below, the mechanism involves three steps. Firstly, the hydride ion acting as a nucleophile attacks the nitrile carbon to form an anion. In the second step, a second equivalent of the hydride ion attacks the anion to...
Aldehydes and Ketones with HCN: Cyanohydrin Formation Mechanism
Electrophilic Aromatic Substitution: Nitration of Benzene
Alkynes to Aldehydes and Ketones: Hydroboration-Oxidation
One of the convenient methods for the preparation of aldehydes and ketones is via hydration of alkynes. Hydroboration-oxidation of alkynes is an indirect hydration reaction in which an alkyne is treated with borane followed by oxidation with alkaline peroxide to form an enol that rapidly converts into an aldehyde or a ketone. Terminal alkynes form aldehydes, whereas internal alkynes give ketones as the final product.
Alkynes to Aldehydes and Ketones: Acid-Catalyzed Hydration
Analogous to alkenes, alkynes also undergo acid-catalyzed hydration. While the addition of water to an alkene gives an alcohol, hydration of alkynes produces different products such as aldehydes and ketones.