Related Experiment Video
Updated: Jun 23, 2025

Fabrication and Testing of Catalytic Aerogels Prepared Via Rapid Supercritical Extraction
Published on: August 31, 2018
Partially oxidized inter-doped RuNi alloy aerogel for the hydrogen evolution reaction in both alkaline and acidic
Taehee Kim1, Hwapyung Jung1, Haryeong Choi1
1Department of Materials Science and Engineering, Yonsei University, Seoul 03722, Republic of Korea. hhpark@yonsei.ac.kr.
Abstract:
A facile reduction and doping process is employed with the supercritical ethanol drying method to form RuNi alloy aerogels. The optimized heterostructure comprising RuNi metal, RuO2, and NiO phases is synthesized through partial oxidation. When applied to the surface of Ni foam, the multiphase aerogels form a morphology of highly porous 0D colloidal aerogel networks on the surface. RuNi alloy-Ni foam oxidized at 350 °C (RuNi-350@NF) has an overpotential of 89 and 61 mV in 1 M KOH and 0.5 M H2SO4 media at 50 mA cm-2, as well as satisfactory long-term stability. Additionally, the Tafel slopes in alkaline and acidic media are found to be 34 and 30.9 mV dec-1, respectively. Furthermore, it exhibits long-term stability (35 h) in alkaline and acidic media at high current densities of 50 mA cm-2, respectively. This study presents a novel strategy for developing exceptionally efficient and free-standing 3D porous aerogel electrocatalysts with potential applications in hydrogen production.
More Related Videos
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...
Oxidation of Alkenes: Syn Dihydroxylation with Osmium Tetraoxide
Alcohols from Carbonyl Compounds: Reduction
Catalytic hydrogenation is similar to the reduction of an alkene or alkyne by adding H2 across the pi bond in the presence of transition metal catalysts like Raney Ni, Pd–C, Pt, or Ru. Aldehydes and ketones can be reduced by this method, often under mild to moderate heat (25–100°C) and...
Acid Halides to Alcohols: LiAlH4 Reduction
The mechanism proceeds in three steps. First, the nucleophilic hydride ion attacks the carbonyl carbon of the acid halide to form a tetrahedral intermediate. Next, the carbonyl group is re-formed, and the halide ion departs as a leaving group, generating an aldehyde. A second nucleophilic attack by the hydride yields an alkoxide ion, which, upon protonation, gives a primary alcohol as...

