Related Experiment Video
Updated: Aug 2, 2026

Facile Preparation of Ultrafine Aluminum Hydroxide Particles with or without Mesoporous MCM-41 in Ambient Environments
Published on: May 11, 2017
Molecular precursor synthesis of the Rh2O3/Fe2O3 spherical architecture for enhanced acidic HER activity and
Muhammad Zulqarnain1, Zheng Wei1, Marcell Hollo2
1Department of Chemistry, University at Albany, SUNY Albany NY 12222 USA edikarev@albany.edu.
Abstract:
Efficient hydrogen evolution catalysts that minimize noble metal content while maintaining high activity and durability are critically needed for scalable water electrolysis. Here, we introduce a molecular precursor strategy to synthesize intimately intermixed Rh2O3/Fe2O3 nanocomposites with precisely controlled 1 : 1 metal ratio. Thermal decomposition of heterobimetallic complex [Rh(acac)3Fe(hfac)2] (acac = acetylacetonate, hfac = hexafluoroacetylacetonate) at 300 °C yields 3D spherical Rh2O3/Fe2O3 architectures without high-temperature sintering. Electrochemical evaluation reveals that Rh2O3/Fe2O3 requires only 32 mV to reach -10 mA cm-2, dramatically lower than Rh/Rh2O3 (140 mV), commercial Rh2O3 (260 mV), or α-Fe2O3 (210 mV). The Tafel slope investigation of Rh2O3/Fe2O3 indicates a Volmer-Heyrovsky mechanism with facile proton adsorption and electron transfer, while electrochemical impedance spectroscopy shows its charge-transfer resistance is an order of magnitude lower than that of Rh/Rh2O3. Importantly, chronopotentiometry at -10 mA cm-2 reveals ultrastable performance with no observable decay over 120 hours, highlighting the exceptional long-term stability of Rh2O3/Fe2O3. Post-stability microscopy exhibits intact spherical architecture with no signs of sintering or Ostwald ripening. By integrating earth-abundant sesquioxide that promotes oxophilicity, oxygen-vacancy generation, and enhanced conductivity, the title Rh2O3/Fe2O3 catalyst uses less than half the Rh loading of Rh/Rh2O3 while delivering both superior activity and unmatched durability. This work establishes that although both individual Rh2O3 and Fe2O3 oxides exhibit poor HER activity and stability in acidic media, their intimately intermixed nanocomposite delivers dramatically enhanced performance and long-term stability. The reported mixed-oxide electrocatalyst overcomes the intrinsic limitations of single-phase oxides and provides general guiding principles for designing future high-performance mixed-oxide systems.
More Related Videos
09:09A Facile Synthetic Method to Obtain Bismuth Oxyiodide Microspheres Highly Functional for the Photocatalytic Processes of Water Depuration
Published on: March 29, 2019
05:52Resource Recycling of Red Soil to Synthesize Fe2O3/FAU-type Zeolite Composite Material for Heavy Metal Removal
Published on: June 2, 2022
Related Concept Videos
Oxidation of Alkenes: Anti Dihydroxylation with Peroxy Acids
Protein Modifications in the RER
Broadly, these modifications can be categorized into four main categories — glycosylation, formation of disulfide bonds, assembly of protein subunits, and specific proteolytic cleavages like removal of signal sequences.
Esters to Carboxylic Acids: Acid-Catalyzed Hydrolysis
During hydrolysis, the ester is first activated towards nucleophilic attack through the protonation of the carboxyl oxygen atom by the acid catalyst. The protonation makes the ester carbonyl carbon more electrophilic. In the next step, water acts as a nucleophile and adds to the...
Radical Reactivity: Steric Effects
Along with electronic factors, steric factors also account...
Carboxylic Acids to Esters: Acid-Catalyzed (Fischer) Esterification Mechanism
Heterogeneous Catalysis