Related Experiment Video
Updated: Apr 8, 2026

Sputter Growth and Characterization of Metamagnetic B2-ordered FeRh Epilayers
Published on: October 5, 2013
Preparation and characterization of RhFe/g-C3N4 nanoparticles for efficient hydrolysis of sodium borohydride
Merve Uçar Kaya1, Mehmet Yurderi2,3, Mehmet Zahmakiran4
1Department of Metallurgical and Materials Engineering, Faculty of Engineering, Architecture and Design, University of Bartın, Bartın, Turkiye.
Abstract:
Highly effective graphitic carbon nitride-supported RhFe nanoparticles (RhFe/g-C3N4) were prepared using a simple wet impregnation-reduction method for the hydrolysis of sodium borohydride (NaBH4). The obtained Rh0.48Fe0.52/g-C3N4 catalyst was characterized using advanced analytical/spectroscopic techniques such as inductively coupled plasma-optical emission spectroscopy, scanning electron microscopy, transmission electron microscopy, powder X-ray diffraction, X-ray spectroscopy, and Fourier transform infrared spectroscopy. The catalytic activities of RhFe/g-C3N4 catalysts with varying Rh/Fe molar ratios were investigated, demonstrating superior catalytic activity compared to monometallic Rh and Fe. The initial turnover frequency value of the Rh0.48Fe0.52/g-C3N4 catalyst was calculated as 33.04 min-1 and it showed an H2 generation rate of at 298 K. Furthermore, the kinetic parameters (E a #, ΔH #, ΔS #) of the hydrolysis of NaBH4 catalyzed by the Rh0.48Fe0.52/g-C3N4 catalyst were elucidated. The findings demonstrated that the resulting Rh0.48Fe0.52/g-C3N4 catalyst was recyclable and retained 80.72% of the initial activity even after 10 runs.
Related Concept Videos
Hydroboration-Oxidation of Alkenes
Regioselectivity and Stereochemistry of Hydroboration
Hydroboration proceeds in a concerted fashion with the attack of borane on the π bond, giving a cyclic four-centered transition state. The –BH2 group is bonded to the less substituted carbon and –H to the more substituted carbon. The concerted nature requires the simultaneous addition of –H and –BH2 across the same face of the alkene giving syn stereochemistry.
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...
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.
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...

