Related Experiment Video
Updated: Jul 4, 2025

A Simple, Low-cost, and Robust System to Measure the Volume of Hydrogen Evolved by Chemical Reactions with Aqueous Solutions
Published on: August 17, 2016
A superior mulberry-like nanoparticle NiB binary catalyst for borohydride oxidation.
Jinliang Cai1, Caini Yi1, Yuxin Xie1
1School of Chemistry and Chemical Engineering, Chongqing University, Chongqing, 401331, P.R. China. yudanmei-1@163.com.
A novel nickel-boron catalyst with a unique morphology shows excellent performance for the borohydride oxidation reaction. This advancement could lead to efficient, metal-free anode catalysts for direct borohydride fuel cells.
Area of Science:
- Electrochemistry
- Materials Science
- Catalysis
Background:
- Direct borohydride fuel cells (DBFCs) offer high energy density but require efficient anode catalysts.
- Noble metal catalysts are effective but costly and scarce.
- Development of cost-effective, high-performance catalysts is crucial for DBFC commercialization.
Purpose of the Study:
- To synthesize and characterize a novel nickel-boron (NiB) binary catalyst with a unique morphology.
- To evaluate the catalytic activity, selectivity, and stability of the NiB catalyst for the borohydride oxidation reaction (BOR).
- To assess the performance of the NiB catalyst as an anode in a direct borohydride fuel cell (DBFC).
Main Methods:
- One-step electrodeposition was used to prepare the NiB binary catalyst with a mulberry-like nanoparticle morphology.
- Electrochemical techniques were employed to study the catalytic properties for the borohydride oxidation reaction.
- A DBFC was assembled with the NiB catalyst as the anode to measure power density and open-circuit voltage.
Main Results:
- The prepared NiB-0.2 catalyst demonstrated excellent catalytic activity, selectivity, and stability for the BOR.
- The DBFC utilizing the NiB-0.2 anode achieved a peak power density of 453 mW cm⁻² and an open-circuit voltage of 1.96 V at 343 K.
- The enhanced performance is attributed to the introduction of boron (B) into the nickel (Ni) structure, creating a unique morphology.
Conclusions:
- The NiB binary catalyst, synthesized via electrodeposition, shows significant promise for the borohydride oxidation reaction.
- The developed catalyst offers a potential noble-metal-free alternative for efficient anode materials in DBFCs.
- This research provides inspiration for designing advanced catalysts for clean energy applications.
More Related Videos
08:40Synthesis of Metal Nanoparticles Supported on Carbon Nanotube with Doped Co and N Atoms and its Catalytic Applications in Hydrogen Production
Published on: December 6, 2021
09:09A Facile Synthetic Method to Obtain Bismuth Oxyiodide Microspheres Highly Functional for the Photocatalytic Processes of Water Depuration
Published on: March 29, 2019
Related Concept Videos
Hydroboration-Oxidation of Alkenes
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.
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...
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...
Preparation of Alcohols via Addition Reactions
The acid-catalyzed addition of water to the double bond of alkenes is a large-scale industrial method used to synthesize low-molecular-weight alcohols. An acidic atmosphere is required to allow the hydrogen in the water molecule to act as an electrophile and attack the double bond in an alkene. The addition of a proton to the double bond creates a carbocation intermediate. The proton preferentially bonds to the less substituted end of the double bond to create a more stable carbocation...
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...