Related Experiment Video
Updated: Nov 24, 2025

Synthesis 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
Coffee ground derived biochar embedded Ov-NiCoO2 nanoparticles for efficiently catalyzing a boron‑hydrogen bond break
Jianan Li1, Wenbo Sun2, Peiling Gao2
1State Environmental Protection Key Laboratory of Environmental Risk Assessment and Control on Chemical Process, School of Resources and Environmental Engineering, East China University of Science and Technology, Shanghai 200237, China; State Key Laboratory of Fine Chemical and Key Laboratory of Industrial Ecology and Environmental Engineering, School of Environmental Sciences and Technology, Dalian University of Technology, Dalian 116024, China.
Researchers developed a novel catalyst from coffee waste and NiCoO2 nanoparticles to efficiently break boron-hydrogen bonds. This sustainable approach enhances catalytic activity for environmental and hydrogen energy applications.
Area of Science:
- Catalysis
- Materials Science
- Environmental Chemistry
Background:
- The boron-hydrogen (B-H) bond break is crucial for environmental treatment and hydrogen energy.
- Noble metal catalysts are effective but costly; transition metal catalysts offer a cost-effective alternative.
- Developing efficient and sustainable catalysts is a key research area.
Purpose of the Study:
- To utilize coffee ground waste as a biochar substrate for catalyst development.
- To synthesize and characterize ultrafine NiCoO2 nanoparticles on biochar for B-H bond activation.
- To investigate the role of oxygen vacancies in enhancing catalytic performance.
Main Methods:
- Coffee grounds were converted into biochar to serve as a support material.
- Ultrafine NiCoO2 nanoparticles were loaded onto the biochar substrate.
- Vacuum-calcination was employed to create oxygen vacancies in the catalyst.
- Catalytic activity was tested for 4-nitrophenol reduction and ammonia borane dehydrogenation.
- Theoretical calculations were used to elucidate the reaction mechanism.
Main Results:
- NiCoO2 nanoparticles were highly dispersed on the biochar due to functional groups.
- Oxygen vacancies were successfully introduced and enhanced catalytic activity.
- The catalyst demonstrated efficient B-H bond breaking in both tested reactions.
- Satisfactory catalytic stability was observed over multiple reaction cycles.
Conclusions:
- Coffee waste can be repurposed into a functional biochar support for catalysts.
- Oxygen vacancies significantly boost the catalytic activity for B-H bond cleavage.
- This approach offers a sustainable method for catalyst design in energy and environmental catalysis.
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 stereochemistry.
Catalysis
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 Benzene to Cyclohexane: Catalytic Hydrogenation

