Related Experiment Video
Updated: Dec 6, 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
Hydrogen Generation upon Nanocatalyzed Hydrolysis of Hydrogen-Rich Boron Derivatives: Recent Developments
Changlong Wang1, Qi Wang1, Fangyu Fu1
1ISM UMR CNRS 5255, Univ. Bordeaux, 351 Cours de la Libération, 33405 Cedex Talence, France.
Abstract:
ConspectusProduction of hydrogen from nonfossil sources is essential toward the generation of sustainable energy. Hydrogen generation upon hydrolysis of stable hydrogen-rich materials has long been proposed as a possibility of hydrogen disposal on site, because transport of explosive hydrogen gas is dangerous. Hydrolysis of some boron derivatives could rapidly produce large amounts of hydrogen, but this requires the presence of very active catalysts. Indeed, late transition-metal nanocatalysts have recently been developed for the hydrolysis of a few hydrogen-rich precursors.Our research group has focused on the improvement and optimization of highly performing Earth-abundant transition-metal-based nanocatalysts, optimization of remarkable synergies between different metals in nanoalloys, supports including positive synergy with nanoparticles (NPs) for rapid hydrogen generation, comparison between various endo- or exoreceptors working as homogeneous and heterogeneous supports, mechanistic research, and comparison of the nanocatalyzed hydrolysis of several boron hydrides.First, hydrogen production upon hydrolysis of ammonia borane, AB (3 mol H2 per mol AB) was examined with heterogeneous endoreceptors. Thus, a highly performing Ni@ZIF-8 nanocatalyst was found to be superior over other Earth-abundant nanocatalysts and supports. With 85.7 molH2·molcat-1·min-1 at 25 °C, this Ni nanocatalyst surpassed the results of previous Earth-abundant nanocatalysts. The presence of NaOH accelerated the reaction, and a remarkable pH-dependent "on-off" control of the H2 production was established. Bimetallic nanoalloys Ni-Pt@ZIF-8 showed a dramatic volcano effect optimized with a nanoalloy containing 2/3 Ni and 1/3 Pt. The rate reached 600 molH2·molcat-1·min-1 and 2222 molH2·molPt-1·min-1 at 20 °C, which much overtook the performances of both related nanocatalysts Ni@ZIF-8 and Pt@ZIF-8. Next, hydrogen production was also researched via hydrolysis of sodium borohydride (4 mol H2 per mol NaBH4) using nanocatalysts in ZIF-8, and, among Earth-abundant nanocatalysts, Co@ZIF-8 showed the best performance, outperforming previous Co nanocatalysts. For exoreceptors, "click" dendrimers containing triazole ligands on their tripodal tethers were used as supports for homogeneous (semiheterogeneous) catalysis of both AB and NaBH4 hydrolysis. For both reactions, Co was found to be the best Earth-abundant metal, Pt the best noble metal, and Co1Pt1 the best nanoalloy, with synergistic effects. Based on kinetic measurements and kinetic isotope effects for all of these reactions, mechanisms are proposed and the hydrogen produced was further used in tandem reactions. Overall, dramatic triple synergies between these nanocatalyst components have allowed hydrogen release within a few seconds under ambient conditions. These nanocatalyst improvements and mechanistic findings should also inspire further nanocatalyst design in various areas of hydrogen production.
More Related Videos
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.
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.
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...
Radical Substitution: Hydrogenolysis of Alkyl Halides with Tributyltin Hydride
The bonds formed in this reaction are stronger than the bonds broken, making it energetically favorable. The reaction follows a radical chain mechanism similar to radical halogenation reactions,...
Reduction of Alkenes: Catalytic Hydrogenation
Metals like palladium, platinum, and nickel are commonly used in their solid forms — fine powder on an inert surface. As these catalysts remain insoluble in the reaction mixture, they are referred to as heterogeneous catalysts.
The hydrogenation process takes place on the...

