Efficient Hydrogen Evolution from Dimethylamine Borane, Ammonia Borane and Sodium Borohydride Catalyzed by Ruthenium and Platinum Nanoparticles Stabilized by an Amine Modified Polymer Immobilized Ionic Liquid: a Comparative Study

• Published in: Catalysis letters Vol. 154; no. 10; pp. 5450 - 5471
• Main Authors: Alharbi, Adhwa A., Wills, Corinne, Dixon, Casey, Arca, Elisabetta, Chamberlain, Thomas W., Griffiths, Anthony, Collins, Sean M., Wu, Kejun, Yan, Han, Bourne, Richard A., Knight, Julian G., Doherty, Simon
• Format: Journal Article
• Language: English
• Published: New York Springer US 01-10-2024; Springer Nature B.V
• Subjects: Activation energy; Ammonia; Boranes; Catalysis; Catalysts; Chemistry; Chemistry and Materials Science; Comparative studies; Dehydrogenation; Hydrogen evolution; Hydrolysis; Industrial Chemistry/Chemical Engineering; Ionic liquids; Nanoparticles; Organometallic Chemistry; Physical Chemistry; Platinum; Polymers; Ruthenium; Substrates; Catalytic dehydrogenation; Dimethylamine borane; Ruthenium and platinum nanoparticles; Ammonia borane; Kinetics and deuterium labelling
• ISSN: 1011-372X; 1572-879X
• DOI: 10.1007/s10562-024-04725-8

Platinum and ruthenium nanoparticles stabilised by an amine modified polymer immobilised ionic liquid (MNP@NH
2
-PEGPIILS, M = Pt, Ru) catalyse the hydrolytic liberation of hydrogen from dimethylamine borane (DMAB), ammonia borane (AB) and NaBH
4
under mild conditions. While RuNP@NH
2
-PEGPIILS and PtNP@NH
2
-PEGPIILS catalyse the hydrolytic evolution of hydrogen from NaBH
4
with comparable initial TOFs of 6,250 molesH
2
.molcat
−1
.h
−1
and 5,900 molesH
2
.molcat
−1
.h
−1
, respectively, based on the total metal content, RuNP@NH
2
-PEGPIILS is a markedly more efficient catalyst for the dehydrogenation of DMAB and AB than its platinum counterpart, as RuNP@NH
2
-PEGPIILS gave initial TOFs of 8,300 molesH
2
.molcat
−1
.h
−1
and 21,200 molesH
2
.molcat
−1
.h
−1
, respectively, compared with 3,050 molesH
2
.molcat
−1
.h
−1
and 8,500 molesH
2
.molcat
−1
.h
−1
, respectively, for PtNP@NH
2
-PEGPIILS. Gratifyingly, for each substrate tested RuNP@NH
2
-PEGPIILS and PtNP@NH
2
-PEGPIILS were markedly more active than commercial 5wt % Ru/C and 5wt% Pt/C, respectively. The apparent activation energies of 55.7 kJ mol
−1
and 27.9 kJ mol
−1
for the catalytic hydrolysis of DMAB and AB, respectively, with RuNP@NH
2
-PEGPIILS are significantly lower than the respective activation energies of 74.6 kJ mol
−1
and 35.7 kJ mol
−1
for its platinum counterpart, commensurate with the markedly higher initial rates obtained with the RuNPs. In comparison, the apparent activation energies of 44.1 kJ mol
−1
and 46.5 kJ mol
−1
, for the hydrolysis NaBH
4
reflect the similar initial TOFs obtained for both catalysts. The difference in apparent activation energies for the hydrolysis of DMAB compared with AB also reflect the higher rates of hydrolysis for the latter. Stability and reuse studies revealed that RuNP@NH
2
-PEGPIILS recycled efficiently as high conversions for the hydrolysis of DMAB were maintained across five runs with the catalyst retaining 97% of its activity.
Graphical Abstract