4.7 Article

Amine-Functionalized Carbon Bowl-Supported Pd-La(OH)3 for Formic Acid Dehydrogenation

Journal

INORGANIC CHEMISTRY
Volume -, Issue -, Pages -

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.inorgchem.2c02672

Keywords

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Funding

  1. National Natural Science Foundation of China [22162014, 22162013]
  2. Natural Science Foundation of Jiangxi Province of China [20212ACB204009]
  3. Sponsored Program for Academic and Technical Leaders of Major Disciplines of Jiangxi Province of China [20212BCJL23059]
  4. Key Laboratory for Environment and Energy Catalysis of Jiangxi Province [20181BCD40004]

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This study presents a facile method to synthesize supported ultrafine metal nanoparticle catalysts for hydrogen generation from formic acid. The catalyst exhibits high selectivity and exceptional catalytic activity, surpassing most reported heterogeneous catalysts.
Formic acid (HCOOH, FA) is emerging as an appealing carrier for hydrogen storage owing to its renewability, a high volumetric capacity of 53 g H-2/L, and convenient storage/transportation as a liquid. It is highly desired but still a challenge to search highly efficient catalysts to realize hydrogen evolution from FA. Here, monodispersed and ultrasmall Pd-La(OH)(3) nanoparticles (NPs) anchored on amine-functionalized N-doped porous carbon bowl (N-PCB-NH2) substrates have been fabricated through a facile wet chemistry approach. As a result of the ultrafine size of Pd-La(OH)(3) NPs (1.6 nm), the deprotonation ability of La(OH)(3) and amine groups, and the strong metal-support interaction between Pd- La(OH)(3) and N-PCB-NH2 , the as-prepared Pd-La(OH)(3)/N-PCB-NH(2 )catalyst exhibits 100% H-2 selectivity and exceptional catalytic property with a high turnover frequency value up to 9585 h(-1) for FA dehydrogenation at 323 K, which is superior to most of the heterogeneous catalysts ever reported. Kinetic isotope effect measurements demonstrate that the C-H bond cleavage is a rate-determining step in the FA dehydrogenation reaction as compared to the O-H bond dissociation. This work presents a feasible approach to synthesize supported ultrafine metal NP catalysts with porous bowl structures for H-2 generation from FA.

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