Mechanistic insights into hydrogen production from formic acid catalyzed by Pd@N-doped graphene : The role of the nitrogen dopant
Research output: Journal Publications and Reviews › RGC 21 - Publication in refereed journal › peer-review
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Detail(s)
Original language | English |
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Pages (from-to) | 16341-16357 |
Journal / Publication | International Journal of Hydrogen Energy |
Volume | 48 |
Issue number | 43 |
Online published | 31 Jan 2023 |
Publication status | Published - 19 May 2023 |
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Abstract
The catalytic decomposition of formic acid (HCOOH) is a crucial process for hydrogen production technologies. Herein, periodic density functional theory (DFT) calculations were employed to explore the effect of N-doping on the decomposition of formic acid. We designed a series of single Pd-atoms deposited in the single vacancy of N-doped graphene sheets, namely Pd-DGr, Pd–N1Gr, Pd–N2Gr, and Pd–N3Gr, as the proposed catalysts. Our findings show that H2 production from HCOOH dehydrogenation on these surfaces proceeds via the formate (HCOO) pathway (Path-I) rather than the carboxylate (COOH) pathway (Path-II). Furthermore, the Pd–N3Gr catalyst shows the greatest catalytic reactivity toward HCOOH dehydrogenation via Path-I, requiring an activation energy (Ea) of 0.38 eV.
On the other hand, the undesirable dehydration of HCOOH to carbon monoxide (CO) through COOH (Path-IIIA) or formyl (HCO) (Path-IIIB) intermediates is unlikely to occur on Pd–N3Gr due to a large activation energy. We found that the active species on the catalyst surface increased with N-doping concentration. Additionally, microkinetic simulations of the HCOOH decomposition on these surfaces confirmed the high activity and selectivity of the Pd–N3Gr catalyst toward HCOOH dehydrogenation (Path-I). These calculated results highlight that the Pd–N3Gr catalyst is a promising candidate for the formic acid decomposition reaction to yield hydrogen.
© 2023 Hydrogen Energy Publications LLC.
On the other hand, the undesirable dehydration of HCOOH to carbon monoxide (CO) through COOH (Path-IIIA) or formyl (HCO) (Path-IIIB) intermediates is unlikely to occur on Pd–N3Gr due to a large activation energy. We found that the active species on the catalyst surface increased with N-doping concentration. Additionally, microkinetic simulations of the HCOOH decomposition on these surfaces confirmed the high activity and selectivity of the Pd–N3Gr catalyst toward HCOOH dehydrogenation (Path-I). These calculated results highlight that the Pd–N3Gr catalyst is a promising candidate for the formic acid decomposition reaction to yield hydrogen.
© 2023 Hydrogen Energy Publications LLC.
Research Area(s)
- Catalyst, Decomposition of formic acid, DFT, Hydrogen energy, N-doped graphene
Citation Format(s)
Mechanistic insights into hydrogen production from formic acid catalyzed by Pd@N-doped graphene: The role of the nitrogen dopant. / Poldorn, Preeyaporn; Wongnongwa, Yutthana; Zhang, Rui-Qin et al.
In: International Journal of Hydrogen Energy, Vol. 48, No. 43, 19.05.2023, p. 16341-16357.
In: International Journal of Hydrogen Energy, Vol. 48, No. 43, 19.05.2023, p. 16341-16357.
Research output: Journal Publications and Reviews › RGC 21 - Publication in refereed journal › peer-review