Carbon dioxide mediated, reversible chemical hydrogen storage using a Pd nanocatalyst supported on mesoporous graphitic carbon nitride

Authors
Lee, Jin HeeRyu, JaeyuneKim, Jin YoungNam, Suk-WooHan, Jong HeeLim, Tae-HoonGautam, SanjeevChae, Keun HwaYoon, Chang Won
Issue Date
2014-07-07
Publisher
ROYAL SOC CHEMISTRY
Citation
JOURNAL OF MATERIALS CHEMISTRY A, v.2, no.25, pp.9490 - 9495
Abstract
Reversible, carbon dioxide mediated chemical hydrogen storage was first demonstrated using a heterogeneous Pd catalyst supported on mesoporous graphitic carbon nitride (Pd/mpg-C3N4). The Pd nanoparticles were found to be uniformly dispersed onto mpg-C3N4 with an average size of 1.7 nm without any agglomeration and further exhibit superior activity for the dehydrogenation of formic acid with a turnover frequency of 144 h(-1) even in the absence of external bases at room temperature. Initial DFT studies suggest that basic sites located at the mpg-C3N4 support play synergetic roles in stabilizing reduced Pd nanoparticles without any surfactant as well as in initiating H-2-release by deprotonation of formic acid, and these potential interactions were further confirmed by X-ray absorption near edge structure (XANES). Along with dehydrogenation. Pd/mpg-C3N4 also proves to catalyze the regeneration of formic acid via CO2 hydrogenation. The governing factors of CO2 hydrogenation are further elucidated to increase the quantity of the desired formic acid with high selectivity.
Keywords
FORMIC-ACID DECOMPOSITION; METAL-ORGANIC FRAMEWORKS; ROOM-TEMPERATURE; AMMONIA-BORANE; ALLOY NANOPARTICLES; EFFICIENT CATALYST; HIGHLY EFFICIENT; IRON CATALYST; GENERATION; DEHYDROGENATION; FORMIC-ACID DECOMPOSITION; METAL-ORGANIC FRAMEWORKS; ROOM-TEMPERATURE; AMMONIA-BORANE; ALLOY NANOPARTICLES; EFFICIENT CATALYST; HIGHLY EFFICIENT; IRON CATALYST; GENERATION; DEHYDROGENATION; Carbon dioxide; Hydrogen storage; Pd catalyst; carbon nitride; Formic acid; Formic acid synthesis; Dehydrogenation
ISSN
2050-7488
URI
https://pubs.kist.re.kr/handle/201004/126598
DOI
10.1039/c4ta01133c
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KIST Article > 2014
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