2021
DOI: 10.1039/d0ta12174f
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Size-dependent hydrogen trapping in palladium nanoparticles

Abstract: We report an experimental study, supported by a theoretical approach based on simulations, to explore the phenomenon of H trapping in small Pd nanoparticles. Hydrogen absorption/desorption of a series of...

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Cited by 17 publications
(24 citation statements)
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“…In the meantime, the number of H atoms dissolved in the α‐PdH phase measured at 0.05 V decreases with the increase in the NPs size, from 0.06 to 0.05 and 0.04 for Pd NPs “S” , “M” , and “L” respectively. This result is in good agreement with the literature, as the solubility of H in the α‐PdH phase is expected to increase with decreasing NPs size, while the H sorption capacity in the β‐PdH phase is expected to decrease [5,29,35] . The observed behaviour is typical of Pd NPs, whereas an opposite trend is expected for Pd thin films.…”
Section: Resultssupporting
confidence: 91%
See 1 more Smart Citation
“…In the meantime, the number of H atoms dissolved in the α‐PdH phase measured at 0.05 V decreases with the increase in the NPs size, from 0.06 to 0.05 and 0.04 for Pd NPs “S” , “M” , and “L” respectively. This result is in good agreement with the literature, as the solubility of H in the α‐PdH phase is expected to increase with decreasing NPs size, while the H sorption capacity in the β‐PdH phase is expected to decrease [5,29,35] . The observed behaviour is typical of Pd NPs, whereas an opposite trend is expected for Pd thin films.…”
Section: Resultssupporting
confidence: 91%
“…The authors also claim that a sublayer rich in H atoms contributes greatly to the global H/Pd ratio in thin films. Some studies describe Pd hydride in NPs as a core‐shell structure, in which the outer shell, i. e. the subsurface, would present interstitial sites less favourable for the H absorption than the ones of the inner core [35] . In such a case, the number of interstitial sites suitable for H absorption decreases with the Pd NPs diameter, which would explain the opposite trend observed.…”
Section: Resultsmentioning
confidence: 99%
“…This is the case for magnesium oxide in Pd/MgO-SiO 2 catalyst, where the MgO is taking care of the CO 2 while the palladium dissociates the H 2 , making the metal-support interface a plausible active site. 281,282 The bifunctional mechanism of this system was confirmed by other works. 277 The replacement of magnesium with nickel or iron does not change significantly the CO 2 conversion.…”
Section: Co 2 Methanation Catalystssupporting
confidence: 82%
“…More importantly, the atomically resolved HAADF-STEM image (Figure i) and the moiré images (Figure j 1 and j 2 ) show that the core–shell interface still remains fully epitaxial and coherent. Hydrogen intercalation can convert Pd to PdH 0.43 and induce a volume expansion of the core, but the Pt shell still maintains the same composition since it is too inert to form the platinum hydride . Therefore, the as-observed continuous lattice at the core–shell interface in c -PdH 0.43 @Pt NPs indicates that the Pt shell is subject to a lattice expansion so that it can match the enlarged lattice of the core very well.…”
Section: Results and Discussionmentioning
confidence: 99%