Separation of temperature effects on double-layer and charge-transfer processes for platinum|solution interphases. Entropy of formation of the double layer and absolute molar entropy of adsorbed hydrogen and OH on Pt(111)
Separation of temperature effects on double-layer and charge-transfer processes for platinum|solution interphases. Entropy of formation of the double layer and absolute molar entropy of adsorbed hydrogen and OH on Pt(111)
The present work combines results from pulsed-laser experiments and a thermodynamic analysis, to separate temperature effects on double-layer and charge-transfer processes. The entropy of formation of the double layer for Pt(111) in 0.1 M HClO4 is evaluated and compared with the corresponding entropy of formation of the overall interphase. The difference between the two quantities is due to the entropy change associated with charge-transfer processes, thus allowing for the evaluation of the absolute molar entropy of adsorbed hydrogen and OH on Pt(111). The results indicate that adsorbed hydrogen on Pt(111) is very mobile, whereas adsorbed OH species are rather immobile. Finally, values of the entropy of formation of the double layer are compared to data for mercury electrodes. It is concluded that the entropy of the interfacial water network on Pt(111) exhibits a nearly symmetrical dependence on charge density. This result contrasts with the behavior observed for mercury electrodes, for which the state of maximum entropy is achieved at clearly negative charge densities
19913-19925
Garcia-Araez, Nuria
9358a0f9-309c-495e-b6bf-da985ad81c37
Climent, Victor
c3ecab58-edb5-4055-8fa0-c0aef0fc60a4
Feliu, Juan
14aa5d27-621c-4999-870d-4856abaf5996
27 October 2009
Garcia-Araez, Nuria
9358a0f9-309c-495e-b6bf-da985ad81c37
Climent, Victor
c3ecab58-edb5-4055-8fa0-c0aef0fc60a4
Feliu, Juan
14aa5d27-621c-4999-870d-4856abaf5996
Garcia-Araez, Nuria, Climent, Victor and Feliu, Juan
(2009)
Separation of temperature effects on double-layer and charge-transfer processes for platinum|solution interphases. Entropy of formation of the double layer and absolute molar entropy of adsorbed hydrogen and OH on Pt(111).
The Journal of Physical Chemistry C, 113 (46), .
(doi:10.1021/jp904638d).
Abstract
The present work combines results from pulsed-laser experiments and a thermodynamic analysis, to separate temperature effects on double-layer and charge-transfer processes. The entropy of formation of the double layer for Pt(111) in 0.1 M HClO4 is evaluated and compared with the corresponding entropy of formation of the overall interphase. The difference between the two quantities is due to the entropy change associated with charge-transfer processes, thus allowing for the evaluation of the absolute molar entropy of adsorbed hydrogen and OH on Pt(111). The results indicate that adsorbed hydrogen on Pt(111) is very mobile, whereas adsorbed OH species are rather immobile. Finally, values of the entropy of formation of the double layer are compared to data for mercury electrodes. It is concluded that the entropy of the interfacial water network on Pt(111) exhibits a nearly symmetrical dependence on charge density. This result contrasts with the behavior observed for mercury electrodes, for which the state of maximum entropy is achieved at clearly negative charge densities
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Published date: 27 October 2009
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Electrochemistry
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Local EPrints ID: 345803
URI: http://eprints.soton.ac.uk/id/eprint/345803
ISSN: 1932-7447
PURE UUID: b5163c63-9b44-4feb-b5bd-7931f525c7be
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Date deposited: 30 Nov 2012 14:37
Last modified: 15 Mar 2024 03:46
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Author:
Victor Climent
Author:
Juan Feliu
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