Cargando…

Analysis of Temperature-Programmed Desorption via Equilibrium Thermodynamics

[Image: see text] Temperature-programmed desorption (TPD) experiments in surface science are usually analyzed using the Polanyi–Wigner equation and/or transition-state theory. These methods are far from straightforward, and the determination of the pre-exponential factor is often problematic. We pre...

Descripción completa

Detalles Bibliográficos
Autores principales: Schmid, Michael, Parkinson, Gareth S., Diebold, Ulrike
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2022
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9881163/
https://www.ncbi.nlm.nih.gov/pubmed/36718262
http://dx.doi.org/10.1021/acsphyschemau.2c00031
_version_ 1784879055367045120
author Schmid, Michael
Parkinson, Gareth S.
Diebold, Ulrike
author_facet Schmid, Michael
Parkinson, Gareth S.
Diebold, Ulrike
author_sort Schmid, Michael
collection PubMed
description [Image: see text] Temperature-programmed desorption (TPD) experiments in surface science are usually analyzed using the Polanyi–Wigner equation and/or transition-state theory. These methods are far from straightforward, and the determination of the pre-exponential factor is often problematic. We present a different method based on equilibrium thermodynamics, which builds on an approach previously used for TPD by Kreuzer et al. (Surf. Sci.1988). Equations for the desorption rate are presented for three different types of surface–adsorbate interactions: (i) a 2D ideal hard-sphere gas with a negligible diffusion barrier, (ii) an ideal lattice gas, that is, fixed adsorption sites without interaction between the adsorbates, and (iii) a lattice gas with a distribution of (site-dependent) adsorption energies. We show that the coverage dependence of the sticking coefficient for adsorption at the desorption temperature determines whether the desorption process can be described by first- or second-order kinetics. The sticking coefficient at the desorption temperature must also be known for a quantitative determination of the adsorption energy, but it has a rather weak influence (like the pre-exponential factor in a traditional TPD analysis). Quantitative analysis is also influenced by the vibrational contributions to the energy and entropy. For the case of a single adsorption energy, we provide equations to directly convert peak temperatures into adsorption energies. These equations also provide an approximation of the desorption energy in cases that cannot be described by a fixed pre-exponential factor. For the case of a distribution of adsorption energies, the desorption spectra cannot be considered a superposition of desorption spectra corresponding to the different energies. Nevertheless, we present a method to extract the distribution of adsorption energies from TPD spectra, and we rationalize the energy resolution of TPD experiments. The analytical results are complemented by a program for simulation and analysis of TPD data.
format Online
Article
Text
id pubmed-9881163
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher American Chemical Society
record_format MEDLINE/PubMed
spelling pubmed-98811632023-01-28 Analysis of Temperature-Programmed Desorption via Equilibrium Thermodynamics Schmid, Michael Parkinson, Gareth S. Diebold, Ulrike ACS Phys Chem Au [Image: see text] Temperature-programmed desorption (TPD) experiments in surface science are usually analyzed using the Polanyi–Wigner equation and/or transition-state theory. These methods are far from straightforward, and the determination of the pre-exponential factor is often problematic. We present a different method based on equilibrium thermodynamics, which builds on an approach previously used for TPD by Kreuzer et al. (Surf. Sci.1988). Equations for the desorption rate are presented for three different types of surface–adsorbate interactions: (i) a 2D ideal hard-sphere gas with a negligible diffusion barrier, (ii) an ideal lattice gas, that is, fixed adsorption sites without interaction between the adsorbates, and (iii) a lattice gas with a distribution of (site-dependent) adsorption energies. We show that the coverage dependence of the sticking coefficient for adsorption at the desorption temperature determines whether the desorption process can be described by first- or second-order kinetics. The sticking coefficient at the desorption temperature must also be known for a quantitative determination of the adsorption energy, but it has a rather weak influence (like the pre-exponential factor in a traditional TPD analysis). Quantitative analysis is also influenced by the vibrational contributions to the energy and entropy. For the case of a single adsorption energy, we provide equations to directly convert peak temperatures into adsorption energies. These equations also provide an approximation of the desorption energy in cases that cannot be described by a fixed pre-exponential factor. For the case of a distribution of adsorption energies, the desorption spectra cannot be considered a superposition of desorption spectra corresponding to the different energies. Nevertheless, we present a method to extract the distribution of adsorption energies from TPD spectra, and we rationalize the energy resolution of TPD experiments. The analytical results are complemented by a program for simulation and analysis of TPD data. American Chemical Society 2022-11-15 /pmc/articles/PMC9881163/ /pubmed/36718262 http://dx.doi.org/10.1021/acsphyschemau.2c00031 Text en © 2022 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by/4.0/Permits the broadest form of re-use including for commercial purposes, provided that author attribution and integrity are maintained (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Schmid, Michael
Parkinson, Gareth S.
Diebold, Ulrike
Analysis of Temperature-Programmed Desorption via Equilibrium Thermodynamics
title Analysis of Temperature-Programmed Desorption via Equilibrium Thermodynamics
title_full Analysis of Temperature-Programmed Desorption via Equilibrium Thermodynamics
title_fullStr Analysis of Temperature-Programmed Desorption via Equilibrium Thermodynamics
title_full_unstemmed Analysis of Temperature-Programmed Desorption via Equilibrium Thermodynamics
title_short Analysis of Temperature-Programmed Desorption via Equilibrium Thermodynamics
title_sort analysis of temperature-programmed desorption via equilibrium thermodynamics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9881163/
https://www.ncbi.nlm.nih.gov/pubmed/36718262
http://dx.doi.org/10.1021/acsphyschemau.2c00031
work_keys_str_mv AT schmidmichael analysisoftemperatureprogrammeddesorptionviaequilibriumthermodynamics
AT parkinsongareths analysisoftemperatureprogrammeddesorptionviaequilibriumthermodynamics
AT dieboldulrike analysisoftemperatureprogrammeddesorptionviaequilibriumthermodynamics