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Using “Tender” X-ray Ambient Pressure X-Ray Photoelectron Spectroscopy as A Direct Probe of Solid-Liquid Interface

We report a new method to probe the solid-liquid interface through the use of a thin liquid layer on a solid surface. An ambient pressure XPS (AP-XPS) endstation that is capable of detecting high kinetic energy photoelectrons (7 keV) at a pressure up to 110 Torr has been constructed and commissioned...

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Detalles Bibliográficos
Autores principales: Axnanda, Stephanus, Crumlin, Ethan J., Mao, Baohua, Rani, Sana, Chang, Rui, Karlsson, Patrik G., Edwards, Mårten O. M., Lundqvist, Måns, Moberg, Robert, Ross, Phil, Hussain, Zahid, Liu, Zhi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4650780/
https://www.ncbi.nlm.nih.gov/pubmed/25950241
http://dx.doi.org/10.1038/srep09788
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author Axnanda, Stephanus
Crumlin, Ethan J.
Mao, Baohua
Rani, Sana
Chang, Rui
Karlsson, Patrik G.
Edwards, Mårten O. M.
Lundqvist, Måns
Moberg, Robert
Ross, Phil
Hussain, Zahid
Liu, Zhi
author_facet Axnanda, Stephanus
Crumlin, Ethan J.
Mao, Baohua
Rani, Sana
Chang, Rui
Karlsson, Patrik G.
Edwards, Mårten O. M.
Lundqvist, Måns
Moberg, Robert
Ross, Phil
Hussain, Zahid
Liu, Zhi
author_sort Axnanda, Stephanus
collection PubMed
description We report a new method to probe the solid-liquid interface through the use of a thin liquid layer on a solid surface. An ambient pressure XPS (AP-XPS) endstation that is capable of detecting high kinetic energy photoelectrons (7 keV) at a pressure up to 110 Torr has been constructed and commissioned. Additionally, we have deployed a “dip & pull” method to create a stable nanometers-thick aqueous electrolyte on platinum working electrode surface. Combining the newly constructed AP-XPS system, “dip & pull” approach, with a “tender” X-ray synchrotron source (2 keV–7 keV), we are able to access the interface between liquid and solid dense phases with photoelectrons and directly probe important phenomena occurring at the narrow solid-liquid interface region in an electrochemical system. Using this approach, we have performed electrochemical oxidation of the Pt electrode at an oxygen evolution reaction (OER) potential. Under this potential, we observe the formation of both Pt(2+) and Pt(4+) interfacial species on the Pt working electrode in situ. We believe this thin-film approach and the use of “tender” AP-XPS highlighted in this study is an innovative new approach to probe this key solid-liquid interface region of electrochemistry.
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spelling pubmed-46507802015-11-24 Using “Tender” X-ray Ambient Pressure X-Ray Photoelectron Spectroscopy as A Direct Probe of Solid-Liquid Interface Axnanda, Stephanus Crumlin, Ethan J. Mao, Baohua Rani, Sana Chang, Rui Karlsson, Patrik G. Edwards, Mårten O. M. Lundqvist, Måns Moberg, Robert Ross, Phil Hussain, Zahid Liu, Zhi Sci Rep Article We report a new method to probe the solid-liquid interface through the use of a thin liquid layer on a solid surface. An ambient pressure XPS (AP-XPS) endstation that is capable of detecting high kinetic energy photoelectrons (7 keV) at a pressure up to 110 Torr has been constructed and commissioned. Additionally, we have deployed a “dip & pull” method to create a stable nanometers-thick aqueous electrolyte on platinum working electrode surface. Combining the newly constructed AP-XPS system, “dip & pull” approach, with a “tender” X-ray synchrotron source (2 keV–7 keV), we are able to access the interface between liquid and solid dense phases with photoelectrons and directly probe important phenomena occurring at the narrow solid-liquid interface region in an electrochemical system. Using this approach, we have performed electrochemical oxidation of the Pt electrode at an oxygen evolution reaction (OER) potential. Under this potential, we observe the formation of both Pt(2+) and Pt(4+) interfacial species on the Pt working electrode in situ. We believe this thin-film approach and the use of “tender” AP-XPS highlighted in this study is an innovative new approach to probe this key solid-liquid interface region of electrochemistry. Nature Publishing Group 2015-05-07 /pmc/articles/PMC4650780/ /pubmed/25950241 http://dx.doi.org/10.1038/srep09788 Text en Copyright © 2015, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Axnanda, Stephanus
Crumlin, Ethan J.
Mao, Baohua
Rani, Sana
Chang, Rui
Karlsson, Patrik G.
Edwards, Mårten O. M.
Lundqvist, Måns
Moberg, Robert
Ross, Phil
Hussain, Zahid
Liu, Zhi
Using “Tender” X-ray Ambient Pressure X-Ray Photoelectron Spectroscopy as A Direct Probe of Solid-Liquid Interface
title Using “Tender” X-ray Ambient Pressure X-Ray Photoelectron Spectroscopy as A Direct Probe of Solid-Liquid Interface
title_full Using “Tender” X-ray Ambient Pressure X-Ray Photoelectron Spectroscopy as A Direct Probe of Solid-Liquid Interface
title_fullStr Using “Tender” X-ray Ambient Pressure X-Ray Photoelectron Spectroscopy as A Direct Probe of Solid-Liquid Interface
title_full_unstemmed Using “Tender” X-ray Ambient Pressure X-Ray Photoelectron Spectroscopy as A Direct Probe of Solid-Liquid Interface
title_short Using “Tender” X-ray Ambient Pressure X-Ray Photoelectron Spectroscopy as A Direct Probe of Solid-Liquid Interface
title_sort using “tender” x-ray ambient pressure x-ray photoelectron spectroscopy as a direct probe of solid-liquid interface
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4650780/
https://www.ncbi.nlm.nih.gov/pubmed/25950241
http://dx.doi.org/10.1038/srep09788
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