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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...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2015
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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. |
format | Online Article Text |
id | pubmed-4650780 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
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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