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Scientific Reports· 2015Q1

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

Stephanus Axnanda, Ethan J. Crumlin, Baohua Mao, Sana Rani et al.

Short summary

A new ambient pressure X-ray photoelectron spectroscopy (AP-XPS) method using a "tender" X-ray source (2-7 keV) and a "dip & pull" technique allows direct in situ observation of solid-liquid interfaces in electrochemical systems.

AI-generated from the title and abstract; the full text is not read.

Key points

  • A new AP-XPS endstation was constructed to probe solid-liquid interfaces.
  • A "dip & pull" method creates stable, nanometer-thick aqueous electrolyte layers on electrodes.
  • The system uses a "tender" X-ray synchrotron source (2-7 keV) to detect high kinetic energy photoelectrons.
  • In situ electrochemical oxidation of a Pt electrode revealed the formation of Pt(2+) and Pt(4+) interfacial species.

AI-generated from the title and abstract; the full text is not read.

Abstract

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.

The authors' abstract, as published at the source. Scientific Reports, 2015 · DOI ↗

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Field: Electrochemistry

ElectrochemistryChemistry