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    Rights statement: This is the author’s version of a work that was accepted for publication in Nano Energy. Changes resulting from the publishing process, such as peer review, editing, corrections, structural formatting, and other quality control mechanisms may not be reflected in this document. Changes may have been made to this work since it was submitted for publication. A definitive version was subsequently published in Nano Energy, 29, 2016 DOI: 10.1016/j.nanoen.2016.04.015

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Ultrahigh vacuum and electrocatalysis: the powers of quantitative surface imaging

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Ultrahigh vacuum and electrocatalysis: the powers of quantitative surface imaging. / Mercer, Michael; Hoster, Harry Ernst.
In: Nano Energy, Vol. 29, 11.2016, p. 394-413.

Research output: Contribution to Journal/MagazineJournal articlepeer-review

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Mercer M, Hoster HE. Ultrahigh vacuum and electrocatalysis: the powers of quantitative surface imaging. Nano Energy. 2016 Nov;29:394-413. Epub 2016 Apr 20. doi: 10.1016/j.nanoen.2016.04.015

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Bibtex

@article{5d93634c6ce54b6b84b390834abc5519,
title = "Ultrahigh vacuum and electrocatalysis: the powers of quantitative surface imaging",
abstract = "We highlight the impact of Ultrahigh Vacuum (UHV)-born surface science on modern electrocatalysis. The microscopic, atomic level picture of surface adsorption and reaction, which was developed in the surface science community in decades of systematic research on single crystals in UHV, has meanwhile become state-of-the-art also in electrochemistry. For the example of CO on Pt(111) single crystals, which has been extensively studied at the solid/gas and the solid/liquid interface using atomic resolution scanning tunnelling microscopy (STM), we highlight how both interfaces may have even more in common than often assumed. We then illustrate how planar model surfaces such as mono- and bimetallic single crystals and surface alloys, prepared and thoroughly analysed in UHV, enabled a systematic search for improved electrocatalysts. Surface alloys, thermodynamically more stable than foreign metal islands, are a particularly important sub-group of model surfaces, which so far have only been fabricated in UHV. We also flag that model surfaces may not always assume the structure anticipated for the respective experiment, regardless of their preparation in UHV or by electrochemical methods. “Accidental” surface alloying may be more common than often assumed, leading to misinterpretations of the structure-property relationships targeted in many model studies. We highlight that controlled surface alloy formation should be a key step in any model study looking at bimetallic systems in order to get an idea what the effect of unintended alloying could possibly be, and to cross-check whether alloyed surfaces may potentially be the better electrocatalysts in the first place. ",
keywords = "Electrochemistry, Electrocatalysis, Surface alloys, Single, Crystals, Ultrahigh vacuum , Scanning tunnelling microscopy",
author = "Michael Mercer and Hoster, {Harry Ernst}",
note = "This is the author{\textquoteright}s version of a work that was accepted for publication in Nano Energy. Changes resulting from the publishing process, such as peer review, editing, corrections, structural formatting, and other quality control mechanisms may not be reflected in this document. Changes may have been made to this work since it was submitted for publication. A definitive version was subsequently published in Nano Energy, 29, 2016 DOI: 10.1016/j.nanoen.2016.04.015",
year = "2016",
month = nov,
doi = "10.1016/j.nanoen.2016.04.015",
language = "English",
volume = "29",
pages = "394--413",
journal = "Nano Energy",
issn = "2211-2855",
publisher = "Elsevier BV",

}

RIS

TY - JOUR

T1 - Ultrahigh vacuum and electrocatalysis

T2 - the powers of quantitative surface imaging

AU - Mercer, Michael

AU - Hoster, Harry Ernst

N1 - This is the author’s version of a work that was accepted for publication in Nano Energy. Changes resulting from the publishing process, such as peer review, editing, corrections, structural formatting, and other quality control mechanisms may not be reflected in this document. Changes may have been made to this work since it was submitted for publication. A definitive version was subsequently published in Nano Energy, 29, 2016 DOI: 10.1016/j.nanoen.2016.04.015

PY - 2016/11

Y1 - 2016/11

N2 - We highlight the impact of Ultrahigh Vacuum (UHV)-born surface science on modern electrocatalysis. The microscopic, atomic level picture of surface adsorption and reaction, which was developed in the surface science community in decades of systematic research on single crystals in UHV, has meanwhile become state-of-the-art also in electrochemistry. For the example of CO on Pt(111) single crystals, which has been extensively studied at the solid/gas and the solid/liquid interface using atomic resolution scanning tunnelling microscopy (STM), we highlight how both interfaces may have even more in common than often assumed. We then illustrate how planar model surfaces such as mono- and bimetallic single crystals and surface alloys, prepared and thoroughly analysed in UHV, enabled a systematic search for improved electrocatalysts. Surface alloys, thermodynamically more stable than foreign metal islands, are a particularly important sub-group of model surfaces, which so far have only been fabricated in UHV. We also flag that model surfaces may not always assume the structure anticipated for the respective experiment, regardless of their preparation in UHV or by electrochemical methods. “Accidental” surface alloying may be more common than often assumed, leading to misinterpretations of the structure-property relationships targeted in many model studies. We highlight that controlled surface alloy formation should be a key step in any model study looking at bimetallic systems in order to get an idea what the effect of unintended alloying could possibly be, and to cross-check whether alloyed surfaces may potentially be the better electrocatalysts in the first place.

AB - We highlight the impact of Ultrahigh Vacuum (UHV)-born surface science on modern electrocatalysis. The microscopic, atomic level picture of surface adsorption and reaction, which was developed in the surface science community in decades of systematic research on single crystals in UHV, has meanwhile become state-of-the-art also in electrochemistry. For the example of CO on Pt(111) single crystals, which has been extensively studied at the solid/gas and the solid/liquid interface using atomic resolution scanning tunnelling microscopy (STM), we highlight how both interfaces may have even more in common than often assumed. We then illustrate how planar model surfaces such as mono- and bimetallic single crystals and surface alloys, prepared and thoroughly analysed in UHV, enabled a systematic search for improved electrocatalysts. Surface alloys, thermodynamically more stable than foreign metal islands, are a particularly important sub-group of model surfaces, which so far have only been fabricated in UHV. We also flag that model surfaces may not always assume the structure anticipated for the respective experiment, regardless of their preparation in UHV or by electrochemical methods. “Accidental” surface alloying may be more common than often assumed, leading to misinterpretations of the structure-property relationships targeted in many model studies. We highlight that controlled surface alloy formation should be a key step in any model study looking at bimetallic systems in order to get an idea what the effect of unintended alloying could possibly be, and to cross-check whether alloyed surfaces may potentially be the better electrocatalysts in the first place.

KW - Electrochemistry

KW - Electrocatalysis

KW - Surface alloys

KW - Single

KW - Crystals

KW - Ultrahigh vacuum

KW - Scanning tunnelling microscopy

U2 - 10.1016/j.nanoen.2016.04.015

DO - 10.1016/j.nanoen.2016.04.015

M3 - Journal article

VL - 29

SP - 394

EP - 413

JO - Nano Energy

JF - Nano Energy

SN - 2211-2855

ER -