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E-SAC SIGNED

Evolving Single-Atom Catalysis: Fundamental Insights for Rational Design

Total Cost €

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EC-Contrib. €

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Partnership

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 E-SAC project word cloud

Explore the words cloud of the E-SAC project. It provides you a very rough idea of what is the project "E-SAC" about.

catalytic    understand    sites    gap    minimising    heterogeneous    recreate    catalysts    combinations    fe3o4    elucidated    xanes    levels    atom    heterogenize    metal    organometallic    tend    robustly    ultrahigh    realistic    cells    energy    structure    selectively    impossible    newly    purpose    catalysis    site    mechanisms    model    replacing    reactions    utilized    atoms    reaction    sacs    vacuum    optimal    conversion    strive    performance    rare    supports    prox    performed    bonds    orr    group    vienna    proves    ultimate    001    metals    fundamental    single    unknown    uhv    methane    resemble    origins    hydrogenation    relationships    pioneered    difficult    chemical    complexes    iras    hydroformylation    technologies    formed    environments    identical    homogeneous    era    pressure    modify    sac    progress    selectivity    mean    precisely    bridge    anchor    expensive    efficiency    active    describe    function    efficient    unravel    environmentally    rational    oxygen    electrochemical    economy    spectra    solution    complexity    designed   

Project "E-SAC" data sheet

The following table provides information about the project.

Coordinator
TECHNISCHE UNIVERSITAET WIEN 

Organization address
address: KARLSPLATZ 13
city: WIEN
postcode: 1040
website: www.tuwien.ac.at

contact info
title: n.a.
name: n.a.
surname: n.a.
function: n.a.
email: n.a.
telephone: n.a.
fax: n.a.

 Coordinator Country Austria [AT]
 Total cost 1˙993˙718 €
 EC max contribution 1˙993˙718 € (100%)
 Programme 1. H2020-EU.1.1. (EXCELLENT SCIENCE - European Research Council (ERC))
 Code Call ERC-2019-COG
 Funding Scheme ERC-COG
 Starting year 2020
 Duration (year-month-day) from 2020-02-01   to  2025-01-31

 Partnership

Take a look of project's partnership.

# participants  country  role  EC contrib. [€] 
1    TECHNISCHE UNIVERSITAET WIEN AT (WIEN) coordinator 1˙993˙718.00

Map

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 Project objective

Rare and expensive metals tend to be the best catalysts, and minimising or replacing them is a major research target as we strive to develop an economy based on more environmentally-friendly, energy-efficient technologies. “Single-atom” catalysis (SAC) represents the ultimate in efficiency, and the chemical bonds formed between the metal atom and the support mean these systems strongly resemble the organometallic complexes utilized in homogeneous catalysis. If all active sites were identical, single-atom catalysts (SACs) could achieve similar levels of selectivity, and even be used to “heterogenize” difficult reactions that must be currently performed in solution. There is a problem however: homogeneous catalysts are designed based on well-understood structure-function relationships. In SAC, the structure of the active site is unknown, thus rational design is impossible. My group in Vienna has pioneered the use of the model supports to understand fundamental mechanisms in SAC. Our work with Fe3O4(001) proves that we can precisely determine and even selectively modify the active site, and unravel the role of structure in catalytic activity. Real progress, however, requires realistic active sites, realistic supports, and realistic environments. In this project, I describe how we will determine the sites that robustly anchor metal atoms on five of the most important supports in ultrahigh vacuum (UHV), and test their performance in newly-developed high-pressure and electrochemical cells. The origins of selectivity for PROX, hydrogenation, hydroformylation, methane conversion, and the oxygen reduction reaction (ORR) will be elucidated, and the best atom/support combinations for each reaction identified. Robust XANES and IRAS spectra will allow us to bridge the complexity gap and recreate the optimal active sites on real SACs and lead the way into a new era in which heterogeneous catalysts are designed for purpose, based on a fundamental understanding of how they work.

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The information about "E-SAC" are provided by the European Opendata Portal: CORDIS opendata.

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