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NitroScission SIGNED

Electrochemical scission of dinitrogen under ambient conditions

Total Cost €

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EC-Contrib. €

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Partnership

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 NitroScission project word cloud

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

electrolytic    metals    hydrogenation    nitride    energy    constraints    interfaces    film    gas    electrochemical    protons    fuel    present    interphases    400    electrolytes    atmospheric    nitroscission    hydrogen    elucidate    observe    dynamically       operando    150    dinitrogen    experiments    deposited    made    ex    never    demonstrating    electrode    facilities    electroreduction    powered    bind    haber    metal    principles    separate    spectroscopy    strategies    air    electrolyte    synthesis    team    place    situ    adsorption    surfaces    leadership    class    preparation    circumvent    occurs    exposure    electrodes    nitrides    subsequent    tested    quantitative    colossal    ambient    oxygen    reactivity    ammonia    tailor    molecular    previously    albeit    water    binding    stronger    breakthrough    shed    fossil    bar    reaction    renewable    evolution    scientific    fabrication    global    gain    thin    centralised    efficiency    consumes    guided    combine    unambiguous    cell    solid    tools    point    looping    pressures    below    catalyse    free    preventing    attractive    reactive    time    ionic    consumption    tests    enabled    first    interface    bosch   

Project "NitroScission" data sheet

The following table provides information about the project.

Coordinator
IMPERIAL COLLEGE OF SCIENCE TECHNOLOGY AND MEDICINE 

Organization address
address: SOUTH KENSINGTON CAMPUS EXHIBITION ROAD
city: LONDON
postcode: SW7 2AZ
website: http://www.imperial.ac.uk/

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 United Kingdom [UK]
 Total cost 2˙744˙880 €
 EC max contribution 2˙744˙880 € (100%)
 Programme 1. H2020-EU.1.1. (EXCELLENT SCIENCE - European Research Council (ERC))
 Code Call ERC-2019-COG
 Funding Scheme ERC-COG
 Starting year 2021
 Duration (year-month-day) from 2021-01-01   to  2025-12-31

 Partnership

Take a look of project's partnership.

# participants  country  role  EC contrib. [€] 
1    IMPERIAL COLLEGE OF SCIENCE TECHNOLOGY AND MEDICINE UK (LONDON) coordinator 2˙744˙880.00

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 Project objective

Present ammonia synthesis, via the Haber-Bosch process, occurs in centralised facilities above 150 bar and above 400 C; it consumes a colossal 1% of our global fossil fuel consumption. Electrolytic ammonia synthesis, i.e. below 100 C and at atmospheric pressures, could be far more attractive: it would be powered by renewable energy and would take place at the point-of-consumption. I have recently made a breakthrough, by demonstrating the first unambiguous and quantitative evidence that dinitrogen electroreduction is possible under ambient conditions on a solid electrode, albeit at low efficiency My aim for NitroScission is to elucidate pathways —at a molecular level— to catalyse the reaction at high efficiency. However, only the most reactive metal or metal nitride surfaces bind to dinitrogen. Such surfaces will bind even stronger to hydrogen or oxygen from water or air. To circumvent these constraints, I will use three strategies: (i) I will tailor the access of protons to the electrode-electrolyte interface, via in-situ deposited ionic interphases, exploiting recent advances in controlling the reactivity of electrolytes. (ii) I will tailor the binding to dinitrogen through oxygen-free fabrication and testing of metals and metal nitrides electrodes. By preventing air exposure, my team will gain access to a class of highly reactive electrodes, never previously tested in an electrochemical cell. (iii) I will use electrochemical looping, to dynamically separate dinitrogen adsorption from its subsequent hydrogenation. These experiments will be enabled by a novel method that allows us to observe gas evolution in real time. I will combine advanced thin film preparation methods, electrochemical tests, and in operando and ex-situ spectroscopy to establish the design principles for this important reaction. Guided by these unique tools and my scientific leadership, my team will shed unique insight into how to tailor electrode-electrolyte interfaces.

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