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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.

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

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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