Interlinking Catalysts, Mechanisms and Reactor Concepts for the Conversion of Dinitrogen by Electrocatalytic, Photocatalytic and Photoelectrocatalytic Methods ("Nitroconversion") (SPP 2370)
Termin:
01.09.2021
Fördergeber:
Deutsche Forschungsgemeinschaft (DFG)
The Senate of the Deutsche Forschungsgemeinschaft (DFG, German Research Foundation) has announced the establishment of a new Priority Programme entitled "Interlinking Catalysts, Mechanisms and Reactor Concepts for the Conversion of Dinitrogen by Electrocatalytic, Photocatalytic and Photoelectrocatalytic Methods ("Nitroconversion")" (SPP 2370). The programme is scheduled to run for six years; the present call invites proposals for the first three-year funding period (2022-2025).
With 945 kJ/mol, the triple bond of the dinitrogen (N2) molecule has one of the highest dissociation enthalpies among covalent bonds. Nowadays, more than 180 million tons of ammonia are produced annually from N2 world-wide based on the Haber-Bosch process, and the rapid growth of the world's population would not have been possible without this industrial "artificial N2 conversion". Downsides of this technology are however the high energy demand, the large CO2 emissions associated to this process (for 1 ton of ammonia 20-40 GJ are required and 1.5 tons of CO2 are produced) and the need of large centralised production sites, impeding decentralisation.
In view of the increasing CO2 concentration in the atmosphere, ongoing energy transitions, and development of alternative concepts for the activation of small molecules, new approaches for artificial N2 conversion are in demand. This includes (photo)electrocatalysis or photocatalysis, which can be operated decentralised under less harsh conditions powered by renewable electricity or light. Although intensely researched, the overall energy demand of these approaches for N2 conversion is still significantly higher, and the space-time yield is far too low to compete with the Haber-Bosch process. Notably, scales of the overall catalytic processes from the nano to the meter level are in most cases investigated isolated from each other, which hampers a disruptive breakthrough.
The Priority Programme focuses on the development of heterogeneous (1) electrocatalytic, (2) photocatalytic and (3) photoelectrochemical N2 conversion reactions for delocalised and sustainable N2 conversion pathways with - as a long-term objective - an overall energy consumption and space-time yield comparable to the Haber-Bosch process.
This is to be achieved by establishing insights into structure/activity relationships for catalysts including experimental and theoretical design strategies, along with developing novel electrode and reactor concepts to overcome N2 mass transfer limitations, and by using novel analytical techniques to investigate the underlying mechanisms to be able to design catalysts rationally, and to develop new reaction pathways. The Priority Programme is explicitly not limited to N2 conversion processes to ammonia but can also include research on oxidative conversions. Moreover, the respective counter reaction should be analysed in detail as well.
Molecular catalysts and immobilised molecular catalysts on surfaces as well as biological approaches are not part of this Priority Programme. Likewise, plasma-enhanced processes are excluded as well.
The Priority Programme focuses on the development of heterogeneous electrocatalytic, photocatalytic and photoelectrochemical N2 conversion reactions. Propositions within this programme should use solid materials for artificial dinitrogen conversion. The formation of consortia of multiple principle investigators (preferably 2-3) is envisioned, and joint proposals should cover at least two of the three following areas:
o catalyst synthesis and their physicochemical characterisation
o experimental and/or theoretical investigation of reaction mechanisms
o reaction engineering
Ideas for novel material classes as absorbers or catalysts are welcome as well as model systems to be studied for the understanding of elementary steps at the solid-liquid interface. The submission of proposals interlinking research on electrocatalysis with photoelectrochemistry and/or photocatalysis to identify common design strategies is greatly encouraged. Proposals should pay special emphasis to the interlink with other projects to strengthen the interdisciplinary character of the programme. Here, we encourage possible principle investigators to discuss and connect complementary project ideas already in the submission phase to form topical clusters. The participation of junior research groups and early career researchers in the consortia is greatly encouraged.
For scientific enquiries, please contact the Priority Programme coordinator:
Professor Dr. Roland Marschall
Universität Bayreuth
Fakultät für Biologie, Chemie und Geowissenschaften
Universitätsstraße 30
95447 Bayreuth
phone +49 921 55-2761
roland.marschall@uni-bayreuth.de
For questions related to the DFG review process, please contact:
Dr. Kerstin Freitag, phone +49 228 885-3084, kerstin.freitag@dfg.de
For administrative questions regarding the DFG application, please contact:
Ralph Kirschbaum, phone +49 228 885-2326, ralph.kirschbaum@dfg.de
Further information:
https://www.dfg.de/en/research_funding/announcements_proposals/2021/info_wissenschaft_21_42
With 945 kJ/mol, the triple bond of the dinitrogen (N2) molecule has one of the highest dissociation enthalpies among covalent bonds. Nowadays, more than 180 million tons of ammonia are produced annually from N2 world-wide based on the Haber-Bosch process, and the rapid growth of the world's population would not have been possible without this industrial "artificial N2 conversion". Downsides of this technology are however the high energy demand, the large CO2 emissions associated to this process (for 1 ton of ammonia 20-40 GJ are required and 1.5 tons of CO2 are produced) and the need of large centralised production sites, impeding decentralisation.
In view of the increasing CO2 concentration in the atmosphere, ongoing energy transitions, and development of alternative concepts for the activation of small molecules, new approaches for artificial N2 conversion are in demand. This includes (photo)electrocatalysis or photocatalysis, which can be operated decentralised under less harsh conditions powered by renewable electricity or light. Although intensely researched, the overall energy demand of these approaches for N2 conversion is still significantly higher, and the space-time yield is far too low to compete with the Haber-Bosch process. Notably, scales of the overall catalytic processes from the nano to the meter level are in most cases investigated isolated from each other, which hampers a disruptive breakthrough.
The Priority Programme focuses on the development of heterogeneous (1) electrocatalytic, (2) photocatalytic and (3) photoelectrochemical N2 conversion reactions for delocalised and sustainable N2 conversion pathways with - as a long-term objective - an overall energy consumption and space-time yield comparable to the Haber-Bosch process.
This is to be achieved by establishing insights into structure/activity relationships for catalysts including experimental and theoretical design strategies, along with developing novel electrode and reactor concepts to overcome N2 mass transfer limitations, and by using novel analytical techniques to investigate the underlying mechanisms to be able to design catalysts rationally, and to develop new reaction pathways. The Priority Programme is explicitly not limited to N2 conversion processes to ammonia but can also include research on oxidative conversions. Moreover, the respective counter reaction should be analysed in detail as well.
Molecular catalysts and immobilised molecular catalysts on surfaces as well as biological approaches are not part of this Priority Programme. Likewise, plasma-enhanced processes are excluded as well.
The Priority Programme focuses on the development of heterogeneous electrocatalytic, photocatalytic and photoelectrochemical N2 conversion reactions. Propositions within this programme should use solid materials for artificial dinitrogen conversion. The formation of consortia of multiple principle investigators (preferably 2-3) is envisioned, and joint proposals should cover at least two of the three following areas:
o catalyst synthesis and their physicochemical characterisation
o experimental and/or theoretical investigation of reaction mechanisms
o reaction engineering
Ideas for novel material classes as absorbers or catalysts are welcome as well as model systems to be studied for the understanding of elementary steps at the solid-liquid interface. The submission of proposals interlinking research on electrocatalysis with photoelectrochemistry and/or photocatalysis to identify common design strategies is greatly encouraged. Proposals should pay special emphasis to the interlink with other projects to strengthen the interdisciplinary character of the programme. Here, we encourage possible principle investigators to discuss and connect complementary project ideas already in the submission phase to form topical clusters. The participation of junior research groups and early career researchers in the consortia is greatly encouraged.
For scientific enquiries, please contact the Priority Programme coordinator:
Professor Dr. Roland Marschall
Universität Bayreuth
Fakultät für Biologie, Chemie und Geowissenschaften
Universitätsstraße 30
95447 Bayreuth
phone +49 921 55-2761
roland.marschall@uni-bayreuth.de
For questions related to the DFG review process, please contact:
Dr. Kerstin Freitag, phone +49 228 885-3084, kerstin.freitag@dfg.de
For administrative questions regarding the DFG application, please contact:
Ralph Kirschbaum, phone +49 228 885-2326, ralph.kirschbaum@dfg.de
Further information:
https://www.dfg.de/en/research_funding/announcements_proposals/2021/info_wissenschaft_21_42