Molecular Design of Electrically Conductive Covalent Organic Frameworks as Efficient Electrodes for Lithium-Ion Batteries
This project aims to design and synthesize new conductive redox-active Covalent Organic Frameworks (COFs) to enhance the electrochemical performance of Lithium-Ion Batteries.
Projectdetails
Introduction
A major breakthrough in chemistry and materials science has been the development of Lithium-Ion Batteries (LIBs), which show great potential for storing energy from renewable sources and as the power sources for electric cars. However, commercially available LIBs are based on transition metal oxide cathodes, presenting limited energy density and raising relevant environmental concerns.
Alternative Materials
Organic materials have received much attention as alternative electrodes because of their high theoretical capacity, resource availability, and sustainability. In particular, Covalent Organic Frameworks (COFs) have emerged in the past few years as promising organic electrode materials due to their high stability, high ionic conductivity, and outstanding chemical and structural versatility.
Challenges
Low electrical conductivity remains the main bottleneck for real applications of COFs as electrode materials, usually addressed by adding in large amounts of conductive carbon additives that decrease the energy density of the battery.
Project Objectives
The overarching objective of this project is to design and synthesize new conductive redox-active COFs as cathode materials to enhance LIBs electrochemical performance. The specific goals are:
- To design a new family of stable redox-active COFs built from unexplored building blocks to achieve an optimal balance between capacity, electrical conductivity, and porosity.
- To investigate the role of the linkages, building blocks, doping, pressure, anisotropy, and morphology on the electrical conductivity, unravelling the fundamental mechanisms of charge transport in COFs.
- To manufacture and test lithium batteries using conductive COFs cathode materials, assessing the influence of the processing techniques on the electrochemical performance.
Financiële details & Tijdlijn
Financiële details
Subsidiebedrag | € 1.498.619 |
Totale projectbegroting | € 1.498.619 |
Tijdlijn
Startdatum | 1-7-2022 |
Einddatum | 30-6-2027 |
Subsidiejaar | 2022 |
Partners & Locaties
Projectpartners
- UNIVERSIDAD DE SANTIAGO DE COMPOSTELApenvoerder
- UNIVERSIDADE DE AVEIRO
Land(en)
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Energy storage with bulk liquid redox materials
The OMICON project aims to develop low molecular weight organic redox materials for efficient, environmentally friendly energy storage in redox flow batteries, enhancing energy density and sustainability.
Highly Redox-active Atomic Centers in Electrode Materials for Rechargeable Batteries
This project aims to develop innovative electrode materials for alkali-ion batteries by combining stable insertion structures with atomic redox centers to enhance energy and power densities.
Design and synthesis of bulk-active polymeric organic electrocatalysts for efficient electroorganic synthesis
PolyElectroCAT aims to develop earth-abundant, carbon-based electrode materials for efficient electroorganic synthesis, enhancing selectivity and reducing reliance on precious metals.
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This project aims to revolutionize Fe-air redox flow batteries by developing advanced porous electrode materials through interdisciplinary methods for enhanced energy storage performance and durability.
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NanOBatt aims to develop innovative redox-active conjugated nanohoops and macrocycles to enhance porosity and ion diffusion in organic electrode materials for next-generation batteries.
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FantastiCOF aims to revolutionize superconducting electronics by developing low-noise Josephson Junctions using novel crystalline moir materials, enhancing performance in various high-tech applications.
Next generation battery production
Dit project ontwikkelt een stabiele silicium-anode voor lithium-ion batterijen met verbeterde prestaties en duurzaamheid, door innovatieve sALD-technologie en industriële schaalproductie te combineren.
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