| 1. |
- Carrod, Andrew J., 1994, et al.
(författare)
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Recent advances in triplet-triplet annihilation upconversion and singlet fission, towards solar energy applications
- 2022
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Ingår i: Energy & Environmental Science. - : Royal Society of Chemistry (RSC). - 1754-5692 .- 1754-5706. ; 15, s. 4982-5016
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Forskningsöversikt (refereegranskat)abstract
- Solar energy is an ample renewable energy resource, with photovoltaic (PV) technology enabling a direct route from light to electricity. Currently, PVs are limited in photon conversion efficiency, due in major part to spectral losses. Mitigation of these losses is therefore important, economically and environmentally. Two processes that aim to increase solar light utilisation are described herein. The first is triplet-triplet annihilation upconversion (TTA-UC), through which two incoherent photons of low energy can produce one of higher energy, reducing below bandgap losses. Secondly, singlet fission (SF), through which two triplet states may be obtained from one initial singlet excited state, in theory allowing two electrons per photon in a PV, reducing thermalisation losses. These fields are often covered seperately, despite being the reverse processes of one another. This work aims to consolidate research in the two fields and highlight their similarities and common challenges, specifically those relevant to PV applications. Herein, we cover systems primarily based on organic small molecules (anthracene, rubrene, tetracene, pentacene), and detail the fabrication of functional materials containing them (MOFs, gels, SAMs on TiO2, thin evaporated and solution cast films, and cavities). We further offer our recommendations for the focus of future work in both the TTA and SF fields, and discuss the need to address current limitations such as poor triplet diffusion, limited charge injection to PVs, and material stability. Specifically, one could do this by cherry picking ideas from other research fields, for example photosensitisers for photodynamic therapy could be used as TTA sensitisers, and molecules having a considerable excited state aromaticity could be considered as SF materials. We hope this review may aid development towards the end goal of an efficient PV, incorporating either, or both, SF and TTA-UC materials.
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| 3. |
- Moth-Poulsen, Kasper, 1978, et al.
(författare)
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Molecular solar thermal (MOST) energy storage and release system
- 2012
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Ingår i: Energy and Environmental Sciences. - : Royal Society of Chemistry (RSC). - 1754-5692 .- 1754-5706. ; 5:9, s. 8534-8537
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Tidskriftsartikel (refereegranskat)abstract
- A device for solar energy storage and release based on a reversible chemical reaction is demonstrated. A highly soluble derivative of a (fulvalene) diruthenium (FvRu(2)) system is synthesized, capable of storing solar energy (110 J g(-1)) in the form of chemical bonds and then releasing it "on demand", when excited thermally or catalytically. A microfluidic device is designed and constructed for both the photo-harvesting and the heat-utilization steps, allowing for the recycling of material.
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| 4. |
- Wang, Zhihang, 1989, et al.
(författare)
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Macroscopic heat release in a molecular solar thermal energy storage system
- 2019
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Ingår i: Energy and Environmental Sciences. - : Royal Society of Chemistry (RSC). - 1754-5692 .- 1754-5706. ; 12:1, s. 187-193
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Tidskriftsartikel (refereegranskat)abstract
- The development of solar energy can potentially meet the growing requirements for a global energy system beyond fossil fuels, but necessitates new scalable technologies for solar energy storage. One approach is the development of energy storage systems based on molecular photoswitches, so-called molecular solar thermal energy storage (MOST). Here we present a novel norbornadiene derivative for this purpose, with a good solar spectral match, high robustness and an energy density of 0.4 MJ kg-1. By the use of heterogeneous catalyst cobalt phthalocyanine on a carbon support, we demonstrate a record high macroscopic heat release in a flow system using a fixed bed catalytic reactor, leading to a temperature increase of up to 63.4 °C (83.2 °C measured temperature). Successful outdoor testing shows proof of concept and illustrates that future implementation is feasible. The mechanism of the catalytic back reaction is modelled using density functional theory (DFT) calculations rationalizing the experimental observations.
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