| 1. |
- Cai, Tianqi, et al.
(författare)
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Low bandgap polymers synthesized by FeCl(3) oxidative polymerization
- 2010
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Ingår i: Solar Energy Materials and Solar Cells. - : Elsevier BV. - 0927-0248. ; 94:7, s. 1275-1281
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Tidskriftsartikel (refereegranskat)abstract
- Four low bandgap polymers, combining an alkyl thiophene donor with benzo[c][1,2,5]thiadiazole, 2,3-diphenylquinoxaline, 2,3-diphenylthieno[3,4-b]pyrazine and 6,7-diphenyl-[1,2,5]thiadiazolo[3,4-g] quinoxaline acceptors in a donor-acceptor-donor architecture, were synthesized via FeCl3 oxidative polymerization. The molecular weights of the polymers were improved by introducing o-dichlor-obenzene (ODCB) as the reaction solvent instead of the commonly used solvent, chloroform. The photophysical, electrochemical and photovoltaic properties of the resulting polymers were investigated and compared. The optical bandgaps of the polymers vary between 1.0 and 1.9 eV, which is promising for solar cells. The devices spin-coated from an ODCB solution of P1DB:[70]PCBM showed a power conversion efficiency of 1.08% with an open-circuit voltage of 0.91 V and a short-circuit current density of 3.36 mA cm(-2) under irradiation from an AM1.5G solar simulator (100 mW cm(-2)). (C) 2010 Elsevier B.V. All rights reserved.
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| 2. |
- Hellström, Stefan, 1978, et al.
(författare)
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Influence of side chains on electrochromic properties of green donor-acceptor-donor polymers
- 2011
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Ingår i: Electrochimica Acta. - : Elsevier BV. - 0013-4686. ; 56:10, s. 3454-3459
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Tidskriftsartikel (refereegranskat)abstract
- Three solution processable cathodically coloring green electrochromic polymers, based on 2,3-diphenyl-5,7-di(thiophen-2-yl)thieno[3,4-b]pyrazine, have been synthesized by oxidative FeCl3 polymerization. The polymers were designed with solubilizing alkyl and oligoethylene oxide side chains to achieve solubility and processability. All three polymers have a small electrochemical bandgap (1.8-1.9 eV) and low oxidation potentials. Spectroelectrochemical studies of polymer films on ITO reveal that the alkyl side chains in head-to-head position on the polymer backbone promote a defined high-energy absorption peak and suppress tailing of charge-carrier absorption into the visible region. Kinetic studies, based on transmission measurements applying a square-wave potential between reduced and oxidized states, show that the polymer with exclusively oligoethylene oxide side chains (P3) had the fastest response times, monitored at the low-energy absorption maxima. The best performing polymer (P1) showed a good optical contrast in the visible region with a Delta T of 26% at 700 nm. An initial test of the electrochemical stability showed that the oligoethylene oxide containing polymers had superior stability over 500 full switches.
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| 3. |
- Lyu, Xiaozan, et al.
(författare)
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A bibliometric evaluation and visualization of global solar power generation research : productivity, contributors and hot topics
- 2024
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Ingår i: Environmental Science and Pollution Research. - : Springer Nature. - 0944-1344 .- 1614-7499. ; 31:5, s. 8274-8290
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Tidskriftsartikel (refereegranskat)abstract
- The demand for sustainable energy is increasingly urgent to mitigate global warming which has been exacerbated by the extensive use of fossil fuels. Solar energy has attracted global attention as a crucial renewable resource. This study conducted a bibliometric analysis based on publication metrics from the Web of Science database to gain insights into global solar power research. The results indicate a stable global increase in publications on solar power generation and a rise in citations, reflecting growing academic interest. Leading contributors include China, the USA, South Korea, Japan, and India, with the Chinese Academy of Sciences emerging as the most prolific institution. Multidisciplinary Materials Science, Applied Physics, Energy and Fuels, Physical Chemistry, and Nanoscience and Nanotechnology were the most used and promising subject categories. Current hot topics include the systematic analysis of photovoltaic systems, perovskite as a solar cell material, and focusing on stability and flexibility issues arising during photovoltaic-grid integration. This study facilitates a comprehensive understanding of the status and trends in solar power research for researchers, stakeholders, and policy-makers.
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| 4. |
- Wang, Linqin, et al.
(författare)
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A crosslinked polymer as dopant-free hole-transport material for efficient n-i-p type perovskite solar cells
- 2021
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Ingår i: Journal of Energy Chemistry. - : Elsevier BV. - 2095-4956 .- 2096-885X. ; 55, s. 211-218
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Tidskriftsartikel (refereegranskat)abstract
- A new crosslinked polymer, called P65, with appropriate photo-electrochemical, opto-electronic, and thermal properties, has been designed and synthesized as an efficient, dopant-free, hole-transport material (HTM) for n-i-p type planar perovskite solar cells (PSCs). P65 is obtained from a low-cost and easily synthesized spiro[fluorene-9,9′-xanthene]-3′,6′-diol (SFX-OH)-based monomer X65 through a free-radical polymerization reaction. The combination of a three-dimensional (3D) SFX core unit, hole-transport methoxydiphenylamine group, and crosslinked polyvinyl network provides P65 with good solubility and excellent film-forming properties. By employing P65 as a dopant-free hole-transport layer in conventional n-i-p type PSCs, a power conversion efficiency (PCE) of up to 17.7% is achieved. To the best of our knowledge, this is the first time a 3D, crosslinked, polymeric dopant-free HTM has been reported for use in conventional n-i-p type PSCs. This study provides a new strategy for the future development of a 3D crosslinked polymeric dopant-free HTM with a simple synthetic route and low-cost for commercial, large-scale applications in future PSCs.
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| 5. |
- Yang, Hao, et al.
(författare)
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Monolithic FAPbBr3 Photoanode for Photoelectrochemical Water Oxidation with Ultralow-Onset-Potential
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Annan publikation (övrigt vetenskapligt/konstnärligt)abstract
- Despite considerable research efforts on photoelectrochemical (PEC) water splitting over the past few decades, its practical application is still impeded by the lack of efficient, stable, and scalable photoelectrodes. Herein, we demonstrate the facile fabrication of a metal-halide perovskite-based photoanode for PEC water oxidation. A hole transport material-free and precious metal-free FAPbBr3 photovoltaic (PV) device is fabricated for the first time to examine the charge separation performance of the FAPbBr3 absorber. With a planar structure using mesoporous carbon as a hole-conducting layer, the device achieved a solar-to-electrical power conversion efficiency of 9.2% and a Voc of 1.4 V. The solar cell architecture is successfully applied to build a monolithic photoanode with the FAPbBr3 absorber, carbon/graphite conductive protection layer, and NiFe catalyst layers for direct photo-driven water oxidation. With suitable energy band alignment and minimal contact loss, the photoanode delivers an ultralow onset potential below 0 V versus a reversible hydrogen electrode and a high applied bias photon-to-current efficiency of 8.5%. Stable operation exceeding 100 h under constant solar illumination is successfully reached by the application of UV filter protection. A detailed photothermal investigation confirms that the photothermal effect can improve the overall performance of the perovskite photoanode. The results in this report are of great significance in guiding the further development of PV material-based photoelectrodes for solar fuel applications.
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| 6. |
- Yang, Hao, et al.
(författare)
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Monolithic FAPbBr3 photoanode for photoelectrochemical water oxidation with low onset-potential and enhanced stability
- 2023
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Ingår i: Nature Communications. - : Springer Nature. - 2041-1723. ; 14:1
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Tidskriftsartikel (refereegranskat)abstract
- Despite considerable research efforts on photoelectrochemical water splitting over the past decades, practical application faces challenges by the absence of efficient, stable, and scalable photoelectrodes. Herein, we report a metal-halide perovskite-based photoanode for photoelectrochemical water oxidation. With a planar structure using mesoporous carbon as a hole-conducting layer, the precious metal-free FAPbBr3 photovoltaic device achieves 9.2% solar-to-electrical power conversion efficiency and 1.4 V open-circuit voltage. The photovoltaic architecture successfully applies to build a monolithic photoanode with the FAPbBr3 absorber, carbon/graphite conductive protection layers, and NiFe catalyst layers for water oxidation. The photoanode delivers ultralow onset potential below 0 V versus the reversible hydrogen electrode and high applied bias photon-to-current efficiency of 8.5%. Stable operation exceeding 100 h under solar illumination by applying ultraviolet-filter protection. The photothermal investigation verifies the performance boost in perovskite photoanode by photothermal effect. This study is significant in guiding the development of photovoltaic material-based photoelectrodes for solar fuel applications.
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