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- Dossow, Marcel, et al.
(författare)
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Electrification of gasification-based biomass-to-X processes - a critical review and in-depth assessment
- 2024
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Ingår i: Energy & Environmental Science. - : Royal Society of Chemistry. - 1754-5692 .- 1754-5706. ; 17:3, s. 925-973
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Forskningsöversikt (refereegranskat)abstract
- To address the impacts of climate change, it is imperative to significantly decrease anthropogenic greenhouse gas emissions. Biomass-based chemicals and fuels will play a crucial role in substituting fossil-based feedstocks and reducing emissions. Gasification-based biomass conversion processes with catalytic synthesis producing chemicals and fuels (Biomass-to-X, BtX) are an innovative and well-proven process route. Since biomass is a scarce resource, its efficient utilization by maximizing product yield is key. In this review, the electrification of BtX processes is presented and discussed as a technological option to enhance chemical and fuel production from biomass. Electrified processes show many advantages compared to BtX and electricity-based processes (Power-to-X, PtX). Electrification options are classified into direct and indirect processes. While indirect electrification comprises mostly the addition of H2 from water electrolysis (Power-and-Biomass-to-X, PBtX), direct electrification refers to power integration into specific processing steps by converting electricity into the required form of energy such as heat, electrochemical energy or plasma used (eBtX). After the in-depth review of state-of-the-art technologies, all technologies are discussed in terms of process performance, maturity, feasibility, plant location, land requirement, and dynamic operation. H2 addition in PBtX processes has been widely investigated in the literature with process simulations showing significantly increased carbon efficiency and product yield. Similar studies on direct electrification (eBtX) are limited in the literature due to low technological maturity. Further research is required on both, equipment level technology development, as well as process and system level, to compare process options and evaluate performance, economics, environmental impact and future legislation.
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- Schmidt, Johannes, et al.
(författare)
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A new perspective on global renewable energy systems : why trade in energy carriers matters
- 2019
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Ingår i: Energy & Environmental Science. - : Royal Society of Chemistry. - 1754-5692 .- 1754-5706. ; 12:7, s. 2022-2029
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Tidskriftsartikel (refereegranskat)abstract
- Recent global modelling studies suggest a decline of long-distance trade in energy carriers in future global renewable energy systems, compared to today's fossil fuel based system. In contrast, we identify four drivers that facilitate trade of renewable energy carriers. These drivers may lead to trade volumes remaining at current levels or even to an increase during the transition to an energy system with very high shares of renewables. First, new land-efficient technologies for renewable fuel production become increasingly available and technically allow for long-distance trade in renewables. Second, regional differences in social acceptance and land availability for energy infrastructure support the development of renewable fuel import and export streams. Third, the economics of renewable energy systems, i.e. the different production conditions globally and the high costs of fully renewable regional electricity systems, will create opportunities for spatial arbitrage. Fourth, a reduction of stranded investments in the fossil fuel sector is possible by switching from fossil fuels to renewable fuel trade. The impact of these drivers on trade in renewable energy carriers is currently under-investigated by the global energy systems research community. The importance of the topic, in particular as trade can redistribute profits and losses of decarbonization and may hence support finding new partners in climate change mitigation negotiations, warrants further research efforts in this area therefore.
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- Vomiero, Alberto, et al.
(författare)
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Flexible dye sensitized solar cells using TiO 2 nanotubes
- 2011
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Ingår i: Energy & Environmental Science. - : Royal Society of Chemistry (RSC). - 1754-5692 .- 1754-5706. ; 4:9, s. 3408-3413
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Tidskriftsartikel (refereegranskat)abstract
- The growth of TiO 2 nanotube arrays on plastic flexible substrates is researched. The approach uses anodization of a titanium thick film for obtaining nanotubes directly on poly(ethylene terephthalate) (PET) and Kapton HN substrate. The morphological features of the tubes can be finely tuned by varying the preparation conditions, and tube morphology affects the functional properties of the nanotube array. Crystallization of the anatase phase in nanotubes on Kapton HN substrate is obtained via post growth annealing. The nanotube arrays have been dye-sensitized using the commercial Ru-based N719 dye. The system was tested as photoanode in a flexible dye sensitized solar cell. Photoconversion efficiency of 3.5% was obtained. © 2011 The Royal Society of Chemistry.
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- Zhao, Haiguang, et al.
(författare)
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Gram-scale synthesis of carbon quantum dots with a large Stokes shift for the fabrication of eco-friendly and high-efficiency luminescent solar concentrators
- 2021
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Ingår i: Energy & Environmental Science. - : Royal Society of Chemistry. - 1754-5692 .- 1754-5706. ; 14:1, s. 396-406
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Tidskriftsartikel (refereegranskat)abstract
- Luminescent solar concentrators (LSCs) are large-area sunlight collectors coupled to small area solar cells, for efficient solar-to-electricity conversion. The three key points for the successful market penetration of LSCs are: (i) removal of light losses due to reabsorption during light collection; (ii) high light-to-electrical power conversion efficiency of the final device; (iii) long-term stability of the LSC structure related to the stability of both the matrix and the luminophores. Among various types of fluorophores, carbon quantum dots (C-dots) offer a wide absorption spectrum, high quantum yield, non-toxicity, environmental friendliness, low-cost, and eco-friendly synthetic methods. However, they are characterized by a relatively small Stokes shift, compared to inorganic quantum dots, which limits the highest external optical efficiency that can be obtained for a large-area single-layer LSC (>100 cm2) based on C-dots below 2%. Herein, we report highly efficient large-area LSCs (100–225 cm2) based on colloidal C-dots synthesized via a space-confined vacuum-heating approach. This one batch reaction could produce Gram-scale C-dots with a high quantum yield (QY) (∼65%) using eco-friendly citric acid and urea as precursors. Thanks to their very narrow size distribution, the C-dots produced via the space-confined vacuum-heating approach had a large Stokes shift of 0.53 eV, 50% larger than C-dots synthesized via a standard solvothermal reaction using the same precursors with a similar absorption range. The large-area LSC (15 × 15 × 0.5 cm3) prepared by using polyvinyl pyrrolidone (PVP) polymer as a matrix exhibited an external optical efficiency of 2.2% (under natural sun irradiation, 60 mW cm−2, uncharacterized spectrum). After coupling to silicon solar cells, the LSC exhibited a power conversion efficiency (PCE) of 1.13% under natural sunlight illumination (20 mW cm−2, uncharacterized spectrum). These unprecedented results were obtained by completely suppressing the reabsorption losses during light collection, as proved by optical spectroscopy. These findings demonstrate the possibility of obtaining eco-friendly, high-efficiency, large-area LSCs through scalable production techniques, paving the way to the lab-to-fab transition of this kind of devices.
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