| 1. |
- Bolívar Caballero, José Juan, et al.
(författare)
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Advanced application of a geometry-enhanced 3D-printed catalytic reformer for syngas production
- 2023
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Ingår i: Energy Conversion and Management. - : Elsevier BV. - 0196-8904 .- 1879-2227. ; 287
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Tidskriftsartikel (refereegranskat)abstract
- Catalyst research on reforming processes for syngas production has mainly focused on the active metals and support materials, while the effect of the catalyst's geometry on the reforming reactions has been poorly studied. The application of 3D-printed materials with enhanced geometries has recently started to be studied in heterogeneous catalysis and is of interest to be implemented for reforming biomass and plastic waste to produce H2-rich syngas. In this study, a geometry-enhanced 3D-printed Ni/Al2O3/FeCrAl-based monolithic catalyst with a periodic open cellular structure (POCS) was designed and fabricated. The catalyst was used for batch steam reforming biomass pyrolysis volatiles for syngas production at different parameters (temperature and steam-to-carbon ratio). The results showed complete reforming of pyrolysis volatiles in all experimental cases, a high H2 yield of ≈ 7.6 wt% of biomass was obtained at the optimized steam-to-carbon ratio of 8 and a reforming temperature of 800 °C, which is a higher yield compared to other batch reforming tests reported in the literature. Moreover, CFD simulation results in COMSOL Multiphysics demonstrated that the POCS configuration improves the reforming of pyrolysis volatiles for tar/bio-oil reforming and H2 production thanks to enhanced mass and heat transfer properties compared to the regular monolithic single-channel configuration.
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| 2. |
- Ganesan, Priya, et al.
(författare)
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Fluorine-Substituted Halide Solid Electrolytes with Enhanced Stability toward the Lithium Metal
- 2023
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Ingår i: ACS Applied Materials and Interfaces. - : American Chemical Society (ACS). - 1944-8244 .- 1944-8252. ; 15:32, s. 38391-38402
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Tidskriftsartikel (refereegranskat)abstract
- The high ionic conductivityand good oxidation stability of halide-basedsolid electrolytes evoke strong interest in this class of materials.Nonetheless, the superior oxidative stability compared to sulfidescomes at the expense of limited stability toward reduction and instabilityagainst metallic lithium anodes, which hinders their practical use.In this context, the gradual fluorination of Li2ZrCl6-x F x (0 & LE; x & LE; 1.2) is proposed to enhance thestability toward lithium-metal anodes. The mechanochemically synthesizedfluorine-substituted compounds show the expected distorted local structure(M2-M3 site disorder) and significant change in the overallLi-ion migration barrier. Theoretical calculations reveal an approximateminimum energy path for Li2ZrCl6-x F x (x = 0 and0.5) with an increase in the Li+ migration energy barrierfor Li2ZrCl5.5F0.5 in comparisonto Li2ZrCl6. However, it is found that the fluorine-substitutedcompound exhibits substantially lower polarization after 800 h oflithium stripping and plating owing to enhanced interfacial stabilityagainst the lithium metal, as revealed by density functional theoryand ex situ X-ray photoelectron spectroscopy, thanks to the formationof a fluorine-rich passivating interphase.
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| 3. |
- Jamal, Ali, et al.
(författare)
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Tris(trimethylsilyl) Phosphite and Lithium Difluoro(oxalato)borate as Electrolyte Additives for LiNi0.5Mn1.5O4-Graphite Lithium-Ion Batteries
- 2023
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Ingår i: ChemElectroChem. - : Wiley-VCH Verlagsgesellschaft. - 2196-0216. ; 10:16
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Tidskriftsartikel (refereegranskat)abstract
- Raising the energy density of lithium-ion batteries (LIBs) through the operation of high-voltage cathodes presents a challenge in terms of practical use due to electrolyte degradation. Consequently, it is imperative to explore new materials to circumvent this issue. In this study, a combination of tris(trimethylsilyl) phosphite (TMSPi) and lithium difluoro(oxalato)borate (LiDFOB) is presented as film-forming additives in a conventional LiPF6-containing carbonate-based electrolyte solution in high-voltage LiNi0.5Mn1.5O4-graphite full cells. At high voltage, TMSPi oxidizes on the LiNi0.5Mn1.5O4 (LNMO) cathode surface prior to the decomposition of electrolyte solvents, promoting the formation of a stable cathode electrolyte interphase (CEI) layer. In tandem, given that LiDFOB has a lower reduction potential than ethylene carbonate (EC), it has the possibility of forming a solid electrolyte interphase (SEI) on the graphite anode surface. Combining the two additives was found to suppress the degradation of the electrolyte to a large extent. Among the investigated concentration of the additives, the combination of 1 wt. % TMSPi and 2 wt. % LiDFOB added to LP40 electrolyte exhibits improved capacity retention of 80 % after 400 cycles at 0.3 C, compared to the electrolyte with no additive with 67 % capacity retention over the same period. Thereby, the combination of TMSPi with LiDFOB provides an improvement for high voltage LIBs.
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| 4. |
- Jin, Yanghao, et al.
(författare)
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Carbon and H-2 recoveries from plastic waste by using a metal-free porous biocarbon catalyst
- 2023
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Ingår i: Journal of Cleaner Production. - : Elsevier BV. - 0959-6526 .- 1879-1786. ; 404
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Tidskriftsartikel (refereegranskat)abstract
- Carbon and H2 recoveries from plastic waste enable high value-added utilizations of plastic waste while mini-mizing its GHG emissions. The objective of this study is to explore the use of a metal-free biocarbon catalyst for waste plastic pyrolysis and in-line catalytic cracking to produce H2-rich gases and carbon. The results show that the biocarbon catalyst exhibits a good catalytic effect and stability for various plastic wastes. Increasing the C/P ratio from 0 to 2, induce an increase in the conversion rate of C and H in plastics to carbon and H2 from 57.1% to 68.7%, and from 22.7% to 53.5%, respectively. Furthermore, a carbon yield as high as 580.6 mg/gplastic and an H2 yield as high as 68.6 mg/gplastic can be obtained. The hierarchical porous structure with tortuous channels of biocarbon extends the residence time of pyrolysis volatiles in the high-temperature catalytic region and thereby significantly promotes cracking reactions.
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| 5. |
- Jin, Yanghao, et al.
(författare)
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From Waste Biomass to Hard Carbon Anodes : Predicting the Relationship between Biomass Processing Parameters and Performance of Hard Carbons in Sodium-Ion Batteries
- 2023
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Ingår i: Processes. - : MDPI AG. - 2227-9717. ; 11:3
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Forskningsöversikt (refereegranskat)abstract
- Sodium-ion batteries (SIBs) serve as the most promising next-generation commercial batteries besides lithium-ion batteries (LIBs). Hard carbon (HC) from renewable biomass resources is the most commonly used anode material in SIBs. In this contribution, we present a review of the latest progress in the conversion of waste biomass to HC materials, and highlight their application in SIBs. Specifically, the following topics are discussed in the review: (1) the mechanism of sodium-ion storage in HC, (2) the HC precursor's sources, (3) the processing methods and conditions of the HCs production, (4) the impact of the biomass types and carbonization temperature on the carbon structure, and (5) the effect of various carbon structures on electrochemical performance. Data from various publications have been analyzed to uncover the relationship between the processing conditions of biomass and the resulting structure of the final HC product, as well as its electrochemical performance. Our results indicate the existence of an ideal temperature range (around 1200 to 1400 degrees C) that enhances the formation of graphitic domains in the final HC anode and reduces the formation of open pores from the biomass precursor. This results in HC anodes with high storage capacity (>300 mAh/g) and high initial coulombic efficiency (ICE) (>80%).
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| 6. |
- Salian, Girish D., et al.
(författare)
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Understanding the electrochemical and interfacial behaviour of sulfolane-based electrolytes in LiNi0.5Mn1.5O4-graphite full-cells
- 2023
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Ingår i: Batteries & Supercaps. - : John Wiley & Sons. - 2566-6223. ; n/a:n/a
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Tidskriftsartikel (refereegranskat)abstract
- An ethylene carbonate-free electrolyte composed of 1 M lithium bis(fluorosulfonyl) imide (LiFSI) in sulfolane (SL) is studied here for LiNi0.5Mn1.5O4-graphite full-cells. An important focus on the evaluation of the anodic stability of the SL electrolyte and the passivation layers formed on LNMO and graphite is being analysed along with intermittent current interruption (ICI) technique to observe the resistance while cycling. The results show that the sulfolane electrolyte shows more degradation at higher potentials unlike previous reports which suggested higher oxidative stability. However, the passivation layers formed due to this electrolyte degradation prevents further degradation. The resistance measurements show that major resistance arises from the cathode. The pressure evolution during the formation cycles suggests that there is lower gas evolution with sulfolane electrolyte than in the conventional electrolyte. The study opens a new outlook on the sulfolane based electrolyte especially regarding its oxidative/anodic stability.
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| 7. |
- Yang, Hanmin, 1992-, et al.
(författare)
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Carbon-negative valorization of biomass waste into affordable green hydrogen and battery anodes
- 2023
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Ingår i: International journal of hydrogen energy. - : Elsevier BV. - 0360-3199 .- 1879-3487.
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Tidskriftsartikel (övrigt vetenskapligt/konstnärligt)abstract
- The global Sustainable Development Goals highlight the necessity for affordable and clean energy, designated as SDG7. A sustainable and feasible biorefinery concept is proposed for the carbon-negative utilization of biomass waste for affordable H2 and battery anode material production. Specifically, an innovative tandem biocarbon + NiAlO + biocarbon catalyst strategy is constructed to realize a complete reforming of biomass pyro-vapors into H2+CO (as a mixture). The solid residues from pyrolysis are upgraded into high-quality hard carbon (HCs), demonstrating potential as sodium ion battery (SIBs) anodes. The product, HC-1600-6h, exhibited great electrochemical performance when employed as (SIBs) anodes (full cell: 263 Wh/kg with ICE of 89%). Ultimately, a comprehensive process is designed, simulated, and evaluated. The process yields 75 kg H2, 169 kg HCs, and 891 kg captured CO2 per ton of biomass achieving approx. 100% carbon and hydrogen utilization efficiencies. A life cycle assessment estimates a biomass valorization process with negative-emissions (−0.81 kg CO2/kg-biomass, reliant on Sweden wind electricity). A techno-economic assessment forecasts a notably profitable process capable of co-producing affordable H2 and hard carbon battery anodes. The payback period of the process is projected to fall within two years, assuming reference prices of 13.7 €/kg for HCs and 5 €/kg for H2. The process contributes to a novel business paradigm for sustainable and commercially viable biorefinery process, achieving carbon-negative valorization of biomass waste into affordable energy and materials.
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