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Sökning: LAR1:ltu > Ji Xiaoyan

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1.
  • Ali, Asad, et al. (författare)
  • Emerging strategies and developments in oxygen reduction reaction using high-performance platinum-based electrocatalysts
  • 2023
  • Ingår i: Nano Reseach. - : Tsinghua University Press. - 1998-0124 .- 1998-0000.
  • Forskningsöversikt (refereegranskat)abstract
    • The global practical implementation of proton exchange membrane fuel cells (PEMFCs) heavily relies on the advancement of highly effective platinum (Pt)-based electrocatalysts for the oxygen reduction reaction (ORR). To achieve high ORR performance, electrocatalysts with highly accessible reactive surfaces are needed to promote the uncovering of active positions for easy mass transportation. In this critical review, we introduce different approaches for the emerging development of effective ORR electrocatalysts, which offer high activity and durability. The strategies, including morphological engineering, geometric configuration modification via supporting materials, alloys regulation, core-shell, and confinement engineering of single atom electrocatalysts (SAEs), are discussed in line with the goals and requirements of ORR performance enhancement. We review the ongoing development of Pt electrocatalysts based on the syntheses, nanoarchitecture, electrochemical performances, and stability. We eventually explore the obstacles and research directions on further developing more effective electrocatalysts. 
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2.
  • Ali, Asad, et al. (författare)
  • Gram-scale production of in-situ generated iron carbide nanoparticles encapsulated via nitrogen and phosphorous co-doped bamboo-like carbon nanotubes for oxygen evolution reaction
  • 2023
  • Ingår i: Materials Science for Energy Technologies. - : Elsevier. - 2589-2991. ; 6, s. 301-309
  • Tidskriftsartikel (refereegranskat)abstract
    • Optimizing electrocatalytic activity and recognizing the most reactive sites for oxygen evolution reaction (OER) electrocatalysts are valuable to the order of renewable power. In this research article, we explored an innovative in-situ annealing technique for constructing iron carbide nanoparticles (Fe3C NPs) encapsulated via nitrogen and phosphorous doped bamboo-shape carbon nanotubes (NP-CNTs) for OER. Interestingly, the constructed Fe3C NPs@NP-CNT-800 composite exhibited remarkable electrochemical operation and offered a stable current density of 10 mA/cm2 at a lower overpotential (280 mV) in an alkaline solution. Furthermore, an innovative Fe3C NPs@N,P-CNT-800 hybrid surpassed the standard RuO2 electrocatalyst in terms of OER performance and showed negligible degradation in chronoamperometric (21 h) and chronopotentiometry (3000 cycles) analyses. The remarkable performance and stability are ascribed to the Fe3C NPs, novel tubular bamboo-like morphology of its carbon materials, and heteroatom doping, which contribute to the electrochemical interfaces, large surface area, active catalytic sites, and rapid charge transfer kinetics.
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3.
  • An, Rong, et al. (författare)
  • Atomic force microscopy probing interactions and microstructures of ionic liquids at solid surfaces
  • 2022
  • Ingår i: Nanoscale. - : Royal Society of Chemistry. - 2040-3364 .- 2040-3372. ; :14, s. 11098-11128
  • Forskningsöversikt (refereegranskat)abstract
    • Ionic liquids (ILs) are room temperature molten salts that possess preeminent physicochemical properties and have shown great potential in many applications. However, the use of ILs in surface-dependent processes, e.g. energy storage, is hindered by the lack of a systematic understanding of the IL interfacial microstructure. ILs on the solid surface display rich ordering, arising from coulombic, van der Waals, solvophobic interactions, etc., all giving near-surface ILs distinct microstructures. Therefore, it is highly important to clarify the interactions of ILs with solid surfaces at the nanoscale to understand the microstructure and mechanism, providing quantitative structure–property relationships. Atomic force microscopy (AFM) opens a surface-sensitive way to probe the interaction force of ILs with solid surfaces in the layers from sub-nanometers to micrometers. Herein, this review showcases the recent progress of AFM in probing interactions and microstructures of ILs at solid interfaces, and the influence of IL characteristics, surface properties and external stimuli is thereafter discussed. Finally, a summary and perspectives are established, in which, the necessities of the quantification of IL–solid interactions at the molecular level, the development of in situ techniques closely coupled with AFM for probing IL–solid interfaces, and the combination of experiments and simulations are argued.
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6.
  • Bao, Ningzhong, et al. (författare)
  • Thermodynamic modeling and experimental verification for ion-exchange synthesis of K2O·6TiO2 and TiO2 fibers from K2O·4TiO2
  • 2002
  • Ingår i: Fluid Phase Equilibria. - 0378-3812 .- 1879-0224. ; 193, s. 229-243
  • Tidskriftsartikel (refereegranskat)abstract
    • A thermodynamic model was established to determine ion-exchange conditions for the synthesis of potassium hexatitanate (K2O·6TiO2) and titanium dioxide (TiO2) from potassium tetratitanate (K2O·4TiO2) fiber. In the proposed model equilibrium species in the solid phase and corresponding ion-exchange equilibrium constants at 298.15 K were determined from the experimental data of Sasaki et al. [Inorg. Chem. 24 (1985) 2265]. In order to verify the proposed model, prediction results were compared with experimental data determined in literature and those measured in this work. The comparison shows a good agreement. Based on this, the proposed model was also used to predict more extensive suitable conditions for the synthesis of K2O·6TiO2 and TiO2.
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7.
  • Bülow, M., et al. (författare)
  • Incorporating a concentration-dependent dielectric constant into ePC-SAFT. An application to binary mixtures containing ionic liquids
  • 2019
  • Ingår i: Fluid Phase Equilibria. - : Elsevier. - 0378-3812 .- 1879-0224. ; 492, s. 26-33
  • Tidskriftsartikel (refereegranskat)abstract
    • Primitive thermodynamic models for electrolyte solutions require the dielectric constant ε. This property strongly depends on the concentration of the electrolytes in the mixture. Neglecting this dependency might be reasonable for modeling solutions at low electrolyte concentrations. However, in solutions containing ionic liquids (ILs) and especially for the calculation of liquid-liquid equilibria (LLE) of systems with ILs, liquid phases often contain high IL concentrations. At such conditions, neglecting the influence of concentration on ε is an oversimplification. In this work, an approach to account for the concentration-dependent dielectric constant within the Debye-Hückel theory was implemented into electrolyte Perturbed-Chain Statistical Associating Fluid Theory (original ePC-SAFT). This new approach was then applied to model LLE of binary mixtures containing water and commonly used hydrophobic ILs. These common ILs are comprised of the IL-cations [C n mim] + , [C n py] + , [C n mpy] + , [C n mpyr] + , [C 4 m 4 py] + and the IL-anions [BF 4 ] - , [NTf 2 ] - , [PF 6 ] - , [TFO] - . The LLE of binary mixtures water + IL were modeled at ambient pressure and different temperatures with the new ePC-SAFT and with the original ePC-SAFT [Ji et al. DOI: 10.1016/j.fluid.2012.05.029] without the concentration-dependent ε. Overall, the new approach within ePC-SAFT shows superior modeling as well as correlation capability compared to original ePC-SAFT, which was concluded by comparing both models with LLE data from literature. 
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8.
  • Cao, Jian, et al. (författare)
  • Heterogeneous consecutive reaction kinetics of direct oxidation of H2 to H2O2: Effect and regulation of confined mass transfer
  • 2023
  • Ingår i: Chemical Engineering Journal. - : Elsevier. - 1385-8947 .- 1873-3212. ; 455
  • Tidskriftsartikel (refereegranskat)abstract
    • Porous catalysts in heterogeneous reactions have played an important role in the modern chemical industry, but it is still challenging to quantitatively describe mass transfer and surface reaction behaviors of reactants in nano-confined space. Direct synthesis of hydrogen peroxide (H2O2) is considered as an attractive alternative to anthraquinone oxidation process, while the confined mass transfer of H2O2 in porous catalysts limits the reactivity. In this work, taking the consecutive reaction of H2O2 synthesis as an example, a quantitative method in modeling the effects of confined mass transfer on the reactivity was studied. More specifically, calorimetry was developed to characterize the confined structures of porous carbon experimentally, the linear nonequilibrium thermodynamics and the statistical mechanics method were further combined. Then, the heterogeneous consecutive reaction kinetics and the Thiele modulus influenced by confined mass transfer were modeled. Consequently, regulation strategies were proposed with the help of theoretical models. The optimized catalyst with biological skeleton carbon support and 0.5 wt% palladium loading shows an excellent catalytic performance. Lastly, for the mesoscience in heterogeneous reaction, the resistance was explored as a quantitative descriptor to compromise in the competition between mass transfer and surface reaction. The mesoscale structures were considered as the dynamic spatiotemporal distribution of substance concentrations, and the resistance minimization multi-scale (RMMS) model was proposed.
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9.
  • Carvalho, Lara, et al. (författare)
  • Alkali enhanced biomass gasification with in situ S capture and a novel syngas cleaning : Part 2: Techno-economic analysis
  • 2018
  • Ingår i: Energy. - : Elsevier. - 0360-5442 .- 1873-6785. ; 165:Part B, s. 471-482
  • Tidskriftsartikel (refereegranskat)abstract
    • Previous research has shown that alkali addition has operational advantages in entrained flow biomass gasification and allows for capture of up to 90% of the biomass sulfur in the slag phase. The resultant low-sulfur content syngas can create new possibilities for syngas cleaning processes. The aim was to assess the techno-economic performance of biofuel production via gasification of alkali impregnated biomass using a novel gas cleaning systemcomprised of (i) entrained flow catalytic gasification with in situ sulfur removal, (ii) further sulfur removal using a zinc bed, (iii) tar removal using a carbon filter, and (iv) CO2 reductionwith zeolite membranes, in comparison to the expensive acid gas removal system (Rectisol technology). The results show that alkali impregnation increases methanol productionallowing for selling prices similar to biofuel production from non-impregnated biomass. It was concluded that the methanol production using the novel cleaning system is comparable to the Rectisol technology in terms of energy efficiency, while showing an economic advantagederived from a methanol selling price reduction of 2–6 €/MWh. The results showed a high level of robustness to changes related to prices and operation. Methanol selling prices could be further reduced by choosing low sulfur content feedstocks.
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10.
  • Chen, Jingjing, et al. (författare)
  • A high efficient heat exchanger with twisted geometries for biogas process with manure slurry
  • 2020
  • Ingår i: Applied Energy. - : Elsevier. - 0306-2619 .- 1872-9118. ; 279
  • Tidskriftsartikel (refereegranskat)abstract
    • Heat-transfer enhancement in manure slurry is crucial for increasing the efficiency and production of biogas during anaerobic digestion in biogas plants. In this study, a novel heat exchanger with an optimal twisted geometry was developed based on the numerical screening of the twisted tubes with equilateral polygons, and experiments were conducted to validate the numerical results. It was observed that the SST k-ω model is more efficient than other turbulence models in representing the heat transfer performance of the twisted tubes, and the numerical model with a thermostatic wall can be used to reliably screen the twisted geometries. The twisted hexagonal tube has the optimal geometry, with enhancement capability of up to 1.4 times compared to that of the circular tube. The formation of high continuity regions with relatively strong heat-transfer rates along the heat-exchange wall is the main reason for the high performance during heat transfer. The external heating process was integrated in a full-scale biogas plant, and the model and algorithm were developed and validated with additional experiments to describe the overall performance of both conventional and screened optimal geometries under different conditions. It was observed that a profit equivalent to 39% of total production for a large-scale biogas plant can be achieved owing to energy conservation in external heating with the twisted hexagonal tubes.
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