Lole Jurado

ORCID: 0000-0003-1908-899X
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About
Contact & Profiles
Research Areas
  • Catalytic Processes in Materials Science
  • Ionic liquids properties and applications
  • Nanomaterials for catalytic reactions
  • Force Microscopy Techniques and Applications
  • Lubricants and Their Additives
  • Catalysts for Methane Reforming
  • Catalysis and Hydrodesulfurization Studies
  • Thermochemical Biomass Conversion Processes
  • Electrocatalysts for Energy Conversion
  • Electrochemical Analysis and Applications
  • Organometallic Complex Synthesis and Catalysis
  • Carbon dioxide utilization in catalysis
  • Advanced battery technologies research
  • Polyoxometalates: Synthesis and Applications
  • Advancements in Battery Materials
  • Metal-Organic Frameworks: Synthesis and Applications
  • Advanced Battery Materials and Technologies
  • Electrochemical sensors and biosensors
  • Advanced Photocatalysis Techniques
  • Advanced Materials Characterization Techniques
  • Catalysis and Oxidation Reactions
  • Nanocluster Synthesis and Applications
  • Supercapacitor Materials and Fabrication
  • Ammonia Synthesis and Nitrogen Reduction

Institut Català d'Investigació Química
2024

Instituto de Ciencia de Materiales de Sevilla
2020-2024

Universidad de Sevilla
2020-2024

Institut National Polytechnique de Toulouse
2023

Université Toulouse III - Paul Sabatier
2023

Université de Toulouse
2023

Laboratoire de Chimie de Coordination
2023

Université de Strasbourg
2020-2023

Institut de Chimie et Procédés pour l'Energie, l'Environnement et la Santé
2020-2023

Centre National de la Recherche Scientifique
2020-2023

Graphene is a promising next-generation conducting material with the potential to replace traditional electrode materials in supercapacitors. Since energy storage supercapacitors relies on electrolyte-electrode interface, here we elucidate interfacial subnanometer structure of single component liquid composed solely cations and anions - an ionic liquid- electrified graphene. We study effect applied interaction between graphene silicon tip describe it within framework...

10.1038/s41598-017-04576-x article EN cc-by Scientific Reports 2017-06-19

A barrier to understanding the factors driving catalysis in oxygen evolution reaction (OER) is multiple overlapping redox transitions OER catalysts. The complexity of these obscure relationship between coverage adsorbates and kinetics, leading an experimental challenge measuring activity descriptors, such as binding energies, well adsorbate interactions, which may destabilize intermediates modulate their energies. Herein, we utilize a newly designed optical spectroelectrochemistry system...

10.1021/jacs.3c11651 article EN cc-by Journal of the American Chemical Society 2024-03-22

Repeatedly applied nanoconfinement of [HMIM] EtSO<sub>4</sub> between mica surfaces induces a long-range liquid-to-solid transition that remains after confinement has been removed.

10.1039/c4cp05592f article EN Physical Chemistry Chemical Physics 2015-01-01

Rhodium single-atoms on carbon nitride are robust and efficient catalysts for the hydroformylation of styrene. Experimental analyses DFT calculations confirm isolated nature Rh atoms their robustness as catalysts.

10.1039/d2cy02094g article EN cc-by-nc Catalysis Science & Technology 2023-01-01

Structural forces reveal the ordered structure of one ionic liquid at rough interfaces well-defined nanoscale roughness, also under nanoconfinement.

10.1039/c5nr07805a article EN Nanoscale 2016-01-01

With reference to our previous surface-force study on 1-hexyl-3-methylimidazolium ethylsulfate ([HMIM] EtSO4) using an extended surface forces apparatus, which showed ordered structure within the nanoconfined dry ionic liquid (IL) between mica surfaces that up ∼60 nm from surface, this work focuses influence of environmental humidity bulk, interfacial and [HMIM] EtSO4. Infrared spectroscopy rheometry reflect changes in chemical physical properties bulk IL due uptake water when exposed...

10.1039/c6cp03777a article EN Physical Chemistry Chemical Physics 2016-01-01

Abstract The development of highly efficient and selective catalysts for carbonylation reactions represents a significant challenge in catalysis. Single‐atom (SACs) have postulated as promising candidates able to combine the strengths both homogeneous heterogeneous catalysts. In this paper, we review recent advances tailoring solid supports SACs enhance their catalytic performance reactions. We first discuss effect on hydroformylation reaction catalysed by SACs, followed methanol, ethanol,...

10.1002/cctc.202400543 article EN cc-by-nc-nd ChemCatChem 2024-05-22

A conventional Pt/CeO2/Al2O3 catalyst physically mixed with an ionic conductor (Mo- or Eu-doped ZrO2) was tested at high space velocity (20,000 h−1 and 80 L gcat−1) under model conditions (only CO H2O) industrial conditions, a realistic feed. The promoted system the showed better catalytic activity associated water dissociation mobility, considered as rate-determining step. activation assessed by operando diffuse reflectance infrared fourier transformed spectroscopy (DRIFTS) studies reaction...

10.3390/catal10080841 article EN Catalysts 2020-07-25

Catalytic structuration on SiC extrudates improves the catalytic performance of Ni based catalysts in toluene reforming, and provides promising materials for hot gas cleaning biomass gasification.

10.1039/d3se00705g article EN cc-by Sustainable Energy & Fuels 2023-01-01

Three Ni-based catalysts (Ni/CY, Ni/LSCF and RuNi/LSCF) were submitted to a pre-treatment in gas atmosphere generated during biomass gasification process. The modifications of the physicochemical properties catalytic performance pre-treated model ex-biomass compared with H2. generation Ni0 through was evidenced. This also provoked formation whisker carbon deposits at surface change Ni dispersion by comparing reduction WGS, CO methanation toluene reforming evaluated. Both exhibited activity...

10.2139/ssrn.4100928 article EN SSRN Electronic Journal 2022-01-01
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