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Sökning: WFRF:(Arán Ais Rosa M.)

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1.
  • Bagger, Alexander, et al. (författare)
  • Ab Initio Cyclic Voltammetry on Cu(111), Cu(100) and Cu(110) in Acidic, Neutral and Alkaline Solutions
  • 2019
  • Ingår i: ChemPhysChem. - : Wiley. - 1439-4235 .- 1439-7641. ; 20
  • Tidskriftsartikel (refereegranskat)abstract
    • Electrochemical reactions depend on the electrochemical interface between the electrode surfaces and the electrolytes. To control and advance electrochemical reactions there is a need to develop realistic simulation models of the electrochemical interface to understand the interface from an atomistic point-of-view. Here we present a method for obtaining thermodynamic realistic interface structures, a procedure we use to derive specific coverages and to obtain ab initio simulated cyclic voltammograms. As a case study, the method and procedure is applied in a matrix study of three Cu facets in three different electrolytes. The results have been validated by direct comparison to experimental cyclic voltammograms. The alkaline (NaOH) cyclic voltammograms are described by H* and OH*, while in neutral medium (KHCO3) the CO3* species are dominating and in acidic (KCl) the Cl* species prevail. An almost one-to-one mapping is observed from simulation to experiments giving an atomistic understanding of the interface structure of the Cu facets. Atomistic understanding of the interface at relevant eletrolyte conditions will further allow realistic modelling of electrochemical reactions of importance for future eletrocatalytic studies.
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2.
  • Björling, Alexander, et al. (författare)
  • Chemical Limits on X-ray Nanobeam Studies in Water
  • 2023
  • Ingår i: Journal of Physical Chemistry C. - 1932-7447. ; 127:28, s. 13877-13885
  • Tidskriftsartikel (refereegranskat)abstract
    • Operando X-ray studies of chemical reactions have gained increasing interest lately, fueled by the emergence of a new generation of powerful focused X-ray sources. Although it is well known that ionizing radiation causes damage to samples via radical chemistry, this effect is often overlooked in studies of working devices or catalysts where intense focused beams are used as nanoscale probes. Here, we show how an X-ray nanobeam directly causes a phase transition in shape-controlled Pd nanoparticles and that a large oxidative potential must be applied to counteract the effect. In addition, we present a chemical reaction-diffusion model that offers a plausible qualitative explanation of the observations, and which also suggests that prohibitive concentrations of reactive species will arise under any focused X-ray probe, calling into question the validity of these methods as applied to aqueous chemical and catalytic systems.
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3.
  • Halldin Stenlid, Joakim, et al. (författare)
  • Uncovering the electrochemical interface of low-index copper surfaces in deep groundwater environments
  • 2020
  • Ingår i: Electrochimica Acta. - : Elsevier BV. - 0013-4686 .- 1873-3859. ; 362
  • Tidskriftsartikel (refereegranskat)abstract
    • Using a combination of a sophisticated modeling protocol and well-established electrochemical techniques, we unravel the chemical composition of the low-index surfaces of copper in groundwater environments at different ion concentrations, pHs, and redox potentials. By carefully linking density functional theory (DFT) and cyclic voltammetry (CV), we are able to extract fundamental information on interfaces of broad significance. Herein, we focus on the case of groundwater found in deep geological environments of importance to the planned constructions of disposal repositories for spent nuclear fuel around the world. Within the error margins of DFT, we can assign adsorption structures and compositions to the current peaks of the CVs. It is found that among the groundwater ions of main interest (i.e. sulfide, bisulfide, sulfate, chloride and bicarbonate), sulfides (HS-, S2-) bind strongest to the surface, and are likely to dominate at the interfaces under the deep geological conditions relevant for repositories of spent nuclear fuel.
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