I20-Scanning-X-ray spectroscopy (XAS/XES)
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Diamond Proposal Number(s):
[25542]
Open Access
Abstract: The realisation of post-combustion CO2 capture (PCCC) at industrial scale remains limited; one challenge is the concerns around capital costs and another concern is corrosion of the system itself. Corrosion resistance and mitigation against the amine solvent monoethanolamine (MEA) was studied, using the inhibitor copper (II) carbonate basic (CC). Carbon steel (C1018) was tested in CO2 loaded, 5M aqueous MEA solution, alone and in the presence of CC, to assess the corrosivity of the solution. Immersion testing used mass loss, Fe and Cu ion concentration in solution via ICP-MS, imaging (SEM) and analytical techniques (XRD and EDX) to investigate the effect of corrosion. Generally, the use of CC improved C1018 corrosion resistance relative to C1018 alone. Even at low concentrations (0.9 mM), CC was effective in inhibiting corrosion against CO2 loaded MEA, as the observed corrosion rate was effectively zero and no dissolved Fe was detected in solution. There was no evidence of copper surface adsorption. To clarify the solution chemistry resulting in corrosion inhibition, the local chemical environment of Fe and Cu were probed by Cu and Fe K-edge X-ray Absorption Spectroscopy, respectively. The Cu K- edge HERFD-XANES spectra reveal that a Cu2+ amine complex forms, critical to understanding the structure which is promoting significant corrosion inhibition.
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Dec 2022
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I18-Microfocus Spectroscopy
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Diamond Proposal Number(s):
[8861]
Open Access
Abstract: Au(I) chloride species are important reactants and intermediates in various processes across the chemical sciences and engineering. Structure and bonding in Au(I) species are often characterized by X-ray absorption spectroscopy (XAS), including measurements under reaction conditions. Previously reported XA spectra for Au(I) chloride species have varied significantly, likely as a result of radiation damage and/or partial disproportionation of [AuCl2]− ions, which are metastable under ambient conditions. By monitoring the decomposition of tetrabutylammonium dichloroaurate(I), TBA[AuCl2], in 1,2-dichlorobenzene we have obtained a reliable X-ray absorption spectrum of [AuCl2]− ions by combining the calculation of difference spectra with an extended X-ray absorption fine-structure (EXAFS) determination of the solution composition. The results show that the X-ray absorption near-edge structure (XANES) of [AuCl2]− is characterized by a weak Au 2p3/2 → 5d (‘white line’) transition, which agrees well with the spectrum predicted by electronic structure calculations using the FEFF8 code. Compared to [AuCl4]−, the determined [AuCl2]− spectrum has several distinctive features of diagnostic analytical value. A more detailed densities of states (DOS) analysis of the electronic structure suggests that the weak white line arises from a hybrid Au 6s/5d DOS band that is partially occupied, up to the level of the highest occupied molecular orbital (HOMO). Correlation of Cl coordination numbers determined from the EXAFS with the intensity of the white line in the XANES indicates that the decomposition is a primarily radiation-induced oxidation to Au(III) species with an average formula of [AuCl3OH]−.
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Dec 2014
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I18-Microfocus Spectroscopy
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Diamond Proposal Number(s):
[8861]
Open Access
Abstract: Electrochemical gold nucleation and nanoparticle growth at a liquid/liquid interface were examined in situ by combined X-ray fluorescence (XRF) mapping with a microfocus X-ray beam and X-ray absorption fine structure (XAFS) spectroscopy. Gold deposition was achieved by reduction of [AuCl4]− with tri-p-tolylamine at a water/1,2-dichlorobenzene interface using a windowless liquid/liquid interface system formed from the contact of aqueous and organic phase droplets. The combination of XRF and XAFS, with a spatial resolution of approximately 70 μm, provided chemical speciation information near the interface under gold deposition conditions. Analysis of the X-ray absorption near-edge structure (XANES) reveals evidence for the presence of Au(I) species as a reduction intermediate, concomitant with a buildup of metallic gold at the interface. Cyclic voltammetry indicates the presence of two ion transfer peaks at the liquid/liquid interface, which are assigned to the transfer of [AuCl4]− and [AuCl2]−. Finally ex situ TEM analysis shows that the resultant nanoparticles have an average size between 3 and 4 nm. In line with this particle size, the XAFS indicates bulk-like structure.
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Jul 2015
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I18-Microfocus Spectroscopy
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Diamond Proposal Number(s):
[8861]
Open Access
Abstract: Voltammetry for charge (ion and electron) transfer at two immiscible electrolyte solutions (VCTIES) has been used to provide insight into the ligand exchange and redox processes taking place during the interfacial reaction of aqueous hexacyanoferrate(II) with tetrachloroaurate ([AuCl4]−) in 1,2-dichloroethane (DCE). VCTIES permitted the detection of the reactants, intermediates and products at the liquid/liquid interface. A model for the sequence of interfacial processes was established with the support of speciation analysis of the key elementary reactions by X-ray absorption spectroscopy (XAS). The potential-driven transfer of [AuCl4]− from the organic into the aqueous phase is followed by reduction and ligand exchange by the aqueous hexacyanoferrate(II) to form dicyanoaurate ([Au(CN)2]−). Inferences from the reactions point to the likely formation of [AuCl2]− during the reduction sequence. The reaction is influenced by ligand exchange equilibria between [AuCl4]−, [AuCl3(OH)]– and [AuCl2(OH)2]–which are shown to be dependent on the chloride ion concentration and pH of the solution. The difference between the Gibbs energy of transfer at the water | DCE interface View the MathML source(ΔGDCEW°)of AuCl4– and [AuCl3(OH)]–, and the difference between [AuCl3(OH)]– and [AuCl2(OH)2]–were found to change by a value close to the difference between View the MathML sourceΔGDCEW° of Cl– and that of OH–. The intermediate Au(I) species, [AuCl2]−, was seen to decompose at neutral pH and in the absence of Cl– in water to form metallic Au, although it was stable in >10 mM HCl for an hour. Time-dependent VCTIES and X-ray absorption fine structure (XAFS) speciation analysis of the homogeneous aqueous phase indicate that reaction between [AuCl4]− and hexacyanoferrate(II) is accompanied by the formation of an intermediate ionic species, formed when the concentration of [AuCl4]− is close to that of hexacyanoferrate(II). This species, whose identity was not precisely determined, was also generated by reaction between [AuCl2]− and hexacyanoferrate(III). The species is shown by VCTIES to be more hydrophilic than [Au(CN)2]−, [AuCl2]− and [AuCl4]−.
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Feb 2016
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I18-Microfocus Spectroscopy
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Diamond Proposal Number(s):
[8861]
Open Access
Abstract: With the advent of high-throughput and imaging core level spectroscopies (including X-ray absorption spectroscopy, XAS, as well as electron energy loss spectroscopy, EELS), automated data processing, visualisation and analytics will become a necessity. As a first step towards these objectives we examined the possibilities and limitations of a simple automated XANES peak fitting procedure written in MATLAB, for the parametrisation of XANES features, including ionisation potentials as well as the energies and intensities of electronic transitions. Using a series of Au L3-edge XANES reference spectra we show that most of the relevant information can be captured through a small number of rules applied to constrain the fits. Uncertainty in this strategy arises mostly when the ionisation potential (IP) overlaps with weak electronic transitions or features in the continuum beyond the IP, which can result in ambiguity through multiple equally good fits.
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May 2016
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I15-1-X-ray Pair Distribution Function (XPDF)
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Diamond Proposal Number(s):
[2257]
Open Access
Abstract: The use of silica as a lithium‐ion battery anode material requires a pretreatment step to induce electrochemical activity. The partially reversible electrochemical reduction reaction between silica and lithium has been postulated to produce silicon, which can subsequently reversibly react with lithium, providing stable capacities higher than graphite materials. Up to now, the electrochemical reduction pathway and the nature of the products were unknown, thereby hampering the design, optimization, and wider uptake of silica‐based anodes. Here, the electrochemical reduction pathway is uncovered and, for the first time, elemental silicon is identified as a reduction product. These insights, gleaned from analysis of the current response and capacity increase during reduction, conclusively demonstrated that silica must be reduced to introduce reversible capacity and the highest capacities of 600 mAh g−1 are achieved by using a constant load discharge at elevated temperature. Characterization via total scattering X‐ray pair distribution function analysis reveal the reduction products are amorphous in nature, highlighting the need for local structural methods to uncover vital information often inaccessible by traditional diffraction. These insights contribute toward understanding the electrochemical reduction of silica and can inform the development of pretreatment processes to enable their incorporation into next‐generation lithium‐ion batteries.
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Sep 2020
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I15-1-X-ray Pair Distribution Function (XPDF)
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Samuel W.
Coles
,
Viktoria
Falkowski
,
Harry S.
Geddes
,
Gabriel E.
Pérez
,
Samuel G.
Booth
,
Alexander G.
Squires
,
Conn
O'Rourke
,
Kit
Mccoll
,
Andrew L.
Goodwin
,
Serena A.
Cussen
,
Simon J.
Clarke
,
Saiful
Islam
,
Benjamin J.
Morgan
Diamond Proposal Number(s):
[27702]
Open Access
Abstract: Short-range ordering in cation-disordered cathodes can have a significant effect on their electrochemical properties. Here, we characterise the cation short-range order in the antiperovskite cathode material Li2FeSO, using density functional theory, Monte Carlo simulations, and synchrotron X-ray pair-distribution-function data. We predict partial short-range cation-ordering, characterised by favourable OLi4Fe2 oxygen coordination with a preference for polar cis-OLi4Fe2 over non-polar trans-OLi4Fe2 configurations. This preference for polar cation configurations produces long-range disorder, in agreement with experimental data. The predicted short-range-order preference contrasts with that for a simple point-charge model, which instead predicts preferential trans-OLi4Fe2 oxygen coordination and corresponding long-range crystallographic order. The absence of long-range order in Li2FeSO can therefore be attributed to the relative stability of cis-OLi4Fe2 and other non-OLi4Fe2 oxygen-coordination motifs. We show that this effect is associated with the polarisation of oxide and sulfide anions in polar coordination environments, which stabilises these polar short-range cation orderings. We propose similar anion-polarisation–directed short-range-ordering may be present in other heterocationic materials that contain cations with different formal charges. Our analysis also illustrates the limitations of using simple point-charge models to predict the structure of cation-disordered materials, where other factors, such as anion polarisation, may play a critical role in directing both short- and long-range structural correlations.
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Apr 2023
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I09-Surface and Interface Structural Analysis
I21-Resonant Inelastic X-ray Scattering (RIXS)
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A. S.
Menon
,
B. J.
Johnston
,
S. G.
Booth
,
L.
Zhang
,
K.
Kress
,
B. E.
Murdock
,
G.
Paez Fajardo
,
N. N.
Anthonisamy
,
N.
Tapia-Ruiz
,
S.
Agrestini
,
M.
Garcia-Fernandez
,
K.
Zhou
,
P. K.
Thakur
,
T. L.
Lee
,
A. J.
Nedoma
,
S. A.
Cussen
,
L. F. J.
Piper
Diamond Proposal Number(s):
[29104, 29113]
Open Access
Abstract: The desire to increase the energy density of stoichiometric layered
Li
TM
O
2
(TM = 3d transition metal) cathode materials has promoted investigation into their properties at high states of charge. Although there is increasing evidence for pronounced oxygen participation in the charge compensation mechanism, questions remain whether this is true
O
-redox, as observed in
Li
-excess cathodes. Through a high-resolution
O
K-edge resonant inelastic x-ray spectroscopy (RIXS) study of the
Mn
-free
Ni
-rich layered oxide
Li
Ni
0.98
W
0.02
O
2
, we demonstrate that the same oxidized oxygen environment exists in both
Li
-excess and non-
Li
-excess systems. The observation of identical RIXS loss features in both classes of compounds is remarkable given the differences in their crystallographic structure and delithiation pathways. This lack of a specific structural motif reveals the importance of electron correlation in the charge compensation mechanism for these systems and indicates how a better description of charge compensation in layered oxides is required to understand anionic redox for energy storage.
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Mar 2023
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B18-Core EXAFS
I18-Microfocus Spectroscopy
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Diamond Proposal Number(s):
[11293, 8861]
Open Access
Abstract: The mechanism of the Brust-Schiffrin gold nanoparticle synthesis has been investigated through the use
of ion transfer voltammetry at the water|1,2-dichloroethane
(DCE) solution interface, combined with X-ray absorption fine structure
(XAFS) of the reaction between [AuCl4]-
and thiol (RSH) in homogeneous toluene (TL) solution. Ion transfer calculations indi-
cate the formation of [AuCl2]- at RSH:Au ratios from 0.2 – 2 with a time-dependent variation observed over several days. At RSH:Au ratios above 2 and after time periods greater than 24 hours, the formation of Au(I)SR is also observed. The relative concentrations of reaction products observed at the liquid/liquid interface are in excellent agreement with those observed by XAFS for the corresponding reaction in a single homogeneous phase. BH4- ion transfer reactions between water and DCE indicate that the reduction of [AuCl4]-
and/or [AuCl2]- to Au nanoparticles by BH4- proceeds in the bulk organic phase. On the other hand, BH4- was unable to reduce the insoluble [Au(I)SR]n species to Au nanoparticles. The number and size of the nanoparticles formed was dependent on the concentration ratio of
RSH:Au, as well as the experimental duration because of the competing
formation of the [Au(I)SR]n
precipitate. Higher concentrations of nanoparticles, with diameters of 1.0 – 1.5 nm, were formed at RSH:Au ratios from 1 to 2.
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Nov 2015
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B18-Core EXAFS
I11-High Resolution Powder Diffraction
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Diamond Proposal Number(s):
[25166]
Open Access
Abstract: Cation migration on electrochemical cycling can significantly influence the performance of li-ion cathode materials. Phases of composition LiFe2–xInxSbO6 (0 < x <1) adopt crystal structures described in space group Pnnm, consisting of a hexagonally close-packed array of oxide ions, with Fe/In and Sb cations ordered on octahedral sites, and lithium cations located within partially occupied tetrahedral sites. NPD, SXRD, and 57Fe Mössbauer data indicate that on reductive lithium insertion (either chemically or electrochemically), LiFe2SbO6 is converted to Li2Fe2SbO6 accompanied by large-scale cation migration, to form a partially Fe/Li cation-ordered and Fe2+/Fe3+ charge-ordered phase from which lithium cations cannot be easily removed, either chemically or electrochemically. Partial substitution of Fe with In suppresses the degree of cation migration that occurs on lithium insertion such that no structural change is observed when LiFeInSbO6 is converted into Li1.5FeInSbO6, allowing the system to be repeatedly electrochemically cycled between these two compositions. Phases with intermediate levels of In substitution exhibit low levels of Fe migration on Li insertion and electrochemical capacities which evolve on cycling. The mechanism by which the In3+ cations suppress the migration of Fe cations is discussed along with the cycling behavior of the LiFe1.5In0.5SbO6–Li1.75Fe1.5In0.5SbO6.
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Dec 2022
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