B18-Core EXAFS
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Open Access
Abstract: Metal nanoparticles are widely considered for heterogeneous catalysis due to their high atomic efficiency and tunable active microenvironment, but their specific functional tendencies are still unclear. Here, we report that a Rh@ZrO2/NC catalyst with only 0.1 wt% Rh exhibits exceptional catalytic performance and high selectivity (p-nitroacetophenone conversion-98.6 %, p-aminoacetophenone selectivity-100 %, r-56.4 molp-nitroacetophenone/(molRh·min)) towards the hydrogenation of the -NO2 group in nitroarene to -NH2. This is because the interaction between Rh species and “ZrO2-N” results in significant hydrogen spillover in the catalyst, as supported by DFT calculations. Extensive characterizations from TG, DTG, NAP-XPS, in-situ Raman spectroscopy, in-situ DRIFT spectroscopy and DFT calculations further confirm the adsorption, activation and dissociation of hydrogen on Rh nanoparticles. The H* species migrate readily over ZrO2-NC, to facilitate the catalytic activity and selectivity for the hydrogenation of nitroarene. This study presents a new approach to develop highly efficient and selective metal nanoparticle-catalysts for cost-effective hydrogenation reactions.
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Dec 2025
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I22-Small angle scattering & Diffraction
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M.
Hassan Sk
,
S. M.
Clarke
,
M.
Woolley
,
A.
Osudare
,
S.
Agrawal
,
N.
Sharifi
,
D.
Eberl-Craske
,
R.
Lindsay
,
M. T. L.
Casford
,
A.
Smith
,
N.
Terrill
Diamond Proposal Number(s):
[23699, 28693, 32669]
Open Access
Abstract: In this study we have investigated the nucleation mechanism of ‘sweet’, CO2 corrosion scale in situ using synchrotron scattering under industrially relevant conditions (CO2 saturated brine, ultra-low oxygen (8–32 ppb), 80 °C, pH 6.8, open-circuit-potential (OCP)). Simultaneous small and wide-angle X-Ray Scattering (SAXS-WAXS) measurement allows the phase and state of the nucleating corrosion scale to be characterised as a function of both immersion time and location with respect to the metal/solution interface. The results indicate that a precursor amorphous phase is formed prior to the emergence of a crystalline iron carbonate scale.
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Dec 2025
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B18-Core EXAFS
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Diamond Proposal Number(s):
[36598]
Open Access
Abstract: O3 phase NiFeMn- based layered transition metal oxides have attracted interest for positive electrode materials for Na-ion batteries. However, they generally suffer from challenges like phase transitions and Fe migration. Recently, the substitution of Ca into the Na layer, serving as a ‘pillar’, has proven to be an effective approach to overcome these challenges. Here, we systematically studied the composition-dependent Ca pillaring effect on the electrochemical performance and structure evolution of two O3 phase NiFeMn-based layered transition metal oxides. It is found that, although moderate Ca doping in high-Ni system - Na1-2xCaxNi0.25Mn0.25Fe0.5O2 (x = 0.00, 0.03) enhances cycling stability and reduces polarization, excessive doping compromises rate capability and does not effectively prevent Fe migration. Conversely, high-Mn system - Na1-2xCaxNi0.17Mn0.33Fe0.5O2 (x = 0.00, 0.04) exhibits a more robust and beneficial response to Ca incorporation, showing enhanced structural integrity, improved redox reversibility, and effective suppression of Fe migration. This study provides insights into the tunable chemical environments of transition metal oxides, thereby advancing the design of high-performance positive electrode materials and contributing to the development of next-generation sodium-ion batteries.
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Dec 2025
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I18-Microfocus Spectroscopy
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Diamond Proposal Number(s):
[34311]
Abstract: Rice is a staple food for over half the world's population. This study uniquely investigates the spatial distribution of key micronutrients (Cu, Mn, Fe, Zn) in cooked brown, white, and parboiled rice using Synchrotron Micro-X-ray Fluorescence (sXRF) for the first time. Complementary analysis with Inductively Coupled Plasma Mass Spectrometry (ICP-MS) validates bulk elemental concentrations. Results from this dual-approach study reveal significantly higher micronutrient concentrations in brown rice compared to white or parboiled rice, with nutrients predominantly localised in the peripheral layers and minimal presence in the endosperm. Notably, sXRF imaging identified nutrient-rich pockets within the grain periphery, offering new perspectives on nutrient distribution beyond peripheral accumulation. Additional insights include the impact of rice section thickness (50 and 150 μm) and beam dwell times (0.5 and 30s) on sXRF sensitivity and resolution, highlighting trade-offs in detection capabilities, advancing our understanding of micronutrient localisation in cooked rice.
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Dec 2025
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I15-1-X-ray Pair Distribution Function (XPDF)
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Diamond Proposal Number(s):
[40520, 38927]
Open Access
Abstract: We employ a combined computational and experimental approach to systematically assess the hydrostatic properties of methanol–ethanol (MeOH–EtOH) mixtures of varying compositions, with the aim of evaluating their suitability as pressure-transmitting mediums (PTMs). PTMs are essential for enabling the characterization of materials properties at high pressure, perhaps most prominently in the context of diffraction measurements, to provide uniform compression and avoid strain on the sample. Molecular dynamics (MD) simulations indicate that the hydrostatic limit and several structural and dynamic properties of the widely used 4:1 MeOH–EtOH volume ratio do not exhibit any significant deviations from the monotonic trends observed as a function of MeOH content within the mixture. These findings are in agreement with X-ray pair distribution function measurements, which show no peculiar structural behaviour for the 4:1 composition. Experimental measurements of the hydrostatic limit confirm this result and demonstrate that, as previously reported, the role of ethanol is primarily to delay MeOH crystallization. However, we find that the same role can be fulfilled by other small molecules, such as propan-2-ol. Additional simulations of several MeOH–X binary mixtures suggest that these results might hold for a variety of similar mixtures. Thus, our findings indicate that the 4:1 ratio is neither peculiar nor optimal in terms of PTM performance; instead, its popularity seems to be mostly due to the influence of previous literature. Indeed, we find that the 9:1 MeOH–EtOH mixture is characterized by a hydrostatic limit which is superior (by nearly 1 GPa) to that observed for the 4:1 ratio. These findings offer a promising alternative PTM composition which is readily available, and pave the way towards future work aimed at the rational design of novel PTMs.
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Dec 2025
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B18-Core EXAFS
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Diamond Proposal Number(s):
[36104]
Abstract: Seawater splitting has been considered an environmentally friendly and cost-effective method for hydrogen production. However, developing efficient electrocatalysts capable of enduring the severe corrosive conditions of natural seawaters for extended durations remains a notable technical challenge. Herein, the Ni3S2 supported NiFe oxalate ((NiFe)C2O4/Ni3S2) nanorod arrays were synthesised through hydrothermal and impregnation precipitation methods. Structural and spectroscopic analyses revealed that the (NiFe)C2O4/Ni3S2 catalyst formed an integrated oxide-sulfide interface with coexisting Ni–O/Ni–S coordination. This dual coordination environment, coupled with the presence of Fe in a higher oxidation state, confirmed interfacial electronic reorganization characterized by directional electron transfer from Ni to Fe. The resulting charge transfer pathway enhanced the electron delocalisation between active centers, thereby improving active site utilization. The obtained (NiFe)C2O4/Ni3S2 demonstrated remarkable catalytic activity for hydrogen evolution reaction (HER) and oxygen evolution reaction (OER) in a simulated alkaline seawater solution (NaCl + KOH), with overpotentials of 363 mV (HER) and 295 mV (OER) at a current density of 500 mA cm−2 for industrial electrolysis requirements and remarkable stability over 100 h of durability testing. Additionally, the (NiFe)C2O4/Ni3S2 electrode pairs only required a cell voltage of 1.81 V to achieve 100 mA cm−2 with Faradaic efficiency of 98 % in 1.0 M KOH + seawater. This study presents a novel approach for fabricating multifunctional electrocatalysts, providing a promising pathway for advancing seawater electrolysis and supporting the development of cost-effective green hydrogen production technologies.
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Nov 2025
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B22-Multimode InfraRed imaging And Microspectroscopy
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Marta
Morana
,
Lorenzo
Barni
,
Haixing
Fang
,
Giulia
Marras
,
Gianfelice
Cinque
,
Antonio
Angellotti
,
Fabrizio
Nestola
,
Alla
Logvinova
,
Denis
Mikhailenko
,
Luca
Bindi
,
Vincenzo
Stagno
Diamond Proposal Number(s):
[35052]
Open Access
Abstract: The investigation of mineral inclusions in diamonds represents a unique tool to better understand the mineralogy and composition of hidden portions of Earth's mantle and, hence, determine conditions of pressure and temperature at the time of diamond formation. Using a combination of experimental techniques and different geothermobarometric approaches, we characterized a natural diamond from Udachnaya kimberlite pipe entrapping nine inclusions; the inclusions are five garnets, three clinopyroxene and one sulfide and represent an eclogitic paragenesis. Here, we adopted, for the first time, the elastic geobarometry method to the garnet-diamond inclusion-host system to calculate the entrapment conditions for the diamond-garnet pair, resulting in 5.7(±0.3) GPa at 1154 °C. These P-T data are compared with estimates obtained through chemical geothermobarometry, employing T projection onto the local geotherm, a common approach used for eclogite xenoliths in absence of robust calibrated barometers. Our data demonstrate that elastic geobarometry for the garnet-diamond pair results to be a very reliable tool to determine the diamond formation also for eclogitic systems and this will allow to expand our knowledge on eclogitic diamonds in terms of depth of formation.
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Nov 2025
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I03-Macromolecular Crystallography
I04-Macromolecular Crystallography
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Diamond Proposal Number(s):
[25402, 33658]
Open Access
Abstract: Environment-sensitive fluorescent probes are indispensable tools for studying biological systems and advancing drug discovery. This study reports the development of 4-sulfamoyl-7-aminobenzoxadiazole (SBD)-based fluorescent probes for the allosteric site of the liver isoform of pyruvate kinase (PKL). By integrating SBD moieties into known activator scaffolds, such as mitapivat and diarylsulfonamide (DASA) ligands, probes for indicator displacement assays were designed to quantify ligand interactions in the allosteric site. Compound 4a displayed dose-dependent fluorescence enhancement in response to PKL binding and was used in a competitive binding assay with unlabelled ligands: mitapivat, TEPP-46, DASA-58 and reported activator 21. Structure–activity relationship (SAR) analysis revealed key structural features influencing activity and fluorescence sensitivity. The probes report selectively on the allosteric site ligands as the binding was not affected by natural ligands, such as ADP, fructose-1,6-bisphosphate (FBP), phosphoenolpyruvate (PEP), and phenylalanine. These findings provide a practical framework for detecting allosteric ligand engagement in PKL and expand the repertoire of molecular tools for advancing PKL-targeted therapies.
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Nov 2025
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DIAD-Dual Imaging and Diffraction Beamline
I12-JEEP: Joint Engineering, Environmental and Processing
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Franck P.
Vidal
,
Shaghayegh
Afshari
,
Sharif
Ahmed
,
Alberto
Albiol
,
Francisco
Albiol
,
Éric
Béchet
,
Alberto Corbí
Bellot
,
Stefan
Bosse
,
Simon
Burkhard
,
Younes
Chahid
,
Cheng-Ying
Chou
,
Robert
Culver
,
Pascal
Desbarats
,
Lewis
Dixon
,
Johan
Friemann
,
Amin
Garbout
,
Marcos
García-Lorenzo
,
Jean-François
Giovannelli
,
Ross
Hanna
,
Clémentine
Hatton
,
Audrey
Henry
,
Graham
Kelly
,
Christophe
Leblanc
,
Alberto
Leonardi
,
Jean Michel
Létang
,
Harry
Lipscomb
,
Tristan
Manchester
,
Bas
Meere
,
Claire
Michelet
,
Simon
Middleburgh
,
Radu P.
Mihail
,
Iwan
Mitchell
,
Liam
Perera
,
Martí
Puig
,
Malek
Racy
,
Ali
Rouwane
,
Hervé
Seznec
,
Aaron
Sújar
,
Jenna
Tugwell-Allsup
,
Pierre-Frédéric
Villard
Diamond Proposal Number(s):
[29820]
Open Access
Abstract: gVirtualXray (gVXR) is an open-source framework that relies on the Beer–Lambert law to simulate X-ray images in real time on a graphics processor unit (GPU) using triangular meshes. A wide range of programming languages is supported (C/C++, Python, R, Ruby, Tcl, C#, Java, and GNU Octave). Simulations generated with gVXR have been benchmarked with clinically realistic phantoms (i.e. complex structures and materials) using Monte Carlo (MC) simulations, real radiographs and real digitally reconstructed radiographs (DRRs), and X-ray computed tomography (XCT). It has been used in a wide range of applications, including real-time medical simulators, proposing a new densitometric radiographic modality in clinical imaging, studying noise removal techniques in fluoroscopy, teaching particle physics and X-ray imaging to undergraduate students in engineering, and XCT to masters students, predicting image quality and artifacts in material science, etc. gVXR has also been used to produce a high number of realistic simulated images in optimisation problems and to train machine learning algorithms. This paper presents a comprehensive review of such applications of gVXR.
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Nov 2025
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B21-High Throughput SAXS
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Diamond Proposal Number(s):
[31850]
Open Access
Abstract: To ensure safety, pharmaceuticals are rigorously tested for lipopolysaccharide (LPS) contamination, as this can trigger severe immune reactions in patients. Low Endotoxin Recovery (LER), describing the masking of spiked LPS controls in Limulus Amebocyte Lysate (LAL) assays, has been associated with the presence of chelating agents and surfactants in pharmaceutical formulations. The addition of excipients, such as Mg2+, have shown the ability to mitigate the effects of LER, however, inconsistencies in various studies regarding the influence of the excipients on LPS aggregate characteristics and LER occurrence hinder a clear understanding of the mechanisms underlying LER. In this study, dynamic light scattering (DLS) and small-angle X-ray scattering (SAXS) were employed to systematically assess the impact of chelating agents, surfactants, and divalent cations on the size and shape of LPS aggregates across various formulations. Our results indicate that surfactant-only formulations generally reduce LPS aggregate size, whereas chelating agent-only formulations do not. Notably, the smallest aggregates were observed when both chelating agents and surfactants were present, with the extent of size reduction being specific to the particular excipients used. Additionally, Mg2+ generally inhibited the excipients’ capacity to decrease aggregate size, most effectively in phosphate-containing samples. Despite these variations in size, the overall aggregate shape remained largely unchanged in all formulations. These findings suggest that LPS aggregate size or shape does not distinguish formulations causing LER; instead, factors such as the characteristics of the LPS aggregate surface in different formulations should be explored in the future.
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Nov 2025
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