B18-Core EXAFS
|
Diamond Proposal Number(s):
[34632]
Abstract: Polychlorinated aromatic hydrocarbons (PCAHs) in flue gas seriously threaten the environment and human health, and Ru-based catalysts exhibit efficient oxidation property for PCAHs removal. However, the current Ru catalysts either have high Ru loading/non-stable structure or are developed empirically whilst lack of design mechanism. Herein, a robust Ru single atom catalyst (0.5 Ru1/TiO2) was designed based on metal-support interaction for o-DCB (o-dichlorobenzene, a typical PCAHs) degradation, and it revealed significantly better oxidation activity with T50 = 207.4 °C and T90 = 243.5 °C than its contrast with weak metal-support interaction (0.5 RuNP/TiO2, T50 = 247.4 °C, T90 > 300 °C). In addition, 0.5 Ru1/TiO2 exhibited much better chlorine resistance stability, maintaining >90% o-DCB conversion for 700 min versus∼70% on 0.5 RuNP/TiO2. The superior performance of 0.5 Ru1/TiO2 was attributed to its stronger metal-support interaction between Ru and TiO2, verified by H2-TPR, which offered higher active oxygen species (22.4%), more Lewis acid (0.675 mmol/g) and higher exposed Ru ratio (> 90.0%) than 0.5 RuNP/TiO2 (15.0%, 0.068 mmol/g, 28.6%, respectively). The above properties can not only enhance o-DCB adsorption/activation and weaken its Csingle bondCl bonds but also favor partial/deep oxidation and remove deposited chlorine on 0.5 Ru1/TiO2, proved by in situ FT-IR. Moreover, notable higher water resistance under different water vapor and applicability under varied pollutant concentration were observed on the robust Ru1/TiO2. This work reveals insightful function-property study on Ru single atom catalysts for PCAHs oxidative removal.
|
May 2026
|
|
I15-1-X-ray Pair Distribution Function (XPDF)
|
Diamond Proposal Number(s):
[345501]
Open Access
Abstract: The Ga₂S₃–Sb₂S₃ quasi-binary system has been investigated for its potential to yield stable chalcogenide glasses with tailored thermal and structural properties. Using melt-quenching techniques, a series of (Ga₂S₃)ₓ(Sb₂S₃)₁₋ₓ compositions (0.0 ≤ x ≤ 0.5) were synthesized, and their glass-forming domain was mapped. The latter extends up to approximately x ≤ 0.40, as confirmed by X-ray diffraction and DSC analyses, with the x = 0.4 composition exhibiting a glass-ceramic character. Density measurements, combined with calculations of molar volume and packing density, revealed a continuous structural densification as Ga₂S₃ content increased. Differential scanning calorimetry showed an increase in glass transition temperature (Tg), with the best thermal stability observed for x = 0.2, as assessed by the Hruby criterion. Electrical conductivity measurements demonstrated thermally activated behaviour following the Arrhenius law, with maximum activation energy also centred at x = 0.2. Raman spectroscopy and DFT modelling were used to decipher the structural contributions of Sb–S and Ga–S bonding. The emergence of vibrational modes characteristic of Ga-based structural units, especially beyond x > 0.2, suggests a structural reorganization from Sb-centred pyramidal units to Ga-centred tetrahedral. This was corroborated by high-energy X-ray diffraction, which showed significant changes in intermediate-range order with increasing Ga content, particularly in the first sharp diffraction peak and partial coordination environments.
|
Apr 2026
|
|
I22-Small angle scattering & Diffraction
|
Tayyaba
Rabnawaz
,
Nathanael
Leung
,
Leonard C.
Nielsen
,
Robert A.
Harper
,
Richard M.
Shelton
,
Gabriel
Landini
,
Tim
Snow
,
Andy
Smith
,
Nick
Terrill
,
Marianne
Liebi
,
Tan
Sui
Diamond Proposal Number(s):
[20285]
Abstract: Dental caries, one of the most prevalent non-communicable diseases worldwide, is characterised by the progressive deterioration of the structure and mechanical properties of dental hard tissues. In human teeth, dentine is the most abundant mineralised tissue, forming the primary support material. To assess changes in the mechanical properties of dentine caused by dental caries and acid erosion, it is crucial to understand the relationship between organic and inorganic dentine components and their organisation into a 3D anisotropic structure at the nanoscale. Over the past 20 years, alterations in dentine structure caused by caries and artificial demineralisation have been reported using conventional microscopy techniques. However, due to the limited spatial resolution of these techniques, the 3D structural organisation including orientation and degree of alignment of mineralised collagen fibrils at the nanoscale, has not been fully explored. This study investigated alterations in the 3D structure of normal, carious and artificially demineralised dentine using SAXS tensor tomography (SASTT). This technique enabled the observation of differences in the local orientation of organic and inorganic components, as well as variations in local scattering intensity, resulting from natural caries and artificial demineralisation. In comparison to normal dentine, caries caused minor orientational differences of both components but had a major impact on the local X-ray scattering intensity. After artificial demineralisation of the dentine, most of the mineral was lost in the outer layers, resulting in a greater reduction in scattering intensity than that caused by caries.
|
Mar 2026
|
|
|
|
Open Access
Abstract: Serial crystallography relies on the reproducible production of high-density suspensions of microcrystals, yet sample optimization remains a resource-intensive bottleneck. While phase diagrams provide a theoretical framework for controlling crystal size and number, experimental mapping is traditionally hindered by relatively high sample consumption. We present an automated microbatch-under-oil crystallization approach that rapidly maps phase boundaries using only 15–60 µl (∼0.15–3.8 mg) of protein. While this workflow is ideally suited for refining existing hits, it serves as a standalone platform for characterizing the crystallization landscape of new protein targets. The power of this approach lies in the integration of three distinct strategies that exploit the stable chemical environment of microbatch-under-oil. Firstly, we utilize an ingenious diagonal sampling strategy that traverses the phase boundary parallel to the solubility curve by systematically varying protein-to-precipitant ratios, identifying primary nucleation zones with far greater efficiency than traditional orthogonal grids. Secondly, we employ a linked variation of multiple precipitants to reveal morphology-specific regions, such as the rod versus plate transitions crucial for time-resolved experiments. Finally, we incorporate automated seed-stock titration to precisely define the metastable zone, enabling the predictive rescue of nucleation-limited systems. The synergy of these three strategies enables the systematic decoupling of nucleation from growth, providing a rational route to optimize microcrystal density, size and lattice order. Crucially, by eliminating the evaporation-related variables inherent in vapor diffusion, this method ensures that the chemical coordinates identified during screening remain constant during scale-up to larger volumes. This workflow transforms empirical serial crystallography sample preparation into a rational, reproducible and highly efficient process applicable to both the optimization of known conditions and the de novo development of microcrystal suspensions, tailored to the rigorous demands of modern serial diffraction experiments.
|
Mar 2026
|
|
I14-Hard X-ray Nanoprobe
|
Diamond Proposal Number(s):
[36126]
Open Access
Abstract: Coal fly ash (CFA), a metal-rich byproduct of coal combustion is produced in vast quantities and poses significant ecological risks. CFA also contains abundant technologically relevant metal oxides and trace metals, including rare earth elements (REE), often at higher concentrations than in primary ores. This makes sustainable recovery strategies a major industrial opportunity. Here, green solvent systems were applied to leach metals from CFA, and the resulting leachates were added to cultures of Magnetospirillum gryphiswaldense (MSR1), a model magnetotactic bacterium that biomineralizes iron into membrane-bound magnetic nanoparticles (magnetosomes) and is capable of interacting with non-iron metals through adsorption and biomineralization. Eleven green solvents, including deep eutectic solvents (DES), were tested for extraction efficiency, with six showing performance comparable to a mineral acid control. Copper (Cu) emerged as the primary toxicant to MSR1, prompting selective precipitation with potassium ferrocyanide trihydrate (PFCT) to reduce its concentration. Cu-depleted lactic acid-based leachates supported MSR1 growth and magnetosome formation even without supplemented iron. Nano-XRF and ICP-MS analysis revealed MSR1 interacts with CFA-derived metals, most significantly showing that produced CFA magnetosomes contained a 5.3–6.1-fold increase in Cu compared to controls. As Cu is both a growth inhibitor and a target pollutant, these findings suggest MSR1 may bioaccumulate Cu within magnetosomes as a detoxification strategy. Overall, this study demonstrates a combined chemical–biological route for CFA valorisation, enabling recovery of diverse metals from waste while producing magnetosomes with distinct compositions.
|
Mar 2026
|
|
I24-Microfocus Macromolecular Crystallography
|
Open Access
Abstract: Serial synchrotron crystallography (SSX) enables structure determination from microcrystals under near-physiological, room-temperature conditions but is limited in part due to the inevitable onset of radiation damage. The ability to reduce the absorbed dose while retaining, or even improving, data quality is an attractive means of mitigating this limitation. Advances in detector technology have made the use of high-energy X-rays a routine approach in MX, improving diffraction efficiency and enhancing overall data quality. Here, we systematically evaluate low-dose SSX data collected at five different X-ray energies from 12.4 to 25 keV using a CdTe Eiger2 detector while maintaining a constant dose. Higher photon energies increased the mean diffracted intensity and signal-to-noise ratio per unit dose, and facilitated higher-resolution structure determination, even with limited crystal numbers. These findings highlight the advantages of high-energy X-rays and provide practical guidance for optimizing SSX experiments in probing protein dynamics.
|
Mar 2026
|
|
I13-2-Diamond Manchester Imaging
|
Mahendra P.
Raut
,
Andrea
Mele
,
Nicholas T. H.
Farr
,
Caroline S.
Taylor
,
David A.
Gregory
,
Jingqiong
Zhang
,
Yufeng
Lai
,
Annabelle
Fricker
,
Jon
Willmott
,
Candice
Majewski
,
Lyudmila
Mihaylova
,
Cornelia
Rodenburg
,
Ipsita
Roy
Diamond Proposal Number(s):
[33034]
Open Access
Abstract: Bone tissue engineering (BTE) aims to address the challenge of repairing critical size bone defects, but effective substitutes with suitable mechanical properties and bioactivity are still needed. Poly(3-hydroxybutyrate), P(3HB)is a sustainable polymer with promising potential but suffers from poor mechanical properties and thermal instability. In this study, P(3HB) was reinforced with various carbon-based materials (CBMs) to evaluate thermomechanical and structural properties as well as biological responses, in composites before and after aging. CBMs with P(3HB) interactions and their spatial distribution were examined using advanced imaging, including Atomic Force Microscopy (AFM), Secondary Electron Hyperspectral Imaging (SEHI), and Short-Wave Infrared (SWIR) analysis. Biological responses were assessed using various biocompatibility assays; cytotoxicity and osteogenicity with primary human osteoblasts (ECACC, 406-05a) and MG63 cells. Aged P(3HB)/inkjet composites showed a 140 % increase in Young's modulus (1.2 GPa), matching trabecular bone stiffness, with a 3 % lower processing temperature than neat P(3HB), enhancing suitability for 3D printing. SEHI revealed elevated OH (4.8 eV) and CO (5.7 eV) functional groups, resulting in increased surface hydrophilicity and promoted cellular responses. P(3HB)/inkjet demonstrated the highest cell attachment (267.5 ± 43.3 cells) and ALP activity (6.3 ± 0.7 nmol PNP/min), outperforming composites with Starbon (150.1 ± 38.3 cells, 6.1 ± 0.8 ALP) and activated carbon (103.4 ± 24.5 cells, 5.7 ± 0.5 ALP). All aged composites showed improved performance over their fresh counterparts. In contrast, TCP and neat P(3HB) exhibited the lowest levels of mineralization. 3D printing offers further potential for enhancing P(3HB)/inkjet composites through precise and bespoke scaffold design and clinical feasibility.
|
Mar 2026
|
|
I11-High Resolution Powder Diffraction
|
Diamond Proposal Number(s):
[33667]
Open Access
Abstract: The use of conventional zirconium alloys at temperatures above 400 °C is limited by high temperature strength and creep resistance. This has prevented the consideration of zirconium alloys for fusion and Generation IV fission plant designs operating at 500 °C–1000 °C. The physical metallurgy of zirconium is similar to titanium which has seen alloying advances allowing application temperatures up to 600 °C. Although the oxidation resistance of zirconium-based alloys is expected to be poor, in a water environment, new Generation-IV and fusion reactors are designed to operate using alternative coolants such as liquid metals and molten salts. Therefore, a new class of zirconium alloys in the Zr-Al-Sn-(Si,Cr,V) system, designed by analogy to near-
titanium alloys, were synthesised by arc melting and processed in a sequence of homogenisation, hot/cold rolling, recrystallisation, and ageing treatments. Microscopy and diffraction identified a refined fully lath grain structure reinforced by nanoscale lamellar or discrete coherent Zr3Al precipitates, with morphology and crystal structure differing with ageing times. Additionally alloying with Si, Cr, and V respectively leads to Zr2Si, ZrCr2, and ZrV2 incoherent precipitates. Tensile testing revealed a strengthening effect by Al, but with significant changes to ductility on ageing depending on the evolution of Zr3Al. Creep testing showed creep rates orders of magnitude better than conventional Zircaloy-4 and nuclear ferritic/martensitic steels, approaching near-
Ti alloys. The present work offers new insights and perspectives into how high-temperature zirconium alloys might be designed to meet the requirements for fusion and Gen-IV fission.
|
Mar 2026
|
|
B21-High Throughput SAXS
|
Diamond Proposal Number(s):
[29895]
Open Access
Abstract: A lipopeptide is designed that contains an epitope from simian virus T-antigen (SV40T, PKKKRKV) conjugated to an N-terminal palmitoyl (C16-) moiety, with the aim to act as an effective cell-penetrating lipopeptide, with additional aggregation propensity conferred by the lipid chain. A combination of cryo-TEM and small-angle X-ray scattering (SAXS) is used to show that the lipopeptide forms micelles, but mixtures with DNA lead to formation of fractal cluster-like co-assemblies due to intercalation of the DNA and peptide. Spectroscopic studies using fluorescence and circular dichroism (along with fiber X-ray diffraction) show that the peptide interacts with DNA and inserts into the groove. Confocal microscopy along with flow cytometry confirms delivery of DNA into both HeLa and mouse embryonic stem cells (mESCs) in pluripotent state, and the system shows excellent cytocompatibility as confirmed by MTT assays. Our data indicate that the lipopeptide may outperform the DNA transfection agent lipofectamine in DNA delivery into these stem cells and it enables DNA delivery into the cytoplasm and nucleus.
|
Mar 2026
|
|
B18-Core EXAFS
|
Yingxiang
Zhao
,
Yingjie
Zhao
,
Xinyue
Zhou
,
Haiwei
Guo
,
Qiqi
Yin
,
Yutao
Jiang
,
Haiyan
He
,
Na
Liu
,
Gengbo
Ren
,
Christopher M. A.
Parlett
,
Changzhi
Li
Diamond Proposal Number(s):
[34632]
Abstract: M–N–C single-atom catalysts (SACs) represent promising candidates owing to their atomically dispersed active sites and tunable catalytic properties and have shown broad potential in various catalysis reactions. However, the mechanisms and true active sites involved in lignin conversion, particularly oxidative depolymerization, remain unclear. Herein, a Ru–N–C SAC with a well-defined configuration, including coordination environment and coordination number, was synthesized via a straightforward ball-milling method for lignin oxidation. The Ru–N–C SAC prepared with 12 h of ball milling demonstrated high catalytic performance in the oxidative depolymerization of various β-O-4 model compounds and diverse lignin feedstocks. Structural analysis via X-ray absorption spectroscopy demonstrated that the Ru–N4 motif constitutes the predominant coordination environment in Ru–N–C, which is regarded as the primary active site in activating O2 into superoxide radicals, as confirmed by free-radical quenching experiments and electron paramagnetic resonance analysis; meanwhile, it also served as a basic site in polarizing Cβ–H bonds in β-O-4 that favored C–O/C–C bond cleavage, which was disclosed by CO2 temperature-programmed desorption and electron localization function analysis. The critical role of Ru–N4 in the activation of O2 and C–O/C–C bond cleavage was further confirmed by density functional theory calculation, which indicated that the Ru–N4 center exhibits strong adsorption toward both the O2 and β-O-4 linkages. This work provides a deep understanding on the active sites within Ru–N–C SACs for lignin oxidative cleavage and offers great potential on the rational design of next-generation SACs in biomass valorization.
|
Feb 2026
|
|
