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In order to explore the changes in the performance of polyester fibers prepared by different processes under alkaline conditions, high tenacity (HT) polyester industrial fiber and fully drawn polyester yarn (FDY) of high speed spinning were selected for artificial accelerated aging tests in alkaline conditions at 85 °C. The mechanical properties of fibers were tested during the processes. Wide-angle X-ray diffraction, small-angle X-ray scattering and intrinsic viscosity were used to study the change in crystalline, lamellar structure and chemical structure of polyester fibers. The results showed that the changes in structure and properties of two polyester fibers in alkaline conditions can be divided into three stages. At the initial stage, the breaking strength and degree of orientation of the fibers first decreased significantly due to the effect of water and heat, while crystallinity remained constant. It was caused by the disorientation of amorphous orientated molecular chain segments in the frozen state, resulting in shrinkage. Then the decrease in breaking strength of fibers was slowed down, which was attributed to the breakage of amorphous molecular chains and the formation of a few new crystal structures. In the final stage of alkaline hydrolysis, the breaking strength of the fibers decreased significantly, while the crystallinity of fibers began to decline and the intrinsic viscosity reduced constantly, indicating that the breakage of amorphous molecular chain became the dominant factor. The alkaline hydrolysis reaction rate and the change degree of microstructure and mechanical property parameters of HT fibers were lower than those of FDY fibers, owing to the greater crystallinity and crystal size of HT fibers, which inhibited the erosion of water and OH-. As a result, HT fibers had a better alkaline hydrolysis resistance than FDY fibers. [ABSTRACT FROM AUTHOR]

Highly concentrated aqueous electrolytes (termed water-in-salt electrolytes, WiSEs) at solid-liquid interfaces are ubiquitous in myriad applications including biological signaling, electrosynthesis, and energy storage. This interface, known as the electrical double layer (EDL), has a different structure in WiSEs than in dilute electrolytes. Here, we investigate how divalent salts [zinc bis(trifluoromethylsulfonyl)imide, Zn(TFSI)2], as well as mixtures of mono-and divalent salts [lithium bis(trifluoromethylsulfonyl) imide (LiTFSI) mixed with Zn(TFSI)2], affect the short-and long-range structure of the EDL under confinement using a multimodal combination of scattering, spectroscopy, and surface forces measurements. Raman spectroscopy of bulk electrolytes suggests that the cation is closely associated with the anion regardless of valency. Wide-angle X-ray scattering reveals that all bulk electrolytes form ion clusters; however, the clusters are suppressed with increasing concentration of the divalent ion. To probe the EDL under confinement, we use a Surface Forces Apparatus and demonstrate that the thickness of the adsorbed layer of ions at the interface grows with increasing divalent ion concentration. Multiple interfacial layers form following this adlayer; their thicknesses appear dependent on anion size, rather than cation. Importantly, all electrolytes exhibit very long electrostatic decay lengths that are insensitive to valency. It is likely that in the WiSE regime, electrostatic screening is mediated by the formation of ion clusters rather than individual well-solvated ions. This work contributes to understanding the structure and charge-neutralization mechanism in this class of electrolytes and the interfacial behavior of mixed-electrolyte systems encountered in electrochemistry and biology. [ABSTRACT FROM AUTHOR]

Orienting polymer semiconductors is desirable to optimize device characteristics, provide insight into microstructure, and magnify subtle phase behavior. Here, a combination of uniaxial strain and subsequent heating of the donor–acceptor (DA) polymer PBnDT‐FTAZ is discovered to lead to exceptional optical dichroic ratios of up to 38 (and close to 50 near the polymer's absorption edge). This alignment is achieved due to the existence of a previously undetected thermotropic liquid crystal (LC) mesophase. The LC transition, not discernable through calorimetry, is uncovered through a combination of in situ UV–vis spectroscopy, X‐ray scattering, and dynamic mechanical analysis (DMA). Comparing PBnDT‐FTAZ to the non‐fluorinated PBnDT‐HTAZ and the homo polymer PBnDT, all of which show similar thermal transitions, reveals that exceptional alignment is only found in PBnDT‐FTAZ. This is attributed to the PBnDT‐FTAZ film having two distinct liquid crystal populations, and the polymer templating to a highly aligned, high‐clearing temperature population when heated. The DMA thermal relaxation behavior observed here is also seen in other DA conjugated polymers suggesting that such thermotropic LC mesophases may be common in these materials. These findings demonstrate a polymer semiconductor with remarkable alignment and uncover phase behavior with broad implications for process‐structure‐property relationships in polymer semiconductors. [ABSTRACT FROM AUTHOR]

In situ ultra-small-angle and wide-angle X-ray scattering enables simultaneous tracking of the structural parameters of mesoporous CeO2 from the atomic scale to the micron-size scale. This multiscale approach provides a path to better understand structure–property relationships in mesoporous polycrystalline materials under dynamic conditions such as high temperature cycling. [ABSTRACT FROM AUTHOR]

In situ ultra-small-angle and wide-angle X-ray scattering enables simultaneous tracking of the structural parameters of mesoporous CeO2 from the atomic scale to the micron-size scale. This multiscale approach provides a path to better understand structure–property relationships in mesoporous polycrystalline materials under dynamic conditions such as high temperature cycling. [ABSTRACT FROM AUTHOR]

Simple Summary: Breast cancer ranks as the most prevalent cancer among women. Current screening includes regular mammography and subsequent biopsy if the mammography results are abnormal. These procedures are costly and uncomfortable. We propose an alternative non-invasive method based on X-ray scattering. Using a machine learning approach, we have examined almost 3000 measurements of cancerous and non-cancerous samples belonging to 110 patients and shown excellent results on cancer/non-cancer separation. This can lead to patient-friendly, fast, and economical solutions for breast cancer screening to complement mammography and reduce biopsy. It should be emphasized that this approach can be readily extended to other types of cancer and even other diseases. With breast cancer being one of the most widespread causes of death for women, there is an unmet need for its early detection. For this purpose, we propose a non-invasive approach based on X-ray scattering. We measured samples from 107 unique patients provided by the Breast Cancer Now Tissue Biobank, with the total dataset containing 2958 entries. Two different sample-to-detector distances, 2 and 16 cm, were used to access various structural biomarkers at distinct ranges of momentum transfer values. The biomarkers related to lipid metabolism are consistent with those of previous studies. Machine learning analysis based on the Random Forest Classifier demonstrates excellent performance metrics for cancer/non-cancer binary decisions. The best sensitivity and specificity values are 80% and 92%, respectively, for the sample-to-detector distance of 2 cm and 86% and 83% for the sample-to-detector distance of 16 cm. [ABSTRACT FROM AUTHOR]

This study presents the characterization of cross-linking parameters of a liquid crystalline epoxy monomer with an aromatic diamine as a curing agent. The mixture tested consisted of bis [4-(10,11-epoxyundecanoyloxy)benzoate] p-phenylene (LCEM) and 1,3-phenylenediamine (1,3-PDA). This paper focuses on the structural characterization of such systems using X-ray analysis. To investigate this, a comprehensive analysis was conducted using Differential Scanning Calorimetry (DSC) and Wide-Angle X-ray Scattering (WAXS). Through DSC analysis, the curing behavior and transition temperature of the liquid crystal epoxy system were established. To fully characterize the cross-linking of the system, a novel technique called DSC-TOPEM® was employed. The use of this technique enabled real-time monitoring of the curing process and provided precise information on the cross-linking energy, which resulted in the finding that the mixture was cross-linking faster than expected. WAXS analysis was performed to assess the structural changes formed during the cross-linking. The results of this analysis confirm that lower cross-linking temperatures of the mixture cause better ordering of mesogens than higher ones. [ABSTRACT FROM AUTHOR]

Cannabis producers, consumers, and regulators need fast, accurate, point‐of‐use sensors to detect Δ9‐tetrahydrocannabinol (THC) and cannabidiol (CBD) from both liquid and vapor source samples, and phthalocyanine‐based organic thin‐film transistors (OTFTs) provide a cost‐effective solution. Chloro aluminum phthalocyanine (Cl‐AlPc) has emerged as a promising material due to its unique coordinating interactions with cannabinoids, allowing for superior sensitivity. This work explores the molecular engineering of AlPc to tune and enhance these interactions, where a series of novel phenxoylated R‐AlPcs are synthesized and integrated into OTFTs, which are then exposed to THC and CBD solution and vapor samples. While the R‐AlPc substituted molecules have a comparable baseline device performance to Cl‐AlPc, their new crystal structures and weakened intermolecular interactions increase sensitivity to THC. Grazing‐incidence wide‐angle X‐ray scattering (GIWAXS) and atomic force microscopy (AFM) are used to investigate this film restructuring, where a significant shift in the crystal structure, grain size, and film roughness is detected for the R‐AlPc molecules that do not occur with Cl‐AlPc. This significant crystal reorganization and film restructuring are the driving force behind the improved sensitivity to cannabinoids relative to Cl‐AlPc and demonstrate that analyte–semiconductor interactions can be enhanced through chemical modification to create more responsive OTFT sensors. [ABSTRACT FROM AUTHOR]

Water interactions with cellulose, hemicellulose, and lignin in cell walls significantly influence their dimensional properties and thus the many applications of wood and other cellulosic materials. The sustainable development and application of wood and cellulosic materials require a better understanding of the mechanisms involved in the deformation with moisture changes. The dimensional changes of multiscale structures of Masson pine were studied during moisture desorption, and the differences at different scales were compared. The confocal laser scanning microscopy (CLSM) was used to observe the deformation of cells. The detail of wood nanostructure was characterized by small-angle X-ray scattering (SAXS) and wide-angle X-ray scattering (WAXS). The molecular interaction between moisture and cell wall was studied using Fourier-transform infrared (FTIR). The results revealed that weakly hydrogen-bonded water molecules and water molecule clusters desorbed from the wood cell walls during moisture loss. The loss of water molecules altered the wood nanostructure, resulting in 12% and 7% reductions in the distances between the elementary fibrils in the latewood (LW) and earlywood (EW) cell walls, respectively. The dimensions of the cellulose crystallites in LW and EW decreased by 5% and 2%, respectively. At the cellular level, the tangential shrinkage of LW and EW were 9% and 6%, respectively. The reduction of the shrinkage at the larger scale can be attributed to the mutual inhibition and fine-tuning of the multi-scale hierarchical structures in wood. These findings provide insight into the instability of wood or natural cellulosic materials during moisture desorption and contribute to developing of more targeted wood-based materials. [ABSTRACT FROM AUTHOR]

A previous study (Paper I) investigated the polarization properties of a variety of simple convex grain shapes, some of which were found to be consistent with the observed polarization properties of interstellar dust from far-ultraviolet to far-infrared. Here, we study the optical properties of 45 nonconvex shapes, all aggregates of N equal-sized spheres. We consider N = 2, N = 3, and N = 256 random aggregates obtained from three different aggregation schemes. We also consider "trimmed" N = 256 aggregates obtained by systematically trimming initially random aggregates to increase either flattening or elongation. The "macroporosities" of the studied aggregates range from P macro = 0.18 (for the N = 2 bisphere) to P macro ≈ 0.85 (for the N = 256 "BA" aggregates). The only aggregates consistent with observations of starlight polarization and polarized thermal emission are shapes that have been trimmed to increase their asymmetry. If interstellar grains are high-porosity aggregates, there must be processes causing extreme elongation or flattening; if not, interstellar grains must be dominated by fairly compact structures, with at most moderate porosities. The ratio of polarization in the 10 μ m silicate feature to starlight polarization in the optical is shown to be insensitive to porosity and shape. X-ray scattering may be the best tool to determine the porosity of interstellar grains. We propose that modest porosities of interstellar grains could be the result of "photolytic densification." High polarization fractions observed in some Class 0 cores require processes to reduce porosities and/or increase asymmetries of aggregates in dense regions. [ABSTRACT FROM AUTHOR]

We report the photon (PL), electron (CL) and X-ray (XEL) induced luminescence characteristics of high aspect ratio ultra-long (~ 50 µm) ZnO nanorods (NRs) and discuss the potential for fast X-ray detection based on the consistent and efficient visible emission (~ 580 nm) from ZnO NRs. Nanostructured ZnO scintillators were rearranged to form a vertically well-aligned NR design in order to help light absorption and coupling resulting in luminescent and fast scintillation properties. The design of the nanorod array combines the key advantages of a low-cost growth technique together with environmentally friendly and widely available materials. A low temperature hydrothermal method was adopted to grow ZnO NRs in one cycle growth and their structural, optical and X-ray scintillation properties were investigated. The relatively short (~ 10 µm) ZnO NRs emitting in the near-band-edge region were found to be almost insensitive to X-rays. On the other hand, the higher XEL response of long ZnO NRs, which is a key parameter for evaluation of materials to be used as scintillators for high quality X-ray detection and imaging, along with a decay time response in the order of ns confirmed promising scintillation properties for fast and high-resolution X-ray detector applications. [ABSTRACT FROM AUTHOR]

Structural colors arise from selective light interaction with (nano)structures, which give them advantages over pigmented colors such as resistance to fading and possibility to be fabricated out of traditional low-cost and non-toxic materials. Since the color arises from the photonic (nano)structures, different structural features can impact their photonic response and thus, their color. Therefore, the detailed characterization of their structural features is crucial for further improvement of structural colors. In this work, we present a detailed multi-scale structural characterization of ceramic-based photonic glasses by using a combination of high-resolution ptychographic X-ray computed tomography and small angle X-ray scattering. Our results uncover the structure-processing-properties' relationships of such nanoparticles-based photonic glasses and point out to the need of a review of the structural features used in simulation models concomitantly with the need for further investigations by experimentalists, where we point out exactly which structural features need to be improved. [ABSTRACT FROM AUTHOR]

The new host materials are reported to boost the multiple resonance‐induced thermally activated delayed fluorescence (MR‐TADF) based pure deep‐blue organic light emitting diodes (OLEDs) toward further shortening the emission full width at the half maximum (FWHM). Based on an unusual asymmetric design concept, two new host compounds Bz2cb and Bz2cbz are synthesized. Despite possessing a compact and rigid molecular packing in crystal, Bz2cbz shows pure amorphous morphology via vapor deposition, as confirmed by the grazing‐incidence wide‐angle X‐ray scattering (GIWAXS) analysis. Via incorporating a promising MR‐TADF emitter, ν‐DABNA‐O‐Me, into Bz2cb and Bz2cbz films, highly pure deep‐blue OLEDs are successfully demonstrated. Remarkably, the Bz2cbz device exhibits a 464 nm electroluminescence (EL) with narrow FWHM of 22 nm, accompanied by the reduction of the 0–1 vibronic sideband, and a maximum external quantum efficiency (EQEmax) of 28.2%, which, overall, reaches the true‐blue Commission Internationale de l'Eclairage coordinates (CIE) of (0.13, 0.07) and the high blue index of 253. The amorphous film formation turns out to be an important factor that is previously unrecognized to externally fine‐tune the MR‐TADF OLEDs toward even higher color purity. [ABSTRACT FROM AUTHOR]

Thin films of crystalline solids with substantial free volume built from organic chromophores and metal secondary building units (SBUs) are promising for engineering new optoelectronic properties through control of interchromophore coupling. Zn‐based SBUs are especially relevant in this case because they avoid quenching the chromophore's luminescence. We find that layer‐by‐layer spin‐coating using Zn acetate dihydrate and benzene‐1,4‐dicarboxylic acid (H2BDC) and biphenyl‐4,4'‐dicarboxylic acid (H2BPDC) linkers readily produces crystalline thin films. However, analysis of the grazing‐incidence wide‐angle X‐ray scattering (GIWAXS) data reveals the structures of these films vary significantly with the linker, and with the metal‐to‐linker molar ratio used for fabrication. Under equimolar conditions, H2BPDC creates a type of structure like that proposed for SURMOF‐2, whereas H2BDC generates a different metal‐hydroxide‐organic framework. Large excess of Zn2+ ions causes the growth of layered zinc hydroxides, irrespective of the linker used. Density functional theory (DFT) calculations provide structural models with minimum total energy that are consistent with the experimentally observed diffractograms. In the broader sense, this work illustrates the importance in this field of careful structure determination, e. g., by utilizing GIWAXS and DFT simulations to determine the structure of the obtained crystalline metal‐organic thin films, such that properties can be rationally engineered and explained. [ABSTRACT FROM AUTHOR]

Ionomers are important to electrode function in energy conversion devices, such as fuel cells and electrolyzers, as the catalyst‐binding nanometer‐thick films under confinement, which compromises mass transport of species. Mitigating confinement effects is necessary for improved performance of polymer electrolyte fuel cells. Studies on perfluorosulfonic acid (PFSA) ionomers provided insights into origins of transport resistances, but limited improvements by current strategies necessitate a need for alternative chemistries to enhance film function. This work investigates new ionomers based on sidechain modifications of PFSA to tune local acidity and structure. Their application‐relevant properties (hydration, thermal‐transition) and nanomorphology are systematically characterized using environmental ellipsometry and grazing‐incidence X‐ray scattering, respectively, to develop chemistry‐structure‐property relationships in thin‐film motif (≤100 nm). Introducing acid sites to sidechains improves hydration and nano‐phase‐separation but reduce chain mobility. Replacing the hydrophilic end‐groups with hydrophobic perfluoro‐groups enhances mobility but disrupts phase‐separation. Although modifying sidechain functional groups alters ionomer‐substrate interactions (Pt/C), chemistry has greater influence on structure‐properties. Proton conductivity correlates with hydration, regardless of chemistry. This work improves the fundamental understanding of chemistry‐function relationships of ionomers by providing a novel means to independently control their side‐chain vs. end‐group and observe resulting effects on interfacial properties to modulate electrode function in electrochemical technologies. [ABSTRACT FROM AUTHOR]

BACKGROUND: X-ray imaging is widely used for the non-destructive detection of defects in industrial products on a conveyor belt. In-line detection requires highly accurate, robust, and fast algorithms. Deep Convolutional Neural Networks (DCNNs) satisfy these requirements when a large amount of labeled data is available. To overcome the challenge of collecting these data, different methods of X-ray image generation are considered. OBJECTIVE: Depending on the desired degree of similarity to real data, different physical effects should either be simulated or can be ignored. X-ray scattering is known to be computationally expensive to simulate, and this effect can greatly affect the accuracy of a generated X-ray image. We aim to quantitatively evaluate the effect of scattering on defect detection. METHODS: Monte-Carlo simulation is used to generate X-ray scattering distribution. DCNNs are trained on the data with and without scattering and applied to the same test datasets. Probability of Detection (POD) curves are computed to compare their performance, characterized by the size of the smallest detectable defect. RESULTS: We apply the methodology to a model problem of defect detection in cylinders. When trained on data without scattering, DCNNs reliably detect defects larger than 1.3 mm, and using data with scattering improves performance by less than 5%. If the analysis is performed on the cases with large scattering-to-primary ratio (1 < SPR < 5), the difference in performance could reach 15% (approx. 0.4 mm). CONCLUSION: Excluding the scattering signal from the training data has the largest effect on the smallest detectable defects, and the difference decreases for larger defects. The scattering-to-primary ratio has a significant effect on detection performance and the required accuracy of data generation. [ABSTRACT FROM AUTHOR]

Increased temperature and high pressure are applied to β‐lactoglobulin fibrils in the autoclave, resulting in the acquisition of a composite material comprised of partially disassembled amyloid fibrils and carbon dots. Confirmation of the preservation of the β‐sheet motif attributed to amyloids in the hydrothermally treated fibrils is obtained through wide‐angle X‐ray scattering and ThT assay. Z‐scan analysis reveals a two‐photon absorption (2PA) enhancement in the low‐lying transition band (La) of tyrosine, while quantum chemical calculations demonstrate a correlation between the yield of 2PA and the interspace distance between aromatic residues. Overall, the intrinsic optical properties of amyloid fibrils treated in a subcritical water environment are found to be linked with the π‐conjugation of tyrosine units and their through‐space coupling. The resulting composite material is employed as a coating for a commercial ultraviolet light‐emitting diode lamp, showcasing the potential utility of sustainable biomaterials with improved optical properties for photonics applications. [ABSTRACT FROM AUTHOR]

In wide-angle X-ray scattering (WAXS) experiments, the use of a one-dimensional arc detector can effectively expand the angle range of collected diffraction or scattering signals. In practice, the relative positions between the centers of arc detector, sample and beam spot may overlap or misalign. Therefore, it is necessary to calibrate the instrument parameters and detection angle of the arc detector. The calibration is routinely performed by standard samples. In this contribution, the equations for angle calibration and error evaluation are constructed based on three standard diffraction peaks, and the corresponding simulation and experiment are performed to verify the feasibility of the calibration. The results indicate that the larger the coverage and the more uniform the dispersion of the three standard diffraction peaks distributed on the detector, the smaller the calibration error. [ABSTRACT FROM AUTHOR]

X‐ray and neutron scattering have long been used for structural characterization of cellulose in plants. Due to averaging over the illuminated sample volume, these measurements traditionally overlooked the compositional and morphological heterogeneity within the sample. Here, a scanning tomographic imaging method is described, using contrast derived from the X‐ray scattering intensity, for virtually sectioning the sample to reveal its internal structure at a resolution of a few micrometres. This method provides a means for retrieving the local scattering signal that corresponds to any voxel within the virtual section, enabling characterization of the local structure using traditional data‐analysis methods. This is accomplished through tomographic reconstruction of the spatial distribution of a handful of mathematical components identified by non‐negative matrix factorization from the large dataset of X‐ray scattering intensity. Joint analysis of multiple datasets, to find similarity between voxels by clustering of the decomposed data, could help elucidate systematic differences between samples, such as those expected from genetic modifications, chemical treatments or fungal decay. The spatial distribution of the microfibril angle can also be analyzed, based on the tomographically reconstructed scattering intensity as a function of the azimuthal angle. [ABSTRACT FROM AUTHOR]

The BL17B beamline at the Shanghai Synchrotron Radiation Facility was first designed as a versatile high‐throughput protein crystallography beamline and one of five beamlines affiliated to the National Facility for Protein Science in Shanghai. It was officially opened to users in July 2015. As a bending magnet beamline, BL17B has the advantages of high photon flux, brightness, energy resolution and continuous adjustable energy between 5 and 23 keV. The experimental station excels in crystal screening and structure determination, providing cost‐effective routine experimental services to numerous users. Given the interdisciplinary and green energy research demands, BL17B beamline has undergone optimization, expanded its range of experimental methods and enhanced sample environments for a more user‐friendly testing mode. These methods include single‐crystal X‐ray diffraction, powder crystal X‐ray diffraction, wide‐angle X‐ray scattering, grazing‐incidence wide‐angle X‐ray scattering (GIWAXS), and fully scattered atom pair distribution function analysis, covering structure detection from crystalline to amorphous states. This paper primarily presents the performance of the BL17B beamline and the application of the GIWAXS methodology at the beamline in the field of perovskite materials. [ABSTRACT FROM AUTHOR]

Understanding and controlling the structure and function of liquid interfaces is a constant challenge in biology, nanoscience and nanotechnology, with applications ranging from molecular electronics to controlled drug release. X‐ray reflectivity and grazing incidence diffraction provide invaluable probes for studying the atomic scale structure at liquid–air interfaces. The new time‐resolved laser system at the LISA liquid diffractometer situated at beamline P08 at the PETRA III synchrotron radiation source in Hamburg provides a laser pump with X‐ray probe. The femtosecond laser combined with the LISA diffractometer allows unique opportunities to investigate photo‐induced structural changes at liquid interfaces on the pico‐ and nanosecond time scales with pump–probe techniques. A time resolution of 38 ps has been achieved and verified with Bi. First experiments include laser‐induced effects on salt solutions and liquid mercury surfaces with static and varied time scales measurements showing the proof of concept for investigations at liquid surfaces. [ABSTRACT FROM AUTHOR]

We calculate electronic structure and spin susceptibility dependencies on doping within the framework of a cluster perturbation theory for strongly correlated electronic systems. The change in the susceptibility with increasing doping is qualitatively consistent with the experimental data on resonant inelastic X-ray scattering and inelastic neutron scattering, as well as with the results of the calculations within the quantum Monte Carlo method. [ABSTRACT FROM AUTHOR]

Fundamental equations describing the X‐ray and electron diffraction scattering in imperfect crystals have been derived in the form of the matrix Fredholm–Volterra integral equation of the second kind. A theoretical approach has been developed using the perfect‐crystal Green function formalism. In contrast, another approach utilizes the wavefield eigenfunctions related to the diagonalized matrix propagators of the conventional Takagi–Taupin and Howie–Whelan equations. Using the Liouville–Neumann‐type series formalism for building up the matrix Fredholm–Volterra integral equation solutions, the general resolvent function solutions of the X‐ray and electron diffraction boundary‐valued Cauchy problems have been obtained. Based on the resolvent‐type solutions, the aim is to reveal the features of the diffraction scattering onto the crystal lattice defects, including the mechanisms of intra‐ and interbranch wave scattering in the strongly deformed regions in the vicinity of crystal lattice defect cores. Using the two‐stage resolvent solution of the second order, this approach has been supported by straightforward calculation of the electron bright‐ and dark‐field contrasts of an edge dislocation in a thick foil. The results obtained for the bright‐ and dark‐field profiles of the edge dislocation are discussed and compared with analogous ones numerically calculated by Howie & Whelan [Proc. R. Soc. A (1962), 267, 206]. [ABSTRACT FROM AUTHOR]

Type I collagen was obtained in gel-like form by enzymatic-acidic extraction from cattle tail tendons and was polymerized at room temperature in ammonia vapor to form a transparent film 60.47–64.9 μm thick with good adhesive properties of 11.6–12.4 kPa and tensile strength 559.5–600.5 kPa. The dependence of the film adhesive properties on its ability to stimulate regenerative processes in tissues was found. The collagen was characterized by X-ray photoelectron spectroscopy. The C 1s spectrum showed peaks for C–C/C–H, C–O–C/C–OH, O=C–N, and O=C–OH groups; the N 1s spectrum for C–NH2, O=C–N, and C–NH3+ groups. [ABSTRACT FROM AUTHOR]

Sortase‐dependent pili are long surface appendages that mediate attachment, colonization and biofilm formation in certain genera and species of Gram‐positive bacteria. Ligilactobacillus ruminis is an autochthonous gut commensal that relies on sortase‐dependent LrpCBA pili for host adherence and persistence. X‐ray crystal structure snapshots of the backbone pilin LrpA were captured in two atypical bent conformations leading to a zigzag morphology in the LrpCBA pilus structure. Small‐angle X‐ray scattering and structural analysis revealed that LrpA also adopts the typical linear conformation, resulting in an elongated pilus morphology. Various conformational analyses and biophysical experiments helped to demonstrate that a hinge region located at the end of the flexible N‐terminal domain of LrpA facilitates a new closure‐and‐twist motion for assembling dynamic pili during the assembly process and host attachment. Further, the incongruent combination of flexible domain‐driven conformational dynamics and rigid isopeptide bond‐driven stability observed in the LrpCBA pilus might also extend to the sortase‐dependent pili of other bacteria colonizing a host. [ABSTRACT FROM AUTHOR]

When solving a structure of a protein from single‐wavelength anomalous diffraction X‐ray data, the initial phases obtained by phasing from an anomalously scattering substructure usually need to be improved by an iterated electron‐density modification. In this manuscript, the use of convolutional neural networks (CNNs) for segmentation of the initial experimental phasing electron‐density maps is proposed. The results reported demonstrate that a CNN with U‐net architecture, trained on several thousands of electron‐density maps generated mainly using X‐ray data from the Protein Data Bank in a supervised learning, can improve current density‐modification methods. [ABSTRACT FROM AUTHOR]

Fat polymorphism plays a crucial role in many fat‐rich food products (e.g., margarine, chocolate). Due to this, polymorphism of triglycerides is widely investigated. During the previous years, the interest of using monoglyceride oleogels to replace margarine is increasing due to its structure, reduced amount of saturated fatty acids, stability and application potential. However, polymorphism of monoglyceride oleogels is less investigated. This research shows the effect of the composition (C18:0 or C18:0 and C16:0), temperature (25°C–20°C–10°C) and production process (static or lab‐scale scraped surface heat exchanger) on the crystallization behavior of monoglyceride oleogels (MO) by using differential scanning calorimetry, (synchrotron) X‐ray scattering and polarized light microscopy. Based on time‐resolved synchrotron WAXS, it was found that the rapeseed oil based MO (MO‐C18) occurred in four different polymorphs. During crystallization, transitions from an inverse lamellar phase (Lα) toward sub‐α1 and sub‐α2 could be established. Upon storage, a polymorphic transition toward β occurred. For the palm oil based MO (MO‐C18/C16), only two polymorphs were found during crystallization (Lα, sub‐α), followed by a polymorphic transition to β upon storage. By applying high shear and cooling rates during the production of MO‐C18 (dynamic production), the polymorphic transition from sub‐α2 to β occurred much faster compared to the static production method. When comparing the dynamically produced MO‐C18 and MO‐C18/C16, the thickness of 1 lamella, the crystal nanoplatelet and the fat crystals were smaller for MO‐C18/C16. This research clearly illustrates that the composition and the applied crystallization conditions have an impact on the properties from nano‐ to microscale. Practical Application: This research illustrates the importance of engineering monoglycerides oleogels to obtain food products with an improved nutritional balance. Hereby, the manuscript focuses on the crystallization behavior of monoglyceride oleogels by changing the composition and the crystallization procedure. The acquired insights go beyond the state of the art. It was found that applying high cooling rates and high shear rates by using a lab‐scale scraped surface heat exchanger affected the crystallization behavior of monoglyceride oleogels. These are crucial experiments to verify the application potential of monoglyceride oleogels in the food industry. Moreover, different polymorphic transitions occurred for the two types of monoglycerides. This is the starting point to investigate the effect of polymorphism on a final food product in order to improve the nutritional balance in fat‐rich food products. [ABSTRACT FROM AUTHOR]

[Display omitted] Understanding and manipulating the oil/water interface is important across various industries, including food, pharmaceuticals, cosmetics, and detergents. Many of these processes occur under elevated pH conditions in buffer systems, where base-catalyzed hydrolysis of triglyceride ester bonds leads to amphiphilic reaction products such as fatty acids. Here, pH-triggered alterations of the triolein/water interface are analyzed in the presence of phosphate (PB) and tris(hydroxymethyl)aminomethane (TRIS). Ellipsometry at the liquid/liquid interface, tensiometry, and scanning small angle X-ray scattering are used to study the formation of structures at the oil/water interface. Confocal Raman microscopy, nuclear magnetic resonance spectroscopy, and in silico modeling analyze compositional changes in the interfacial region. pH and buffer ions were discovered to significantly modify the triglyceride/water interface, contrary to the decane/water control. Decreasing interfacial tensions from 32.4 to 2.2 mN/m upon pH increase from 6.5 to 9.5 is seen with multilamellar interfacial layers forming at pH around 9.0 in the presence of TRIS. Oleic acid from triolein hydrolysis and its further interaction with TRIS is held responsible for this. The new understanding can guide the design of pH- and ion-responsive functional materials and optimize industrial processes involving triglyceride/water interfaces. [ABSTRACT FROM AUTHOR]

Pulsed underwater direct current discharge is considered as a tool for a one-step process for ferrite synthesis and organic dye removal. The formation of cobalt, nickel and titanium ferrites during the discharge firing process was confirmed by methods of dynamic light scattering and X-ray phase analysis. The transformation of dye molecules (fluorescein, methylene green) during the combined action of plasma and ferrites was detected by UV absorption spectroscopy. The contributions of the separate action of plasma and ferrites to the process of dye removal from the solution were investigated. It was found that the synthesized structures have a high sorption capacity. It was found that fluorescein can be used as an indicator for the presence of nickel ferrites. [ABSTRACT FROM AUTHOR]

Here, the effect of thermal annealing (TA) on the stability of solution‐sheared thin films of the semiconducting polymer poly[2,5‐bis(2‐octyldodecyl)pyrrolo[3,4‐c]pyrrole‐1,4(2H,5H)‐dione‐3,6‐diyl)‐alt‐(2,2′;5′,2′';5′',2′"‐quaterthiophen‐5,5′"‐diyl)] (PDPP4T) against the original coating solvent is studied, and it is shown that TA significantly improves the solvent resistance of semiconducting polymer films. Specifically, after the thin films are annealed at or above a critical temperature, the thin film thickness is largely retained when exposed to the original solvent, while for lower annealing temperatures material loss occurs, i.e., the thin film thickness is reduced due to rapid dissolution. The results of various techniques including grazing‐incidence wide‐angle x‐ray scattering (GIWAXS), atomic force microscopy (AFM), and ultraviolet‐visible‐near infrared (UV–vis‐NIR) absorption spectroscopy suggest physical changes as the cause for the increased solvent resistance. Such annealed films also show stable electrical characteristics in bottom‐gate, top‐contact (BGTC) organic field‐effect transistors (OFETs) even after solvent exposure. In initial tests, a multitude of technologically relevant polymers show such behavior, underlining the potential impact of such temperature treatments for the fabrication of multi‐layer polymer devices. [ABSTRACT FROM AUTHOR]

We present in situ measurements of spectrally resolved X-ray scattering and X-ray diffraction from monocrystalline diamond samples heated with an intense pulse of heavy ions. In this way, we determine the samples' heating dynamics and their microscopic and macroscopic structural integrity over a timespan of several microseconds. Connecting the ratio of elastic to inelastic scattering with state-of-the-art density functional theory molecular dynamics simulations allows the inference of average temperatures around 1300 K, in agreement with predictions from stopping power calculations. The simultaneous diffraction measurements show no hints of any volumetric graphitization of the material, but do indicate the onset of fracture in the diamond sample. Our experiments pave the way for future studies at the Facility for Antiproton and Ion Research, where a substantially increased intensity of the heavy ion beam will be available. [ABSTRACT FROM AUTHOR]

The molecular structure of a crystalline monolayer of hydrocarbon chains was modeled and studied via computer simulation using the Metropolis Monte Carlo algorithm at a temperature T = 300 K. The only interactions in this system occur through Lennard‐Jones dispersion forces and short‐range atom‐atom repulsion. The intent was to establish whether the chains were either rigidly extended or twisted via the thermal formation of gauche bonds and apply the results to understand observations made on two possible oleogelators: triacontane and stearic acid. Specifically, we aimed to understand if their observed crystalline monolayer thicknesses are due to gauche‐bond‐shortened hydrocarbon chains oriented perpendicular to the monolayer surface, or to fully extended rigid chains oriented at a tilt angle with respect to the surface. The results showed that crystals of hydrocarbon chains did not include significant gauche bonds, so that all molecules were rigidly extended, thus explaining the experimental data previously reported. Accordingly, TC and SA dimer molecules are packed in crystalline multilayers with tilt angles in relation to the methyl group plane. [ABSTRACT FROM AUTHOR]

Wood is a complex, multi‐component material with a variety of applications. The properties of wood are especially sensitive to its moisture content and comprehending wood–water interactions is thus paramount. Understanding of the moisture interactions of the wood polysaccharide components, cellulose microfibrils and hemicelluloses, is improving. However, the role of lignin remains less clear. In this work, X‐ray scattering measurements were carried out on delignified spruce undergoing a desorption‐adsorption cycle, and the results were compared to previous data from untreated wood. In addition, a molecular model of the cell wall nanostructure, including the main chemical components, was used to support the experimental results. Based on the small‐angle scattering, delignification affects the arrangement of cellulose microfibrils in the cell wall by increasing their packing distance. Wide‐angle scattering shows that delignification has no substantial effect on the cellulose crystal structure and how it changes with moisture. Both the scattering results and simulations suggest that lignin is a passive, rather than an active participant in the moisture response of microfibril bundles in wood cell walls. Small‐angle scattering from fully wet delignified wood reveals a contribution that can be assigned to aligned nanometer scale pores which close during drying.

This study combines molecular dynamics (MD) simulations with small angle x-ray scattering (SAXS) measurements to investigate the range of conformations that can be adopted by a pH/ionic strength (IS) sensitive protein and to quantify its distinct populations in solution. To explore how the conformational distribution of proteins may be modified in the environmental niches of biological media, we focus on the periplasmic ferric binding protein A (FbpA) from Haemophilus influenzae involved in the mechanism by which bacteria capture iron from higher organisms. We examine iron-binding/release mechanisms of FbpA in varying conditions simulating its biological environment. While we show that these changes fall within the detectable range for SAXS as evidenced by differences observed in the theoretical scattering patterns calculated from the crystal structure models of apo and holo forms, detection of conformational changes due to the point mutation D52A and changes in ionic strength (IS) from SAXS scattering profiles have been challenging. Here, to reach conclusions, statistical analyses with SAXS profiles and results from different techniques were combined in a complementary fashion. The SAXS data complemented by size exclusion chromatography point to multiple and/or alternative conformations at physiological IS, whereas they are well-explained by single crystallographic structures in low IS buffers. By fitting the SAXS data with unique conformations sampled by a series of MD simulations under conditions mimicking the buffers, we quantify the populations of the occupied substates. We also find that the D52A mutant that we predicted by coarse-grained computational modeling to allosterically control the iron binding site in FbpA, responds to the environmental changes in our experiments with conformational selection scenarios that differ from those of the wild type. [ABSTRACT FROM AUTHOR]

We present a sub-picosecond resolved investigation of the structural solvent reorganization and geminate recombination dynamics following 400 nm two-photon excitation and photodetachment of a valence p electron from the aqueous atomic solute, I−(aq). The measurements utilized time-resolved X-ray Absorption Near Edge Structure (TR-XANES) spectroscopy and X-ray Solution Scattering (TR-XSS) at the Linac Coherent Light Source x-ray free electron laser in a laser pump/x-ray probe experiment. The XANES measurements around the L1-edge of the generated nascent iodine atoms (I0) yield an average electron ejection distance from the iodine parent of 7.4 ± 1.5 Å with an excitation yield of about 1/3 of the 0.1M NaI aqueous solution. The kinetic traces of the XANES measurement are in agreement with a purely diffusion-driven geminate iodine–electron recombination model without the need for a long-lived (I0:e−) contact pair. Nonequilibrium classical molecular dynamics simulations indicate a delayed response of the caging H2O solvent shell and this is supported by the structural analysis of the XSS data: We identify a two-step process exhibiting a 0.1 ps delayed solvent shell reorganization time within the tight H-bond network and a 0.3 ps time constant for the mean iodine–oxygen distance changes. The results indicate that most of the reorganization can be explained classically by a transition from a hydrophilic cavity with a well-ordered first solvation shell (hydrogens pointing toward I−) to an expanded cavity around I0 with a more random orientation of the H2O molecules in a broadened first solvation shell. [ABSTRACT FROM AUTHOR]

The results of a combined experimental and computational investigation of the structural evolution of Au81Si19, Pd82Si18, and Pd77Cu6Si17 metallic glass forming liquids are presented. Electrostatically levitated metallic liquids are prepared, and synchrotron x-ray scattering studies are combined with embedded atom method molecular dynamics simulations to probe the distribution of relevant structural units. Metal–metalloid based metallic glass forming systems are an extremely important class of materials with varied glass forming ability and mechanical processibility. High quality experimental x-ray scattering data are in poor agreement with the data from the molecular dynamics simulations, demonstrating the need for improved interatomic potentials. The first peak in the x-ray static structure factor in Pd77Cu6Si17 displays evidence for a Curie–Weiss type behavior but also a peak in the effective Curie temperature. A proposed order parameter distinguishing glass forming ability, 1 / S T , q 1 − 1 , shows a peak in the effective Curie temperature near a crossover temperature established by the behavior of the viscosity, TA. [ABSTRACT FROM AUTHOR]

We have observed details of the internal motion and dissociation channels in photoexcited carbon disulfide (CS2) using time-resolved x-ray scattering (TRXS). Photoexcitation of gas-phase CS2 with a 200 nm laser pulse launches oscillatory bending and stretching motion, leading to dissociation of atomic sulfur in under a picosecond. During the first 300 fs following excitation, we observe significant changes in the vibrational frequency as well as some dissociation of the C–S bond, leading to atomic sulfur in the both 1D and 3P states. Beyond 1400 fs, the dissociation is consistent with primarily 3P atomic sulfur dissociation. This channel-resolved measurement of the dissociation time is based on our analysis of the time-windowed dissociation radial velocity distribution, which is measured using the temporal Fourier transform of the TRXS data aided by a Hough transform that extracts the slopes of linear features in an image. The relative strength of the two dissociation channels reflects both their branching ratio and differences in the spread of their dissociation times. Measuring the time-resolved dissociation radial velocity distribution aids the resolution of discrepancies between models for dissociation proposed by prior photoelectron spectroscopy work. [ABSTRACT FROM AUTHOR]

We present a formally exact and simulation-free approach for the normalization of X-ray Thomson scattering (XRTS) spectra based on the f-sum rule of the imaginary-time correlation function (ITCF). Our method works for any degree of collectivity, over a broad range of temperatures, and is applicable even in nonequilibrium situations. In addition to giving us model-free access to electronic correlations, this new approach opens up the intriguing possibility to extract a plethora of physical properties from the ITCF based on XRTS experiments. [ABSTRACT FROM AUTHOR]

Quantum fluctuations in low-dimensional systems and near quantum phase transitions have significant influences on material properties. Yet, it is difficult to experimentally gauge the strength and importance of quantum fluctuations. Here we provide a resonant inelastic x-ray scattering study of magnon excitations in Mott insulating cuprates. From the thin film of SrCuO2, single- and bi-magnon dispersions are derived. Using an effective Heisenberg Hamiltonian generated from the Hubbard model, we show that the single-magnon dispersion is only described satisfactorily when including significant quantum corrections stemming from magnon-magnon interactions. Comparative results on La2CuO4 indicate that quantum fluctuations are much stronger in SrCuO2 suggesting closer proximity to a magnetic quantum critical point. Monte Carlo calculations reveal that other magnetic orders may compete with the antiferromagnetic Néel order as the ground state. Our results indicate that SrCuO2—due to strong quantum fluctuations—is a unique starting point for the exploration of novel magnetic ground states. Magnetic excitations in infinite-layer cuprates have been intensively studied. Here the authors use resonant inelastic x-ray scattering and theoretical calculations to study magnons in thin films of SrCuO2, finding distinct magnon dispersion attributed to renormalization due to quantum fluctuations. [ABSTRACT FROM AUTHOR]

The synergistic utilization of low‐dimensional perovskites with 3D perovskite architectures represents a pervasive approach for fabrication of high‐performance and enduring perovskite solar cells (PSCs). In this work, four distinct ionic liquids (ILs) with distinct cations, were introduced on the surface of 3D perovskite to induce the formation of 1D perovskite.Starting with the analysis of 1D/3D heterojunction structures, the assessment foucsed on the binding energies in four ILs‐induced 1D/3D heterojunctions, comparing electron cloud density within 1D/3D structures, and calculating the formation energies associated with iodine and lead defects within these four 1D/3D perovskite structures via DFT calculations. Furthermore, the time‐resolved grazing‐incidence wide‐angle X‐ray scattering technique, as employed in this study, offers real‐time insights into the phase‐transition occurring during the process of ILs coating and the formation of 1D/3D heterojunctions. The well‐designed and optimized 1D perovskite layer significantly reduces the residual lead iodide (PbI2), modulates the work function of the perovskite, and passivates defects in the 3D perovskite, thereby reducing non‐radiative recombination and enhancing charge transport. With the assistance of 1D/3D hybrid films, we achieved an exceptional power conversion efficiency (PCE) of 24.75% in the generated PSCs with remarkable stability. [ABSTRACT FROM AUTHOR]

Femtosecond high-intensity laser pulses at intensities surpassing 1014 W/cm2 can generate a diverse range of functional surface nanostructures. Achieving precise control over the production of these functional structures necessitates a thorough understanding of the surface morphology dynamics with nanometer-scale spatial resolution and picosecond-scale temporal resolution. In this study, we show that single XFEL pulses can elucidate structural changes on surfaces induced by laser-generated plasmas using grazing-incidence small-angle X-ray scattering (GISAXS). Using aluminium-coated multilayer samples we distinguish between sub-picosecond (ps) surface morphology dynamics and subsequent multi-ps subsurface density dynamics with nanometer-depth sensitivity. The observed subsurface density dynamics serve to validate advanced simulation models representing matter under extreme conditions. Our findings promise to open new avenues for laser material-nanoprocessing and high-energy-density science. [ABSTRACT FROM AUTHOR]

This work presents the design and construction of an automated industrial injection moulding apparatus that can be used with a typical multi-user beamline such as the NCD-SWEET small-angle X-ray scattering at the ALBA Synchrotron Light Source. This apparatus is focused on developing an understanding of how the mould temperature and the injection temperature and pressure affect both the orientation and morphology of the semi-crystalline polymer used to fabricate the injected parts. The system design follows current industrial practice and enables the collection of time-resolved X-ray scattering data at several points within the mould cavity, so we can understand the 4D morphology. In this work we show the effectiveness of the equipment using some results from the injection moulding of a random copolymer of polypropylene and that it can be used with a more demanding material such as polyhydroxybutyrate. This can be seen as the first step toward a multiscale digital twin for injection moulding. [ABSTRACT FROM AUTHOR]

Operando studies using high‐energy X‐rays from synchrotron sources are essential for unraveling the complex material transformation that electrocatalysts undergo under operating conditions. This article explores key considerations to perform these experiments and the insights gained from such studies on nanostructured electrocatalysts. Critical factors include optimizing electrochemical performance while obtaining high‐quality X‐ray signals, which often require compromises. The electrochemical operando cell design is crucial, and several different cells are discussed here. Working electrode geometries parallel to the X‐ray beam, probed with a microfocused beam, are emerging as promising solutions for realistic electrochemical performance in operando cells. Careful attention must also be paid to the electrochemical measuring conditions, electrode loading, and beam damage to ensure reliable experiments. When carefully performed and by combining multiple characterization techniques, operando studies with high‐energy X‐rays offer the unique possibility to fully understand the structure of the active electrocatalyst. [ABSTRACT FROM AUTHOR]

Purpose. Fast kV-switching (FKS) and dual-layer flat-panel detector (DL-FPD) technologies have been actively studied as promising dual-energy spectral imaging solutions for FPD-based cone-beam computed tomography (CT). However, cone-beam CT (CBCT) spectral imaging is known to face challenges in obtaining accurate and robust material discrimination performance. That is because the energy separation by either FKS or DL-FPD, alone, is still limited, along with apparently unpaired signal levels in the effective low- and high-energy projections in real applications, not to mention the x-ray scatter in cone-beam scan which will make the material decomposition almost impossible if no correction is applied. To further improve CBCT spectral imaging capability, this work aims to promote a source-detector joint multi-energy spectral imaging solution which takes advantages of both FKS and DL-FPD, and to conduct a feasibility study on the first tabletop CBCT system with the joint spectral imaging capability developed. Methods. For CBCT, development of multi-energy spectral imaging can be jointly realized by using an x-ray source with a generator whose kilo-voltages can alternate in tens of Hertz (i.e. FKS), and a DL-FPD whose top- and bottom-layer projections corresponds to different effective energy levels. Thanks to the complimentary characteristics inherent in FKS and DL-FPD, the overall energy separation will be significantly better when compared with FKS or DL-FPD alone, and the x-ray photon detection efficiency will be also improved when compared with FKS alone. In this work, a noise performance analysis using the Cramér–Rao lower bound (CRLB) method is conducted. The CRLB for basis material after a projection-domain material decomposition is derived, followed by a set of numerical calculations of CRLBs, for the FKS, the DL-FPD and the joint solution, respectively. To compensate for the slightly angular mismatch between low- and high- projections in FKS, a dual-domain projection completion scheme is implemented. Afterwards material decomposition from the complete projection data is carried out by using the maximum-likelihood method, followed by reconstruction of basis material and virtual monochromatic images (VMI). In this work, the first FKS and DL-FPD jointly enabled multi-energy tabletop CBCT system, to the best of our knowledge, has been developed in our laboratory. To evaluate its spectral imaging performance, a set of physics experiments are conducted, where the multi-energy and head phantoms are scanned using the 80/105/130 kVp switching pairs and projection data are collected using a prototype DL-FPD, whose both top and bottom layer of panels are composed of 550 μ m of cesium iodine (CsI) scintillators with no intermediate metal filter in-between. Results. The numerical simulations show that the joint spectral imaging solution can lead to a significant improvement in energy separation and lower noise levels in most of material decomposition cases. The physics experiments confirmed the feasibility and superiority of the joint spectral imaging, whose CNRs in the selected regions of interest of the multi-energy phantom were boosted by an average improvement of 21.9%, 20.4% for water basis images and 32.8%, 62.8% for iodine images when compared with that of the FKS and DL-FPD, respectively. For the head phantom case, the joint spectral imaging can effectively reduce the streaking artifacts as well, and the standard deviation in the selected regions of interest are reduced by an average decrement of 19.5% and 8.1% for VMI when compared with that of the FKS and DL-FPD, respectively. Conclusions. A feasibility study of the joint spectral imaging solution for CBCT by utilizing both the FKS and DL-FPD was conducted, with the first tabletop CBCT system having such a capability being developed, which exhibits improved CNR and is more effective in avoiding streaking artifacts as expected. [ABSTRACT FROM AUTHOR]

Sub‐monolayer networks of the electron‐transporting semiconducting polymer poly([N,N'‐bis(2‐octyldodecyl)‐naphthalene‐1,4,5,8‐bis(dicarboximide)−2,6‐diyl]‐alt‐5,5′‐(2,2′‐bithiophene)) (P(NDI2OD‐T2)) are realized through judicious choice of spin‐coating solvent and control of solution concentration. These sub‐monolayer networks provide a platform to study the effects of surface coverage, network connectivity, and orientational order on charge transport. It is found that charge transport through semiconducting polymer networks depends not only on the coverage/concentration of the material but also on the nature of the conduction paths themselves. Down to 40% surface coverage, current measured in a field‐effect architecture decreases in line with the decrease in surface coverage, but drops precipitously below a surface coverage of 40%. Below 40% surface coverage, there is a marked decrease in network connectivity (quantified through the branching point density) and a decrease in orientational order. Furthermore, an increase in the density of dangling branches (dead ends) is also seen with decreasing surface coverage. Additional supporting data in the form of grazing incidence wide‐angle X‐ray scattering (GIWAXS), optical spectroscopy, and charge modulation spectroscopy are presented, which help to establish that long‐range interconnectivity rather than local morphology dominates charge transport in P(NDI2OD‐T2) sub‐monolayers as well as thin films. [ABSTRACT FROM AUTHOR]