Operando Neutron Imaging.

In the past, neutron imaging has been the little brother of advanced neutron spectroscopy techniques due to its apparent simplicity. However, this simplicity allows the studying of complex chemical and electrochemical processes and related devices even under harsh reaction conditions such as high pressure, high temperature, corrosive and/or air sensitive environments. We review a number of highly relevant case studies as archetypal examples of modern energy technology; that is heat storage, power-to-X, batteries, fuel cells, and catalysis. The promising results trigger the further development of neutron imaging towards a chemical imaging method.

Phase-contrast neutron imaging compared with wave propagation and McStas simulations.

Propagation-based phase contrast, for example in the form of edge enhancement contrast, is well established within X-ray imaging but is not widely used in neutron imaging. This technique can help increase the contrast of low-attenuation samples but may confuse quantitative absorption measurements. Therefore, it is important to understand the experimental parameters that cause and amplify or dampen this effect in order to optimize future experiments properly. Two simulation approaches have been investigated, a wave-based simulation and a particle-based simulation conducted in McStas [Willendrup & Lefmann (2020). J. Neutron Res. 22, 1-16], and they are compared with experimental data. The experiment was done on a sample of metal foils with weakly and strongly neutron absorbing layers, which were measured while varying the rotation angle and propagation distance from the sample. The experimental data show multiple signals: attenuation, phase contrast and reflection. The wave model reproduces the sample attenuation and the phase peaks but it does not reproduce the behavior of these peaks as a function of rotation angle. The McStas simulation agrees better with the experimental data, as it reproduces attenuation, phase peaks and reflection, as well as the change in these signals as a function of rotation angle and distance. This suggests that the McStas simulation approach, where the particle description of the neutron facilitates the incorporation of multiple effects, is the most convenient way of modeling edge enhancement in neutron imaging.

Who made the noise? Systematic approach for the assessment of neutron imaging scintillators.

We propose a method to analyze the characteristics of scintillator screens for neutron imaging applications. Using calculations based on the theory of cascaded linear steps as well as experimental measurements, we compared the characteristics of different lithium- and gadolinium-based scintillator screens. Our results show that, despite their much lower light output, gadolinium-based scintillators outperform lithium-based scintillators in terms of noise characteristics for a variety of imaging setups. However, the relative performance of scintillator screens is highly dependent on the other setup characteristics such as the beam spectrum, field of view, used optical lens and size of the camera sensor. Consequently, the selection of the best scintillator screen - as well as the scintillator characteristics assessment in new developments - requires a systematic consideration of all these elements, as enabled by the framework presented here.

Chloride-induced corrosion of steel in concrete-insights from bimodal neutron and X-ray microtomography combined with ex-situ microscopy.

The steel-concrete interface (SCI) is known to play a major role in corrosion of steel in concrete, but a fundamental understanding is still lacking. One reason is that concrete's opacity complicates the study of internal processes. Here, we report on the application of bimodal X-ray and neutron microtomography as in-situ imaging techniques to elucidate the mechanism of steel corrosion in concrete. The study demonstrates that the segmentation of the specimen components of relevance-steel, cementitious matrix, aggregates, voids, corrosion products-obtained through bimodal X-ray and neutron imaging is more reliable than that based on the results of each of the two techniques separately. Further, we suggest the combination of tomographic in-situ imaging with ex-situ SEM analysis of targeted sections, selected based on the segmented tomograms. These in-situ and ex-situ characterization techniques were applied to study localized corrosion in a very early stage under laboratory chloride-exposure conditions, using reinforced concrete cores retrieved from a concrete bridge. Several interesting observations were made. First, the acquired images revealed the formation of several corrosion sites close to each other. Second, the morphology of the corrosion pits was relatively shallow. Finally, only about half of the total 31 corrosion initiation spots were in close proximity to interfacial macroscopic air voids, and > 90% of the more than 160 interfacial macroscopic air voids were free from corrosion. The findings have implications for the mechanistic understanding of corrosion of steel in concrete and suggest that multimodal in-situ imaging is a valuable technique for further related studies. Supplementary Information: The online version contains supplementary material available at 10.1617/s11527-024-02337-7.

Neutron radiography of an anisotropic drainage flow.

Liquid drainage through foam is dominated by gravity, capillary, and viscous forces. The liquid is conducted by an isotropic network of Plateau borders; however, imposed stress changes the alignment of the foam's structural elements. Previous numerical simulations predicted that a vertical drainage flow will be deflected horizontally if the foam is sheared. We investigated this phenomenon by measuring the distribution of the liquid fraction within a foam formed in a flat rectangular cell. The foam was subjected to shear stress under a forced liquid supply from the top of the cell. Neutron radiographies of unchanged and sheared foam were analyzed to extract measurements of the liquid fraction. Deflections in the distribution of the drainage liquid were detected and found to be positively correlated with increasing foam shear.

LiOH Decomposition by NiO/ZrO2 in Li-Air Battery: Chemical Imaging with Operando Synchrotron Diffraction and Correlative Neutron/X-Ray Computed-Tomography Analysis.

Li-air batteries attract significant attention due to their highest theoretical energy density among all existing energy storage technologies. Currently, challenges related to extending lifetime and long-term stability limit their practical application. To overcome these issues and enhance the total capacity of Li-air batteries, this study introduces an innovative approach with NiO/ZrO2 catalysts. Operando advanced chemical imaging with micrometer spatial resolution unveils that NiO/ZrO2 catalysts substantially change the kinetics of crystalline lithium hydroxide (LiOH) formation and facilitate its rapid decomposition with heterogeneous distribution. Moreover, ex situ combined neutron and X-ray computed tomography (CT) analysis, provide evidence of distinct lithium phases homogeneously distributed in the presence of NiO/ZrO2 . These findings underscore the material's superior physico-chemical and electronic properties, with more efficient oxygen diffusion and indications of lower obstruction to its active sites, avoiding clogging in the active electrode, a common cause of capacity loss. Electrochemical tests conducted at high current density demonstrated a significant kinetic enhancement of the oxygen reduction and evolution reactions, resulting in improved charge and discharge processes with low overpotential. This pioneering approach using NiO/ZrO2 catalysts represents a step toward on developing the full potential of Li-air batteries as high-energy-density energy storage systems.

Neutron radiography of liquid foam structure near a vertical wall.

At a solid boundary, the structural formation of bubbles is different from that in the bulk of a liquid foam. The presence of a solid boundary imposes additional constraints, resulting in a crystalline arrangement of the bubbles. For dry and monodisperse foam, the Kelvin and Fejes-Tóth structure is expected in the vicinity of the wall, while a random ordering should occur in the bulk. In this study, we investigate the transition from a crystalline to a random structure near a vertical wall located in the middle of a flat foam cell. The corresponding layering of the liquid was quantified by measuring the distribution of liquid fraction within the cell using neutron radiography. The amplitude of the liquid fraction distribution and its decay with distance from the solid boundary were correlated with the foam bubble size and polydispersity. Furthermore, by applying forced drainage, we measured the corresponding permeability and wetting front velocity near the vertical wall. We found that the crystalline sorting reduces the permeability and wetting front velocity compared to a randomly packed foam.

Hydrogen Transport and Evolution in Ni-MH Batteries by Neutron Imaging.

Efficiency losses due to side reactions are one of the main challenges in battery development. Despite providing valuable insights, the results of standard analysis on the individual components cannot be simply extrapolated to the full operating system. Therefore, non-destructive, and high resolution approaches that allow the investigation of the full system are desired. Herein, we combined neutron radiography and tomography with electrical monitoring of the state of charge of commercial Ni-mischmetal hydride batteries, to track the exchange and transport of hydrogen under operating conditions. This non-destructive approach allowed both the quantification of the hydrogen distribution in the electrodes in 4D, and the distinction between the electrochemically exchanged hydrogen and the hydrogen gas pressure generated by side reactions, as a function of the applied potential and current. One of the most counter-intuitive observation is that the generation of hydrogen gas during discharge depends on the charging state of the battery. The results presented provide critical new insights in the mechanisms governing the electrochemical processes during Nimischmetal hydride battery operation, and also pave the way for the extrapolation of this approach to the investigation of state-of-the-art Li-ions batteries.

From superhydrophilicity to superhydrophobicity: high-resolution neutron imaging and modeling of water imbibition through porous surfaces treated with engineered nano-coatings.

This paper reports on a superhydrophilic to superhydrophobic transformation of TiO2 nanoparticles doped zinc phosphate coating systems when a hydrophobic agent is applied. The objective of the reported research was to demonstrate the feasibility of a neutron imaging technique for evaluating the performance of the proposed nano-coating system and reveal the differences in water ingress mechanisms which are specific to plain, superhydrophilic, overhydrophobic, and superhydrophobic specimens. The engineered nano-coatings were designed to improve hydrophobic response with inducing the required roughness pattern and introducing the photocatalytic performance. The effectiveness of the coatings was assessed using high-resolution neutron imaging (HR-NI), SEM, CLSM, and XRD techniques. High-resolution neutron imaging revealed that the superhydrophobic coating effectively prevents water ingress into the porous ceramic substrate, whereas water imbibition was observed for superhydrophilic coating during the test duration. The moisture transport kinetics was modeled based on the Richards equation for plain ceramic and superhydrophilic specimens using obtained penetration depth values from HR-NI. SEM, CLSM, and XRD studies confirm the desired TiO2-doped zinc phosphate coatings with increased surface roughness, photocatalytic reactivity, and chemical bonding. The research results demonstrated that a two-layer superhydrophobic system is capable of creating effective water barriers on the surface with contact angles of 153°, which remained effective even after surface damage.

4D nanoimaging of early age cement hydration.

Despite a century of research, our understanding of cement dissolution and precipitation processes at early ages is very limited. This is due to the lack of methods that can image these processes with enough spatial resolution, contrast and field of view. Here, we adapt near-field ptychographic nanotomography to in situ visualise the hydration of commercial Portland cement in a record-thick capillary. At 19 h, porous C-S-H gel shell, thickness of 500 nm, covers every alite grain enclosing a water gap. The spatial dissolution rate of small alite grains in the acceleration period, ∼100 nm/h, is approximately four times faster than that of large alite grains in the deceleration stage, ∼25 nm/h. Etch-pit development has also been mapped out. This work is complemented by laboratory and synchrotron microtomographies, allowing to measure the particle size distributions with time. 4D nanoimaging will allow mechanistically study dissolution-precipitation processes including the roles of accelerators and superplasticizers.

Using micro-XRF to characterize chloride ingress through cold joints in 3D printed concrete.

Digital fabrication methods with concrete have been rapidly developing, with many problems related to component production and material control being solved in recent years. These processes produce inherently layered cementitious components that are anisotropic, and in many cases, produces a weak interface between layers, which are generally referred to as cold joints. While material strength at these interfaces has been well studied in recent years, durability has received less attention, even though cold joints can function as channels for aggressive agents, such as chlorides. This work presents a method using micro-X-ray fluorescence (µXRF) to image chloride ingress into layer interfaces of 3D printed fine-grained concrete specimens produced with varying layer deposition time intervals, and also compares it to neutron imaging of moisture uptake. The results show that cold joints formed after a 1 day time interval are highly susceptible to chloride ingress, and that curing conditions play a major role in how quickly interfacial transport can take place. The µXRF method is also shown to be useful for study of transport of chlorides in cold joints, due to its spatial resolution and direct analysis of an aggressive species of interest.

Absorption of pressurized methane in normal and supercooled p-xylene revealed via high-resolution neutron imaging.

Supercooling of liquids leads to peculiarities which are scarcely studied under high-pressure conditions. Here, we report the surface tension, solubility, diffusivity, and partial molar volume for normal and supercooled liquid solutions of methane with p-xylene. Liquid bodies of perdeuterated p-xylene (p-C8D10), and, for comparison, o-xylene (o-C8D10), were exposed to pressurized methane (CH4, up to 101 bar) at temperatures ranging 7.0-30.0 °C and observed at high spatial resolution (pixel size 20.3 µm) using a non-tactile neutron imaging method. Supercooling led to the increase of diffusivity and partial molar volume of methane. Solubility and surface tension were insensitive to supercooling, the latter substantially depended on methane pressure. Overall, neutron imaging enabled to reveal and quantify multiple phenomena occurring in supercooled liquid p-xylene solutions of methane under pressures relevant to the freeze-out in the production of liquefied natural gas.

Combinatorial neutron imaging methods for hydrogenation catalysts.

Heterogeneous catalysts are materials with a complex structure at the atomic to mesoscopic scale, which depends on a variety of empirical parameters applied during preparation and processing. Although model systems clarified the general physical and chemical phenomena relevant to catalysis, such as hydrogen spillover, a rational design of heterogeneous catalysts is impeded by the sheer number of parameters. Combinatorial methods and high-throughput techniques have the potential of accelerating the development of optimal catalysts. We describe here a combinatorial approach based on hydrogen adsorption/absorption and hydrogen-deuterium exchange quantified by neutron imaging. The method coined CONI is capable of measuring more than 50 samples simultaneously. As a proof of concept, we study Pt catalyzed WO3 as an archetypal spillover system, and a Ni-catalyst supported on Al2O3 and SiO2. CONI is ideally suited to distinguish between irreversible surface adsorption and reversible bulk absorption, providing quantitative information. Concretely, CONI yields the number of reversibly adsorbed/absorbed hydrogen atoms in and on a great number of various catalysts in a single experiment.

Highly Concentrated, Zwitterionic Ligand-Capped Mn2+:CsPb(Br x Cl1-x )3 Nanocrystals as Bright Scintillators for Fast Neutron Imaging.

Fast neutron imaging is a nondestructive technique for large-scale objects such as nuclear fuel rods. However, present detectors are based on conventional phosphors (typically microcrystalline ZnS:Cu) that have intrinsic drawbacks, including light scattering, γ-ray sensitivity, and afterglow. Fast neutron imaging with colloidal nanocrystals (NCs) was demonstrated to eliminate light scattering. While lead halide perovskite (LHP) FAPbBr3 NCs emitting brightly showed poor spatial resolution due to reabsorption, the Mn2+-doped CsPb(BrCl)3 NCs with oleyl ligands had higher resolution because of large apparent Stokes shift but insufficient concentration for high light yield. In this work, we demonstrate a NC scintillator that features simultaneously high quantum yields, high concentrations, and a large apparent Stokes shift. In particular, we use long-chain zwitterionic ligand capping in the synthesis of Mn2+-doped CsPb(BrCl)3 NCs that allows for attaining very high concentrations (>100 mg/mL) of colloids. The emissive behavior of these ASC18-capped NCs was carefully controlled by compositional tuning that permitted us to select for high quantum yields (>50%) coinciding with Mn-dominated emission for minimal self-absorption. These tailored Mn2+:CsPb(BrCl)3 NCs demonstrated over 8 times brighter light yield than their oleyl-capped variants under fast neutron irradiation, which is competitive with that of near-unity FAPbBr3 NCs, while essentially eliminating self-absorption. Because of their rare combination of concentrations above 100 mg/mL and high quantum yields, along with minimal self-absorption for good spatial resolution, Mn2+:CsPb(BrCl)3 NCs have the potential to displace ZnS:Cu as the leading scintillator for fast neutron imaging.

Luminescent Lead Halide Ionic Liquids for High-Spatial-Resolution Fast Neutron Imaging.

The fast neutron imaging technique with recoil proton detection harbors significant potential for imaging of thick, large-scale objects containing high-Z elements. However, the challenge to find efficient fast neutron scintillators with high spatial resolution is ongoing. The list of requirements for such scintillators is long and demanding: a proton-rich, scattering-free material combining high light yield with the absence of light reabsorption. To meet these challenges, we look for a suitable material among a rising class of 0D organic-inorganic Pb(II) halide hybrids. The use of large organic cations, e.g., trihexyltetradecylphosphonium, results in room-temperature ionic liquids that combine highly Stokes-shifted (up to 1.7 eV), reabsorption-free, and efficient emission (photoluminescence quantum yield up to 60%) from molecularly small and dense (PbX2 molar fraction up to 0.33) emitting centers. We investigate the optical properties of the resulting ionic liquids and showcase their utility as fast neutron imaging scintillators. Concomitantly with good light yield, such fast-neutron scintillators exhibit both higher spatial resolution and lower γ-ray sensitivity compared with commercial ZnS:Cu-based screens.

Neutron Imaging of Paramagnetic Ions: Electrosorption by Carbon Aerogels and Macroscopic Magnetic Forces.

The electrosorption of Gd3+ ions from an aqueous 70 mM Gd(NO3)3 solution in monolithic carbon aerogel electrodes was recorded by dynamic neutron imaging. The aerogels have a bimodal pore size distribution consisting of macropores and mesopores centered at 115 and 15 nm, respectively. After the uptake of Gd3+ ions by the negatively charged surface of the porous structure, an inhomogeneous magnetic field was applied to the system of discharging electrodes. This led to a convective flow and confinement of Gd(NO3)3 solution in the magnetic field gradient. Thus, a way to desalt and capture paramagnetic ions from an initially homogeneous solution is established.

NEURAP-A Dedicated Neutron-Imaging Facility for Highly Radioactive Samples.

NEURAP is a dedicated set-up at the Swiss neutron spallation source (SINQ) at the Paul Scherrer Institut (PSI), optionally implemented as a special configuration of the neutron-imaging station NEUTRA. It is one of very few instrumentations available worldwide enabling neutron-imaging of highly radioactive samples to be performed routinely, with special precautions and following a specific procedure. Since the relevant objects are strong γ-sources, dedicated techniques are needed to handle the samples and to perform neutron-imaging despite the radiation background. Dysprosium (Dy)-loaded imaging plates, effectively made sensitive to neutrons only, are employed. Neutrons are captured by Dy during neutron irradiation. Then the imaging plate is erased removing gamma detections. A subsequent relatively long self-exposure by the radiation from the intrinsic neutron-activated Dy within the imaging plate yields the neutron-only radiograph that is finally read out. During more than 20 years of NEURAP operation, images have been obtained for two major applications: (a) highly radioactive SINQ target components were investigated after long-term operation life; and (b) spent fuel rods and their cladding from Swiss nuclear power plants were characterized. Quantitative analysis of the image data demonstrated the accumulation of spallation products in the lead filled "Cannelloni" Zircaloy tubes of the SINQ target and the aggregation of hydrogen at specific sites in used fuel pins of power plants and their cladding, respectively. These results continue to help understanding material degradation and optimizing the operational regimes, which might lead to extending the safe lifetimes of these components.

Hydrogen in methanol catalysts by neutron imaging.

Although of pivotal importance in heterogeneous hydrogenation reactions, the amount of hydrogen on catalysts during reactions is seldom known. We demonstrate the use of neutron imaging to follow and quantify hydrogen containing species in Cu/ZnO catalysts operando during methanol synthesis. The steady-state measurements reveal that the amount of hydrogen containing intermediates is related to the reaction yields of CO and methanol, as expected from simple considerations of the likely reaction mechanism. The time-resolved measurements indicate that these intermediates, despite indispensable within the course of the reaction, slow down the overall reaction steps. Hydrogen-deuterium exchange experiments indicate that hydrogen reduction of Cu/ZnO nano-composites modifies the catalyst in such a way that at operating temperatures, hydrogen is dynamically absorbed in the ZnO-nanoparticles. This explains the extraordinary good catalysis of copper if supported on ZnO by its ability to act as a hydrogen reservoir supplying hydrogen to the surface covered by CO2, intermediates, and products during catalysis.

One-pot neutron imaging of surface phenomena, swelling and diffusion during methane absorption in ethanol and n-decane under high pressure.

We report a powerful method for capturing the time-resolved concentration profiles, liquid swelling and surface phenomena during the absorption of methane (CH4) in still liquid ethanol (C2D6O) and n-decane (n-C10D22) and at high spatial resolution (pixel size 21.07 µm) using neutron imaging. Absorption of supercritical methane was followed at two temperatures and two pressures of methane, namely 7.0, 37.8 °C and 80, 120 bar. Fick's second law, which was used in the liquid-fixed coordinates, enabled for an adequate parameterization of the observed concentration profiles and liquid levels using simple analytical expressions. For both studied liquids, anomalously slow diffusion was observed in the initial stage of the absorption experiment. This was ascribed to the slow formation of the surface excess on the interface, time constant ranged 130-275 s. The axial symmetry of the cell allowed for the tomographic reconstructions of the profiles of the menisci. Based on these profiles, contact angle and surface tension were evaluated using the Young-Laplace equation. Overall, neutron imaging made it possible to capture time- and space-resolved information from which the methane concentration, liquid level and meniscus shape under high-pressure conditions inside a cylindrical titanium vessel were quantitatively derived. Multiple characteristics of ethanol, a methane hydrate inhibitor, and n-decane, a model constituent of crude oil, were thus measured for the first time under industrially relevant conditions in a one-pot experiment.

Sample container for high-resolution neutron imaging of spent nuclear fuel cladding sections.

In this work, for the first time, high-resolution neutron imaging (true spatial resolution of 13 µm) is used for irradiated nuclear fuel cladding, applying an adapted procedure for transfer, handling, and measurements of highly radioactive samples in combination with the neutron microscope detector at Paul Scherrer Institut. A sample container referred to as an active box for high-resolution neutron imaging of highly active spent nuclear fuel cladding sections was developed. Sections of unirradiated and irradiated cladding of duplex type, having a liner, with hydrogen average concentrations of 420 wppm and 450 wppm were investigated using this device. The irradiated cladding originated from a fuel rod operated for five cycles in a Swiss pressurized water reactor. The irradiated cladding sample was measured inside the active box. Long circumferential hydride accumulations were revealed together with notable hydride precipitation at the liner-substrate interface. Measurements of the unirradiated cladding in air and inside the active box delivered consistent results, confirming the applicability of the developed device for high-resolution neutron imaging.