High Energy Resolution Research Articles

Structural, spectroscopi c and laser properties of transparent Tm:YScO3 ceramic based on gas-phase synthesized nanoparticles

Owing to the combination of good thermo-optical properties and inhomogeneously broadened fluorescence spectra suitable for ultrashort laser pulse generation, rare-earth doped solid solutions of sesquioxides (Y,Lu,Sc)2O3 have attracted considerable interest in recent years. In this study, compositionally disordered Tm3+-doped YScO3 transparent ceramic was fabricated using solid-state vacuum sintering of nanopowder produced using laser ablation of solid target in air flow. The as-synthesized powder consisted of weakly aggregated spherical particles having 20 nm diameter and a mostly monoclinic (space group C2/m) crystal structure, whose symmetry was transformed into cubic (space group Ia-3) by calcination at 1050 °C. From high resolution transmission electron microscopy (HRTEM) and energy dispersive X-ray analysis (EDX), we observed a homogeneous distribution of components both throughout individual nanoparticles and 100-nm-thick ceramic foil resulting in high structural and optical quality of the obtained samples. The sintered ceramic featured an optical transmission of 77% at 600 nm and above 81% near 2 μm, an average grain size of 24.2 μm and a content of scattering centers of 26.1 ppm. The absorption spectra at several temperatures, from 93 K to 293 K, were measured and the corresponding absorption coefficients were obtained by Lambert-Beer formula in the range from 600 nm to 900 nm and from 1400 nm to 2100 nm. In particular, the room temperature absorption cross section at 794 nm and 1634 nm were determined to be σabs = 4.25 × 10−21 cm2 and σabs = 5.01 × 10−21 cm2 respectively. Concerning the emission cross section it was calculated by Fuchtbauer-Ladenburg equation starting from the fluorescence spectrum acquired at the laser work temperature: at 1951 nm and 2106 nm corresponding to the main two emission peaks belonging the curve, it was found σem = 9.2 × 10−21 cm2 and σem = 4.9 × 10−21 cm2, respectively. Finally, it was tested the laser behavior of the ceramic: pumped at 793 nm in quasi-CW mode it delivered 1.27 W of output power with a slope efficiency of 10.33% at 2081 nm. The tunability curve spans from 1942 nm to 2110 nm (i.e. 168 nm).

A Monte Carlo simulation study for designing collimators for a CZT-based spent nuclear fuel characterization system

As an attempt to develop a spent nuclear fuel characterization system that can acquire both high-resolution gamma-ray energy spectrum and neutron flux simultaneously at multiple positions around the spent nuclear fuel assembly and provide more information compared to conventional equipment, simulation study was conducted to design a collimator around a gamma-ray detector to obtain high-resolution gamma-ray spectra in a high-flux gamma-ray environment. The ORIGEN depletion code was used to evaluate the source terms of spent nuclear fuel, and MCNP 6.2, the Monte Carlo simulation code, was used to simulate the detector response. Considering the realistic operating conditions of Korea's pressurized light water reactor, the source term for the ACE7 17×17 nuclear fuel assembly was derived under the conditions of initial enrichment ranging from 3 to 5%, burnup ranging from 30 to 60 GWd/MTU, and maximum cooling time of 30 years. MCNP 6.2, the Monte Carlo simulation code, was used to design a spent nuclear fuel characterization system using a CZT detector as a gamma-ray detector to obtain a high-resolution gamma-ray energy spectrum. In particular, the research focused on designing collimators to be used in high-flux radiation environments, such as spent nuclear fuel inspection, with CZT detectors. A simulation model of the CZT detector to be installed internally was made and the validity of the detector simulation model was confirmed by comparing simulation results with the measurement experiment results. Finally, the response of the CZT detector was calculated by changing various setting parameters of the collimator. By comparing the calculated detector response with the design standard count rate, the design of a collimator that can utilize the CZT detector in a spent nuclear fuel inspection environment was derived.

Gauging Iron-Sulfur Cubane Reactivity from Covalency: Trends with Oxidation State.

We investigated room-temperature metal and ligand K-edge X-ray absorption (XAS) spectra of a complete redox series of cubane-type iron-sulfur clusters. The Fe K-edge position provides a qualitative but convenient alternative to the traditional spectroscopic descriptors used to identify oxidation states in these systems, which we demonstrate by providing a calibration curve based on two analytic methods. Furthermore, high energy resolution fluorescence detected XAS (HERFD-XAS) at the S K-edge was used to measure Fe-S bond covalencies and record their variation with the average valence of the Fe atoms. While the Fe-S(thiolate) covalency evolves linearly, gaining 11 ± 0.4% per bond and hole, the Fe-S(μ3) covalency evolves asystematically, reflecting changes in the magnetic exchange mechanism. A strong discontinuity manifested for superoxidation to the all-ferric state, distinguishing its electronic structure and its potential (bio)chemical role from those of its redox congeners. We highlight the functional implications of these trends for the reactivity of iron-sulfur cubanes.

Energy spectra of energetic neutral hydrogen backscattered and sputtered from the lunar regolith by the solar wind

Context. The solar wind impinging on the lunar surface results in the emission of energetic neutral atoms. This particle population is one of the sources of the lunar exosphere. Aims. We present a semi-empirical model to describe the energy spectra of the neutral emitted atoms. Methods. We used data from the Advanced Small Analyzer for Neutrals (ASAN) on board the Yutu-2 rover of the Chang’E-4 mission to calculate high-resolution average energy spectra of the energetic neutral hydrogen flux from the surface. We then constructed a semi-empirical model to describe these spectra. Results. Excellent agreement between the model and the observed energetic neutral hydrogen data was achieved. The model is also suitable for describing heavier neutral species emitted from the surface. Conclusions. A semi-analytical model describing the energy spectrum of energetic neutral atoms emitted from the lunar surface has been developed and validated by data obtained from the lunar surface.

Comparison between conventional Si and new generation of SiC detector for high proton energy spectrometry

A SiC Schottky diode and a Si surface barrier detector have been compared during Rutherford backscattering spectrometry (RBS) using 2–3 MeV proton beams. Both detectors are suited to detect high energetic ions with high-energy resolution for spectroscopic analysis. The correlations between the detector parameters and the surface passivating layers, ion energy and current dependence, ion penetration depth, detection efficiency and energy resolution, are outlined. Comparative RBS analysis performed using SiC and Si detectors has been investigated to highlight the advantages and disadvantages of the use of SiC with respect to the traditional Si junction detector. RBS spectrometry has been carried out using projectiles of proton incident on different targets to analyse their composition and thickness by the detection of the backscattered ions revealed by Si and SiC detectors.

Unveiling diverse coordination-defined electronic structures of reconstructed anatase TiO2(001)-(1 × 4) surface

Transition metal oxides (TMOs) exhibit fascinating physicochemical properties, which originate from the diverse coordination structures between the transition metal and oxygen atoms. Accurate determination of such structure-property relationships of TMOs requires to correlate structural and electronic properties by capturing the global parameters with high resolution in energy, real, and momentum spaces, but it is still challenging. Herein, we report the determination of characteristic electronic structures from diverse coordination environments on the prototypical anatase-TiO2(001) with (1 × 4) reconstruction, using high-resolution angle-resolved photoemission spectroscopy and scanning tunneling microscopy/atomic force microscopy, in combination with density functional theory calculation. We unveil that the shifted positions of O 2s and 2p levels and the gap-state Ti 3p levels can sensitively characterize the O and Ti coordination environments in the (1 × 4) reconstructed surface, which show distinguishable features from those in bulk. Our findings provide a paradigm to interrogate the intricate reconstruction-relevant properties in many other TMO surfaces.

Clickable X-ray Nanoprobes for Nanoscopic Bioimaging of Cellular Structures.

Synchrotron-based X-ray microscopy (XRM) has garnered widespread attention from researchers due to its high spatial resolution and excellent energy (element) resolution. Existing molecular probes suitable for XRM include immune probes and genetic labeling probes, enabling the precise imaging of various biological targets within cells. However, immune labeling techniques are prone to cross-interference between antigens and antibodies. Genetic labeling technologies have limited systems that allow express markers independently, and moreover, genetically encoded labels based on catalytic polymerization lack a fixed morphology. When applied to cell imaging, this can result in reduced localization accuracy due to the diffusion of labels within the cells. Therefore, both techniques face challenges in simultaneously labeling multiple biotargets within cells and achieving high-precision imaging. In this work, we applied the click reaction and developed a third category of imaging probes suitable for XRM, termed clickable X-ray nanoprobes (Click-XRN). Click-XRN consists of two components: an X-ray-sensitive multicolor imaging module and a particle-size-controllable morphology module. Efficient identification of intra- and extracellular biotargets is achieved through click reactions between the probe and biomolecules. Click-XRN possesses a controllable particle size, and its loading of various metal ions provides distinctive signals for imaging under XRM. Based on this, we optimized the imaging energy of Click-XRN with different particle sizes, enabling single-color and two-color imaging of the cell membrane, cell nucleus, and mitochondria with nanoscale spatial nanometers. Our work provides a potent molecular tool for investigating cellular activities through XRM.

Unveiling Hidden Shake-Up Features in the Uranyl M4-Edge Spectrum.

The M4,5-edge high energy resolution X-ray absorption near-edge structure (HR-XANES) spectra of actinyls offer valuable insights into the electronic structure and bonding properties of heavy-element complexes. To conduct a comprehensive spectral analysis, it is essential to employ computational methods that accurately account for relativistic effects and electron correlation. In this work, we utilize variational relativistic multireference configurational interaction methods to compute and analyze the X-ray M4-edge absorption spectrum of uranyl. By employing these advanced computational techniques, we achieve excellent agreement between the calculated spectral features and experimental observations. Moreover, the calculations unveil significant shake-up features, which arise from the intricate interplay between strongly correlated 3d core-electron and ligand excitations. This research provides important theoretical insights into the spectral characteristics of heavy-element complexes. Furthermore, it establishes the foundation for utilizing M4,5-edge spectroscopy as a means to investigate the chemical activities of such complexes. By leveraging this technique, we can gain a deeper understanding of the bonding behavior and reactivity of heavy-element compounds.

Design and fabrication of low background, high energy resolution thermal bonding Micromegas detectors for the PandaX-III experiment

The high-pressure xenon time projection chamber (TPC) utilizing micro-pattern gaseous detector readout has emerged as a highly promising technical solution for the search of neutrino-less double beta decay events. This approach offers exceptional features, including high energy resolution, fine granularity, low background radioactivity, and scalability for large-scale experiments. In line with these advantages, the PandaX-III experiment aims to implement a 10 bar Xe136 TPC, employing a readout plane comprising 52 194 × 194 mm2 Micromegas detectors, within the China Jinping Underground Laboratory.To fulfill the stringent experimental requirements of PandaX-III, a low-background Micromegas detector with high energy resolution was proposed and developed using the thermal bonding method. The performance of the thermal bonding Micromegas prototypes was investigated using X-ray characterization under various gas mixtures with argon and isobutane from 1 bar to 10 bars. Remarkable results were presented at 1 bar gas pressure, where a maximum gas gain of ∼8 × 104 and the best energy resolution (FWHM @5.9 keV) of 13.6% is obtained, and at 10 bar pressure, where maximum gas gain exceeding 104, the best energy resolution of 19%, and excellent stability over a test duration exceeding 150 h is achieved.

Design and performance of an ultrahigh vacuum spectroscopic-imaging scanning tunneling microscope with a hybrid vibration isolation system.

A spectroscopic imaging-scanning tunneling microscope (SI-STM) allows for the atomic scale visualization of the surface electronic and magnetic structure of novel quantum materials with a high energy resolution. To achieve the optimal performance, a low vibration facility is required. Here, we describe the design and performance of an ultrahigh vacuum STM system supported by a hybrid vibration isolation system that consists of a pneumatic passive and a piezoelectric active vibration isolation stage. We present the detailed vibrational noise analysis of the hybrid vibration isolation system, which shows that the vibration level can be suppressed below 10-8 m/sec/√Hz for most frequencies up to 100Hz. Combined with a rigid STM design, vibrational noise can be successfully removed from the tunneling current. We demonstrate the performance of our STM system by taking high resolution spectroscopic maps and topographic images on several quantum materials. Our results establish a new strategy to achieve an effective vibration isolation system for high-resolution STM and other scanning probe microscopies to investigate the nanoscale quantum phenomena.

A versatile laser-based apparatus for time-resolved ARPES with micro-scale spatial resolution.

We present the development of a versatile apparatus for 6.2eV laser-based time and angle-resolved photoemission spectroscopy with micrometer spatial resolution (time-resolved μ-ARPES). With a combination of tunable spatial resolution down to ∼11 μm, high energy resolution (∼11meV), near-transform-limited temporal resolution (∼280fs), and tunable 1.55eV pump fluence up to 3 mJ/cm2, this time-resolved μ-ARPES system enables the measurement of ultrafast electron dynamics in exfoliated and inhomogeneous materials. We demonstrate the performance of our system by correlating the spectral broadening of the topological surface state of Bi2Se3 with the spatial dimension of the probe pulse, as well as resolving the spatial inhomogeneity contribution to the observed spectral broadening. Finally, after in situ exfoliation, we performed time-resolved μ-ARPES on a ∼30 μm flake of transition metal dichalcogenide WTe2, thus demonstrating the ability to access ultrafast electron dynamics with momentum resolution on micro-exfoliated materials.

Understanding the catalysis of chromium trioxide added magnesium hydride for hydrogen storage and Li ion battery applications

This study explores how the chemical interaction between magnesium hydride (MgH2) and the additive CrO3 influences the hydrogen/lithium storage characteristics of MgH2. We have observed that a 5 wt.% CrO3 additive reduces the dehydrogenation activation energy of MgH2 by 68 kJ/mol and lowers the required dehydrogenation temperature by 80 °C. CrO3 added MgH2 was also tested as an anode in an Li ion battery, and it is possible to deliver over 90% of the total theoretical capacity (2038 mAh/g). Evidence for improved reversibility in the battery reaction is found only after the incorporation of additives with MgH2. In depth characterization study by X-ray diffraction (XRD) technique provides convincing evidence that the CrO3 additive interacts with MgH2 and produces Cr / MgO byproducts. Gibbs free energy analyses confirm the thermodynamic feasibility of conversion from MgH2/CrO3 to MgO/Cr, which is well supported by the identification of Cr(0) in the powder by X ray photoelectron spectroscopy (XPS) technique. Through high resolution transmission electron microscopy (HRTEM) and energy dispersive spectroscopy (EDS) we found evidence for the presence of 5 nm size Cr nanocrystals on the surface of MgO rock salt nanoparticles. There is also convincing ground to consider that MgO rock salt accommodates Cr in the lattice. These observations support the argument that creation of active metal – metal dissolved rock salt oxide interface may be vital for improving the reactivity of MgH2, both for the improved storage of hydrogen and lithium.

Optical properties of InSb derived from reflection electron energy loss spectroscopy spectrum

The energy loss function (ELF) of the narrow bandgap semiconductor, InSb, was derived from the reflection electron energy loss spectroscopy (REELS) spectrum measured at 4 keV incident electron energy in an energy loss range of 1.6–200 eV using a high energy resolution electron spectrometer. The experimental spectrum was analyzed with the reverse Monte Carlo (RMC) method, which integrates the classical trajectory Monte Carlo simulation with the simulated annealing method for optimizing the trial ELF. Subsequently, the complex dielectric function ε(ω), refractive index and extinction coefficient were determined from the obtained ELF in the energy loss (i.e. photon energy) range of 1.6–200 eV. The validity of the obtained data was verified by the f-sum rule, ps-sum rule, inertial sum rule and dc-conductivity sum rule. We found that our calculated data of InSb fulfill the sum rules with very high accuracy; therefore, the use of these calculated optical data in material science and surface analysis is highly recommended for further applications.

Local defect and mid-gap state analysis of GaN using monochromated EELS combined with nanodiffraction and atomic-resolution imaging

Defects in semiconductor materials significantly impact their inherent properties, making the evaluation of local defects and their energy levels crucial for controlling device performance. With advancements in monochromators, electron energy loss spectroscopy (EELS) combined with scanning transmission electron microscopy (STEM) has emerged as a promising approach for assessing crystal and band structures of semiconductor materials at the nanoscale. However, there is limited experimental research investigating the relationship between actual defective structures in local regions and mid-gap states. In this study, we conducted high-energy resolution EELS (HR-EELS) measurements with an energy resolution of less than 100 meV to detect the mid-gap states of GaN. Various defects were intentionally induced through Ga-ion implantation, and the defect concentration varied in the depth direction. To understand the origin of the mid-gap states, we performed 4D-STEM analysis and atomic-resolution STEM observations. The HR-EELS measurements provided insights into the depth-dependent valence-loss spectra, revealing that the intensities corresponding to mid-gap states gradually increased toward the surface, whereas the slope at the onsets corresponding to interband transition decreased. Furthermore, local structural analysis unveiled the presence of structural disorder and defective structures, indicating the existence of extended defects such as stacking faults and domain boundaries. Observably, these defective structures were abundant near the surface and less pronounced in deeper regions. Based on these experimental findings, we concluded that the variations in valence-loss spectra can be utilized to qualitatively evaluate the crystal imperfections at the nanoscale.

Quantification in high-energy resolution Auger electron spectroscopy; Proposal of a reference target convolution technique for direct spectra

Currently, high-energy resolution Auger electron spectroscopy (AES) is utilized for chemical-state qualitative analysis, such as x-ray photoelectron spectroscopy. It is highly desirable to perform quantitative analysis using the high-energy resolution direct spectra used for qualitative analysis. However, AES analysis parameters, such as relative sensitivity factors (RSFs), derived from conventional-energy resolution differentiated spectra cannot be adopted for high-energy resolution direct spectra. Furthermore, for quantification by high-energy resolution direct spectra, there is no established method for determining peak intensity, and no database of RSFs is available in surface analysis communities. Therefore, we tasked ourselves with investigating the use of the analysis parameters obtained from conventional-energy resolution-differentiated spectra obtained with a cylindrical mirror analyzer (CMA)-type AES instrument for high-energy resolution direct spectra measured with a spherical capacitor analyzer (SCA)-type AES instrument. The convolution technique proposed here is achieved by using a conventional-energy resolution spectral dataset obtained with CMA-AES as a target. By applying the convolution with the window function of the convoluted function of the Gaussian function and rectangular function, high-energy resolution direct spectra containing the inherent nature of fine structures are converted to the similar shapes of conventional-energy resolution direct spectra after the Shirley type background subtraction [Watanabe et al., J. Vac. Sci. Technol. A 41, 043209 (2023)]. Results revealed that for all spectra of conventional-energy resolution spectra taken with CMA-AES, as well as high-energy resolution spectra taken with SCA-AES with various energy resolutions, the ratios of the background-subtracted direct peak areas and the differentiated peak-to-peak intensities were well-aligned along the identical parabolic curve as a function of the kinetic energy (KE). Experimental results also revealed that the generalized conversion function f(KE;ΔE)=IareacmaIareaconv.sca(KE;ΔE), which is the ratio of the conventional-energy resolution spectral area (Iareacma) and the convoluted high-energy resolution spectral area (Iareaconv.sca), which can transform differentiated intensities of convoluted high-energy resolution spectra, such that they are similar to those of conventional-energy resolution spectra obtained using the CMA-AES instrument, being a function of KE and the energy resolution ΔE. By applying the conversion function, the historically accumulated AES analysis parameters for conventional-energy resolution differentiated spectra can be adopted to differentiated high-energy resolution spectra. Finally, the results revealed the sufficiency of the conversion function obtained by the actual measurements of the four reference specimens for the practical quantification of high-energy resolution AES direct spectra.

Evaluating the capability of detecting recoil-electron tracks using an electron-tracking Compton camera with a silicon-on-insulator pixel sensor

Sub-MeV gamma-ray line observations are crucial for the understanding of high-energy astrophysical processes. In this energy range, the presence of a significant amount of background poses a serious problem. Therefore, it is essential to reduce this background to achieve high-sensitivity observations. An electron-tracking Compton camera can efficiently mitigate the impact of background on scientific results thanks to its ability to fully resolve the Compton process. In addition if we utilize a semiconductor detector as the sensor, the electron-tracking Compton camera can achieve high-energy resolution for the detection of gamma-ray lines. To operate the electron-tracking Compton camera effectively, the sensor needs to coincidence events for each detection signal and resolve the complex structure of recoiled-electron tracks of a few hundred μm. We focused on the silicon-on-insulator pixel sensor XRPIX2b developed for X-ray observations, which satisfies requirements. We developed a prototype electron-tracking Compton camera using XRPIX2b and carried out a quantitative evaluation of its detection capability for estimating the recoil directions of electrons at various angles. As a result, we successfully detected short recoil-electron tracks with a length of 100μm corresponded to scattering angles of 30°-40° for 511 keV gamma rays entering the sensor. In term of angular resolution measure and scatter plane deviation of a reconstructed image, the evaluations showed results of 15° and 40° (full width at half maximum), respectively, in cases where 511 keV gamma rays were scattered at 90° and recoil electrons tracked the surface of the sensor detection plane. We confirmed that these results were consistent with simulation results, within approximately a 15% margin.

Self-powered 4 H-SiC charged particle detector with 1 cm2 sensitive area and 0.63% energy resolution

Silicon carbide (SiC) detector, one of important charged particle detectors with good endurance in high-temperature and harsh-radiation environment, is highly demanded for high energy resolution and large sensitive area, but is hardly to acquire for decades. In this paper, a SiC charged particle detector was fabricated using high-quality homogenous epitaxial 4 H-SiC wafer with thickness of 150 μm and in vertical PIN diode structure; high-performance of low dark current (0.60 nA/cm2 within reverse bias of 600 V), large sensitive area (1 cm2) and high energy resolution (0.63%) were successfully achieved; furthermore, the detector was proven as self-powered charged particle detector for high charge collection efficiency of 95.96% and proper energy resolution at a bias voltage of 0 V. We envision that SiC charged particle detector would promote further development of radiation detection and charged particle spectrometer.

Insights into uranium sequestration by coal fly-ash-derived zeolites: Understanding via wet chemistry, and advanced spectroscopies

The operation of nuclear power plants requires a supply of nuclear fuel where uranium plays a substantial role as a primary fissile material. Its extraction from U-bearing minerals and handling may cause a leakage of heavily toxic radioactive pollution, which ends up in water bodies and soil. Therefore, tackling U-contaminated water is crucial to preserve water integrity and quality. Zeolites are known as profound ion exchangers with great affinity towards cationic species present in polluted waters. Various zeolite synthesis routes have made this group of aluminosilicates even more promising to be applied as water purification materials. Here, the synthetic gismondite, faujasite, and Linde type-A zeolites from coal fly-ash were synthesized via tailored, coupled fusion-hydrothermal method and applied to remove aqueous uranium (primarily as 238U) under varying pH, time (sorption kinetics), and initial U concentrations (sorption isotherms). The maximum U uptake was observed for Na–P1 (GIS) zeolite, which equals 48.72 mg U/g, the highest reported value on maximum U adsorption capacity for zeolitic materials. The U adsorption kinetics showed that equilibrium is reached after approximately 3 h of adsorption and that the removal process follows a Freundlich isothermal model for all zeolites, thus preferential adsorption onto heterogeneous surfaces. Advanced spectroscopic studies, including laboratory-scale X-ray Photoelectron Spectroscopy with synchrotron light X-ray Absorption Near Edge Structure in High Energy Resolution Fluorescence Detection mode, revealed that at acidic pH, predominantly an ion exchange between Na+ ions with hexavalent uranyl species takes place. In contrast, in the neutral pH region, the U is immobilized via precipitation in the form of μm-scale mineral aggregates of Na-schoepite: Na[(UO2)4O2(OH)5](H2O)5↓. The outcomes of the research study has demonstrated that synthetic zeolites, obtained from industrial by-products such as coal fly-ash, can be successfully valorized to efficient U adsorbents while unveiling the insights to understand the zeolites/U interactions at the nanoscale level.

Consideration of the Potential of High Energy Resolution X-ray Absorption and X-ray Emission Experiments to Track Changes in Oxidation States on Nanoparticle Materials

Consideration of the Potential of High Energy Resolution X-ray Absorption and X-ray Emission Experiments to Track Changes in Oxidation States on Nanoparticle Materials

First measurements with a new β-electron detector for spectral shape studies

The shape of the electron spectrum emitted in β decay carries a wealth of information about nuclear structure and fundamental physics. In spite of that, few dedicated measurements have been made of β-spectrum shapes. In this work we present a newly developed detector for β electrons based on a telescope concept. A thick plastic scintillator is employed in coincidence with a thin silicon detector. The first measurements employing this detector have been carried out with mono-energetic electrons from the high-energy resolution electron-beam spectrometer at Bordeaux. Here we report on the good reproduction of the experimental spectra of mono-energetic electrons using Monte Carlo simulations. This is a crucial step for future experiments, where a detailed Monte Carlo characterization of the detector is needed to determine the shape of the β-electron spectra by deconvolution of the measured spectra with the response function of the detector. A chamber to contain two telescope assemblies has been designed for future β-decay experiments at the Ion Guide Isotope Separator On-Line facility in Jyväskylä, aimed at improving our understanding of reactor antineutrino spectra.