Energy Filtering Research Articles

Enhancement of the Seebeck Coefficient by Energy Filtering in Mixed-Phase Cu2−xS Films at Room Temperature

Enhancement of the Seebeck Coefficient by Energy Filtering in Mixed-Phase Cu2−xS Films at Room Temperature

Power Quality Improvement for Hybrid Microgrid Integrated with Renewable Energy Sources

Given the present energy crisis and depletion of fossil fuel reserves, there is a pressing need to enhance the integration of Renewable Energy Sources (RES) into the power system. This research focuses on designing and managing a Hybrid Microgrid (HMG) in fluctuating RES. The Direct Current (DC) sub-grid comprises a Wind Turbine (WT), a solar Photovoltaic (PV) array equipped with a Perturb-and-Observation (P&O) Maximum Power Point Tracking (MPPT) method, a boost conversion, and a Battery Energy Storage System (B-ESS) connected to DC demands. The Alternative Current (AC) sub-grid comprises a Permanent Magnet Synchronous Generator (PMSG) WT and a Fuel Cell (FC) integrated with an inverter circuit synced with the grid to fulfill its load requirements. A reversible Interlinking Conversion (IC) connects the AC and DC sub-grid, enabling efficient power interchange across the two grids. The IC's control technique allows it to function as an active energy filter and exchange operator. The IC's active energy filtering function ensures that the power supply of the microgrid complies with the criteria set by IEEE 519. It does this by offering reactive power assistance and decreasing the harmonic levels to below 5%. The suggested method enables the HMG to function in grid-connected and islanded states. During grid-connected operation, power is transferred across the DC and AC sub-grids, ensuring that all load requirements are fulfilled. In the islanded method, a diesel generator provides power to the AC sub-grid to fulfill the needs of essential loads, while the B-ESS sustains the DC microgrid. The suggested model is constructed and simulated with MATLAB, and its outcomes are examined.

Tailoring Single-Electron Emission Distributions in the Time-Energy Phase Space.

The precise characterization and control of single-electron wave functions emitted from a single-electron source are essential for advancing electron quantum optics. Here, we introduce a method for tailoring a single-electron emission distribution using energy filtering, enabling selective control of the distribution under various energy barrier conditions of the filter. The tailored electron is studied by reconstructing its Wigner distribution in the time-energy phase space using the continuous-variable tomography method. Our results reveal that the filtering cuts the portion of the distribution below the energy-barrier height of the filter in the time-energy space. While the filtering is demonstrated in a classical regime of the emitted electrons, we expect that this study significantly contributes to the design and implementation of advanced experiments toward quantum information processing based on single electrons.

Multi‐Photon 3D Laser Micro‐Printed Plastic Scintillators for Applications in Low‐Energy Particle Physics

AbstractPlastic scintillators are inexpensive to manufacture and therefore a popular alternative to inorganic crystalline scintillators. For many applications, their advantages outweigh their lower light yield. Additionally, it is easier to structure plastic scintillators with well‐developed processing techniques which is of growing relevance in modern applications. One technique to structure plastic material is 3D printing, with noteworthy recent advances in one‐photon‐based approaches. However, some applications require high spatial resolution and optically smooth surfaces, which can be achieved by multi‐photon 3D laser micro‐printing. One application example is the improvement of sensitivity of the Karlsruhe Tritium Neutrino (KATRIN) experiment. This improvement can be realized by printing a 3D scintillator structure as an active transverse energy filter directly onto the detector. Herein, the first two‐photon printable plastic scintillator providing a printing resolution in the micrometer regime is presented. Using the benefits of two‐photon grayscale lithography, optical‐grade surfaces are achieved. The light output is estimated to be 930 photons MeV−1. A prototype structure printed directly on a single‐photon avalanche diode array is demonstrated.

A strategy to fabricate nanostructures with sub-nanometer line edge roughness

Line edge roughness (LER) has been an important issue in the nanofabrication research, especially in integrated circuits. Despite numerous research studies has made efforts on achieving smaller LER value, a strategy to achieve sub-nanometer level LER still remains challenging due to inability to deposit energy with a profile of sub-nanometer LER. In this work, we introduce a strategy to fabricate structures with sub-nanometer LER, specifically, we use scanning helium ion beam to expose hydrogen silsesquioxane (HSQ) resist on thin SiNx membrane (∼20 nm) and present the 0.16 nm spatial imaging resolution based on this suspended membrane geometric construction, which is characterized by scanning transmission electron microscope (STEM). The suspended membrane serves as an energy filter of helium ion beam and due to the elimination of backscattering induced secondary electrons, we can systematically study the factors that influences the LER of the fabricated nanostructures. Furthermore, we explore the parameters including step size, designed exposure linewidth (DEL), delivered dosage and resist thickness and choosing the high contrast developer, the process window allows to fabricate lines with 0.2 nm LER is determined. AFM measurement and simulation work further reveal that at specific beam step size and DEL, the nanostructures with minimum LER can only be fabricated at specific resist thickness and dosage.

Enhancing the thermoelectric properties of PEDOT:PSS films through the incorporation of g-C3N4 nanosheets and carbon nanotubes

Present study focuses on the synthesis of flexible nanocomposite film made of poly(3,4-ethylenedioxythiophene)-poly(styrenesulfonate) (PEDOT:PSS), graphitic carbon nitride (g-C3N4) nanosheets, and carbon nanotubes (CNTs) and how the g-C3N4 nanosheets and CNTs affect the thermoelectric properties of PEDOT:PSS. Incorporating 10 wt% of g-C3N4 nanosheets to PEDOT:PSS improved the Seebeck coefficient to 74.3 μVK−1, ∼5 times higher than the PEDOT:PSS film. However, this led to a decrease in electrical conductivity, limiting the power factor to 335.4 μWm−1K−2. In order to address this, CNTs were added as conductive fillers. The resulting PEDOT:PSS composite, with 10 wt% of g-C3N4 and 10 wt% CNTs, showed a significant power factor of 589.8 μWm−1K−2, an electrical conductivity of 810.6 Scm−1, and a Seebeck coefficient of 84.5 μVK−1, indicating a substantial improvement in the thermoelectric performance of pristine PEDOT:PSS. The increased Seebeck coefficient in the PEDOT:PSS and g-C3N4 composite is due to reduced carrier concentration and energy filtering at the interfaces. The enhancement in electrical conductivity and the Seebeck coefficient after adding CNTs is attributed to the formation of conductive networks, increased mobility, and energy filtering at the interfaces between PEDOT:PSS and CNTs. The study suggests that combining g-C3N4 nanosheets and CNTs with PEDOT:PSS could enhance the thermoelectric performance of PEDOT:PSS-based materials.

Testing the optical components for the National Ignition Facility time-resolved soft x-ray opacity spectrometer (OpSpecTR).

Opacity measurements are being carried out at the Z-facility at Sandia National Laboratories and at the National Ignition Facility (NIF) at Lawrence Livermore National Laboratory. The current soft x-ray Opacity Spectrometer (OpSpec) used on the NIF uses two elliptically bent crystals in time-integrated mode on either an image plate or a film. Plans are under way to expand these opacity measurements into a mode of time-resolved detection, called OpSpecTR. Previously, considerations for the available hCMOS detector size and photometrics led to a crystal geometry redesign and the use of a grazing angle x-ray mirror. The mirror acts as a low-pass x-ray energy filter, reducing the contribution of higher energy x rays. The first tests of the mirror and the crystal for OpSpecTR are presented here. The size of the mirror reflection and the reflectivity is tested using a Manson x-ray source. The mirror coupled with the new elliptical crystal shape demonstrates OpSpecTR's spectral coverage. The results from the x-ray optics performance testing are shown along with the intended design.

Determining pair distribution functions of thin films using laboratory-based X-ray sources.

This article demonstrates the feasibility of obtaining accurate pair distribution functions of thin amorphous films down to 80 nm, using modern laboratory-based X-ray sources. The pair distribution functions are obtained using a single diffraction scan without the requirement of additional scans of the substrate or of the air. By using a crystalline substrate combined with an oblique scattering geometry, most of the Bragg scattering of the substrate is avoided, rendering the substrate Compton scattering the primary contribution. By utilizing a discriminating energy filter, available in the latest generation of modern detectors, it is demonstrated that the Compton intensity can further be reduced to negligible levels at higher wavevector values. Scattering from the sample holder and the air is minimized by the systematic selection of pixels in the detector image based on the projected detection footprint of the sample and the use of a 3D-printed sample holder. Finally, X-ray optical effects in the absorption factors and the ratios between the Compton intensity of the substrate and film are taken into account by using a theoretical tool that simulates the electric field inside the film and the substrate, which aids in planning both the sample design and the measurement protocol.

Energy filtering enables macromolecular MicroED data at sub-atomic resolution.

High resolution information is important for accurate structure modelling. However, this level of detail is typically difficult to attain in macromolecular crystallography because the diffracted intensities rapidly fade with increasing resolution. The problem cannot be circumvented by increasing the fluence as this leads to detrimental radiation damage. Previously, we demonstrated that high quality MicroED data can be obtained at low flux conditions using electron counting with direct electron detectors. The improved sensitivity and accuracy of these detectors essentially eliminate the read-out noise, such that the measurement of faint high-resolution reflections is limited by other sources of noise. Inelastic scattering is a major contributor of such noise, increasing background counts and broadening diffraction spots. Here, we demonstrate that a substantial improvement in signal-to-noise ratio can be achieved using an energy filter to largely remove the inelastically scattered electrons. This strategy resulted in sub-atomic resolution MicroED data from proteinase K crystals, enabling accurate structure modelling and the visualization of detailed features. Interestingly, filtering out the noise revealed diffuse scattering phenomena that can hold additional structural information. Our findings suggest that combining energy filtering and electron counting can provide more accurate measurements at higher resolution, providing better insights into protein function and facilitating more precise model refinement.

Achieving quantized transport in Floquet topological insulators via energy filters

Achieving quantized transport in Floquet topological insulators via energy filters

A TEM Study of Structural Degradation in LiFePO4 Batteries after Hybrid Vehicle Use

Establishing a robust, efficient circular economy for batteries hinges on understanding how they decay over time under various conditions. This understanding is crucial to maximize material use before recycling or disposal. A key aspect of this endeavor is the study of lithium iron phosphate (LiFePO4), a pivotal battery technology whose structural integrity over time remains a subject of inquiry.1 Known aging mechanisms in LiFePO4 (LFP) batteries include electrode degradation, SEI growth, and electrolyte decomposition.1 These processes extend to the cathode, where degradation can manifest as Fe dissolution, Li inventory loss, Fe/Li anti-site defects, and LFP amorphization.1–3 However, these mechanisms are typically studied in lab-aged cells under controlled conditions, leaving a gap in our understanding of their behavior in real-life, commercialized applications.Our research aims to bridge this gap by characterizing the degradation mechanisms of LFP cathode material in various states of health (SOH) after use in a hybrid vehicle. We sourced our cathode samples from 26650 cells extracted from a BAE ESS-A123 hybrid bus battery pack. After selecting cells with drastically different SOHs based on previous analyses,4 we employed transmission electron microscopy (TEM) for detailed characterization.In this talk, we will share insights gained from high-resolution TEM characterization, alongside chemical analysis using energy-filtered TEM and electron energy loss spectroscopy (EELS). Our focus will be on changes in the olivine structure, including lattice parameter alterations, Li and Fe migration, and Fe oxidation. By combining cell-level SOH analyses with TEM characterization, we will highlight how electrochemical test results correlate with material degradation mechanisms, enhancing our understanding of battery health, longevity, and diagnostics. Wang, L. et al. Insights for understanding multiscale degradation of LiFePO4 cathodes. eScience 2, 125–137 (2022). Li, X. et al. First Atomic-Scale Insight into Degradation in Lithium Iron Phosphate Cathodes by Transmission Electron Microscopy. J. Phys. Chem. Lett. 11, 4608–4617 (2020). Xu, P. et al. Efficient Direct Recycling of Lithium-Ion Battery Cathodes by Targeted Healing. Joule 4, 2609–2626 (2020). Ramirez-Meyers, K., Rawn, B. & Whitacre, J. F. A statistical assessment of the state-of-health of LiFePO4 cells harvested from a hybrid-electric vehicle battery pack. J. Energy Storage 59, 106472 (2023).

(Invited) Epitaxial Growth of Quasi-Low Dimensional Materials for Novel Thermoelectric Films

Thermoelectric conversion devices or modules with high performance have been expected for the electrical power generation from wasted heat. Then, thermoelectric materials with high dimensionless figure of merit zT at temperature T , described as S 2 σT/κ have been intensively sought, where S is Seebeck coefficient, σ is electrical conductivity, and κ is thermal conductivity. Therein, intercorrelation among three thermoelectric properties has been a big barrier against high zT. In conventional approach, the heavy elements such as rare metals are used because they inherently bring small κ in the materials. Now, ecofriendly ubiquitous element materials without toxic, rare, or high cost elements, showing high zT, are expected in the application view.Introduction of nanostructures into materials is one of the promising ways to increase zT because of phonon scattering [1], quantum confinement effect in low dimensional materials and by energy filtering [2], and so on. Therein, structure design determines the properties, and then, this method can be expected to bring high zT in the ecofriendly and low-cost ubiquitous element materials. Furthermore, it is recently found that low dimensional materials and quasi-low dimensional materials such as layered materials with 2D structures in the unit cell show high zT values. Therefore, low and quasi-low dimensional materials for extraordinarily high zT values have been expected to be developed.We have been developing a lot of kinds of well-controlled nanostructure films by SiO2 film technique. One of the examples: Si-based films including ultrasmall semiconductor nanodots with controlled interfaces, strains, crystal orientations, and compositions [3]. Furthermore, we have developed the epitaxial growth method of quasi-low dimensional material films composed of ecofriendly group IV elements on Si substrates: FeGeγ including 1D Ge helical structure and Ca-intercalated multi-layered silicene films. Here, we will introduce the epitaxial growth results of quasi-low dimensional material films. Epitaxial growth of FeGeγ films on Si were achieved by using Ge epitaxial nanodots as seed crystals[4]. In the case of Ca-intercalated multi-layered silicene, silicene bucked structure was found to be deformed. The deformation enhanced Seebeck coefficient. As a result, this sub-angstrom atomic displacement brought power factor enhancement while keeping high electrical conductivity [5]. In this talk, we will present the epitaxial growth process of quasi-low-dimensional material films on Si substrates for thermoelectric film devices composed of ecofriendly and low-cost thermoelectric materials .[1] Y. Nakamura, et al., Nano Energy 12, 845 (2015).[2] T. Ishibe, et al., ACS Appl. Mater. Inter. 10, 37709 (2018).[3] Y. Nakamura, et al., Sci. Technol. Adv. Mater. 19, 31 (2018).[4] T. Terada, Acta Materialia 236, 118130 (2022).[4] T. Terada, et al., Adv. Mater. Inter. 9, 2101752 (2022).

Quantum Dots and Molecular Junctions as Energy Filters for Thermal-to-Electric Energy Conversion

The thermoelectric conversion of heat into electricity requires a form of energy filtering, that allows hot electrons to pass while blocking cold electrons. The energy conversion efficiency is determined by the details of the energy filtering, with an infinitely sharp (delta function) transmission spectrum allowing near ideal (Carnot) efficiency. [1]I will introduce this concept and report on a proof-of-performance experiment based on a quantum dot embedded into a single, semiconductor nanowire. This near-ideal quantum-dot heat engine realized power production at maximum power with Curzon-Ahlborn efficiency as well more than 70% of Carnot efficiency at maximum efficiency settings [2].To further enhance efficiency at maximum power one wishes to shape the transmission function to allow a spectrum of warmer electrons to pass while still completely blocking cold electrons. This may be achieved by exploiting quantum interference phenomena to block low-energy electron transmission by destructive interference, and to thus sculpt the transmission function of quantum dots or molecular junctions.[4] In contrast to quantum dots, molecular junctions have the advantage that they can be used at room temperature and can be produced, in principle, cheaply and scalable. To systematically explore the effect of quantum interferences, we designed and synthesized a new class of porphyrins that are expected to feature destructive quantum interference in single molecule junctions with gold electrodes and may thus show high thermopower, as well as a control that does not. We performed detailed experimental single-molecule break-junction studies of conductance and thermopower on porphyrin molecular junctions. We find a somewhat better thermoelectric performance for the porphyrin where we expect destructive interference. However, the predicted large difference in conductance and thermopower is not supported by our experimental findings.[4]Finally, I will also briefly discuss the potential application of the concepts and systems presented here in hot-carrier photovoltaics, as an approach to increasing photovoltaic energy conversion efficiency beyond current limits.[1] T.E. Humphrey et al., Reversible Quantum Brownian Heat Engines for Electrons. Phys. Rev. Lett., 89, 116801 (2002)[2] M. Josefsson et al. A quantum-dot heat engine operated close to thermodynamic efficiency limits. Nature Nanotechn. 13, 920 (2018)[3] O Karlström et al. Increasing thermoelectric performance using coherent transport. Phys. Rev. B 84, 113415 (2011)[4] H. Xu et al. Electrical Conductance and Thermopower of β-Substituted Porphyrin Molecular Junctions Synthesis and Transport. JACS 145 , 23541 (2023) Figure 1

Optimization of three-dimensional electron diffuse scattering data acquisition

The diffraction patterns of crystalline materials with local order contain sharp Bragg reflections as well as highly structured diffuse scattering. In this study, we quantitatively show how the diffuse scattering in three-dimensional electron diffraction (3D ED) data is influenced by various parameters, including the data acquisition mode, the detector type and the use of an energy filter. We found that diffuse scattering data used for quantitative analysis are preferably acquired in selected area electron diffraction (SAED) mode using a CCD and an energy filter. In this study, we also show that the diffuse scattering in 3D ED data can be obtained with a quality comparable to that from single-crystal X-ray diffraction. As electron diffraction requires much smaller crystal sizes than X-ray diffraction, this opens up the possibility to investigate the local structure of many technologically relevant materials for which no crystals large enough for single-crystal X-ray diffraction are available.

Probing Enzyme@Metal-Organic Framework Interactions for Enhanced Stability and Catalytic Efficiency Using Cryogenic Electron Energy Loss Spectroscopy (CryoEELS) and Energy-Filtered TEM (EF-TEM)

Probing Enzyme@Metal-Organic Framework Interactions for Enhanced Stability and Catalytic Efficiency Using Cryogenic Electron Energy Loss Spectroscopy (CryoEELS) and Energy-Filtered TEM (EF-TEM)

Phase interface engineering enables state-of-the-art half-Heusler thermoelectrics

In thermoelectric, phase interface engineering proves effective in reducing the lattice thermal conductivity via interface scattering and amplifying the density-of-states effective mass by energy filtering. However, the indiscriminate introduction of phase interfaces inevitably leads to diminished carrier mobility. Moreover, relying on a singular energy barrier is insufficient for comprehensive filtration of low-energy carriers throughout the entire temperature range. Addressing these challenges, we advocate the establishment of a composite phase interface using atomic layer deposition (ALD) technology. This design aims to effectively decouple the interrelated thermoelectric parameters in ZrNiSn. The engineered coherent dual-interface energy barriers substantially enhance the density-of-states effective mass across the entire temperature spectrum while preser carrier mobility. Simultaneously, the strong interface scattering on phonons is crucial for curtailing lattice thermal conductivity. Consequently, a 40-cycles TiO2 coating on ZrNi1.03Sn0.99Sb0.01 achieves an unprecedented zT value of 1.3 at 873 K. These findings deepen the understanding of coherent composite-phase interface engineering.

Decoupling Plasmonic Hot Carrier from Thermal Catalysis via Electrode Engineering.

Increased attention has been directed toward generating nonequilibrium hot carriers resulting from the decay of collective electronic oscillations on metal known as surface plasmons. Despite numerous experimental endeavors, demonstrating hot carrier-mediated photocatalysis without a heating contribution has proven challenging, particularly for single electron transfer reactions where the thermal contribution is generally detrimental. An innovative engineering solution is proposed to enable single electron transfer reactions with plasmonics. It consists of a photoelectrode designed as an energy filter and photocatalysis performed with light function modulation instead of continuously. The photoelectrode, consisting of FTO/TiO2 amorphous (10 nm)/Au nanoparticles, with TiO2 acting as a step-shape energy filter to enhance hot electron extraction and charge-separated state lifetime. The extracted hot electrons were directed toward the counter electrode, while the hot holes performed a single electron transfer oxidation reaction. Light modulation prevented local heat accumulation, effectively decoupling hot carrier catalysis from the thermal contribution.

Asymmetric electrostatic dodecapole: compact bandpass filter with low aberrations for momentum microscopy.

Imaging energy filters in photoelectron microscopes and momentum microscopes use spherical fields with deflection angles of 90°, 180° and even 2 × 180°. These instruments are optimized for high energy resolution, and exhibit image aberrations when operated in high transmission mode at medium energy resolution. Here, a new approach is presented for bandpass-filtered imaging in real or reciprocal space using an electrostatic dodecapole with an asymmetric electrode array. In addition to energy-dispersive beam deflection, this multipole allows aberration correction up to the third order. Here, its use is described as a bandpass prefilter in a time-of-flight momentum microscope at the hard X-ray beamline P22 of PETRA III. The entire instrument is housed in a straight vacuum tube because the deflection angle is only 4° and the beam displacement in the filter is only ∼8 mm. The multipole is framed by transfer lenses in the entrance and exit branches. Two sets of 16 different-sized entrance and exit apertures on piezomotor-driven mounts allow selection of the desired bandpass. For pass energies between 100 and 1400 eV and slit widths between 0.5 and 4 mm, the transmitted kinetic energy intervals are between 10 eV and a few hundred electronvolts (full width at half-maximum). The filter eliminates all higher or lower energy signals outside the selected bandpass, significantly improving the signal-to-background ratio in the time-of-flight analyzer.

Physicochemical Properties of Cellulose Nanocrystals Extracted from Postconsumer Polyester/Cotton-Blended Fabrics and Their Effects on PVA Composite Films.

The utilisation of cotton waste as precursors in the synthesis of nanocrystalline cellulose has gained significant attention. This approach suggests a sustainable solution to address the growing concern of textile waste accumulation while simultaneously producing a valuable material. The main aim of this study is to examine the properties of cellulose nanocrystals (CNCs) obtained from postconsumer polyester-cotton waste and assess the effect of different fabric structures on the extraction and these properties. To acquire nanocellulose, a thorough decolourisation pretreatment process was utilised, which involved the treatment of polyester-cotton waste with sodium dithionite and hydrogen peroxide. Consequently, the postconsumer material was then treated with an acid hydrolysis method employing a 64% (v/v) sulphuric acid solution at 50 °C for 75 min, resulting in the formation of CNCs with average yield percentages ranging from 38.1% to 69.9%. Separation of the acid from the CNC was facilitated by a centrifugation process followed by dialysis against deionised water. Uniform dispersion was then achieved using ultrasonication. A variety of analytical techniques were employed to investigate the morphological, chemical, thermal, and physical properties of the isolated CNCs. Among these techniques, attenuated total reflection-Fourier-transform infrared spectroscopy (ATR-FTIR), energy-filtered transmission electron microscopy (EF-TEM), thermogravimetric analysis (TGA), and X-ray diffraction (XRD) were utilised to analyse the CNCs. The findings indicated that the separated CNCs exhibited a rod-shaped morphology, measuring between 78 and 358 nm in length and 5 and 16 nm in diameter, and also exhibited high crystallinity (75-89%) and good thermal stability. The extracted CNCs were mixed with polyvinyl alcohol (PVA) and glycerol to assess their reinforcing effect on plastic films. The prepared composite film exhibited improved mechanical properties and thermal stability. Incorporating CNCs led to a 31.9% increase in the tensile strength and a 42.33% rise in the modulus of elasticity. The results from this research proved that CNCs can be extracted from postconsumer mixed fabrics as a potential solution to effectively address the mounting concerns surrounding waste management in the textile industry and also provide avenues for enhancing the qualities of eco-friendly composite films.

Weak interlayer interactions and nearly temperature independent electrical transport in p-type 1T′-MoTe2/Sb2Te3 superlattice-like films

Thermoelectric superlattices (SLs) are one of the important focuses in the thermoelectric field due to their ordered stacking structure and the potential to obtain extremely high thermoelectric performance. To understand the critical effects of interlayer interactions, this work fabricates p-type (1T′-MoTe2)x(Sb2Te3)y SLs and investigates their electrical properties as functions of SL period and temperature. The results discovered that the weak interlayer interactions could be driven by both the small work function difference and temperature. This brings forth hole donation and energy filtering and leads to increased hole density and the carrier effective mass of (1T′-MoTe2)x(Sb2Te3)y SLs. Strikingly, the SL structure is beneficial for achieving temperature independent electrical properties, owing to the temperature driven interlayer interaction. Several SLs acquire the largest average power factor among all SLs, which is about 1.10 mWm−1K−2 within 300∼473 K, favorable for thermoelectric applications near room temperature. This work points out the beneficial effect of the SL structure on obtaining high thermoelectric properties in a wide temperature range.