Search Results (539)

The effects of Fe non-stoichiometry on crystal structure, microstructural evolution, and thermoelectric transport properties were systematically investigated in bornite (Cu₅Fe_1+yS₄; −0.06 ≤ y ≤ 0.06) synthesized by mechanical alloying followed by hot pressing. X-ray diffraction analysis confirmed the formation of a single-phase orthorhombic bornite structure over the entire composition range. Anisotropic lattice distortion was observed with increasing Fe non-stoichiometry, manifested as contraction along the a-axis and expansion along the b- and c-axes, with a non-linear dependence on composition. Crystallite sizes estimated from Lorentzian peak fitting increased from 64.1 nm for the stoichiometric composition to 70.6–76.3 nm for Fe-deficient samples and 73.2–90.9 nm for Fe-excess samples. Hall-effect measurements revealed p-type semiconducting behavior for the stoichiometric composition, degenerate p-type transport with increased hole concentration under Fe-deficient conditions, and a transition to n-type behavior with reduced carrier mobility under Fe-excess conditions. While Fe-deficient samples retained high electrical conductivity and positive Seebeck coefficients, Fe-excess samples exhibited negative Seebeck coefficients at low temperatures with sign reversal at elevated temperatures. As a consequence, the power factor of Fe-deficient samples was enhanced by approximately 20–30% relative to the stoichiometric composition. In addition, the total thermal conductivity remained below 0.8 W·m⁻¹·K⁻¹ for all samples, and Fe non-stoichiometry effectively suppressed lattice thermal conductivity. Consequently, the Cu₅Fe_0.94S₄ composition achieved a maximum dimensionless figure of merit of ZT = 0.61 at 673 K, representing a performance enhancement of approximately 30–70% compared with the stoichiometric composition (ZT = 0.36 at 673 K and 0.47 at 723 K). Full article

This study aims to develop high-performance hybrid nanocomposites for solid-state energy conversion. We achieved this by improving charge transport and thermoelectric efficiency through the interaction of polymers, nanoparticles, and ionic liquids. Nickel oxide nanoparticles (NiO NPs) were synthesized via a sonochemical route using a novel ionic liquid, 1,2-(propan). In our recent work, this approach enabled the formation of a hybrid [NiO NPs + IL] system, which was subsequently incorporated at different loadings (8, 15, and 30 wt.%) and coated with polyethylene glycol (PEG). The resulting nanocomposites were investigated to elucidate charge-transport mechanisms and assess the influence of the polymer coating on their optical, electrical, and thermal transport properties. Optical measurements showed a shift in the band gap due to π–π* electronic transitions. This effect indicates strong interface interactions. The PEG-coated [NiO NPs + IL] nanocomposites exhibited significantly enhanced charge-carrier mobility, resulting in improved electrical conductivity. Remarkably, a high Seebeck coefficient of 720 μV/K and an electrical conductivity of 0.35 S/cm were achieved, resulting in a maximum power factor of 24.74 μW/m·K², surpassing many recently reported polymer-based nanocomposites. PEG-coated [NiO NPs + IL] systems offer tunable optical properties and superior thermoelectric performance. Consequently, they are a promising alternative to conventional nanocomposites for sustainable energy conversion. Full article

In this work, we develop a three-dimensional thermoelectric (TE) numerical model of a commercial 127-thermocouple TEG, incorporating the temperature-dependent Seebeck coefficient, electrical resistivity, and thermal conductivity. The model is validated against manufacturer data, achieving average errors below 5% in internal resistance, voltage, current, and power output. Using this validated model, we propose a hybrid TEG composed of Bi₂Te₃, PbTe, and skutterudite legs electrically connected in series. This multi-material configuration enables each leg to operate near its optimal hot-side temperature, extending the usable temperature range beyond that of conventional Bi₂Te₃ modules. Multiple uniform and non-uniform hot-side thermal boundary configurations are examined, including diagonal, rectangular, and cavity-inspired arched thermal regions. Under uniform hot-side temperatures (200 °C and 230 °C), the commercial Bi₂Te₃ module outperforms the hybrid material design. However, when non-uniform hot-side boundary conditions align with the material-specific optimal temperature ranges, the hybrid TEG delivers up to 17.37 W (Case F), representing a 135.3% increase in power relative to the commercial module. The highest-temperature cases exceed the thermal operating limits of Bi₂Te₃ modules, demonstrating the advantage of hybrid material TEGs. Full article

Reliable and real-time environmental monitoring is essential for controlling pollution and protecting public health. However, conventional station-based measurements are expensive and often lack spatial and temporal resolution. This paper proposes a low-cost multimodal environmental monitoring system. Experiments verified that thin-film thermocouples exhibit near-linear voltage–temperature characteristics ($R^2>0.99$). Integration of the AI data pipeline substantially enhances monitoring accuracy: the proposed fusion strategy reduces relative error to approximately 2.3% under typical noise conditions, with a correlation coefficient of 0.79 between predicted and observed PM2.5 values. This research provides a scalable blueprint for edge-deployable environmental monitoring. A thin-film thermocouple with a fast response time is used as a temperature sensor and is statically calibrated against a K-type reference. To improve dynamic tracking and reduce measurement noise, a Kalman filter-based fusion strategy is employed, which is then compared with weighted averaging and Bayesian fusion. Simulation-driven validation is performed for thermocouple linearity, PID-based temperature control, micro-signal filtering and system-level latency and robustness. The results demonstrate that thin-film thermocouples exhibit near-linear voltage–temperature characteristics (R² > 0.99) with Seebeck coefficients ranging from 40.92 to 42.08 μV/°C, close to the theoretical K-type value of 42.87 μV/°C. The proposed fusion strategy reduces relative error to ~2.3% under typical noise conditions, enabling stable, real-time processing with near-second latency for 10,000-point batches. This study summarizes the design considerations for selecting and calibrating sensors and for achieving AI robustness in the presence of drift and faults. It provides a scalable blueprint for edge-deployable environmental monitoring. Full article

At present, the advancement of thermoelectric technology remains largely focused on developing high-performance thermoelectric materials, while comparatively little attention is directed towards its fundamental principles. To address this gap, this study introduces a new physical quantity, the “thermoelectric diffusion potential”, which clarifies the physical interpretations of various thermoelectric coefficients. Analyses reveal that, within a thermoelectric element, the Seebeck coefficient represents a balance between the thermoelectric diffusion field and electrostatic field, rather than between temperature and voltage differences. Using the thermoelectric diffusion potential, the relationship between the Seebeck and Peltier coefficients can be derived directly. Building on this framework, two additional physical quantities, namely the “thermoelectric energy” and “thermoelectric energy flow”, associated with the thermoelectric diffusion potential, are introduced. The formulation of thermoelectric energy flow helps derive the energy conversion relationship at the interface on a macroscopic level. Specifically, energy conversion at the interface occurs between thermoelectric and thermal energy flows, while within the element, it takes place between thermoelectric and electrical energy flows. Owing to the dual nature of internal energy in thermoelectric materials, manifesting as both thermal and electrical energy, the conversion within the element can also be regarded as one between thermal and electrical energy flows. The proposed quantities constitute an important complementary interpretation for the existing thermoelectric framework. Full article

In this work, the deposition of graphene coatings on substrates of an ELI grade Ti-6Al-4V alloy was carried out using the Plasma Enhanced Chemical Vapor Deposition (PECVD) technique. The purpose of this study was to improve the surface properties of the material. The characterization of the material was carried out by non-destructive techniques, such as Raman Spectroscopy and Thermoelectric Potential. A preliminary characterization of Ti substrates was carried out by Raman spectroscopy. Conversely, thermoelectric potential tests were conducted using three distinct tip systems and four different temperature gradients. Lastly, some surface roughness measurements were conducted on all samples, both coated and uncoated. Graphene micro-structured coatings were obtained using a plasma-activated mixture of hydrogen and methane gases with an equimolar feed ratio (1:1 H₂:CH₄) at a temperature of 850 °C and a plasma exposure of 150 Watts and duration of 15 min. Raman spectra verified the presence of uniform micrometric graphene on the surface of Ti substrates. Graphene-coated Ti-6Al-4V ELI substrates exhibited Seebeck coefficient values indicating metallic-like behavior and suitability for thermoelectric sensing. In the eddy current analyses, it was found that low frequencies provided the highest sensitivity for differentiating between samples. An inverse relationship was identified between substrate thickness and phase angle, and a direct relationship with calculated electrical conductivity was also identified. This direct relation is attributed to penetration depth and interactions due to the chemical nature of the substrate and coating. Despite a slight increase in surface roughness after graphene deposition, values remained comparable to the base alloy, preserving compatibility for biomedical integration. Thermoelectric potential measurements revealed enhanced sensitivity to surface morphology and interfacial effects when high-sensitivity probe configurations were employed. These results support potential applications in implantable or wearable temperature sensors, energy harvesting devices, and smart biomedical interfaces. The thickness of the graphene coating was also characterized by SEM, which showed that the films deposited by PECVD are about 1 micron thick. Full article

The pursuit of energy-efficient technologies is crucial for achieving sustainability amid rising global energy demands and climate concerns. MXenes—a class of two-dimensional (2D) transition metal carbides, nitrides, and carbonitrides—have recently attracted significant attention in thermoelectric (TE) research due to their outstanding electrical conductivity, tunable surface chemistry, and unique layered structures. This review uniquely focuses on the integration of MXenes into flexible and wearable platforms, offering a systematic analysis of material innovations specifically tailored to mechanical compliance. Beyond material-level transport properties, we critically evaluate actual device-level demonstrations, including fabrication strategies for flexible TE generators (f-TEGs), that achieve impressive outputs, such as Seebeck voltages of up to 399.9 mV for 200 p-n modules. To assist readers in gauging progress, we provide a comprehensive comparative analysis of diverse MXene architectures, summarized in a quantitative benchmark table covering Seebeck coefficients (S), electrical conductivity (σ), power factor (PF), and ZT values. Notably, experimental optimization has led to performance breakthroughs, with MXene-based flexible films exhibiting power factors exceeding 2100 µW m⁻¹ K⁻² and ZT values as high as 1.33 at room temperature. Finally, critical challenges, including environmental stability and large-scale manufacturing, are discussed alongside future perspectives on multifunctional MXene systems. Full article

To address the trade-off between thermoelectric efficiency in oxide thermoelectric materials used in Aiye Processing Equipment, this study investigates the effect of La doping on the thermoelectric properties of indium oxide (In₂O₃) through experimental characterization and mechanism analysis. The results show that La doping induces synergistic optimization of the electronic structure, lattice dynamics, and defect state of In₂O₃, leading to simultaneous enhancements in thermoelectric and mechanical properties. Specifically, La³⁺ substitution for In³⁺ significantly increases carrier concentration, which, combined with the band convergence-induced elevation of density of states (DOS) near the Fermi level, results in a remarkable improvement in power factor (from the intrinsic enhancement driven by electrical conductivity) while mitigating the reduction in Seebeck coefficient. Meanwhile, lattice distortion caused by ionic radius mismatch and decreased Young’s modulus (due to weakened In-O bonds) jointly enhance phonon scattering and reduce phonon propagation velocity, leading to a significant decrease in lattice thermal conductivity and total thermal conductivity. Consequently, the thermoelectric figure of merit (ZT) of La-doped In₂O₃ increases from 0.055 to 0.358, a six-fold enhancement. Additionally, La doping improves Vickers hardness through three synergistic mechanisms: internal stress from lattice distortion, enhanced interatomic bonding (synergistic reinforcement of ionic and covalent bond components), and dislocation pinning by substitutional defects (La_In). This study demonstrates that La doping achieves the dual regulation of “promoting electrical transport, suppressing thermal conduction, and enhancing mechanical strength” in In₂O₃, breaking the traditional trade-off between thermoelectric and mechanical properties. The findings provide a feasible strategy for the performance optimization of oxide thermoelectrics and lay a foundation for their practical applications in energy conversion systems requiring high efficiency and structural reliability. Full article

Topological semimetals with nontrivial band structures host a variety of unconventional transport phenomena and have attracted significant attention in condensed matter physics. SnTaS₂, a recently proposed topological nodal-line superconductor with a centrosymmetric layered structure, provides an ideal platform to explore the interplay between topology and electronic transport. Here, we report a comprehensive study of the normal-state magnetotransport and magneto-thermoelectric properties of SnTaS₂ single crystals. We observed large magnetoresistance and nonlinear Hall resistivity at low temperatures, which can be well described by a two-band model, indicating the coexistence of electron and hole carriers. The Seebeck and Nernst coefficients were found to exhibit pronounced and nonmonotonic magnetic field dependences at low temperatures, consistent with multiband transport behavior. Moreover, clear quantum oscillations with a single frequency are detected in both electrical and thermoelectric measurements. Analysis of the oscillations reveals a small effective mass and a nontrivial Berry phase, suggesting that the corresponding Fermi surface arises from a topologically nontrivial band. These findings shed light on the normal-state electronic structure of SnTaS₂ and highlight the important role of topological bands in shaping its transport properties. Full article

The thermoelectric (TE) performance of iron silicide (β-FeSi₂) can be enhanced by introducing metal dopants. However, such doping often leads to the emergence of secondary phases, which negatively affect the Seebeck coefficient and overall TE efficiency. Consequently, it is crucial to understand the phase transitions involved and how they influence the transport properties in order to optimize the material’s performance. This work investigates the influence of Mn-doping on the phase change and properties of p-type β-Fe_1−xMn_xSi₂. The findings show that the semiconducting β-phase decreases sharply when x ≥ 0.09, indicating that the optimal doping concentration lies below this level. As a result, the maximum power factor of 970 μW m⁻¹ K⁻² and a dimensionless figure of merit (ZT) value of 0.12 are achieved at x = 0.03. This study clarifies how the phase composition relates to the thermoelectric properties of p-type β-FeSi₂. Full article

Nanostructured semiconductors have emerged as transformative materials for enhancing the efficiency of waste heat-to-electricity conversion through thermoelectric (TE) processes. By altering structural features at the nanoscale, these materials can simultaneously reduce lattice thermal conductivity and optimize electronic transport properties, thereby significantly improving the thermoelectric figure of merit (ZT). Recent studies have demonstrated that introducing periodic twin planes in III–V semiconductor nanowires can achieve a tenfold reduction in thermal conductivity while maintaining excellent electrical performance. Similarly, Pb_1−xGe_xTe alloys, through controlled spinodal decomposition, form stable nanostructures that maintain low thermal conductivity even after thermal cycling, crucial for high-temperature applications. Enhancing electrical properties is another key advantage of nanostructuring. PbTe-based materials, when heavily doped and engineered with nanoscale inclusions, have achieved a ZT of approximately 1.9 and a thermoelectric efficiency of around 12% over a 590 K temperature difference. Single-walled carbon nanotubes (SWCNTs) also show strong correlations between their electronic structure and thermoelectric conductivity, highlighting their potential for next-generation devices. Two-dimensional silicon–germanium (Si_xGe_γ) compounds offer ultra-low lattice thermal conductivity and high Seebeck coefficients, providing a promising pathway for future TE applications. Despite these advancements, challenges remain, particularly regarding scalability and integration into existing energy recovery systems. Techniques such as focused ion beam milling and solution-based synthesis of porous nanostructures are being developed to fabricate high-performance materials on a commercial scale. Moreover, integrating nanostructured semiconductors into real-world systems, such as automotive exhaust heat recovery units, requires improvements in material durability, fabrication efficiency, and device compatibility. In conclusion, nanostructured semiconductors offer a powerful route for enhancing waste heat-to-electricity conversion. Their ability to decouple electrical and thermal transport at the nanoscale opens new opportunities for high-efficiency, sustainable energy harvesting technologies. Continued research into scalable manufacturing techniques, material stability, and system integration is essential to fully unlock their potential for commercial thermoelectric applications. Full article

Bismuth–telluride-based alloys are excellent thermoelectric materials for Peltier modules and thermoelectric generators (TEGs). Owing to the emergence of the Internet of Things (IoT), the demand for sensors has increased considerably and self-power supplies to sensors using TEGs are garnering attention. To apply TEGs to IoT sensors, the thermoelectric materials used must be sufficiently small and thin while exhibiting high thermoelectric performance. In this study, Bi_0.5Sb_1.5Te₃ thin films were prepared using a pressure-gradient sputtering system. The obtained films exhibit a nanocrystalline structure with a significantly smooth surface and no preferred crystal orientation. Because the Bi_0.5Sb_1.5Te₃ thin films exhibit a high Seebeck coefficient and low thermal conductivity, the in-plane dimensionless figure of merit is 0.98, which is one of the highest values reported for thermoelectric materials measured near 300 K. Furthermore, the phonon mean-free path is 0.19 nm, as estimated using the 3ω method and nanoindentation. This value is significantly smaller than the average crystallite size of the thin film, thus indicating that phonon scattering occurs more frequently via ternary-alloy scattering inside the crystallites than via boundary scattering at the crystallite boundaries. The results of this study can advance thin-film TEGs as a source of self-sustaining power for IoT systems. Full article

A deterministic platform for engineering epitaxial strain in CaMnO_3-δ (CMO) thermoelectric thin films is demonstrated using pulsed laser deposition, enabling precise control of the interplay between strain state and oxygen vacancy formation. High-quality epitaxial CMO films are grown on four different single crystalline substrates, which impose fully relaxed, partially relaxed, low tensile, and high tensile strain states, respectively. Increasing tensile strain induces a monotonic expansion of the unit cell volume and a systematic rise in oxygen vacancy concentration. Oxygen vacancies increase carrier concentration but decrease mobility due to enhanced scattering. Reducing tensile strain suppresses scattering of electrons by oxygen vacancies and increases both electrical conductivity (σ) and the Seebeck coefficient (S), mitigating the conventional inverse relationship between S and σ. Fully relaxed films exhibit σ approximately four orders of magnitude higher at room temperature than highly tensile strained films. These relaxed films also show the highest power factor (PF = S²·σ), exceeding strained films by up to six orders of magnitude. Strain-controlled oxygen vacancies thus provide a direct route to optimize charge transport and maximize the thermoelectric performance of CMO thin films. Full article

To improve the comprehensive performance of indium oxide (In₂O₃) thermoelectric materials, this study systematically investigates the regulatory effects of tantalum (Ta) doping on their electrical transport characteristics, thermoelectric conversion efficiency, and mechanical properties. The results show that Ta doping achieves synchronous optimization of multiple properties through precise regulation of crystal structure, electronic structure, and microdefects. In terms of electrical transport, the electron doping effect of Ta⁵⁺ substituting In³⁺ and the introduction of impurity levels lead to a continuous increase in carrier concentration; lattice relaxation and impurity band formation at high doping concentrations promote mobility to first decrease and then increase, resulting in a significant growth in electrical conductivity. Although the absolute value of the Seebeck coefficient slightly decreases, the growth rate of electrical conductivity far exceeds the attenuation rate of its square, increasing the power factor from 1.83 to 5.26 μWcm⁻¹K⁻² (973 K). The enhancement of density of states near the Fermi level not only optimizes carrier transport efficiency but also provides electronic structure support for synergistic performance improvement. For thermoelectric conversion efficiency, the substantial increase in power factor collaborates with thermal conductivity suppression induced by lattice distortion and impurity scattering, leading to a leapfrog increase in ZT value from 0.055 to 0.329 (973 K). In terms of mechanical properties, lattice distortion strengthening, formation of strong Ta-O covalent bonds, and dispersion strengthening effect significantly improve the Vickers hardness of the material. Ta doping breaks the bottleneck of mutual property constraints in traditional modification through an integrated mechanism of “electronic structure regulation-carrier transport optimization-multiple performance synergistic enhancement”, providing a key strategy for designing high-performance indium oxide-based thermoelectric materials and facilitating their practical application in the field of green energy conversion. Full article

Carbon nanocomposites have gained interest due to the rapid development of nanotechnology. The graphite-based composites have been demonstrated to possess unique mechanical, electrical, and thermal properties. This paper presents a facile one-step sonochemical synthesis of antimony sulfoiodide (SbSI)/graphite nanocomposite. The weight concentrations of graphite in the prepared material varied from 0% to 33.3%. The morphology and chemical composition of the SbSI/graphite nanocomposites are studied with scanning electron microscopy (SEM) and energy-dispersive X-ray spectroscopy (EDS), respectively. SEM examination shows that SbSI/graphite nanocomposite consists of one-dimensional SbSI nanostructures and graphite microparticles. The influence of graphite concentration on the energy band gap of SbSI/graphite nanocomposite is investigated using diffuse reflectance spectroscopy (DRS). The prepared materials are cold-pressed to obtain the bulk samples. They are characterized by direct current (DC) electrical measurements and thermoelectric examination. The increase in the graphite concentration in the SbSI/graphite nanocomposite resulted in a significant reduction in the electrical resistivity of the material. The Seebeck coefficients of the pristine SbSI nanowires and SbSI/graphite nanocomposite are determined for the first time. The investigations of the thermoelectric effect reveal that these nanomaterials exhibited p-type electrical conductivity. The thermoelectric power factor of the SbSI/graphite nanocomposite is examined as a function of the graphite concentration. The presented work demonstrates the comprehensive optical, electrical, and thermoelectric characterization of novel hybrid SbSI/graphite nanocomposites, which has not been studied before. Full article