Seebeck Coefficient Measurements Research Articles

Thermoelectric and electrical properties of triple-conducting multicomponent oxides based on substituted barium cerate-zirconate.

Multicomponent oxides often have exceptional thermal stability and interesting electronic properties. The present work presents the thermoelectric and electrical properties of the Ba(Zr0.2Hf0.2Sn0.2Ti0.2Fe0.2)O3-δ and Ba(Zr0.1Hf0.1Sn0.1Ti0.1Co0.1Ce0.1Bi0.1Fe0.1Y0.1Zn0.1)O3-δ multicomponent perovskites. Single-phase cubic perovskites were synthesized using the solid-state reaction method. They were characterized using X-ray diffraction, drop-solution calorimetry, and thermogravimetry methods. The total electrical conductivity and Seebeck coefficient measurements were performed in dry and wet air at temperatures between 600 and 1050 K. It was found that Ba(Zr0.1Hf0.1Sn0.1Ti0.1Co0.1Ce0.1Bi0.1Fe0.1Y0.1Zn0.1)O3-δ is thermodynamically less stable than Ba(Zr0.2Hf0.2Sn0.2Ti0.2Fe0.2)O3-δ. Moreover, this oxide incorporates a higher amount of water and exhibits higher conductivity and lower Seebeck coefficient. Charge transport in both perovskites can be assigned to the small-polaron hopping process via electron holes. An interesting temperature dependence of the Seebeck coefficient was found and, at temperatures above 750 K, related to hopping between energetically inequivalent states.

(Invited) Molecular Thermoelectricity

The field of molecular thermoelectricity focuses on the Seebeck effect occurring in electrode-molecule-electrode junction. The field is of fundamental interest to study structure-thermopower relationship at the atomic level and develop nanoscale thermoelectric devices. Research in molecular thermoelectricity is highly challenging. This is because, among others, i) heat can dissipate in an uncontrollable manner through nearly all matters, ii) it is difficult to create and define reliably temperature differentials across ~1 nm gap, iii) organic molecules may undergo thermal degradation, iv) it is non-trivial to connect soft, floppy organic molecules with hard electrodes in a non-invasive manner with reproducibility, and v) charges move in a quantum-mechanical regime. This presentation will discuss our recent efforts in the field of molecular thermoelectricity. We have developed a new metrology technique for reliably measuring Seebeck coefficient over molecular monolayers. Using this technique, we have begun to probe how thermopower is related to the structure of molecule and how to enhance the thermoelectric performance of molecular-scale device in a quantum-tunneling regime.

Discovery of superconductivity and electron-phonon drag in the non-centrosymmetric Weyl semimetal LaRhGe3

We present an exploration of the effect of electron-phonon coupling and broken inversion symmetry on the electronic and thermal properties of the semimetal LaRhGe3. Our transport measurements reveal evidence for electron-hole compensation at low temperatures, resulting in a large magnetoresistance of 3000% at 1.8 K and 14 T. The carrier concentration is on the order of 1021/cm3 with high carrier mobilities of 2000 cm2/Vs. When coupled to our theoretical demonstration of symmetry-protected almost movable Weyl nodal lines, we conclude that LaRhGe3 supports a Weyl semimetallic state. We discover superconductivity in this compound with a Tc of 0.39(1) K and Bc(0) of 2.2(1) mT, with evidence from specific heat and transverse-field muon spin relaxation. We find an exponential dependence in the normal state electrical resistivity below ~50 K, while Seebeck coefficient and thermal conductivity measurements each reveal a prominent peak at low temperatures, indicative of strong electron-phonon interactions. To this end, we examine the temperature-dependent Raman spectra of LaRhGe3 and find that the lifetime of the lowest energy A1 phonon is dominated by phonon-electron scattering instead of anharmonic decay. We conclude that LaRhGe3 has strong electron-phonon coupling in the normal state, while the superconductivity emerges from weak electron-phonon coupling. These results open up the investigation of electron-phonon interactions in the normal state of superconducting non-centrosymmetric Weyl semimetals.

Effects of lattice instability on the thermoelectric behavior of kagome metal ScV6Sn6

Kagome metal ScV6Sn6 has been a subject of interest due to the emergence of a first-order structural phase transition with intriguing charge density wave behavior below the transition temperature Tc ∼ 92 K. To explore the thermoelectric properties and provide experimental insights into the nature of the phase transition, we have carried out a combined study by means of the electrical resistivity, Seebeck coefficient, and thermal conductivity measurements on single crystalline ScV6Sn6. Pronounced features near Tc have been characterized by all measured physical quantities. In particular, the Seebeck coefficient exhibits a marked reduction as lowering temperature across Tc, attributed to an imbalance of the contribution from different type of carriers induced by the structural phase transition. From the examination of the electronic and lattice thermal conductivities, we obtained a confirmation that the observed enhancement at Tc is essentially caused by the change of the lattice thermal conductivity, demonstrating the primary importance of lattice distortions for the heat transport of ScV6Sn6. In addition, the lattice thermal conductivity above Tc was found to increase monotonically with temperature. We associated the peculiar phenomenon with lattice fluctuations, highlighting the essence of structural instability in the kagome lattice ScV6Sn6. These results add to the knowledge about the thermal transport properties in kagome materials with a hexagonal HfFe6Ge6-type structure.

How Oxygen Deficiency and Its Ordering Control Electrical Conductivity in Sr2-x Ca x Fe2O6-δ Perovskites as Related to Water Oxidation Electrocatalysis.

We report on the analysis of oxygen vacancies (OVs) content and ordering of Sr2-x Ca x Fe2O6-δ perovskites and explain how OVs change the electrical conductivity and oxygen evolution catalytic activity of these compounds. The structure and OV content are tuned by controlling the A-site composition and the reaction atmosphere. X-ray diffraction (XRD) and thermogravimetric analysis (TGA) are used to identify the crystal structures and to quantify bulk oxygen vacancy contents. Our analysis shows that OV content and crystal structure govern the electronic transport properties of the Sr2-x Ca x Fe2O6-δ system. The electrical conductivity of oxygen-deficient perovskites (ODPs) is significantly higher than those in brownmillerites (by at least 2 orders of magnitude). Seebeck coefficient measurements identified that the Sr-rich ODPs and brownmillerites are p-type semiconductors, while Ca-rich brownmillerites are either insulators (within the experimental temperature range) or p-type semiconductors at lower temperatures (<750 K). Electrical conductivity of p-type semiconductors (Sr-rich compounds) reduces with higher OV content, and in brownmillerites with x ≥ 1.25, a transition to n-type semiconductor is observed at temperatures above 750 K. Our analysis shows that the hole and electron concentrations are similar in these brownmillerites, indicating major contributions from ionic transport. Finally, we show how oxygen deficiency alters the electrical conductivity and catalytic activity of the Sr2-x Ca x Fe2O6-δ system in noncomplementary ways.

Tuning conduction properties and clarifying thermoelectric performance of P-type half-heusler alloys TiNi1−xCoxSn (0 ≤ x ≤ 0.15)

TiNiSn is an N-type thermoelectric material with a high-power factor composed of low toxicity and abundant elements. TiNiSn also shows P-type electrical conduction by hole doping. In this study, we tune the conduction properties of TiNi1−xCoxSn (0 ≤ x ≤ 0.15) with Co substitution at the Ni site. The samples were prepared by the arc melting method, and thermoelectric properties were investigated up to 800 K. The results of the Hall effect and the Seebeck coefficient measurements indicate that the majority of charge carriers changes from electrons to holes at x ≥ 0.03, suggesting that Co acts as an acceptor. We report for the first time that Ti0.994Ni1.00Co0.051Sn1.01 exhibits ZT = 0.12 at 675 K. This work reveals that Ti0.994Ni1.00Co0.051Sn1.01 could be a potential P-type thermoelectric material operating at high temperatures.

Hot probe technique for thin films Seebeck coefficient measurement

A new experimental method using a 50 μm diameter hand fabricated hot probe of Pt90/10Rh alloy is proposed as a tool to measure the Seebeck coefficient of thin films deposited onto electrically insulated substrates. A thermal model for heat transfer inside the probe and to the sample was developed to simulate the corresponding temperature distributions. Simulations showed that the ratio of the temperature rise in the contact point to the average temperature of the probe evolves basically independent on electrical current and film-substrate properties. Moreover, the values of contact radius and thermal contact resistance should not be necessary known, but only the pairs which are best fitting the probe thermal resistance in contact with the film-substrate. This brings a great simplification in respect with certain AFM based hot probe methods for which is necessary to determine these two parameters by calibration of the two substrates with known thermal conductivity. The values can be further used to evaluate the Seebeck coefficient of the sample with a macroscopic probe, within 1 % precision. By variance to the classical measuring methods, which resort to a heater-heat sink ensemble instrumented with thermocouples, heated metallic rods with built-in thermocouples or microfabricated structures, the proposed method is fast, reliable and of higher spatial resolution. The method was validated by measuring the Seebeck coefficient on CdS, Bi and Cr thin films reference samples, respectively.

Exploring the effect of strong electronic correlations in Seebeck Coefficient of the NdCoO3 compound : Using experimental and DFT+U approach

The presence of complexity in the electronic structure of strongly correlated electron system NdCoO3 (NCO) have sparked interest in the investigation of its physical properties. Here, we study the Seebeck coefficient (α) of NCO by using the combined experimental and DFT+U based methods. The experimentally measured Seebeck coefficient is found to be ∼444 μ V/K at 300 K, which decreases to 109.8 μ V/K at 600 K. In order to understand the measured Seebeck coefficient, we have calculated the PDOS and band structure of the NCO. Furthermore, the calculated occupancy of 6.4 for Co 3d orbitals and presence of large unoccupied O 2p states indicate the covalent nature of the bonding. Apart from this, the maximum effective mass is found to be 36.75 (28.13) me for the spin-up (dn) channel in conduction band indicates the n-type behaviour of the compound in contrast to our experimentally observed p-type behaviour. While, the calculated Seebeck coefficient at the temperature-dependent chemical potential (μ) at 300 K shows the p-type behaviour of the compound. Fairly good agreement is seen between the calculated and measured values of α at U ff = 5.5 eV and U dd = 2.7 eV. The maximum power factor (PF) is found to be 47.6 (114.4)×1014 μW K −2cm−1 s −1 at 1100 K, which corresponds to p (n)-type doping of ∼1.4 (0.7)×1021 cm−3. This study suggests the importance of strong on-site electron correlation in understanding the thermoelectric property of the compound

Enhanced magnon thermal transport in yttrium-doped spin ladder compounds Sr14−xYxCu24O41

Magnons are quasiparticles of spin waves, carrying both thermal energy and spin information. Controlling magnon transport processes is critical for developing innovative magnonic devices used in data processing and thermal management applications in microelectronics. The spin ladder compound Sr14Cu24O41 with large magnon thermal conductivity offers a valuable platform for investigating magnon transport. However, there are limited studies on enhancing its magnon thermal conductivity. Herein, we report the modification of magnon thermal transport through partial substitution of strontium with yttrium (Y) in both polycrystalline and single crystalline Sr14−xYxCu24O41. At room temperature, the lightly Y-doped polycrystalline sample exhibits 430% enhancement in thermal conductivity compared to the undoped sample. This large enhancement can be attributed to reduced magnon-hole scattering, as confirmed by the Seebeck coefficient measurement. Further increasing the doping level results in negligible change and eventually suppression of magnon thermal transport due to increased magnon-defect and magnon-hole scattering. By minimizing defect and boundary scattering, the single crystal sample with x = 2 demonstrates a further enhanced room-temperature magnon thermal conductivity of 19Wm−1K−1, which is more than ten times larger than that of the undoped polycrystalline material. This study reveals the interplay between magnon-hole scattering and magnon-defect scattering in modifying magnon thermal transport, providing valuable insights into the control of magnon transport properties in magnetic materials.

Direct Measurement of the Absolute Seebeck Coefficient Using Graphene as a Zero Coefficient Reference

Direct Measurement of the Absolute Seebeck Coefficient Using Graphene as a Zero Coefficient Reference

Exploring electrical transport in thin film and bulk thermoelectric materials with an automated Seebeck coefficient and resistivity measurement platform

Accurate assessment of electrical properties, particularly the Seebeck coefficient and electrical resistivity, is critical in thermoelectric energy harvesting research, which involves converting thermal energy into electricity. This study presents an innovative automated system designed for the simultaneous measurement of the Seebeck coefficient and electrical resistivity as a function of temperature in both film and bulk samples. The system exhibits high precision across a wide range of electrical resistance, from milli Ohm (mΩ) to giga Ohm (GΩ). Furthermore, and in contrast with commercial systems, it provides excellent flexibility in accommodating samples with diverse lateral dimensions and thicknesses, ranging from a few millimetres to several centimetres. The measurement principle is based on analysing the current–voltage (I-V) characteristic of the samples. To ensure seamless monitoring and control of the measurement process, a user-friendly and adaptable Graphical User Interface (GUI) is integrated into the system, enhancing its overall user-friendliness and convenience.

Physical properties of rutile-TiO2 Nanoparticles and effect on PVA/SiO2 hybrid films synthesized by sol-gel method

We use an ab-initio approach to analyze the structural, electronic band structure, and thermoelectric properties of titanium dioxide (TiO2 in rutile phase), and we then use rutile-TiO2 nanoparticles to determine its effects on sol-gel-produced polyvinyl alcohol/silicon dioxide (PVA/SiO2) hybrid films. The synthesis of hybrid films involved the incorporation of 1 % rutile-TiO2 nanoparticles in the PVA/SiO2 matrix. The thermoelectric properties of the resulting hybrid films were characterized by Seebeck coefficient measurements, as well as electrical and thermal conductivities. The synthesis of PVA/SiO2/Nano-TiO2 films was accomplished with success. The chemical bonds have amply demonstrated that the PVA backbone is connected to the (SiO2-TiO2) network. TGA testing indicates that hybrid films are more resistant to higher temperatures than pure PVA films. SiO2 nanoparticles reveal more effective loading to improve dielectric characteristics compared to TiO2. The best results are obtained in cases of mechanical, thermal and electrical insulation when both nanofillers are integrated into the polymer matrix. The findings show that the thermoelectric performance of PVA/SiO2 hybrid films is improved by the addition of (1 %) rutile-TiO2 nanoparticles in the rutile phase. This study provides insights into the potential applications of rutile-TiO2 nanoparticles in enhancing the thermoelectric properties of hybrid materials and opens up avenues for further research in this area, and contributes to the growing body of knowledge on enhancing the thermoelectric properties of materials by incorporating rutile-TiO2 nanoparticles into hybrid films synthesized by the sol-gel method.

Cu1.3Mn1.7O4/LaNi0.6Fe0.4O3 composite with prospects for IT-SOFC/SOEC applications

Composite materials with the composition (100-x)Cu1.3Mn1.7O4/xLaNi0.6Fe0.4O3 (CMxLNF, where: x = 5, 10, 15, 20, 30, 40 and 50 wt%) were evaluated as possible coating materials for SOFC/SOEC metallic interconnects. The introduction of LaNi0.6Fe0.4O3 into spinel matrices improved electrical conductivity compared to pure Cu1.3Mn1.7O4. The measured Seebeck coefficient values indicate that carrier concentration increased with LaNi0.6Fe0.4O3 content, yet the activation energy of the carriers' mobility decreased. Extensive structural and microstructural studies of selected CM/LNF systems showed that composite material components exhibited high stability in relation to one another. Additionally, LaNi0.6Fe0.4O3 significantly improved the chemical stability of Cu1.3Mn1.7O4 in the presence of chromia, as tested after 150 h of exposure to air at 800 °C. Finally, coatings based on selected composite powders were deposited electrophoretically on the steel and were oxidized for 1500 h in air at 750 °C, confirming that CM10LNF can be applied as effective protective-conducting coatings on low-chromium ferritic steel.

Thermoelectric Properties of Spray Coated n-Type PEDOT:PSS Film

Inorganic thermoelectric (TE) materials have gained significant attention because of their salient properties. However, they possess some significant drawbacks, including high production costs, high heat loss, and fragility. Recently, Organic conducting polymers presented a promising platform as an alternative TE material because of their great mechanical flexibility, high stretchability, and environmental friendliness. In this work, we report for the first time on the TE properties of n-PEDOT:PSS film prepared using spray coating technique. The structural, optical and TE properties of the obtained n-PEDOT:PSS thin film was investigated using X-ray diffraction spectroscopy, UV-vis spectroscopy and Seebeck coefficient measurement systems, respectively. The n-PEDOT:PSS layer showed excellent optical properties with a band gap ranges from 3.91 to 3.78. In addition, the Seebeck coefficient and power factor (PF) were obtained to be 1096.77 µVK-1 and 298.59 µWm-1K-2 respectively, making n-PEDOT:P PSS to be regarded as efficient TE material.

Novel methodology for characterization of thermoelectric modules and materials

The document presents an innovative methodology that combines forced response and natural response theories in thermoelectric materials and devices. It stands out for expressing the thermoelectric figure of merit in terms of the ratio of two temperatures ZT푇̅=∆T′/∆T, enabling comprehensive testing and precise characterization of thermoelectric modules and materials, including measurements of thermal conductance, electrical resistance, Seebeck coefficient, and figure of merit. Additionally, it addresses the determination of thermal resistances and thermal capacitances related to thermal contacts, as well as the derivation of characteristic time constants and angular frequencies. This approach, applicable to both modular devices and individual samples, allows for the simultaneous measurement of all parameters on a single sample. The experiments considered non-ideal contacts and non-adiabatic conditions at room temperature T= 300K, enhancing the feasibility of in-situ characterization and positioning this methodology as a key tool in thermoelectric research.

Improved thermoelectric properties by copolymerization of conducting with insulating monomers on carbon nanotubes

In the present work, development of carbon nanotube (CNT)/poly(conducting-co-insulating monomer) structures was proposed to improve the thermoelectric (TE) performance in CNT/polyaniline (PANI) composites. To check the validity of this idea, we prepared multiwalled carbon nanotube (MWNT)/poly(aniline-co-acrylonitrile) composites by in-situ inverted emulsion copolymerization, and applied secondary doping with camphorsulfonic acid in m-cresol medium prior to the investigation of TE properties. The samples were characterized by FT-IR, UV–Vis, 1H NMR, DSC, GPC, CHNS elemental analysis, intrinsic viscosity, SEM, XRD, electrical resistance, Seebeck coefficient, thickness, and Hall measurements. We report that nitrile groups were hydrolyzed during the polymerization reactions to provide a polymer structure exhibiting aniline, acrylamide, acrylic acid, and glutarimide groups. Further, the poly(aniline-co-acrylonitrile) that prepared in the present work were random copolymers. Importantly, we found that 30 % MWNT/70 % poly(90ANI-co-10AN) composite exhibited a 63 % higher power factor (PF) of 5.48 μW/mK2 (σ: 225 S/cm, S: 15.6 μV/K) at 35 °C than that of 30 % MWNT/70 % PANI, which exhibited a PF of about 3.37 μW/mK2 (σ: 238 S/cm, S: 11.9 μV/K). This was ascribed to the decrease of carrier concentration together with the increase of carrier mobility in the 30 % MWNT/70 % poly(90ANI-co-10AN) composite as compared to the 30 % MWNT/70 % PANI.

Three-Dimensional Graphene Sheet-Carbon Veil Thermoelectric Composite with Microinterfaces for Energy Applications.

Over the years, various processing techniques have been explored to synthesize three-dimensional graphene (3DG) composites with tunable properties for advanced applications. In this work, we have demonstrated a new procedure to join a 3D graphene sheet (3DGS) synthesized by chemical vapor deposition (CVD) with a commercially available carbon veil (CV) via cold rolling to create 3DGS-CV composites. Characterization techniques such as scanning electron microscopy (SEM), Raman mapping, X-ray diffraction (XRD), electrical resistance, tensile strength, and Seebeck coefficient measurements were performed to understand various properties of the 3DGS-CV composite. Extrusion of 3DGS into the pores of CV with multiple microinterfaces between 3DGS and the graphitic fibers of CV was observed, which was facilitated by cold rolling. The extruded 3D graphene revealed pristine-like behavior with no change in the shape of the Raman 2D peak and Seebeck coefficient. Thermoelectric (TE) power generation and photothermoelectric responses have been demonstrated with in-plane TE devices of various designs made of p-type 3DGS and n-type CV couples yielding a Seebeck coefficient of 32.5 μV K-1. Unlike various TE materials, 3DGS, CV, and the 3DGS-CV composite were very stable at high relative humidity. The 3DGS-CV composite revealed a thin, flexible profile, good moisture and thermal stability, and scalability for fabrication. These qualities allowed it to be successfully tested for temperature monitoring of a Li-ion battery during charging cycles and for large-area temperature mapping.

Kaolin Clay-Based Geopolymer for Ionic Thermoelectric Energy Harvesting.

Geopolymers, a class of sustainable inorganic materials derived from natural and recycled resources, hold promise for various applications, including thermoelectric power generation. This study delves into the thermoelectric properties of Ikere white (IKW)-geopolymer, derived from kaolin clay, by employing rigorous measurements of thermal conductivity, electrical conductivity, and Seebeck coefficient. The investigation elucidates the pivotal role of temperature and ions in shaping the thermoelectric performance of IKW-geopolymer. Electrical conductivity analysis pinpoints ions within the geopolymer's channels as primary contributors. Beyond a critical temperature, the evaporation of bulk water triggers a transition of charge carriers from one- to three-dimensional motion, resulting in reduced conductivity. The Seebeck coefficient exhibits a range from -182 to 42 μV/K, with its time-dependent profile suggesting that ions potentially drive thermoelectricity in cementitious materials. Notably, a unique transition from n-type to p-type behavior was observed in the geopolymer, opening new avenues for ionic thermoelectric capacitors. These insights advance our understanding of thermoelectric behavior in geopolymers and have the potential to propel the development of novel building materials for energy conversion applications.

Large thermoelectric effects in p-SiC/p-Si and n-SiC/p-Si heterojunctions

The thermoelectric effect is important for thermal sensing, energy harvesting and other applications. This paper investigates the Seebeck coefficient of silicon carbide (SiC) on silicon (Si) heterojunctions and discusses the mechanism underlying the observed effects. The measured Seebeck coefficients of p‐3C‐SiC/p‐Si and n‐3C‐SiC/p‐Si heterojunctions are much higher than other reported values for SiC materials. The maximum Seebeck coefficients of p‐3C‐SiC/p‐Si and n‐3C‐SiC/p‐Si obtained were 1720 µV/K at 383 K and –421 µV/K at 396 K, respectively. These values are almost three times higher than those of other p-SiC and n-SiC materials. The high Seebeck coefficient in SiC/Si heterojunctions is attributed to the unique structure of the heterojunctions, which enables thermally activated charge carriers to migrate from Si to SiC. The results suggest that these heterojunctions can be exploited to develop highly sensitive self-powered thermal sensors.

Independent enhancement of the in-plane Seebeck effect in 2D PtSe2/PtSe2 homostructures via a facile interface tuning method

Atomically thin two-dimensional (2D) transition-metal dichalcogenide (TMDC) films have emerged as promising semiconducting materials for use in thermoelectric (TE) applications. However, the utilization of such materials remains challenging owing to the relatively high intrinsic resistance as the size of the TMDC thin films increases to the centimeter scale. These 2D TMDC films can also form vertically stacked homo- or heterostructures at large interfaces with other 2D TMDC films, resulting in unique TE properties at room temperature. This article reports on the in-plane TE properties when the interfaces formed within a PtSe2/PtSe2 (3 nm/3 nm) homostructure are modulated as a function of O2 plasma treatment time. The results show enhanced Seebeck coefficients compared with that of the single-layer PtSe2 with the same thickness. The independent enhancement in the Seebeck coefficient while keeping the electrical conductivity leads to a substantial increase in the power factor. Such extra Seebeck voltage in 2D PtSe2/PtSe2 homostructures is mainly as a result of momentum exchange by charge carriers caused by the temperature gradient in the vertical direction, which occurs in-plane Seebeck coefficient measurements, at the interface between the PtSe2 layers in the in-plane temperature gradient along the samples. These results resemble the characteristics of the phonon drag effect at low temperatures, which can independently increase the Seebeck coefficient at room temperature.