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Recently, photothermoelectric effect of thermoelectric materials has been hotly explored to develop self-powered and large bandwidth photodetectors working at ambient conditions. However, the key parameters for optimized photothermoelectric effect are still elusive. Here, based on the two-temperature model under static condition, we theoretically studied the key parameters to optimize the photothermoelectric performance of thermoelectric materials. Results verify that when the incident electromagnetic wave only generates electronic intra-band excitation, there is an ideal carrier concentration to optimize the photothermoelectric voltage; when the wavelength of a detected electromagnetic wave can resonantly excite quasi-particle (like phonons) except electrons, the photothermoelectric voltage can be enhanced significantly around the resonant wavelength regime; and when the electronic inter-band transition can be excited by an electromagnetic wave, photothermoelectric voltage is significantly increased due to the high optical absorption. As an example, the theoretical dependence of the photothermoelectric voltage of SnSe on wavelength is in line with the experimental result. This work elucidates the crucial parameters of thermoelectric materials to achieve the ideal photothermoelectric performance. [ABSTRACT FROM AUTHOR]

GeSe, composed of ecofriendly and earth-abundant elements, presents a promising alternative to conventional toxic lead-chalcogenides and earth-scarce tellurides as mid-temperature thermoelectric applications. This review comprehensively examines recent advancements in GeSe-based thermoelectric materials, focusing on their crystal structure, chemical bond, phase transition, and the correlations between chemical bonding mechanism and crystal structure. Additionally, the band structure and phonon dispersion of these materials are also explored. These unique features of GeSe provide diverse avenues for tuning the transport properties of both electrons and phonons. To optimize electrical transport properties, the strategies of carrier concentration engineering, multi-valence band convergence, and band degeneracy established on the phase modulation are underscored. To reduce the lattice thermal conductivity, emphasis is placed on intrinsic weak chemical bonds and anharmonicity related to chemical bonding mechanisms. Furthermore, extra-phonon scattering mechanisms, such as the point defects, ferroelectric domains, boundaries, nano-precipitates, and the phonon mismatch originating from the composite engineering, are highlighted. Additionally, an analysis of mechanical properties is performed to assess the long-term service of thermoelectric devices based on GeSe-based compounds, and correspondingly, the theoretical energy-conversion efficiency is discussed based on the present zT values of GeSe. This review provides an in-depth insight into GeSe by retrospectively examining the development process and proposing future research directions, which could accelerate the exploitation of GeSe and elucidate the development of broader thermoelectric materials. [ABSTRACT FROM AUTHOR]

This study introduces the synthesis of a hybrid thermoelectric material with enhanced conductivity and a high Seebeck coefficient, leveraging the properties of Te nanowires (NWs) and the conductive polymer PEDOT:PSS. Te NWs were synthesized using the galvanic displacement reaction. To further enhance conductivity, Ag-Te NWs were synthesized under optimized conditions via the Ag topotactic reaction, achieving desired results within 7 min using ethylene glycol and AgNO3. This hybrid material exhibited an electrical conductivity of 463 S/cm, a Seebeck coefficient of 69.5 μV/K at 300 K, and a power factor of 260 μW/mK2. These metrics surpassed those of conventional Te/PEDOT:PSS hybrids by a factor of 3.6, highlighting the superior performance of our approach. This study represents a significant advancement in thermoelectric materials, improving both conductivity and efficiency. [ABSTRACT FROM AUTHOR]

This study introduces the synthesis of a hybrid thermoelectric material with enhanced conductivity and a high Seebeck coefficient, leveraging the properties of Te nanowires (NWs) and the conductive polymer PEDOT:PSS. Te NWs were synthesized using the galvanic displacement reaction. To further enhance conductivity, Ag-Te NWs were synthesized under optimized conditions via the Ag topotactic reaction, achieving desired results within 7 min using ethylene glycol and AgNO3. This hybrid material exhibited an electrical conductivity of 463 S/cm, a Seebeck coefficient of 69.5 µV/K at 300 K, and a power factor of 260 µW/Mk². These metrics surpassed those of conventional Te/PEDOT:PSS hybrids by a factor of 3.6, highlighting the superior performance of our approach. This study represents a significant advancement in thermoelectric materials, improving both conductivity and efficiency. [ABSTRACT FROM AUTHOR]

This review explores the state‐of‐the‐art of thermoelectric materials, covering different crystalline structures and material families (e.g., chalcogenides, Zintl phases, skutterudites, clathrates, oxides, half‐Heusler, organic–inorganic composites, metal–organic frameworks, and silicides). It examines their corresponding thermoelectric properties while considering the synthesis methods employed, paying significant attention to those that particularly follow sustainable routes. Additionally, the work addresses current challenges in the field, such as enhancing stability at high temperatures and reducing manufacturing costs. The understanding gained in this field opens avenues for designing more efficient and sustainable devices to convert waste heat into electrical energy, thereby advancing cleaner technologies.

In this paper, the redox behaviour of Bi(III) unitary, Te(IV) unitary, Bi(III)-Te(IV) (Bi-Te) binary and Bi(III)-Te(IV)-graphene oxide (Bi-Te-GO) ternary solution using dimethyl sulphoxide as solvent was analysed by cyclic voltammetry and linear sweep voltammetry. On this basis, Bi2Te3 and Bi2Te3/reduced graphene oxide(Bi2Te3/rGO) thermoelectric thin films were prepared by potentiostatic electrodeposition. The phase structure, microstructure, elemental composition and thermoelectric properties of the composites were characterised by X-ray diffraction, scanning electron microscopy, energy dispersive spectrometer and Seebeck coefficient tests. The results show that the redox processes of Bi(III) unitary, Te(IV) unitary, Bi-Te binary and Bi-Te-GO ternary solution in DMSO are all irreversible. The reduction of Bi(III) ions is more difficult than that of Te(IV) ions, but at a certain potential, co-reduction of Bi(III) ions, Te(IV) ions and GO can occur. The surface roughness of the prepared thin film thermoelectric material increases with the negative shift of the deposition potential. The Bi2Te3 and Bi2Te3/rGO film materials prepared at different potentials all exhibit P-type characteristics, with the highest Seebeck coefficient of about 29.7 μV K−1. [ABSTRACT FROM AUTHOR]

In this study, the fabricated Hf-free N-type (Zr,Ti)Ni(Sn,Sb) and P-type (Zr,Ti)Co(Sn,Sb) thermoelectric materials were subjected to cyclic oxidation testing at 500 °C for 10, 30, and 50 cycles. The oxidation behaviour of the materials was systematically investigated by evaluating mass gain to study the oxidation kinetics and by analysing surface morphology, phase constitution and elemental distribution to investigate the oxidation mechanism. The results indicated that both of the materials were severely oxidised during the cyclic oxidation testing, and the mass gain followed the parabolic kinetics and the parabolic rate constant (kp) being 0.006165 mg2cm−4s−1 and 0.000109 mg2cm−4s−1 for the N-type and the P-type TE materials, respectively. Alternated multilayers of Ni3Sn4+SnO2+(Zr,Ti)O2 and CoSb + SnO2+Sb2O4+(Zr,Ti)O2 were identified on the surface of the N-type and P-type materials, respectively, after the cyclic testing, which would deteriorate the thermoelectric performance of the materials. The outcome of this study strongly suggests that it is essential to improve the oxidation resistance and the thermal stability of the N-type (Zr,Ti)Ni(Sn,Sb) and P-type (Zr,Ti)Co(Sn,Sb) thermoelectric materials for high-temperature applications.

Wearable electronic devices have emerged as a pivotal technology in healthcare and artificial intelligence robots. Among the materials that are employed in wearable electronic devices, organic thermoelectric materials possess great application potential due to their advantages such as flexibility, easy processing ability, no working noise, being self-powered, applicable in a wide range of scenarios, etc. However, compared with classic conductive materials and inorganic thermoelectric materials, the research on organic thermoelectric materials is still insufficient. In order to improve our understanding of the potential of organic thermoelectric materials in wearable electronic devices, this paper reviews the types of organic thermoelectric materials and composites, their assembly strategies, and their potential applications in wearable electronic devices. This review aims to guide new researchers and offer strategic insights into wearable electronic device development. [ABSTRACT FROM AUTHOR]

Production of thermoelectric materials from solution‐processed particles involves the synthesis of particles, their purification and densification into pelletized material. Chemical changes that occur during each one of these steps render them performance determining. Particularly the purification steps, bypassed in conventional solid‐state synthesis, are the cause for large discrepancies among similar solution‐processed materials. In present work, the investigation focuses on a water‐based surfactant free solution synthesis of SnSe, a highly relevant thermoelectric material. We show and rationalize that the number of leaching steps, purification solvent, annealing, and annealing atmosphere have significant influence on the Sn : Se ratio and impurity content in the powder. Such compositional changes that are undetectable by conventional characterization techniques lead to distinct consolidated materials with different types and concentration of defects. Additionally, the profound effect on their transport properties is demonstrated. We emphasize that understanding the chemistry and identifying key chemical species and their role throughout the process is paramount for optimizing material performance. Furthermore, we aim to demonstrate the necessity of comprehensive reporting of these steps as a standard practice to ensure material reproducibility. [ABSTRACT FROM AUTHOR]

Due to their broad range of uses in thermo-electric devices, aerospace, and other industries, thermoelectric materials have garnered much attention. To expand the scope of their applications, thermoelectric materials’ thermoelectric characteristics must be effectively improved. Improved thermoelectrical properties with advancement is one of the critical strategies. Even though it is challenging to do small-scale measurements, it is crucial to precisely gauge the thermoelectric characteristics of varying materials (organic/inorganic/MXenes). Two-dimensional materials have drawn much interest for technological applications because of their unique properties. MXenes are a class of two-dimensional (2D) transition metal carbides, nitrides, and carbonitrides that have garnered significant attention for their promising properties by showing high electrical conductivity, controllable thermal conductivity, and high Seebeck coefficient value making suitable candidates for thermoelectric energy conversion. Thermal and electrical parameters are currently measured using a variety of techniques. However, the advanced thermoelectric properties with advanced thermoelectric materials, such as thermopower, thermal conductance, and electrical conductivity, are compiled in this review. Also outlined are measurement techniques for thermoelectric properties of selected advanced and 2D materials. Lastly, the challenges of integrated measurement methods are suggested, and a few integrated measurement solutions that work well with many inorganic/organic composites and two-dimensional materials MXenes are most proposed.

Thermoelectric materials can efficiently and cleanly convert between electrical and thermal energy，offering significant prospects in waste heat recovery and electronic cooling applications. Lead telluride（PbTe）materials were used in thermoelectric power sources for deep space exploration. Lead selenide（PbSe），a homologue of PbTe，shows potential as a more abundant and cost-effective alternative for mid-temperature thermoelectric power generation. Recently，research in PbSe thermoelectric has shifted from mid-temperature power generation to near-room-temperature cooling，driven by the growing demand for Te-free thermoelectric cooling materials and devices. This paper reviewed the typical optimization strategies used in the research of p-type PbSe，summarized the key research progress in thermoelectric devices based on this material，and highlighted its significant development prospects. Finally，we provide a personal outlook on developing the near-room-temperature thermoelectric performance of p-type PbSe materials and manufacturing high-performance cooling devices，which includes integrating various optimization strategies，optimizing device assembly techniques，identifying suitable contact materials，and developing Te-free thermoelectric devices based on PbSe，with the goal of advancing their application in critical fields such as deep space exploration and laser cooling.

This study examines the oxidation behavior of skutterudite materials fabricated using a rapid self-propagating high-temperature synthesis and pulse plasma sintering route. Pure Co 4 Sb 12 and Co 4 Sb 10.8 Se 0.6 Te 0.6 were oxidized in the air at 773 K for up to 500 h. Skutterudites modified with Se and Te had a lower oxidation resistance than that of pure Co 4 Sb 12 and also showed a lower decomposition temperature. This changed the oxidation mechanism, as manifested by the different roles of the Sb 2 O 3 phase during oxide scale formation and the CoSb 2 -like phase in the modified near-surface region. The unusual mass loss by the Co 4 Sb 10.8 Se 0.6 Te 0.6 alloy during the first 100 h of oxidation was also revealed. Despite the evident changes at the surface of the samples, no visible grain growth was noted in both skutterudites. The electrical properties of the samples were also stable. [ABSTRACT FROM AUTHOR]

This scientometric study looks at the current trend in thermoelectric materials research and explores the evolving domain of thermoelectric materials research using a combination of bibliometric and scientometric methodologies. The analysis examines global research trends from a dataset of over 37,739 research articles, focusing on thematic evolution, annual growth rates, and significant contributions. Six principal research clusters were identified, encompassing energy conversion, material synthesis and nanostructures (the most prominent cluster), computational modeling and material properties, measurement and characterization, material performance enhancement, and material processing and microstructure. Each cluster highlights a critical aspect of the field, reflecting its broad scope and depth. The key findings reveal a marked annual increase in research output, highlighting the growing global importance of thermoelectric materials in sustainable energy solutions. This is especially evident in the significant contributions from China and the USA, emphasizing their leadership in the field. The study also highlights the collaborative nature of thermoelectric research, showing the impact of global partnerships and the synergistic effects of international collaboration in advancing the field. Overall, this analysis provides a comprehensive overview of the thermoelectric materials research landscape over the past decade, offering insights into trends, geographic contributions, collaborative networks, and research growth. The findings underscore thermoelectric materials’ vital role in addressing global energy challenges, highlighting recent advancements and industrial applications for energy efficiency and sustainability.

In this study, advanced oxidation-protective CrSi coatings were developed and deposited on N-type (Zr,Ti)Ni(Sn,Sb) and P-type (Zr,Ti)Co(Sn,Sb) thermoelectric (TE) materials using an environmentally friendly closed field unbalanced magnetron sputtering PVD system. The oxidation behaviour of the CrSi-coated and uncoated samples was evaluated through static oxidation tests at 500 °C and 600 °C for 10h and 50 h, respectively. In addition, the samples were exposed to cyclic oxidation tests between 25 °C and 500 °C for 10, 30 and 50 cycles, with each cycle consisting of 1h of oxidation at 500 °C, to examine the coating ability to withstand thermal shock, which is involved in the service of TE devices. The surface morphology, cross-section layer structure, elemental distribution and phase constitution were analysed using scanning electron microscopy (SEM), energy dispersive spectroscopy (EDX) and X-ray diffraction (XRD). The mass gain after the oxidation tests was measured and calculated for each sample to study the oxidation kinetics. The uncoated samples exhibited a considerable amount of oxidation, leading to change in the surface morphologies, and the formation of alternated layers including oxide products (Zr(Ti)O2, SnO2) and Ni3Sn4 compound for the N-type and (Zr(Ti)O2, SnO2, Sb2O4) and CoSb compound for the P-type material, after static and cyclic oxidation tests. The experimental work in this study has, for the first time, demonstrated that the CrSi coatings developed with very high thermal stability and oxidation resistance can effectively protect both the N-type and P-type materials from oxidation and sublimation even during cyclic oxidation tests. The strong affinity of Cr and Si to oxygen can trap oxygen, retard its inward diffusion and thus protect the TE material substrate from oxidation. This finding could pave the way towards the further development of long-life high-performance TE generators and devices, thus contributing to the net zero target.

Screen printing technology is employed to prepare poly(3,4‐ethylenedioxythiophene):poly(styrenesulfonate) (PEDOT:PSS)/double‐walled carbon nanotubes (DWCNT) films as active p‐type material for flexible thermoelectric generators (TEGs). Performance of the PEDOT:PSS/CNT composites have been optimized by changing the formulation inks to make them suitable for screen printing, by varying the CNT concentrations and by treating the printed polymeric films in ethylene glycol (EG). The purpose of this work is finding the processing conditions that optimize conductivity, Seebeck coefficient, and the power factor of the fully printed material. From experimental data, the composite with 10% by weight of DWCNT chemically treated in EG maximizes conductivity, Seebeck coefficient, and power factor of the material. [ABSTRACT FROM AUTHOR]

In2O3 based materials are one of the most promising high-temperature thermoelectric materials for application. Herein, Sm doped In2O3 samples were prepared by mechanical alloying, high-temperature calcination, and discharge plasma sintering, and the influence mechanism of rare earth element doping on the thermoelectric properties of In2O3 based semiconductors was studied. The results indicate that the electrical conductivity increased significantly. Due to the introduction of Sm impurity levels, the density of states near the Fermi level significantly increases. The bandgap widens, and the mobility first decreases and then increases. Due to the increase in carrier concentration, the absolute value of the Seebeck coefficient decreases, but the gain effect caused by the increase in conductivity is greater than the debuff caused by the decrease in the absolute value of the Seebeck coefficient. The power factor increases after Sm doping.The thermal conductivity decreases due to the decrease in Young's modulus, enhanced heterogeneous scattering, and enhanced heavy element scattering. The ZT value was raised to ∼0.327 at 973 K, obtained by Sm doped In2O3 sample with x = 0.060, which is ∼6 times as that of the pristine In2O3 sample.