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There is evidence that magnetism can potentially increase the thermopower of materials, most likely due to magnon scattering, suggesting the incorporation of intrinsic magnetic semiconductors in non-magnetic thermoelectric materials. Here, samples of p-type Bi0.5Sb1.5Te3 with 10 at. % excess Te are ball-milled with varying ratios of the antiferromagnetic semiconductor CrSb (0, 0.125, 0.5, and 1 wt. %) to prepare bulk samples by spark plasma sintering technique. The thermopower of samples containing CrSb is increased due to an increase in the effective mass of the charge carriers, indicating that there is a drag effect originating from the magnetic particles. However, this was at the expense of reduced electrical conductivity caused by reduced charge carrier mobility. While overall only marginal improvements in power factors were observed, these samples exhibited significantly lower thermal conductivity compared to the single-phase material. As a result, a peak zT value of ∼1.4 was achieved at 325 K for the sample with 0.125 wt. % CrSb. These results highlight the potential of incorporating magnetic secondary phases to enhance the thermoelectric performance of materials. [ABSTRACT FROM AUTHOR]

Oxides are of interest for thermoelectrics due to their high thermal stability, chemical inertness, low cost, and eco‐friendly constituting elements. Here, adopting a unique synthesis route via chemical co‐precipitation at strongly alkaline conditions, one of the highest thermoelectric performances for ZnO ceramics (PFmax=$PF_{\text{max}} =$ 21.5 µW cm−1 K−2 and zTmax=$zT_{\text{max}} =$ 0.5 at 1100 K in Zn0.96Al0.04O${\rm Zn}_{0.96} {\rm Al}_{0.04}{\rm O}$) is achieved. These results are linked to a distinct modification of the electronic structure: charge carriers become trapped at the edge of the conduction band due to Anderson localization, evidenced by an anomalously low carrier mobility, and characteristic temperature and doping dependencies of charge transport. The bi‐dimensional optimization of doping and carrier localization enable a simultaneous improvement of the Seebeck coefficient and electrical conductivity, opening a novel pathway to advance ZnO thermoelectrics. [ABSTRACT FROM AUTHOR]

In-filled skutterudites InxCo4Sb12 have attracted much attention due to their relatively high thermoelectric performance, which, in turn, is attributed to the In atoms acting as rattlers in the skutterudite voids and to the formation of InSb precipitates when the In solubility limit is exceeded (0.22 ≤ xmax ≤ 0.27). In this work, to suppress the formation of the unwanted CoSb2 phase and favor the formation of InSb precipitates, the following composition of In1Co4Sb12+δ with In concentration much higher than the solubility limit and Sb overstoichiometry was used. Three sets of bulk specimens with a nominal composition of In1Co4Sb12+δ were synthesized by conventional induction melting followed by (1) ball milling (BM) and spark plasma sintering (SPS), (2) BM and SPS followed by high-temperature annealing, and (3) melt spinning and SPS. The utilization of different sample preparation methods and processing conditions leads to samples with different microstructures and InSb precipitates of different shapes, sizes, and distributions. Thus, for all samples with the same nominal composition of In1Co4Sb12+δ, zTmax varies from 0.7 to 1.3 at 673 K only because of microstructural modification. A maximum zT value of around 1.3 was obtained at 673 K for the sample prepared using induction melting followed by annealing, melt spinning, and SPS. [ABSTRACT FROM AUTHOR]

Bi2SeO2 is a promising n‐type semiconductor to pair with p‐type BiCuSeO in a thermoelectric (TE) device. The TE figure of merit zT and, therefore, the device efficiency must be optimized by tuning the carrier concentration. However, electron concentrations in self‐doped n‐type Bi2SeO2 span several orders of magnitude, even in samples with the same nominal compositions. Such unsystematic variations in the electron concentration have a thermodynamic origin related to the variations in native defect concentrations. In this study, first‐principles calculations are used to show that the selenium vacancy, which is the source of n‐type conductivity in Bi2SeO2, varies by 1–2 orders of magnitude depending on the thermodynamic conditions. It is predicted that the electron concentration can be enhanced by synthesizing under more Se‐poor conditions and/or at higher solid‐state reaction temperatures (TSSR), which promote the formation of selenium vacancies without introducing extrinsic dopants. The computational predictions are validated through solid‐state synthesis of Bi2SeO2. More than two orders of magnitude increase are observed in the electron concentration simply by adjusting the synthesis conditions. Additionally, a significant effect of grain boundary scattering on the electron mobility in Bi2SeO2 is revealed, which can also be controlled by adjusting TSSR. By simultaneously optimizing the electron concentration and mobility, a zT of ≈0.2 is achieved at 773 K for self‐doped n‐type Bi2SeO2. The study highlights the need for careful control of thermodynamic growth conditions and demonstrates TE performance improvement by varying synthesis parameters according to thermodynamic guidelines. [ABSTRACT FROM AUTHOR]

Bismuth telluride-based alloys possess the highest efficiencies for the low-temperature-range (<500 K) applications among thermoelectric materials. Despite significant advances in the efficiency of p-type Bi 2 Te 3 -based materials through engineering the electronic band structure by convergence of multiple bands, the n - type pair still suffers from poor efficiency due to a lower number of electron pockets near the conduction band edge than the valence band. To overcome the persistent low efficiency of n-type Bi 2 Te 3 -based materials, we have fabricated multiphase pseudobinary Bi 2 Te 3 -Bi 2 S 3 compounds to take advantages of phonon scattering and energy filtering at interfaces, enhancing the efficiency of these materials. The energy barrier generated at the interface of the secondary phase of Bi 14 Te 13 S 8 in the Bi 2 Te 3 matrix resulted in a higher Seebeck coefficient and consequently a higher power factor in multiphase compounds than the single-phase alloys. This effect was combined with low thermal conductivity achieved through phonon scattering at the interfaces of finely structured multiphase compounds and resulted in a relatively high thermoelectric figure of merit of ∼0.7 over the 300-550 K temperature range for the multiphase sample of n-type Bi 2 Te 2.75 S 0.25 , double the efficiency of single-phase Bi 2 Te 3 . Our results inform an alternative alloy design to enhance the performance of thermoelectric materials.