- Anion-cation co-doping with NaCl optimises carrier concentration and mobility and suppresses bipolar conduction, yielding maximum ZT ≈1.49 at 350 K.
- Higher NaCl content produces nanoscale precipitates that enhance phonon scattering without degrading electronic transport.
- Dicing-free, mechanically robust module using electrically insulating PEEK support enables a 31-pair module with performance competitive to commercial Bi2Te3 modules.
Small. 2026 Aug 20:e74188. doi: 10.1002/smll.74188. Online ahead of print.
ABSTRACT
We present a thermoelectric performance enhancement by anion-cation co-doping in p-type bismuth tellurides with a cost-effective and mechanically robust thermoelectric module fabrication process. Polycrystalline (BST)1 – x(NaCl)x (0 ≤ x ≤ 5.0 mol%) samples were synthesized via melting and hot-press sintering, and their anisotropic transport properties were investigated. At low NaCl concentrations, Na+ and Cl– act as effective substitutional dopants, optimizing carrier concentration and mobility while suppressing bipolar thermal conduction via local lattice strain. At higher NaCl contents, nanoscale precipitates form, providing additional phonon scattering without degrading electronic transport. Consequently, a maximum ZT ≈ 1.49 at 350 K and an average ZTavg ≈ 1.4(300-425 K) were achieved. In parallel, a mechanically robust module architecture using an electrically insulating, low-thermal-conductivity PEEK support eliminates wafering and dicing processes. A 31-pair module fabricated with optimized p-type (BST)1 – x(NaCl)x and n-type (CuI)0.3 Bi2 Te2.7 Se0.3 materials exhibit competitive thermoelectric performance to that of commercial Bi2 Te3-based modules. These results demonstrate a pathway toward economically competitive and mechanically robust next-generation thermoelectric modules.
PMID:42622341 | DOI:10.1002/smll.74188
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