News Release

Efficient power generation and cooling in cubic tin selenide

Peer-Reviewed Publication

Maximum Academic Press

Figure 1

image: 

Figure 1. (a) Our optimization mechanism for p-type polycrystalline SnSe with a cubic structure. The isoelectronic doping of Pb and Ge promoted band divergence, reduced the effective mass m*, and enhanced the carrier mobility μ. Substitution of Pb and Ge at cation sites with unequal atomic numbers generated numerous cation vacancies, which induced various defects, effectively reducing thermal conductivity and enabling carrier–phonon decoupling. (b) The maximum cooling temperature difference ΔTmax and maximum conversion efficiency ηmax for cubic SnSe/Bi2 (Te, Se)3 (BTS)-based devices. The inset shows the thermoelectric devices. The thermoelectric properties of (SnSe)0.6(Ag1-4xPbxGexSbTe2)0.4 (x = 0, 0.02, 0.04, 0.06, and 0.08) are as follows: (c) Power factor, PF. (d) Total thermal conductivity, κtot. (e) ZT and ZTave (300–673 K) values. (f, g) Electronic band structures calculated for (f) (SnSe)0.6(AgSbTe2)0.4 and (g) (SnSe)0.6(Ag0.84Pb0.04Ge0.04SbTe2)0.4. (h) The corresponding density of states.

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Credit: Originality

Thermoelectrics are regarded as potential materials in energy technology because they can enable direct and reversible conversion between heat and electricity. A new study advances this promise by redesigning polycrystalline tin selenide (SnSe), which is easier to manufacture than fragile single crystals but has historically shown limited room-temperature thermoelectric performance. By co-doping cubic SnSe with lead (Pb) and germanium (Ge), the researchers introduced beneficial vacancy defects that promote electron-phonon decoupling. The optimized polycrystalline SnSe exhibited high room-temperature thermoelectric performance, enhanced mechanical robustness, and demonstrated device-level cooling and power generation, suggesting a practical route toward cleaner thermal management and waste-heat recovery.

Thermoelectric technology relies on the Seebeck and Peltier effects, which enable the direct interconversion of heat and electricity. The conversion efficiency of a thermoelectric material is determined by the dimensionless figure of merit ZT, defined as ZT=(S2σ/k)⋅T, where S, σ, k, and T represent the Seebeck coefficient, electrical conductivity, thermal conductivity, and temperature in kelvin. However, these thermoelectric parameters are strongly coupled with each other as a result of their mutual dependence on the dynamic carrier concentration n, which is usually limiting for thermoelectric optimization. Crystalline SnSe exhibits excellent thermoelectric potential, but its long fabrication cycle. Polycrystalline SnSe is more scalable, yet grain-boundary scattering and oxidation have restricted its performance. Given these challenges, further research on high-performance polycrystalline SnSe for cooling and power-generation applications is urgently needed.

In a study published in Originality, a research team led by Li-Dong Zhao from  Beihang University reported “High-performance thermoelectric power generation and cooling realized in cubic polycrystalline SnSe”  (https://doi.org/10.1016/j.orig.2026.05.001). The study addresses an important issue in SnSe thermoelectrics: How to achieve high device-level conversion efficiency and reliable device operation in polycrystalline SnSe. The team developed a non-equivalent isoelectronic co-doping strategy using Pb and Ge at cation sites in polycrystalline SnSe with cubic structure, achieving excellent near-room-temperature thermoelectric performance as well as outstanding power-generation and cooling performance.

The key advance lies in a defect-engineering strategy that turns atomic-scale defects into beneficial features for performance enhancement. In cubic polycrystalline SnSe, substitutional doping with lead (Pb) and germanium (Ge) disrupts the cation balance and generates abundant cation vacancies. These vacancies further coalesce into micro-and nanoscale defect regions, forming hierarchical phonon-scattering centers that suppress phonon transport and reduce lattice thermal conductivity. Simultaneously, Pb/Ge co-doping reshapes the valence-band structure, increases band divergence, lowers the effective mass, and enhances carrier mobility by nearly fourfold. As a result, the cubic SnSe achieved a room-temperature ZT of ~0.5 and an average ZT (ZTave) of ~0.9 from 300 to 673 K. When paired with n-type bismuth telluride selenide (Bi2(Te,Se)3) in a full thermoelectric device, the optimized p-type cubic SnSe polycrystal delivered a maximum cooling temperature difference (ΔTmax) of ~47.3 K and a maximum conversion efficiency (ηmax) of ~4.6%. Moreover, the cubic polycrystalline SnSe exhibits isotropic transport behavior and higher hardness than pristine polycrystalline SnSe, which could make it easier to cut, polish, assemble, and integrate into thermoelectric devices.

These findings provide a new materials basis for near-room-temperature thermoelectric cooling and waste-heat power generation, and are expected to meet the needs of industrial equipment, electronic devices, and compact thermal-management systems for localized cooling, precise temperature control, and waste-heat recovery. Meanwhile, the study also shows that the synergistic design of band engineering and vacancy manipulation may offer new insights for polycrystalline thermoelectric materials to overcome the traditional trade-off between thermoelectric performance and mechanical durability.

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References

DOI

10.1016/j.orig.2026.05.001

Original Source URL

https://doi.org/10.1016/j.orig.2026.05.001

About Originality

Originality (ISSN: 3051-2700) is an international, peer-reviewed journal co-owned by the University of Science and Technology Beijing, Peking University, and China Rural Special Technology Association, and is globally published by KeAi. Dedicated to originality and interdisciplinary innovation, the journal aims to build a world-class academic platform spanning Life Sciences, Agriculture and Food Systems, Physical Sciences, Engineering, Earth and Environmental Sciences, and Interdisciplinary Sciences. Originality welcomes original research that inspires and leads future scientific innovation in both specialized and interdisciplinary fields.https://www.sciencedirect.com/journal/originality


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