Abstract

The high potential of polycrystalline Ge as a thin-film thermoelectric material was demonstrated. We synthesize a polycrystalline Ge layer on an insulating substrate at 450 °C via advanced solid-phase crystallization and control its carrier concentration through the solid-phase diffusion of various p- and n-type dopants. The heating deposition (150 °C) of the amorphous precursor considerably improves the crystal quality of the polycrystalline Ge layer as well as the doping properties. The solid-phase diffusion of Ga and P dopants onto the Ge layers allows for control of the carrier concentration in the ranges of 1017–1020 cm−3 for p-type and 1018–1019 cm−3 for n-type, respectively, by modulating the diffusion annealing temperature and time. Because of the high electrical conductivities reflecting the carrier mobilities and carrier concentrations, the maximum power factors reach a value of 1080 μW m−1 K−2 for p-type and 2300 μW m−1 K−2 for n-type at room temperature. These power factors are higher than those of most polycrystalline semiconductor thin films formed at temperatures below 1000 °C. Therefore, this study serves as a milestone toward high-performance and reliable thin-film thermoelectric generators based on an environmentally friendly semiconductor.

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