CuSe-based thermoelectric materials exhibit high dimensionless figure of merit () values at elevated temperatures (900-1000 K) but relatively lower values at intermediate temperatures, approximately 500 K. We synthesized a series of polycrystalline CuSeTeI/CuO composites (where = 0.00, 0.01, 0.02, and 0.03) using an energy-efficient synthesis method conducted at room temperature, followed by heat treatment at 923 K for 6 h. X-ray diffraction (XRD) analysis confirmed the monoclinic crystal structure of the α phase. The introduction of iodine doping at Te sites introduced electron carriers to p-type CuSeTe, reducing the hole carrier concentration. Consequently, the electrical resistivity increased, and the thermopower exhibited a significant increase. The incorporation of electron carriers into the p-type CuSeTe/CuO composites resulted in an enhanced power factor within the medium-temperature range. Specifically, at 500 K, the CuSeTeI/CuO ( = 0.02) composites demonstrated the highest power factor among the series of CuSeTeI/CuO composites, measuring 9.1 μW cm K. According to the weighted mobility analysis, it is clear that the = 0.02 composite possesses the optimal carrier concentration, which accounts for its superior power factor compared to the other composites in the series. Furthermore, the CuSeTeI/CuO composites and CuSeTe/CuO composites displayed values of 0.49 and 0.33, respectively, at 550 K. Additionally, iodine doping led to an enhancement in the average values between 450 and 550 K. Therefore, electron doping in p-type materials presents itself as a viable strategy for shifting the operating temperature of a thermoelectric device from high to medium temperature. We successfully fabricated a thermoelectric generator comprising 6 pairs of p-leg CuSeTeI/CuO composites and n-leg InSbBi. This TEG achieved impressive results, including a maximum output voltage, power output, power density, and efficiency of 0.115 V, 10.6 μW, 35.1 μW cm, and 1.74% at a temperature difference (Δ) of 120 K.

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http://dx.doi.org/10.1021/acs.inorgchem.3c03774DOI Listing

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