Zong-Ren Yang

Optimization and Analysis of Thermoelectric Properties of Unfilled Co1–x–yNixFeySb3 Synthesized via a Rapid Hydrothermal Procedure

A series of nanostructured co-doped Co(1-x-y)Ni(x)Fe(y)Sb3 were fabricated using a rapid hydrothermal method at 170 °C for a duration of 12 h, followed by evacuated-and-encapsulated heating at 580 °C for a short period of 5 h. The resulting samples were characterized using powder X-ray diffraction, field emission scanning electron microscopy, bulk density, electronic and thermal transport measurements. The power factor of Co(1-x-y)Ni(x)Fe(y)Sb3 is significantly enhanced in the high-temperature region due to significant enhancement of the electrical conductivity and absolute value of thermopower. The latter arises from the onset of bipolar effect being shifted to higher temperatures as compared with the non-doped CoSb3. The room temperature thermal conductivity falls in the range between 1.22 and 1.67 W m(-1) K(-1) for Co(1-x-y)Ni(x)Fe(y)Sb3. The thermal conductivity of both the (x,y) = (0.14,10) and (0.14,12) samples is measured up to 600 K and found to decrease with increasing temperature. The thermal conductivity of the (0.14,10) sample goes down to ∼1.02 W m(-1) K(-1). As a result, zT = 0.68 is attained at 600 K. The lattice thermal conductivity is analyzed to gain insight into the contribution of various scattering processes that suppress the heat transfer through the phonons in Co(1-x-y)Ni(x)Fe(y)Sb3. The effect of the simultaneous presence of Co, Ni, and Fe elements on the electronic structure and transport properties of Co(1-x-y)Ni(x)Fe(y)Sb3 is described using the quantum mechanical tunneling theory of electron transmission among the potential barriers.

A facile energy-saving route of fabricating thermoelectric Sb2Te3-Te nanocomposites and nanosized Te

A facile energy-saving route is developed for fabricating Sb2Te3-Te nanocomposites and nanosized Te powders. The fabrication route not only avoids using organic chemicals, but also keeps the energy consumption to a minimum. The fabrication procedure involves two steps. Energetic precursors of nanosized powders of Sb and Te are produced at room temperature followed by hot pressing at 400°C under 70 MPa for 1 h. The resulting Sb2Te3-Te nanocomposite exhibits enhanced power factor. The dimensionless figure of merit zT value of the Sb2Te3-Te nanocomposite is 0.29 at 475 K.

Enhanced thermoelectric properties of hydrothermally synthesized Bi0.88−xZnxSb0.12 nanoalloys below the semiconductor–semimetal transition temperature

Bi0.88−xZnxSb0.12 alloys with x = 0.00, 0.05, 0.10, and 0.15 were prepared using hydrothermal synthesis in combination with evacuating-and-encapsulating sintering. The effects of partial Zn substitution for Bi and different sintering temperatures on the thermoelectric properties of Bi0.88−xZnxSb0.12 alloys were investigated between 25 K and 425 K. Both the electrical conductivity and absolute thermopower are enhanced for the set of alloys sintered at 250 °C. The maximum power factor of 57.60 μW cm−1 K−2 is attained for the x = 0.05 alloy sintered at 250 °C. As compared with Zn-free Bi0.88Sb0.12, both the total thermal conductivity and lattice component are reduced upon Zn doping. Bipolar conduction is observed in both electronic and thermal transport. The maximum zT of 0.47 is attained at 275 K for the x = 0.05 alloy sintered at 250 °C.