Abundant conducting polymers are promising organic substances
for
low-temperature thermoelectric applications due to their inherently
low thermal conductivities. By introducing a conducting polymer filler
(PEDOT:PSSpoly(3,4-ethylenedioxythiophene):poly(4-styrenesulfonic
acid)) into a representative inorganic thermoelectric matrix (Bi2Te3), a bulk-phase composite (i.e., inorganic matrix/organic
filler) for low-temperature thermoelectric applications is proposed.
This composite hosts an interfacial energy barrier between the inorganic
and organic components, facilitating controlled carrier transport
based on its energy level, known as the energy filtering effect, and
thus the composite exhibits a highly improved Seebeck coefficient
compared to pristine Bi2Te3. The composite also
displays a completely different temperature dependence on the Seebeck
coefficient from Bi2Te3 due to its distinct
bipolar conduction tendency. By regulation of the energy filtering
effect and bipolar conduction tendency, the composite undergoes noticeable
variations in the Seebeck coefficient, resulting in a significantly
enhanced power factor. Furthermore, the composite shows a substantially
reduced thermal conductivity compared to Bi2Te3 because it has lower carrier/lattice thermal contributions, possibly
attributed to its high carrier/phonon scattering probabilities. Owing
to the superior power factor and reduced thermal conductivity, the
composite exhibits markedly enhanced thermoelectric performance, achieving
a maximum figure of merit of approximately 1.26 at 380 K and an average
figure of merit of approximately 1.23 in the temperature range of
323–423 K. The performance of the composite is competitive
with previously reported n-type Bi2Te3 binary
or ternary analogues. Therefore, the composite is highly expected
to be a promising n-type counterpart of p-type Bi2Te3-based alloys for various low-temperature thermoelectric applications.