Interfacial effects in an inorganic/organic composite based on Bi2Te3 inducing decoupled transport properties and enhanced thermoelectric performance. Issue 26 (9th June 2022)

• Record Type: Journal Article
• Authors: Kim, Cham; Cho, Jaehun; Kim, Taewook; Lopez, David Humberto
• Is Part Of: Journal of materials chemistry. Volume 10:Issue 26(2022)
• Page Start: 13780
• Page End: 13792
• Publication Date: 2022-06-09
• Subjects: Materials -- Research -- Periodicals; Chemistry, Analytic -- Periodicals; Environmental sciences -- Research -- Periodicals; 543.0284
• DOI: 10.1039/d2ta02334b
• Languages: English
• ISSNs: 2050-7488

Abstract

Abstract : Conducting polymer fillers are added to a Bi2 Te3 matrix to develop an inorganic/organic composite including the interface, where an energy filtering effect occurs along with phonon scattering, resulting in greatly enhanced thermoelectric performance. Abstract : An inorganic/organic composite is suggested for low-temperature thermoelectric applications. An abundant and inexpensive conducting polymer, poly(3, 4-ethylenedioxythiophene):poly(styrenesulfonate) (PEDOT:PSS), is introduced into n-type Bi2 Te3, thus affording a bulk-phase composite, in which an interfacial energy barrier may occur at the component interfaces. These interfaces interfere with charge carrier transport, and thus the composite exhibits somewhat higher electrical resistivity than pristine Bi2 Te3 . However, the interfacial energy barrier can cause an energy filtering effect; thus, the composite exhibits a higher Seebeck coefficient than the pristine Bi2 Te3 . This Seebeck coefficient improvement is high enough to compensate for the resistivity increase, and thus the composite affords a significantly higher power factor than Bi2 Te3 . The composite exhibits lower lattice and carrier thermal conductivities than Bi2 Te3, because the composite includes the interfaces possibly causing vigorous phonon scattering, and it exhibits relatively low carrier mobility. The composite is observed to show much lower total thermal conductivity than Bi2 Te3 . Consequently, the electrical and thermal properties are decoupled in the composite, resulting in remarkably enhanced thermoelectric performance (ZTmax ∼ 1.19@132 °C; ZTave ∼ 1.14@50–150 °C), which is approximately double that of Bi2 Te3 . Not only are the ZT values predominant among those of n-type Bi2 Te3 analogues but they are also as competent as those of n-type Bi2 Te3 -based ternary substances. The composite is expected to be an excellent counterpart of p-type Bi2 Te3, and thus it should be highly applicable to promising low-temperature thermoelectric operations, such as sustainable energy harvesting devices and systems.