Abstract
Hybrid inorganic-organic superlattice with an electron-transmitting but phonon-blocking structure has emerged as a promising flexible thin film thermoelectric material. However, the substantial challenge in optimizing carrier concentration without disrupting the superlattice structure prevents further improvement of the thermoelectric performance. Here we demonstrate a strategy for carrier optimization in a hybrid inorganic-organic superlattice of TiS2[tetrabutylammonium] x [hexylammonium] y, where the organic layers are composed of a random mixture of tetrabutylammonium and hexylammonium molecules. By vacuum heating the hybrid materials at an intermediate temperature, the hexylammonium molecules with a lower boiling point are selectively de-intercalated, which reduces the electron density due to the requirement of electroneutrality. The tetrabutylammonium molecules with a higher boiling point remain to support and stabilize the superlattice structure. The carrier concentration can thus be effectively reduced, resulting in a remarkably high power factor of 904 uW m-1 K-2 at 300 K for flexible thermoelectrics, approaching the values achieved in conventional inorganic semiconductors.
Original language | American English |
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Number of pages | 9 |
Journal | Nature Communications |
Volume | 8 |
DOIs | |
State | Published - 2017 |
NREL Publication Number
- NREL/JA-5500-70434
Keywords
- organic-inorganic nanostructures
- thermoelectrics
- two-dimensional materials