Organic-inorganic hybrids have recently emerged as a class of high-performing thermoelectric materials that are lightweight and mechanically flexible. However, the fundamental electrical and thermal transport in these materials has remained elusive due to the heterogeneity of bulk, polycrystalline, thin films reported thus far. Here, we systematically investigate a model hybrid comprising a single core/shell nanowire of Te-PEDOT:PSS. We show that as the nanowire diameter is reduced, the electrical conductivity increases and the thermal conductivity decreases, while the Seebeck coefficient remains nearly constant-this collectively results in a figure of merit, ZT, of 0.54 at 400 K. The origin of the decoupling of charge and heat transport lies in the fact that electrical transport occurs through the organic shell, while thermal transport is driven by the inorganic core. This study establishes design principles for high-performing thermoelectrics that leverage the unique interactions occurring at the interfaces of hybrid nanowires.

Organic–inorganic hybrids offer great promise as solution-processable thermoelectric materials. However, they have struggled to surpass the performance of their rigid inorganic counterparts due, in part, to a lack of synthetic control and limited understanding of how inorganic nanostructure dimensions impact overall charge transport. While it has been hypothesized that length, diameter, and aspect ratio (AR) all impact electronic transport in hybrid nanowires, the field lacks clarity on the relative role of each. In this study, the experimental parameter of ligand molecular weight (MW) is investigated as a synthetic knob for modulating nanowire dimensions, as well as the deconvolution of nanowire length versus diameter impacts on electron transport. By increasing ligand MW, larger nanowire AR dispersions occur and an optimal power factor of ≈130 μWm−1 K−2 is achieved for a modest AR of 73. Power factors of this magnitude are thought to only be achievable in ultrahigh AR systems; representing a 183% increase in performance over literature reports with similar AR. Additionally, nanowire diameter is demonstrated to be a far more sensitive parameter for enhancing performance than modulating length. This study provides improved fundamental insight into rational synthetic design avenues for future enhancements in the performance of hybrid materials.

A high-performance, wearable thermoelectric generator (TEG) was fabricated with a highly aligned carbon nanotube (CNT) sheet. The aligned CNT sheet exhibits extraordinary electrical conductivity compared to disordered CNT sheets and also can be directly fabricated as a continuous TEG without metal electrode interconnects. This provides a significant reduction in contact resistance between TE legs and electrodes compared to traditional TEGs, resulting in higher power output. In addition, the continuity of the module without any disconnected parts provides high degrees of mechanical stability and durability. This robust and scalable approach to flexible TEG fabrication paves the way for CNT applications in lightweight, flexible, and wearable electronics.