of clean energy. In recent years, there has been considerable progress in the development of conducting polymers (CPs) for TE applications and the performance of p-type CPs is comparable to that of inorganic TE materials. [1][2][3] Despite their promise, one critical issue with the implementation of organic TE materials is that they tend to exhibit inefficient n-doping and unstable electron transport in most n-type polymers, significantly limiting their application, as both efficient p-type and n-type materials with comparable performance are required for practical TE applications. [4][5][6] Thereby, further development of efficient n-type materials is needed for the advancement of the field.During the last decade, composite and hybrid organic/inorganic materials have been developed in an attempt to mitigate the difficulties of enhancing the TE performance arising from the interrelation of the electrical conductivity (σ), Seebeck coefficient (S), and thermal conductivity (κ) through the charge carrier concentration (n). [7] These hybrid systems can not only inherit the individual strengths of each component, such as the high σ and S of inorganic materials and the low κ of organic materials, but they also possess interesting interfacial effects at the soft-hard interface that enables decoupling of the thermal and electrical transport, offering the opportunity Hybrid organic/inorganic materials have emerged as promising thermoelectric (TE) materials since they inherit the individual strengths of each component, enabling rational materials design with enhanced TE performance. The doping of hybrid TE materials via post-treatment processes is used to improve their performance, but there is still an incomplete understanding of the elicited effects. Here, the impact of different doping methods on the thin film TE performance of p-type Te/poly(3,4-ethylenedioxythiophene):poly(styre nesulfonate) (PEDOT:PSS) and n-type Ag 2 Te/PEDOT:PSS hybrid materials is investigated. Primary doping through acid-base and charge transfer processes using H 2 SO 4 and tetrakis(dimethylamino)ethylene, respectively, and the effects of secondary doping using ethylene glycol is examined. Through a combination of Hall effect measurements, hard X-ray photoelectron spectroscopy, and Raman spectroscopy, variations in the charge carrier concentration, mobility, and overall TE performance are related to the morphological and chemical structure of the hybrid materials. This study provides an improved understanding of the effects that different post-treatments have on hybrid materials and shows that the impact of these post-treatments on pure PEDOT:PSS does not always apply to hybrid systems. These new insights into post-treatment effects on hybrid materials is expected to facilitate further enhancement of their performance as electronic materials in general and thermoelectric materials in particular.