Emeraldine-based polyaniline (EB-PANI) was synthesized via oxidative polymerization of aniline in aqueous acid. Various aliquots of graphene oxide (GO) aqueous dispersion were added to aniline during polymerization to achieve a… Click to show full abstract
Emeraldine-based polyaniline (EB-PANI) was synthesized via oxidative polymerization of aniline in aqueous acid. Various aliquots of graphene oxide (GO) aqueous dispersion were added to aniline during polymerization to achieve a mass percent of GO in the PANI:GO nanocomposites of 0%, 0.49%, 2.4%, 4.9%, 7.3%, 9.8%, 12.2%, and 24.5%, respectively. TEM images of the GO taken from different locations showed that most of the GO is either a double layer or multilayer graphene sheet—although some of the locations showed a single-layer graphene sheet. Raman shift of GO presents the G band located at 1591 cm−1 and the D band located at 1321 cm−1. The thermogravimetric analysis (TGA) of the PANI:GO nanocomposite showed the evidence of existing GO in PANI. The X-ray photoelectron spectroscopy (XPS) narrow scans of EB-PANI, GO, and PANI:GO showed a maximum that is assigned to the C–C peak position (284.8 eV). The deconvolution of the C1s peak in EB-PANI reveals the presence of C–N/C=N species (285.8 eV) assigned to the amine and imine nitrogens in polyaniline. The acid-free hole transport layer (HTL) synthesized from PANI:GO composites was used in two different types of organic solar cells (OPVs), i.e., P3HT:PC60BM (1:0.6) and PCDTBT:PC70BM (1:4). The highest power conversion efficiency (PCE) as a function of GO loadings in the PANI:GO nanocomposites for P3HT:PCBM cells was for the nanocomposite PANI:GO-7.5 with an average of ~ 0.2%, where the GO loading was 7.3% w/w. Equivalently, the PCDTBT:PCBM cells exhibited the highest PCE for PANI:GO-7.5 nanocomposite (~ 0.5%), as well.
               
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