ABSTRACT
A simple, inexpensive in situ oxidative polymerization of aniline and pyrrole using ammonium persulfate (APS) as oxidant and hydrochloric acid (HCl) as dopant has been used to synthesize a hybrid (PAni-Co-PPy)@TiO2 nanocomposite with titanium oxide (TiO2) nanoparticles (NPs) wrapped into (PAni-Co-PPy) copolymer. The synthesized nanocomposite has been shown with higher oxygen reduction reactions (ORR) as an excellent cathode material for higher performance in the complex of (PAni-Co-PPy)+/TiO2(O-). The charge transport phenomenon between TiO2 and (PAni-Co-PPy)+ were found adequate with subsequent delocalization of electron/s at PAni and PPy. The self-doping nature of TiO2 (O-) played a vital role in oxygen adsorption and desorption process. With higher electrical conductivity and surface area, these were tested in microbial fuel cells (MFCs) for ORRs at cathode. This yielded a relatively higher current and power density output as compared to PAni@TiO2, PPy@TiO2, and commercially available Pt/C cathode catalysts in MFC system. In overall, the prepared (PAni-Co-PPy)@TiO2 nano-hybrid cathode delivered ~2.03 fold higher power density as compared to Pt/C catalyst, i.e. ~987.36 ± 49 mW/m2 against ~481.02 ± 24 mW/m2. The properties of electro-catalysts established an improved synergetic effect between TiO2 NPs and (PAni-Co-PPy). In effect, the enhanced surface area and electrochemical properties of the prepared (PAni-Co-PPy)@TiO2 nano-hybrid system is depicted here as an effective cathode catalyst in MFCs for improved performance.
Subject(s)
Bioelectric Energy Sources , Nanocomposites , Aniline Compounds , Electrodes , Pyrroles , TitaniumABSTRACT
In this study, sulfonated graphene oxide (SGO) was synthesized as potential conducting matrix to improve the properties of catalyst for single chamber microbial fuel cells (SC-MFCs). Here, TiO2 and Polyaniline (PAni) nanoparticles were anchored over SGO and the resulting SGO-TiO2-PAni nanocomposites were used as a potential cathode catalyst in MFCs. We have also examined the performance of SGO-TiO2-PAni compared to GO-TiO2-PAni and TiO2-PAni catalyst. The structural and morphological analyses were examined using a variety of characterization techniques. TiO2 nanoparticles bridged PAni and SGO through hydrogen bonding/electrostatic interaction and improved the thermal stability of SGO-TiO2-PAni catalyst. The electrochemical characterizations of these nanocatalysts suggest that the SGO-TiO2-PAni showed higher reduction current value (-0.46 mA), enhanced stability, and lower internal resistance (46.2 Ω) in comparison to GO-TiO2-PAni and TiO2-PAni towards oxygen reduction reactions (ORR). Consequently, MFC using SGO-TiO2-PAni demonstrated a maximum power density of 904.18 mWm-2 than that of GO-TiO2-PAni (734.12 mWm-2), TiO2-PAni (561.5 mWm-2) and Pt/C (483.5 mWm-2). The enhanced catalytic activity of SGO-TiO2-PAni catalyst was ascribed to the high electronic conductivity and long-term permanence of the nanocomposite. These superior electrochemical results suggested that the SGO-TiO2-PAni catalyst could be applied as a potential alternative to the commercial Pt/C cathode catalyst for the application of MFCs.