Photoelectrochemical cells based on bis-aniline-crosslinked CdS nanoparticle–carbon nanotube matrices associated with electrodes

Abstract

The electrochemical preparation of a bis-aniline-crosslinked CdS nanoparticle–carbon nanotube matrix on electrode surfaces is described. The optimal electrode was prepared by the electropolymerization of thioaniline-functionalized CdS nanoparticles (NPs) and aniline-tethered carbon nanotubes (CNTs), using 80 electropolymerization cycles at a CdS NPs:CNTs (w/w) ratio of 5.5. The photocurrent generated by the electrode, in the presence of triethanolamine as electron-donor, reveals a quantum yield of ϕ = 2.4%, ca. seven-fold higher than for a monolayer of CdS NPs crosslinked to the electrode by bis-aniline bridges. The enhanced photocurrents in the CdS NP–CNT composite were attributed to the trapping of the photogenerated conduction-band electrons in the semiconductor NPs by the CNTs, and their effective transport to the electrode, a process that facilitated charge separation. The bias potential applied to the electrodes affected the resulting photocurrents, and enhanced photocurrents were observed when the bis-aniline bridges existed in their oxidized quinoid state. This was attributed to the improved trapping of the conduction-band electrons by the electron-acceptor (relay) bridging units. The supramolecular association of N,N′-dimethyl-4,4′-bipyridinium, MV²⁺, to the π-donor bis-aniline bridging units resulted in a photocurrent quantum yield of ϕ = 6.1%. The enhanced quantum yield was attributed to the effective trapping of the conduction-band electrons by the π-acceptor MV²⁺ relay units associated with the π-donor bridging elements, and the efficient transport of the electrons to the electrode by the conductive CNT matrix. These processes facilitated and improved charge separation and provided a competitive path to degradative electron–hole recombination in the semiconductor particles.