A new strategy for co-assembling π-conjugated polymer/cadmium sulfide hybrids into an efficient charge-transporting nanochannel array by using an all-conjugated diblock copolymer motif

Abstract

In this study, a novel organic/inorganic hybrid material containing cadmium sulfide (CdS) nanoparticles was synthesized in situ by using an all π-conjugated block copolymer as both a synergistic long-range ordered structure-directing template and an efficient exciton quencher for the nanohybrid. The conducting–conducting block copolymer of poly(2,5-dihexyloxy-para-phenylene)-b-poly(3-hexyl thiophene) (PPP-P3HT) was used as a linear nanoreactor for the quantum dot synthesis to yield nanohybrids with highly ordered donor/acceptor (D/A) nanowire morphology that exhibit enhanced optoelectronic properties. The synthesized PPP-P3HT/CdS-OH nanohybrid possessed a one-dimensional D/A coaxial nanowire structure of uniform width (∼10 nm), wherein the synthesized CdS quantum dots were embedded, resulting in a display of superior long-term stability in a solution medium. By a simple drop casting process, the hybrid materials with highly ordered organic/inorganic nanochannel arrays could also be preserved in a thin film state, as evidenced by TEM and X-ray measurements, for device applications. The PPP-P3HT block copolymer exhibited significantly better hole mobility than its P3HT homopolymer counterpart. In addition, the resulting PPP-P3HT/CdS-OH hybrid systems displayed a considerably enhanced PL quench effect and shorter exciton lifetime due to efficient charge transfer between the P3HT block and the confining CdS nanoparticles in the P3HT/CdS coaxial domain of the hybrid nanowire structure. Therefore, the PPP-P3HT/CdS-OH nanohybrids can be used as bicontinuous nanochannels for efficient charge separation and charge transport, which show potential for use in future optoelectronic applications.