In-Situ Construction Of Novel Naphthalenediimide/Metal-Iodide Hybrid Heterostructures For Enhanced Photoreduction Of Cr (Vi)

The organic-inorganic donor-acceptor (D-A) hybrid hetemstructures, an emerging class of hybrid complexes containing semiconductive organic dyes and inorganic pigments at a molecular level, have displayed extraordinary optoelectronic properties and applications. Herein, we demonstrated that the combination of dipyridylnaphthalene diimide tecton (DPNDI) with CuI (or AgOOCF3) resulted in two isostructural D-A hybrid heterostructures based on 1D [Cu8I14](6) or [Ag8I14](6) polyanions surrounded by an interwoven network of in situ N-methylated DPNDI cations. Due to the compact contact between these two semiconductive components by the charge-assisted anion-ic and C-H center dot center dot center dot I hydrogen-bonding interactions, the obtained hybrid materials not only display high chemical stability but also exhibit high efficiency and moderate stability in the photoreduction of Cr (VI) upon visible light irradiation. The influences of various experimental conditions on the photocatalytic reactions including pH value and hole scavenger have been investigated. In addition, the possible mechanism studied shows that photogenerated electrons are the main active substances in the photoreduction of Cr(VI). This study suggests that constructing D-A hybrids heterostructures by two functional components with noncovalent interactions are promising for developing the hybrids used in the reduction of Cr(VI) in the future.