Solution processable photovoltaic devices based on an organic donor (D) and organic/inorganic acceptor (A) offers promise for development of low cost, light weight flexible energy sources. [1][2] The performance of such devices (which have recently exceeded power conversion efficiencies of 7% [3] ) is based on (1) the generation of bound electron-hole pairs (excitons) upon photoexcitation, (2) the dissociation of these excitons generated within the exciton diffusion length from the D-A interface (3) transportation of the free holes and electrons and (4) extraction of these charges at the anode and cathode respectively. While organic semiconductors are commonly used as the donor, [1][2] fullerene derivatives [4][5] , n-type conjugated polymers [6] or inorganic nanostructures [7][8] have been employed as acceptors. The potential advantage in the use of inorganic systems compared to the more widely used organic materials includes a high dielectric constant which facilitates effective exciton dissociation by reducing Coulombic interaction between the electron and the hole in an exciton as well as high carrier mobility. [7] Among the inorganic materials systems widely studied, ZnO with its wide (bulk) band gap of ~3.4 eV, [9] high electron mobility [10] combined with the capability to form nanocrystallites at low temperatures through the use of metallorganic precursors [11] 2 allows it to be incorporated into organic donors that are known only to withstand low temperature annealing processes. [12] Initial investigations on hybrid organic/inorganic photovoltaic systems focused on the addition of quantum dots, nanorods, multipods and nanoparticles into the organic donor. [13] However, difficulty in identification of a suitable solvent for accommodating both the organic and inorganic components as well as the lack of a bicontinous network upon spin casting the hybrid mixture led to poor device efficiencies. [14][15][16] In order to overcome the above technical difficulties, Beek et al [17] proposed the use of diethyl zinc (DEZ), a molecular precursor that is readily soluble in organic media and converts to ZnO upon exposure to moisture at temperatures compatible with organic photovoltaic device fabrication. Since then, the use of DEZ has led to several reports on ZnO incorporated organic-inorganic hybrid photovoltaics. [7,[18][19][20] In addition to the above mentioned advantages, the non-formation of ZnO at room temperature compared to other zinc containing metallorganic precursors [21] as well as the possibility of forming a bicontinous network [7] makes the use of DEZ an attractive route towards forming hybrid organic/inorganic photovoltaic cells. In addition to changing the nature through which the acceptor phase is incorporated, recent investigations have also focused on the use of modified organic donors for inorganic acceptor (Table S1). However as of present, efficiencies comparable to hybrid systems prepared using rr-P3HT and DEZ basedZnO is yet to be achieved.Despite the advantages noted above, as well as the ...