文摘
This paper reports the chemical modification effects at charge separation interface on the performance of the hybrid solar cells consisting of poly(2-methoxy-5-(2-ethylhexyloxy)-1,4-phenylenevinylene) (MEH-PPV) as an electron donor (D) and vertically aligned ZnO nanorod arrays as an electron acceptor (A). Results show that, with increasing the modification time Ts for grafting dye Z907 onto the ZnO surface from 0 to 8 h, the charge transfer efficiency at the MEH-PPV/ZnO interface keeps increasing, the short circuit current (Jsc) increases and reaches a peak value at Ts = 8 h, but the open circuit voltage (Voc) increases within Ts = 1鈭? h and reduces with further increasing Ts up to 鈮? h. By controlling the Ts, a peak power conversion efficiency of 畏 = 0.61% at AM 1.5 illumination (100 mW/cm2) is obtained for Ts = 6 h. It is revealed that the Z907 modification mainly contributes to the enhanced Jsc by increasing the charge separation efficiency as a result of the improved electronic coupling property at the D/A interface rather than the light harvesting; on the other hand, the Z907 modification reduces (Ts = 1鈭? h) or increases (Ts 鈮?6 h) the surface defect concentration of the ZnO nanorods, resulting in the increased or reduced Voc (or electron lifetime 蟿e). It is demonstrated that trapping electrons by the surface defects may facilitate the charge separation at the D/A interface in the MEH-PPV/ZnO devices, and both Voc and 蟿e correlate to the occupation of injected electrons in conduction band and surface defects. Further analysis provides the relation between Voc and 蟿e in those devices.