In the present article bulk heterojunction (BHJ) solution processed organic solar cells have been prepared using mono(carboxy)porphyrin-triazine-(Bodipy) 2 triad (PorCOOH)(BDP) 2 as a donor and ([6,6]-phenyl C 71 butyric acid methyl ester) (PC 71 BM) as an acceptor. This donor/acceptor system aims at the of increasing the light capturing process efficiency of the device. The solution processed BHJ organic solar cell with an optimized weight ratio of 1:1 (PorCOOH)(BDP) 2 :PC 71 BM processed with THF as a solvent showed an overall power conversion efficiency (PCE) of 3.48 % with short circuit current J sc = 8.04 mA/cm 2 , open circuit voltage V oc = 0.94 V and fill factor FF =0.46. The relatively high value of V oc was attributed to the deeper highest occupied molecular orbital energy level of (PorCOOH)(BDP) 2 . When the active layer of the solar cell was processed from a mixture of 4% v/v of pyridine in THF solvent, it achieved a PCE value of 5.29 % with J sc =10.48 mA/cm 2 , V oc =0.90 V and FF=0.56. This was ascribed to the enhancement of both the J sc and the FF values. The higher value of J sc is explained by the increased absorption profile of the blend, the stronger incident photon to current efficiency (IPCE) response and the higher crystallinity of the active layer, induced by the solvent additive while the enhancement of FF may be due to the better charge transport capability and the charge collection efficiency in the later device.

A novel BODIPY-porphyrin triad is prepared with two BODIPY molecules covalently attached via a 1,3,5-triazine molecule to a free-base carboxyphenyl meso-substituted porphyrin.