Abstract
This study first demonstrates the potential of organic photoabsorbing blends in overcoming a critical limitation of metal oxide photoanodes in tandem modules: insufficient photogenerated current. Various organic blends, including PTB7‐Th:FOIC, PTB7‐Th:O6T‐4F, PM6:Y6, and PM6:FM, were systematically tested. When coupled with electron transport layer (ETL) contacts, these blends exhibit exceptional charge separation and extraction, with PM6:Y6 achieving saturation photocurrents up to 16.8 mA cm−2 at 1.23 VRHE (oxygen evolution thermodynamic potential). For the first time, a tandem structure utilizing organic photoanodes has been computationally designed and fabricated and the implementation of a double PM6:Y6 photoanode/photovoltaic structure resulted in photogenerated currents exceeding 7 mA cm−2 at 0 VRHE (hydrogen evolution thermodynamic potential) and anodic current onset potentials as low as −0.5 VRHE. The herein‐presented organic‐based approach paves the way for further exploration of different blend combinations to target specific oxidative reactions by selecting precise donor/acceptor candidates among the multiple existing ones.
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