Neutral water splitting catalysis with a high FF triple junction polymer cell

This document is the Accepted Manuscript version of a Published Work that appeared in final form in CS catalysis, copyright © American Chemical Society, after peer review and technical editing by the publisher and may be found at http://dx.doi.org/10.1021/acscatal.6b01036We report a photovoltaics-electrochemical (PV-EC) assembly based on a compact and easily processable triple homojunction polymer cell with high fill factor (76%), optimized conversion efficiencies up to 8.7%, and enough potential for the energetically demanding water splitting reaction (V-oc = 2.1 V). A platinum-free cathode made of abundant materials is coupled to a ruthenium oxide on glassy carbon anode (GC-RuO2) to perform the reaction at optimum potential (Delta E = 1.70-1.78 V, overpotential = 470-550 mV). The GC-RuO2 anode contains a single monolayer of catalyst corresponding to a superficial concentration (Gamma) of 0.15 nmol cm(-2) and is highly active at pH 7. The PV-EC cell achieves solar to hydrogen conversion efficiencies (STH) ranging from 5.6 to 6.0%. As a result of the solar cell's high fill factor, the optimal photovoltaic response is found at 1.70 V, the minimum potential at which the electrodes used perform the water splitting reaction. This allows generating hydrogen at efficiencies that would be very similar (96%) to those obtained as if the system were to be operating at 1.23 V, the thermodynamic potential threshold for the water splitting reaction.Peer ReviewedPostprint (author's final draft

4‑Terminal Tandem Photovoltaic Cell Using Two Layers of PTB7:PC₇₁BM for Optimal Light Absorption

A 4-terminal architecture is proposed in which two thin active layers (<100 nm) of PTB7:PC₇₁BM are deposited on a two-sided ITO covered glass substrate. By modeling the electric field distribution inside the multilayer structure and applying an inverse solving problem procedure, we designed an optimal device architecture tailored to extract the highest photocurrent possible. By adopting such a 4-terminal configuration, we numerically demonstrated that even when the two subcells use identical absorber materials, the performance of the 4-terminal device may overcome the performance of the best equivalent single-junction device. In an experimental implementation of such a 4-terminal device, we demonstrate the viability of the approach and find a very good match with the trend of the numerical predictions