Scalable Perovskite-BiVO4 Photoelectrochemical Devices for Solar Fuel Production
Virgil Andrei a, Haijiao Lu a, Sebastian D. Pike a, Robert L. Z. Hoye b, Bertrand Reuillard a, Shahab Ahmad c, Dominic S. Wright a, Michael De Volder c, Richard H. Friend b, Erwin Reisner a
a University of Cambridge , Department of Chemistry, United Kingdom, Lensfield Road, United Kingdom
b Optoelectronics Group, Cavendish Laboratory, University of Cambridge, UK., J.J. Thomson Avenue, Cambridge, United Kingdom
c NanoManufacturing Group, University of Cambridge, Department of Engineering, United Kingdom., Charles Babbage Road, 17, United Kingdom
International Conference on Hybrid and Organic Photovoltaics
Proceedings of Online International Conference on Hybrid and Organic Photovoltaics (OnlineHOPV20)
Online, Spain, 2020 May 26th - 29th
Organizers: Tracey Clarke, James Durrant, Annamaria Petrozza and Trystan Watson
Poster, Virgil Andrei, 086
Publication date: 22nd May 2020
ePoster: 

The light-driven conversion of small molecules such as water and CO2 into higher-value chemicals (e.g. H2, CO) represents an attractive alternative for simultaneous energy harvesting and storage.[1,2] While great progress has been made in the development of suitable light absorbers, their integration with catalysts into photoelectrochemical (PEC) devices for the production of the so-called solar fuels still poses challenges. Beside the performance and stability of small prototypes, their scalability is a major factor which must be considered for commercial applications.

In this contribution, we address those issues by developing approaches to synthesize and characterize such devices on a medium- and large-scale. For this purpose, the water splitting performance of 0.25-10 cm2 perovskite-BiVO4 PEC tandems is investigated in a versatile 3D-printed PEC cell.[3,4] By employing state-of-the-art triple cation perovskite photoabsorbers, a solar-to-hydrogen conversion of 0.35% can be achieved under no applied bias. Their potential for further up-scaling is exemplified by fabricating 25 and 300 cm2 doped BiVO4 panels from bismuth (transition metal) polyoxovanadate single-source precursors (SSPs).[5]

Looking beyond water splitting, we will also discuss our recent progress on the development of PEC devices that can couple the more challenging CO2 reduction to water oxidation. By interfacing the perovskite photocathodes with an earth abundant molecular cobalt catalyst, selective aqueous CO2 reduction can be maintained for one day at light intensities as low as 0.1 Sun, providing potential pathways for maximizing daylight utilisation. The resulting perovskite-BiVO4 PEC tandems sustain an unprecedented bias-free syngas production for three days, operating as standalone artificial leaves in neutral pH solution.[6] The overall findings are applicable to a wide range of photoelectrochemical systems,[7] with the ultimate goal of contributing towards a circular carbon economy via photoelectrocatalysis.

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