A scale-up-led approach to photoelectrochemical water splitting: from nanomaterials optimisation to field testing
George H. Creasey a b, Arend W. Moelich c, Craig McGregor c, Katie Shanks d, Andreas Kafizas b, Anna Hankin a
a Department of Chemical Engineering, Imperial College London, London SW7 2AZ, UK
b Department of Chemistry, Imperial College London, W12 OBZ, UK
c Department of Mechanical and Mechatronic Engineering, Joubert Street, Stellenbosch, 7602, South Africa
d Environment & Sustainability Institute, University of Exeter, Penryn, Cornwall, TR10 9FE, UK
Proceedings of MATSUS Fall 2026 Conference (MATSUSFall26)
E2 Solar fuels and chemicals: from devices to discoveries in unconventional environments
Palma, Spain, 2026 October 26th - 30th
Organizers: Franky Esteban Bedoya Lora, Katharina Brinkert and Anna Hankin
Oral, George H. Creasey, presentation 155
Publication date: 22nd July 2026

Scaling-up photoelectrochemical (PEC) water splitting requires an end-to-end approach that encompasses photoelectrode fabrication, reactor design, optical coupling and operating strategy, yet few studies address these constraints simultaneously.[1] Our strategy involves a scale-up-led workflow, from materials optimisation in deployment-relevant conditions to field testing and life cycle assessment (LCA).

 

We developed up-scalable FTO|WO3|BiVO4|NiFeOOH photoanodes, mechanically stable under electrolyte flow, sustaining a photocurrent density of 1.75 mA cm-2 for 24 hours.[2] Elevated temperature stability tests revealed that a WO3 seed layer between the FTO and nanostructured WO3 improves adhesion and mechanical robustness under flow-induced shear stress.[3] Next, we developed an up-scaled PV-PEC reactor (30 cm2 photoanode + Ni cathode + 30 cm2 c-Si PV), characterised outdoors on a dual-axis tracking platform. Sunlight was concentrated (up to 4×) laterally onto the photoanode and PV using linear Fresnel lenses and aluminium lightguides, delivering photocurrents up to 77.5 mA.[4] Returning to the 1 cm2 scale, we integrated wide-angle (± 30°) crossed-compound parabolic concentrators (CCPCs, 3.6× optical concentration) with the PEC reactor. We demonstrated broad-angular light concentration, enhancing photocurrent (up to 3×) and enabling simplified solar tracking or stationary configurations, akin to those deployed for solar photovoltaics.[5,6] Finally, annual hydrogen production was modelled for a theoretical pilot-scale PEC plant. Cradle-to-gate LCA showed that CCPC integration reduces the global warming potential by 21% (from 50.6 to 40.2 kg CO2-eq. kg-1 H2), with further reductions with single-axis tracking.[5]

 

I shall present results from materials development to field testing, highlighting operability challenges and how optics-coupled modules can enhance performance with reduced balance-of-system complexity.

The authors thank the UKRI-EPSRC Solar Chemicals Network (EP/X035301/1) for a Scientific Exchange/Collaboration Award. A. K. thanks the Grantham Institute for Climate Change and the Environment for a pump-priming grant and the EPSRC for a Programme Grant (EP/W017075/1). K. S. thanks the EPSRC for David Clarke Fellowship (EP/V043617/1). A. H. thanks the Department of Chemical Engineering at Imperial College London for an EPSRC DTP PhD scholarship (EP/W524323/1) for G. H. C. and for a lectureship start-up grant.

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