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Citation for published item:rrenD FgF nd o¤ %t hovskyD uF nd hot nD rF nd veroyD gFwF nd gornuzD wF nd tell iD pF nd r¡ e ertD gF nd oths hildD eF nd qr¤ tzelD wF @PHIQA 9sdentifying h mpion n nostru tures for sol r w terEsplittingF9D x ture m teri lsFD IP @WAF ppF VRPEVRWF Further information on publisher's website: httpXGGdxFdoiForgGIHFIHQVGnm tQTVR Publisher's copyright statement: Use policyThe full-text may be used and/or reproduced, and given to third parties in any format or medium, without prior permission or charge, for personal research or study, educational, or not-for-pro t purposes provided that:• a full bibliographic reference is made to the original source • a link is made to the metadata record in DRO • the full-text is not changed in any way The full-text must not be sold in any format or medium without the formal permission of the copyright holders.Please consult the full DRO policy for further details. Charge transport in nanoparticle-based materials underlies many emerging energy conversion technologies, yet assessing the impact of nanometer-scale structure on charge transport across micron-scale distances remains a challenge. Here we develop an approach for correlating the spatial distribution of crystalline and current-carrying domains in entire nanoparticle aggregates. We apply this approach to nanoparticle-based α-Fe 2 O 3 electrodes that are of interest in solar-to-hydrogen energy conversion. In correlating structure and charge transport with nanometer resolution across micron-scale distances, we have identified the existence of champion nanoparticle aggregates that are most responsible for the high photoelectrochemical activity of the present electrodes. Indeed, when electrodes are fabricated with a high proportion of these champion nanostructures, the electrodes achieve the highest photocurrent of any metal oxide photoanode for photoelectrochemical water splitting under 100 mW cm -2 air mass 1.5 global sunlight.Batteries, fuel cells, and solar energy conversion devices have emerged as a class of important technologies that increasingly rely upon electrodes derived from nanoparticles 1 . These nanoparticle-based materials provide a unique challenge in assessing structure-property relationships because of the disordered arrangement of nanocrystals that results when nanoparticles collide and aggregate [2][3][4][5][6] . The morphological evolution that follows aggregation further obscures the influence of particle size, shape, and interfacial characteristics in defining the physical properties of these materials 7,8 . For the nanoparticle-based electrodes used in solar energy conversion, structural defects such as grain boundaries define pathways for charge transport by creating potential barriers and by promoting recombination 9 . Because of the complexity of these materials, within a single electrode there may exist a small proportion of "champion" nanostructures-by analogy with champion solar cells 10,11 , these are nanostructures that provide the highest solar conversion efficiencies-th...

Semiconductor photoelectrodes for solar hydrogen production by water photoelectrolysis must employ stable, non-toxic, abundant and inexpensive visible-light absorbers. Iron oxide (α-Fe(2)O(3)) is one of few materials meeting these requirements, but its poor transport properties present challenges for efficient charge-carrier generation, separation, collection and injection. Here we show that these challenges can be addressed by means of resonant light trapping in ultrathin films designed as optical cavities. Interference between forward- and backward-propagating waves enhances the light absorption in quarter-wave or, in some cases, deeper subwavelength films, amplifying the intensity close to the surface wherein photogenerated minority charge carriers (holes) can reach the surface and oxidize water before recombination takes place. Combining this effect with photon retrapping schemes, such as using V-shaped cells, provides efficient light harvesting in ultrathin films of high internal quantum efficiency, overcoming the trade-off between light absorption and charge collection. A water photo-oxidation current density of 4 mA cm(-2) was achieved using a V-shaped cell comprising ~26-nm-thick Ti-doped α-Fe(2)O(3) films on back-reflector substrates coated with silver-gold alloy.

Solar water splitting provides a promising path for sustainable hydrogen production and solar energy storage. One of the greatest challenges towards large-scale utilization of this technology is reducing the hydrogen production cost. The conventional electrolyser architecture, where hydrogen and oxygen are co-produced in the same cell, gives rise to critical challenges in photoelectrochemical water splitting cells that directly convert solar energy and water to hydrogen. Here we overcome these challenges by separating the hydrogen and oxygen cells. The ion exchange in our cells is mediated by auxiliary electrodes, and the cells are connected to each other only by metal wires, enabling centralized hydrogen production. We demonstrate hydrogen generation in separate cells with solar-to-hydrogen conversion efficiency of 7.5%, which can readily surpass 10% using standard commercial components. A basic cost comparison shows that our approach is competitive with conventional photoelectrochemical systems, enabling safe and potentially affordable solar hydrogen production.

A 2-nm thick Nb(2)O(5) underlayer deposited by atomic layer deposition increases the charge separation efficiency and the photovoltage of ultrathin hematite films by suppressing electron back injection. Absorbed photon-to-current efficiencies (APCE) as high as 40%, which are one of the highest ever reported with hematite photoanodes, are obtained at 400 nm at +1.43 V vs. RHE.

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We introduce an empirical in operando analysis of the charge carrier dynamics in hematite photoanodes by PEIS, IMPS and IMVS.

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