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Journal ArticleDOI

Water photolysis at 12.3% efficiency via perovskite photovoltaics and Earth-abundant catalysts

TLDR
It is shown that a pair of perovskite cells connected in series can power the electrochemical breakdown of water into hydrogen and oxygen efficiently, and the combination of the two yields a water-splitting photocurrent density and a solar-to-hydrogen efficiency of 12.3%.
Abstract
Although sunlight-driven water splitting is a promising route to sustainable hydrogen fuel production, widespread implementation is hampered by the expense of the necessary photovoltaic and photoelectrochemical apparatus. Here, we describe a highly efficient and low-cost water-splitting cell combining a state-of-the-art solution-processed perovskite tandem solar cell and a bifunctional Earth-abundant catalyst. The catalyst electrode, a NiFe layered double hydroxide, exhibits high activity toward both the oxygen and hydrogen evolution reactions in alkaline electrolyte. The combination of the two yields a water-splitting photocurrent density of around 10 milliamperes per square centimeter, corresponding to a solar-to-hydrogen efficiency of 12.3%. Currently, the perovskite instability limits the cell lifetime.

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Citations
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Journal ArticleDOI

Oxygen evolution on Fe-doped NiO electrocatalysts deposited via microplasma

TL;DR: This work highlights that microplasma-based deposition is a general approach to realize conformal coatings of nanostructured, doped oxides with high activity for OER under alkaline conditions.
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An Integrated Device View on Photo-Electrochemical Solar-Hydrogen Generation

TL;DR: Parts of overall component integration in photo-electrochemical water-splitting devices that ultimately can lead to deployable devices are reviewed, providing the grounds to draw conclusions on the overall technological outlook.
Journal ArticleDOI

Interfacial synergy between dispersed Ru sub-nanoclusters and porous NiFe layered double hydroxide on accelerated overall water splitting by intermediate modulation

TL;DR: In this article, the authors proposed a rational interface-engineering strategy to optimize the adsorption energy of H* and OH* species at the atomic/molecular level for water splitting.
Journal ArticleDOI

Localized dielectric breakdown and antireflection coating in metal–oxide–semiconductor photoelectrodes

TL;DR: This work proposes and demonstrates a general method to decouple the two roles of the insulator by employing localized dielectric breakdown, which allows the insulators to be thick, which enhances stability, while enabling low-resistance carrier transport as required for efficiency.
Journal ArticleDOI

Enhancing hydrogen generation via fabricating peroxide decomposition layer over NiSe/MnO2-CdS catalyst

TL;DR: In this paper, the peroxide decomposing active MnO2 thin-layer over CdS nanowires and assembling oxygen separation artificial gill to remove nascent formed oxygen in the dispersion was used to overcome the disadvantage of Cds photocorrosion.
References
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Journal ArticleDOI

Electrochemical Photolysis of Water at a Semiconductor Electrode

TL;DR: Water photolysis is investigated by exploiting the fact that water is transparent to visible light and cannot be decomposed directly, but only by radiation with wavelengths shorter than 190 nm.
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A low-cost, high-efficiency solar cell based on dye-sensitized colloidal TiO2 films

TL;DR: In this article, the authors describe a photovoltaic cell, created from low-to medium-purity materials through low-cost processes, which exhibits a commercially realistic energy-conversion efficiency.
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Organometal Halide Perovskites as Visible-Light Sensitizers for Photovoltaic Cells

TL;DR: Two organolead halide perovskite nanocrystals were found to efficiently sensitize TiO(2) for visible-light conversion in photoelectrochemical cells, which exhibit strong band-gap absorptions as semiconductors.
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Efficient Hybrid Solar Cells Based on Meso-Superstructured Organometal Halide Perovskites

TL;DR: A low-cost, solution-processable solar cell, based on a highly crystalline perovskite absorber with intense visible to near-infrared absorptivity, that has a power conversion efficiency of 10.9% in a single-junction device under simulated full sunlight is reported.
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Sequential deposition as a route to high-performance perovskite-sensitized solar cells

TL;DR: A sequential deposition method for the formation of the perovskite pigment within the porous metal oxide film that greatly increases the reproducibility of their performance and allows the fabrication of solid-state mesoscopic solar cells with unprecedented power conversion efficiencies and high stability.
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