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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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Ultrathin cobalt phosphide nanosheets as efficient bifunctional catalysts for a water electrolysis cell and the origin for cell performance degradation

TL;DR: In this paper, ultrathin CoP nanosheets (CoP NS) were used as bifunctional catalysts for electrochemical water splitting and achieved a current density of 335 mA cm−2 at 1.8 V, which is rather competitive to the state-of-the-art Pt/IrO2 catalyst.
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Karst landform-featured monolithic electrode for water electrolysis in neutral media

TL;DR: In this paper, a nickel foam-based monolithic electrode with high performance for both hydrogen and oxygen evolution reactions in neutral media is reported with the capability to switch between HER and OER reversibly and flexibly with longterm viability.
Journal ArticleDOI

Upscaling of integrated photoelectrochemical water-splitting devices to large areas

TL;DR: The concept of a fully integrated, wireless device which, by design, is scalable to large areas and is compatible with multiple thin-film photovoltaic technologies, and its successful realization may be an important contribution towards the large-scale application of artificial photosynthesis.
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In situ engineering bi-metallic phospho-nitride bi-functional electrocatalysts for overall water splitting

TL;DR: In this paper, a polyhedron N-doped Ni-Co phosphide (N-NiCoP/NCF) was used to construct a bi-functional electrocatalyst for hydrogen evolution reaction and oxygen evolution reaction.
Journal ArticleDOI

Synergistic coupling of NiTe nanoarrays with RuO2 and NiFe-LDH layers for high-efficiency electrochemical-/photovoltage-driven overall water splitting

TL;DR: In this article, the authors constructed full electrochemical cells for overall water splitting using NiTe@RuO2 as the cathode and NiTe-NiFe-LDH as the anode, which delivered a current density of 200'mA'cm−2 under a voltage of 1.63'V.
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.
Journal ArticleDOI

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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