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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

Composition-Dependent Catalytic Activities of Noble-Metal-Free NiS/Ni3S4 for Hydrogen Evolution Reaction

TL;DR: In this paper, NiSx with tunable NiS/Ni3S4 molar ratios were synthesized via a simple hydrothermal method, and detailed electrochemical studies under neutral conditions indicated that the electrocatalytic property of NiSX catalysts was determined by the composition.
Journal ArticleDOI

One-pot hydrothermal fabrication of layered β-Ni(OH)2/g-C3N4 nanohybrids for enhanced photocatalytic water splitting

TL;DR: In this article, a simple and green hydrothermal process was introduced to fabricate ultrathin layered β-Ni(OH)2/g-C3N4 nanohybrids for photocatalytic water splitting application.
Journal ArticleDOI

Enabling practical electrocatalyst-assisted photoelectron-chemical water splitting with earth abundant materials

TL;DR: In this paper, the authors provide a concise review of the key issues encountered in carrying out photoelectrochemical water splitting, focusing on the balance of considerations such as stability, earth abundance, and efficiency.
Journal ArticleDOI

Device Fabrication for Water Oxidation, Hydrogen Generation, and CO2 Reduction via Molecular Engineering

TL;DR: In this article, the authors summarize recent developments in operation and fabrication strategies for various water-splitting devices constructed from electrodes (electrochemical cells) or photoelectrodes (photoelectrondes) using molecular engineering and provide insights into the factors that influence device efficiency and stability.
Journal ArticleDOI

One-step solid phase synthesis of a highly efficient and robust cobalt pentlandite electrocatalyst for the oxygen evolution reaction

TL;DR: In this paper, a facile one-step solid phase calcination approach is presented in which Co9S8 nanoparticles (NPs) were concurrently synthesised on carbon nanosheets (CNSs).
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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