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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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Bifunctional Nickel Phosphide Nanocatalysts Supported on Carbon Fiber Paper for Highly Efficient and Stable Overall Water Splitting

TL;DR: In this article, a self-supported electrodes comprising carbon fiber paper (CP) integrated with bifunctional nickel phosphide (Ni-P) electrocatalysts are fabricated by electrodeposition of Ni on functionalized CP, followed by a convenient one-step phosphorization treatment in phosphorus vapor at 500 °C.
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Non-noble metal-nitride based electrocatalysts for high-performance alkaline seawater electrolysis

TL;DR: A three-dimensional core-shell metal-nitride catalyst consisting of NiFeN nanoparticles uniformly decorated on NiMoN nanorods supported on Ni foam serves as an eminently active and durable oxygen evolution reaction catalyst for alkaline seawater electrolysis.
Journal ArticleDOI

Smart Utilization of Carbon Dots in Semiconductor Photocatalysis.

TL;DR: Carbon dots have emerged as a promising new class of metal-free photocatalyst, displaying semiconductor-like photoelectric properties and showing excellent performance in a wide variety of photoelectrochemical and photocatalytic applications owing to their ease of synthesis.
Journal ArticleDOI

Recent Progress in Energy-Driven Water Splitting

TL;DR: This review briefly summarizes thermolytic, electrolytic, photolytic and biolytic water splitting, which highlights photonic and electrical driven water splitting together with photovoltaic‐integrated solar‐driven water electrolysis.
Journal ArticleDOI

Recent developments of carbon-based electrocatalysts for hydrogen evolution reaction

TL;DR: In this article, the authors reviewed the research progress in the development of carbon-based electrocatalysts toward hydrogen evolution reaction (HER) in acid electrolytes throughout the past few years.
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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