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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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Vanadium nanobelts coated nickel foam 3D bifunctional electrode with excellent catalytic activity and stability for water electrolysis

TL;DR: A vanadium nanobelts coating on a nickel foam is proposed as an excellent 3D bifunctional electrode for water electrolysis here, which exhibits high activities with overpotentials of 292 and 176 mV at 10 mA cm(-2) for OER and HER, respectively.
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Alignment of Redox Levels at Semiconductor-Water Interfaces

TL;DR: In this article, the band alignment between various semiconductors and liquid water was determined by combining molecular dynamics simulations of atomistic interface models, electronic-structure calculations at the hybrid functional and GW level, and a computational standard hydrogen electrode.
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Surface plasmon-driven photoelectrochemical water splitting of TiO 2 nanowires decorated with Ag nanoparticles under visible light illumination

TL;DR: In this paper, the authors demonstrate that TiO 2 nanowires (NWs) can be significantly driven by visible light through the decoration with Ag nanoparticles (NPs) (Ag-decorated TiO2 NWs) showed remarkably photoelectrochemical (PEC) water splitting performance under illumination with λ −>-420 visible light due to surface plasmon resonance (SPR) of Ag NPs.
Journal ArticleDOI

Strategies to improve light utilization in solar fuel synthesis

TL;DR: In this paper, the authors review recent progress on emerging complementary approaches to better modify, enhance or distribute solar energy for sunlight-to-fuel conversion, including advanced light management, integrated thermal approaches and solar concentrators, which can improve the efficiency and production rates of existing photo-electrochemical systems and, therefore, the overall economics of solar fuel production.
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.
Journal ArticleDOI

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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