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      Hematite heterostructures for photoelectrochemical water splitting: rational materials design and charge carrier dynamics

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          Abstract

          Different approaches to improving photoelectrochemical performance through α-Fe 2O 3 heterostructure design.

          Abstract

          Hematite (α-Fe 2O 3), with a bandgap suitable for absorption of the solar spectrum, is ideally suited for use as a photoanode material in photoelectrochemical (PEC) conversion of solar light into hydrogen fuel via water splitting. However, low hole mobility, short hole lifetime, high density of surface states, and slow kinetics for oxygen evolution at the α-Fe 2O 3/electrolyte interface have limited the PEC performance of α-Fe 2O 3 photoanodes to date. Along with numerous reports on doping and nanostructuring of α-Fe 2O 3, increased attention has been paid to α-Fe 2O 3 heterostructure design for improved PEC performance. This review article provides an overview of four main approaches to rational heterostructure design: coupling α-Fe 2O 3 with (1) an n- or p-type semiconductor for promoting charge separation; (2) a nanotextured conductive substrate for efficient charge collection; (3) a surface/interface passivation layer for reduced surface/interface charge recombination; (4) a catalyst for accelerated water oxidation kinetics. The achievements to date demonstrate that high PEC performance may be accessed with these designs. In addition, we review time-resolved laser techniques used to probe the charge carrier dynamics of these heterostructures. Dynamic studies have provided insight into the mechanisms responsible for the improved PEC performance in these materials and helped to guide continued design of α-Fe 2O 3 heterostructures for further enhancement of PEC water splitting. As summarized in this review article, rational heterostructure design is a promising strategy to push forward the application of α-Fe 2O 3 for potential low cost and high efficiency solar hydrogen conversion. A better fundamental understanding of the charge carrier dynamics in these structures in turn helps to guide and improve the heterostructure design.

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          Titanium dioxide-based nanomaterials for photocatalytic fuel generations.

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            Solar water splitting: progress using hematite (α-Fe(2) O(3) ) photoelectrodes.

            Photoelectrochemical (PEC) cells offer the ability to convert electromagnetic energy from our largest renewable source, the Sun, to stored chemical energy through the splitting of water into molecular oxygen and hydrogen. Hematite (α-Fe(2)O(3)) has emerged as a promising photo-electrode material due to its significant light absorption, chemical stability in aqueous environments, and ample abundance. However, its performance as a water-oxidizing photoanode has been crucially limited by poor optoelectronic properties that lead to both low light harvesting efficiencies and a large requisite overpotential for photoassisted water oxidation. Recently, the application of nanostructuring techniques and advanced interfacial engineering has afforded landmark improvements in the performance of hematite photoanodes. In this review, new insights into the basic material properties, the attractive aspects, and the challenges in using hematite for photoelectrochemical (PEC) water splitting are first examined. Next, recent progress enhancing the photocurrent by precise morphology control and reducing the overpotential with surface treatments are critically detailed and compared. The latest efforts using advanced characterization techniques, particularly electrochemical impedance spectroscopy, are finally presented. These methods help to define the obstacles that remain to be surmounted in order to fully exploit the potential of this promising material for solar energy conversion. Copyright © 2011 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.
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              Highly active oxide photocathode for photoelectrochemical water reduction.

              A clean and efficient way to overcome the limited supply of fossil fuels and the greenhouse effect is the production of hydrogen fuel from sunlight and water through the semiconductor/water junction of a photoelectrochemical cell, where energy collection and water electrolysis are combined into a single semiconductor electrode. We present a highly active photocathode for solar H(2) production, consisting of electrodeposited cuprous oxide, which was protected against photocathodic decomposition in water by nanolayers of Al-doped zinc oxide and titanium oxide and activated for hydrogen evolution with electrodeposited Pt nanoparticles. The roles of the different surface protection components were investigated, and in the best case electrodes showed photocurrents of up to -7.6 mA cm(-2) at a potential of 0 V versus the reversible hydrogen electrode at mild pH. The electrodes remained active after 1 h of testing, cuprous oxide was found to be stable during the water reduction reaction and the Faradaic efficiency was estimated to be close to 100%. © 2011 Macmillan Publishers Limited. All rights reserved
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                Author and article information

                Journal
                EESNBY
                Energy & Environmental Science
                Energy Environ. Sci.
                Royal Society of Chemistry (RSC)
                1754-5692
                1754-5706
                2016
                2016
                : 9
                : 9
                : 2744-2775
                Article
                10.1039/C6EE01845A
                85e13108-51f3-4e37-9fbe-e85bed56b8fe
                © 2016
                History

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