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      TiO 2/BiVO 4 Nanowire Heterostructure Photoanodes Based on Type II Band Alignment

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          Abstract

          Metal oxides that absorb visible light are attractive for use as photoanodes in photoelectrosynthetic cells. However, their performance is often limited by poor charge carrier transport. We show that this problem can be addressed by using separate materials for light absorption and carrier transport. Here, we report a Ta:TiO 2|BiVO 4 nanowire photoanode, in which BiVO 4 acts as a visible light-absorber and Ta:TiO 2 acts as a high surface area electron conductor. Electrochemical and spectroscopic measurements provide experimental evidence for the type II band alignment necessary for favorable electron transfer from BiVO 4 to TiO 2. The host–guest nanowire architecture presented here allows for simultaneously high light absorption and carrier collection efficiency, with an onset of anodic photocurrent near 0.2 V vs RHE, and a photocurrent density of 2.1 mA/cm 2 at 1.23 V vs RHE.

          Abstract

          We report the use of Ta:TiO 2|BiVO 4 as a photoanode for use in solar water splitting cells. This host−guest system makes use of the favorable band alignment between the two semiconductors. The nanowire architecture allows for simultaneously high light absorption and carrier collection for efficient solar water oxidation.

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          Atomic layer deposition: an overview.

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            A review and recent developments in photocatalytic water-splitting using TiO2 for hydrogen production

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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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                Author and article information

                Journal
                ACS Cent Sci
                ACS Cent Sci
                oc
                acscii
                ACS Central Science
                American Chemical Society
                2374-7943
                2374-7951
                03 February 2016
                24 February 2016
                : 2
                : 2
                : 80-88
                Affiliations
                [1] Department of Chemical Engineering and Department of Chemistry, University of California , Berkeley, California 94720, United States
                [§ ]Department of Physics, Kangwon National University , Chuncheon-si, Gangwon-do 200-701, South Korea
                []Advanced Light Source, Lawrence Berkeley National Laboratory , Berkeley, California 94720, United States
                []Department of Polymer Science & Engineering, Conte Polymer Research Center, University of Massachusetts , Amherst, Massachusetts 01003, United States
                [5] #Materials Sciences Division and Kavli Energy NanoSciences Institute, Lawrence Berkeley National Laboratory , Berkeley, California 94720, United States
                Author notes
                Article
                10.1021/acscentsci.5b00402
                4827543
                27163032
                50dd3f9f-229d-43d4-8ebe-bb8644d6db7e
                Copyright © 2016 American Chemical Society

                This is an open access article published under an ACS AuthorChoice License, which permits copying and redistribution of the article or any adaptations for non-commercial purposes.

                History
                : 26 December 2015
                Categories
                Research Article
                Custom metadata
                oc5b00402
                oc-2015-004025

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