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      Improved Water Oxidation of Fe 2O 3/Fe 2TiO 5 Photoanode by Functionalizing with a Hydrophilic Organic Hole Storage Overlayer

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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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            MOF-Derived Bifunctional Cu3 P Nanoparticles Coated by a N,P-Codoped Carbon Shell for Hydrogen Evolution and Oxygen Reduction

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              Is Open Access

              Single-crystalline, wormlike hematite photoanodes for efficient solar water splitting

              A hematite photoanode showing a stable, record-breaking performance of 4.32 mA/cm2 photoelectrochemical water oxidation current at 1.23 V vs. RHE under simulated 1-sun (100 mW/cm2) irradiation is reported. This photocurrent corresponds to ca. 34% of the maximum theoretical limit expected for hematite with a band gap of 2.1 V. The photoanode produced stoichiometric hydrogen and oxygen gases in amounts close to the expected values from the photocurrent. The hematitle has a unique single-crystalline “wormlike” morphology produced by in-situ two-step annealing at 550°C and 800°C of β-FeOOH nanorods grown directly on a transparent conducting oxide glass via an all-solution method. In addition, it is modified by platinum doping to improve the charge transfer characteristics of hematite and an oxygen-evolving co-catalyst on the surface.
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                Author and article information

                Contributors
                Journal
                ACS Catalysis
                ACS Catal.
                American Chemical Society (ACS)
                2155-5435
                2155-5435
                July 01 2022
                June 17 2022
                July 01 2022
                : 12
                : 13
                : 7833-7842
                Affiliations
                [1 ]Institute for Energy Research, Automotive Engineering Research Institute, Jiangsu University, Zhenjiang 212013, China
                [2 ]Institute of Functional Nano and Soft Materials Laboratory, Jiangsu Key Laboratory for Carbon-Based Functional Materials & Devices, Soochow University, Suzhou 215123, China
                [3 ]Institute of High Energy Physics, Chinese Academy of Sciences, Beijing 100049, China
                Article
                10.1021/acscatal.2c01328
                52394878-efee-4ff8-a6f5-602658bee82d
                © 2022

                https://doi.org/10.15223/policy-029

                https://doi.org/10.15223/policy-037

                https://doi.org/10.15223/policy-045

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