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      Co-Catalyst Ti3C2TX MXene-Modified ZnO Nanorods Photoanode for Enhanced Photoelectrochemical Water Splitting

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          Electrochemical Photolysis of Water at a Semiconductor Electrode

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            Two-dimensional nanocrystals produced by exfoliation of Ti3 AlC2.

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              Nitrogen-doped ZnO nanowire arrays for photoelectrochemical water splitting.

              We report the rational synthesis of nitrogen-doped zinc oxide (ZnO:N) nanowire arrays, and their implementation as photoanodes in photoelectrochemical (PEC) cells for hydrogen generation from water splitting. Dense and vertically aligned ZnO nanowires were first prepared from a hydrothermal method, followed by annealing in ammonia to incorporate N as a dopant. Nanowires with a controlled N concentration (atomic ratio of N to Zn) up to approximately 4% were prepared by varying the annealing time. X-ray photoelectron spectroscopy studies confirm N substitution at O sites in ZnO nanowires up to approximately 4%. Incident-photon-to-current-efficiency measurements carried out on PEC cell with ZnO:N nanowire arrays as photoanodes demonstrate a significant increase of photoresponse in the visible region compared to undoped ZnO nanowires prepared at similar conditions. Mott-Schottky measurements on a representative 3.7% ZnO:N sample give a flat-band potential of -0.58 V, a carrier density of approximately 4.6 x 10(18) cm(-3), and a space-charge layer of approximately 22 nm. Upon illumination at a power density of 100 mW/cm(2) (AM 1.5), water splitting is observed in both ZnO and ZnO:N nanowires. In comparison to ZnO nanowires without N-doping, ZnO:N nanowires show an order of magnitude increase in photocurrent density with photo-to-hydrogen conversion efficiency of 0.15% at an applied potential of +0.5 V (versus Ag/AgCl). These results suggest substantial potential of metal oxide nanowire arrays with controlled doping in PEC water splitting applications.
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                Author and article information

                Contributors
                Journal
                Topics in Catalysis
                Top Catal
                Springer Science and Business Media LLC
                1022-5528
                1572-9028
                May 05 2022
                Article
                10.1007/s11244-022-01619-0
                fbe809e1-c6b9-4614-af05-f189dfa349e0
                © 2022

                https://www.springer.com/tdm

                https://www.springer.com/tdm

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