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      Synthesis of ZnO doped high valence S element and study of photogenerated charges properties†

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      RSC Advances
      The Royal Society of Chemistry

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          Abstract

          Nonmetal doping is an efficient way to increase the photoresponse range of ZnO. However, the mechanism for improving the light response range of ZnO with nonmetal doping is not clear. Herein, ZnO doped with S was successfully prepared by ion exchange and calcination methods, which resulted in the uniform distribution of sulfur ions in ZnO. The S element doped was mainly S 4+ and S 6+, which was identified by XPS. We studied the influence of S on the photogenerated charge characteristics of ZnO with SPS. Results indicated that the uniform distribution of S dopants elevated the valence band maximum by mixing S 3p with the upper valence band states of ZnO. The valence band maxima of S–ZnO was 0.37 eV higher than that of ZnO. This result was the main reason for the improvement in the light response. We also studied the photocatalytic activity of Ag/S–ZnO. Ag/S–ZnO with 10 wt% Ag loading showed the highest photocatalytic degradation rate for MO. In this paper, a potential photocatalytic mechanism has been proposed.

          Abstract

          The uniform distribution of S dopants elevated the valence band maximum by mixing S 3p with the upper valence band states of ZnO. The valence band maxima of S–ZnO was 0.37 eV higher than that of ZnO.

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          Visible-light photocatalysis in nitrogen-doped titanium oxides.

          To use solar irradiation or interior lighting efficiently, we sought a photocatalyst with high reactivity under visible light. Films and powders of TiO(2-x)N(x) have revealed an improvement over titanium dioxide (TiO2) under visible light (wavelength < 500 nanometers) in optical absorption and photocatalytic activity such as photodegradations of methylene blue and gaseous acetaldehyde and hydrophilicity of the film surface. Nitrogen doped into substitutional sites of TiO2 has proven to be indispensable for band-gap narrowing and photocatalytic activity, as assessed by first-principles calculations and x-ray photoemission spectroscopy.
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            Unique electronic structure induced high photoreactivity of sulfur-doped graphitic C3N4.

            Electronic structure intrinsically controls the light absorbance, redox potential, charge-carrier mobility, and consequently, photoreactivity of semiconductor photocatalysts. The conventional approach of modifying the electronic structure of a semiconductor photocatalyst for a wider absorption range by anion doping operates at the cost of reduced redox potentials and/or charge-carrier mobility, so that its photoreactivity is usually limited and some important reactions may not occur at all. Here, we report sulfur-doped graphitic C(3)N(4) (C(3)N(4-x)S(x)) with a unique electronic structure that displays an increased valence bandwidth in combination with an elevated conduction band minimum and a slightly reduced absorbance. The C(3)N(4-x)S(x) shows a photoreactivity of H(2) evolution 7.2 and 8.0 times higher than C(3)N(4) under lambda > 300 and 420 nm, respectively. More strikingly, the complete oxidation process of phenol under lambda > 400 nm can occur for sulfur-doped C(3)N(4), which is impossible for C(3)N(4) even under lambda > 300 nm. The homogeneous substitution of sulfur for lattice nitrogen and a concomitant quantum confinement effect are identified as the cause of this unique electronic structure and, consequently, the excellent photoreactivity of C(3)N(4-x)S(x). The results acquired may shed light on general doping strategies for designing potentially efficient photocatalysts.
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              Significantly enhanced photocatalytic performance of ZnO via graphene hybridization and the mechanism study

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                Author and article information

                Journal
                RSC Adv
                RSC Adv
                RA
                RSCACL
                RSC Advances
                The Royal Society of Chemistry
                2046-2069
                5 February 2019
                30 January 2019
                5 February 2019
                : 9
                : 8
                : 4422-4427
                Affiliations
                [a] College of Chemical Engineering, Key Laboratory for Palygorskite Science and Applied Technology of Jiangsu Province, Huaiyin Institute of Technology Huaian 223003 China lijingz16@ 123456hyit.edu.cn
                Author information
                https://orcid.org/0000-0003-1995-0412
                https://orcid.org/0000-0003-1799-610X
                Article
                c8ra07751g
                10.1039/c8ra07751g
                9060612
                35520177
                b309a72c-916c-4498-bb72-8ccc6fa504e5
                This journal is © The Royal Society of Chemistry
                History
                : 18 September 2018
                : 24 December 2018
                Page count
                Pages: 6
                Funding
                Funded by: National Natural Science Foundation of China, doi 10.13039/501100001809;
                Award ID: 51574130
                Categories
                Chemistry
                Custom metadata
                Paginated Article

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