Journal
APPLIED SURFACE SCIENCE
Volume 539, Issue -, Pages -Publisher
ELSEVIER
DOI: 10.1016/j.apsusc.2020.148267
Keywords
Zinc foil; Inorganic-organic hybrid ZnS(en)(0.5) nanosheet; Dual nanoarchitecture; Hydrogen production
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Funding
- Korea Research Fellowship Program through the National Research Foundation of Korea (NRF) - Ministry of Science and ICT [2017H1D3A1A02014020]
- National Research Foundation of Korea (NRF) - Korea government (MSIT) [2019R1A2C1006402, 2018R1D1A1B07043453]
- National Research Foundation of Korea [2019R1A2C1006402, 2018R1D1A1B07043453] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)
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Dual nanostructured ZnO nanorod-Zn1-xCdxS porous nanosheet photoanodes were successfully synthesized on a zinc foil through cation exchange reaction. The optimized photoanode exhibited high photocurrent density and hydrogen production at 0 V vs. Ag/AgCl, with efficient charge separation mechanism.
Herein, dual nanostructured ZnO nanorod (NR)-Zn1-xCdxS porous nanosheet (PNS) photoanodes were produced on a zinc foil through cation exchange reaction of inorganic-organic hybrid ZnS(en)(0.5) nanosheets. ZnS(en)(0.5) NS's photoanodes have been synthesized via a facile solvothermal method followed by a series of cadmium (Cd2(+)) ion-exchange using various ion-exchange reaction times and temperatures. During Cd2(+) ion-exchange, the Zn1-xCdxS PNS and a new type of vertically aligned ZnO NR were subsequently grown on the zinc foil substrate. The different exposed surfaces of the vertically aligned hexagonal ZnO NR and Zn1-xCdxS PNS photoanodes contribute to appropriate morphology, effective light harvesting, and efficient charge separation in ZnO-NR-Zn1-xCdxS PNS160C. The optimum ZnO NR-Zn1-xCdxS PNS160C photoanode contributed the highest photocurrent density of 6.60 mA center dot cm(-2) and hydrogen production of 250.65 mu mol center dot cm(-2) at 0 V vs. Ag/AgCl. Finally, the charge transfer mechanism in the optimum photoanode is discussed in detail.
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