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Chemical synthesis of ZnO nanorods: Investigations of electrochemical performance and photo-electrochemical water splitting applications
Zinc Oxide (ZnO) nanorods were prepared by facile and inexpensive chemical route at low temperature. X-ray diffraction study confirms the formation of hexagonal wurtzite crystal structure with high orientation along the c-axis. FE-SEM images show a vertical alignment of ZnO nanorods to the substrate...
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Published in: | Journal of alloys and compounds 2017-07, Vol.711, p.573-580 |
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Main Authors: | , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | Zinc Oxide (ZnO) nanorods were prepared by facile and inexpensive chemical route at low temperature. X-ray diffraction study confirms the formation of hexagonal wurtzite crystal structure with high orientation along the c-axis. FE-SEM images show a vertical alignment of ZnO nanorods to the substrate surface, whose average diameter and length is 1.33 and 15 μm, respectively. Electrochemical performance and photo-electrochemical water splitting of ZnO nanorods are investigated in 1 M Na2SO4 electrolyte using the different electrochemical techniques. Electrochemical study of ZnO nanorods exhibits the maximum areal capacitance of 29.36 mFcm−2 in the negative potential window, which is higher than the areal capacitance of 10.84 mFcm−2 in the positive potential window at the scan rate of 5 mVs−1. ZnO nanorods show the excellent stability of 97% over the 3000 cycles in both potential windows. Photo-electrochemical water splitting demonstrates the fast photo-response with 0.098% photo-conversion efficiency.
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•Low temperature chemical synthesis of ZnO nanorods.•Study of ZnO nanorods in electrochemical and PEC water splitting applications.•ZnO nanorods exhibits the maximum areal capacitance of 29.36 mFcm−2.•ZnO nanorods demonstrated the superb 97% stability over 3000 cycles.•PEC water splitting showed the fast photoresponse and photo conversion efficiency. |
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ISSN: | 0925-8388 1873-4669 |
DOI: | 10.1016/j.jallcom.2017.04.030 |