Effect of Mn doping on structural, optical and photocatalytic behaviors of hydrothermal Zn1−xMnxS nanocrystals
•ZnS nanocrystals doped with Mn2+ were synthesized from hydrothermal method.•Structural behaviors are analyzed from XRD, Raman and PL measurements.•We report on long PL lifetimes of Mn levels due to excitation transfer from ZnS.•High photocatalytic efficiency was reported for ZnS-doped 3%Mn. Undoped...
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Published in | Applied surface science Vol. 351; pp. 1122 - 1130 |
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Main Authors | , , |
Format | Journal Article |
Language | English |
Published |
Elsevier B.V
01.10.2015
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Subjects | |
Online Access | Get full text |
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Summary: | •ZnS nanocrystals doped with Mn2+ were synthesized from hydrothermal method.•Structural behaviors are analyzed from XRD, Raman and PL measurements.•We report on long PL lifetimes of Mn levels due to excitation transfer from ZnS.•High photocatalytic efficiency was reported for ZnS-doped 3%Mn.
Undoped and Mn-doped ZnS nanocrystals (Ncs) have been synthesized by using the hydrothermal method at 200°C. X-ray diffraction (XRD) patterns revealed that the synthesized Ncs have cubic zinc blende structure. Typical SEM images show that undoped and Mn-doped ZnS Ncs are agglomerated in microspheres. Raman spectra informed that the Mn doping has improved the crystallinity of the ZnS Ncs up to the concentration 3%. The optical properties of Mn-doped ZnS Ncs were studied through UV–vis diffuse reflection spectroscopy, photoluminescence (PL), PL decay and PL excitation (PLE) measurements. The optical band gap was found to decrease from 3.59 to 3.35eV with increasing the Mn doping concentration. PL spectra demonstrate clearly that Mn2+ ions reduce the density of defect in both ZnS lattice and surface. An efficient excitation transfer from the ZnS host to Mn2+ ions is evidenced from PL decays.
ZnS:Mn Ncs were found to be good photocatalyst for sunlight degradation of Rhodamine B. The optimum Mn dopant concentration was 3%, above which photocatalytic activity decreased. The degradation reaction obeyed pseudo-first-order kinetics. |
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ISSN: | 0169-4332 1873-5584 |
DOI: | 10.1016/j.apsusc.2015.06.096 |