Hostname: page-component-77c89778f8-vsgnj Total loading time: 0 Render date: 2024-07-18T17:14:14.160Z Has data issue: false hasContentIssue false

Effects of Mn2+ Distribution Controlled by Carboxylic Acids on Photoluminescence Intensity of Nanosized ZnS:Mn Particles

Published online by Cambridge University Press:  15 February 2011

T. Isobe
Affiliation:
Department of Applied Chemistry, Keio University, 3–14–1 Hiyoshi, Kohoku-ku, Yokohama 223, Japan. isobe@appIc.keio.ac.jp
T. Igarashi
Affiliation:
Department of Applied Chemistry, Keio University, 3–14–1 Hiyoshi, Kohoku-ku, Yokohama 223, Japan. isobe@appIc.keio.ac.jp
M. Senna
Affiliation:
Department of Applied Chemistry, Keio University, 3–14–1 Hiyoshi, Kohoku-ku, Yokohama 223, Japan. isobe@appIc.keio.ac.jp
Get access

Abstract

Addition of methacrylic acid (MA) during preparation of ZnS doped with Mn2+ (ZnS:Mn) increased the photoluminescence (PL) due to 4T1-6A1 transition of Mn2+. According to X-ray fluorescence analysis and electron paramagnetic resonance spectroscopy, ion exchange between Zn2+ and Mn2+ through a preferential dissolution of Mn2+ was promoted by acidic additives. This caused that Mn ions were isolatedly incorporated into ZnS. The X-ray photoelectron spectra show that the intensity of S 2p3/2 peak due to S6+ increased relative to that of S2- by virtue of carboxylic groups. The intensities of PL peaks at 450 and 580 nm, corresponding to polymethacrylic acid and Mn2+, respectively, increased after heating at 80°C for 1 week. We conclude that MA plays important roles on selective leaching to increase the amount of isolated Mn2+ ions, chemical interaction between ZnS:Mn and MA and energy transfer to Mn2+, leading to the increase in PL intensity.

Type
Research Article
Copyright
Copyright © Materials Research Society 1997

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

REFERENCES

[1]Bhargava, R.N., Gallagher, D. and Welker, T., J. Lumin. 60&61, 275 (1994).Google Scholar
[2]Yu, I., Isobe, T. and Senna, M., J. Phys. Chem. Solids 54, 373 (1996).Google Scholar
[3]Yu, I., Isobe, T., Senna, M. and Takahashi, S., Mater. Sci. Eng. B38, 177 (1996).Google Scholar
[4]Yu, I. and Senna, M., Appl. Phys. Lett. 66, 424 (1995).Google Scholar
[5]Baláz, P., Basti, Z., Briancin, J., Ebert, I. and Lipka, J., J. Mater. Sci. 27, 653 (1992).Google Scholar
[6]Gallagher, D., Heady, W.E., Racz, J.M. and Bhargava, R.N., J. Mater. Res. 10, 870 (1995).Google Scholar