Hostname: page-component-78c5997874-s2hrs Total loading time: 0 Render date: 2024-11-19T22:08:30.654Z Has data issue: false hasContentIssue false

Low-temperature route to nanoscale P3N5 hollow spheres

Published online by Cambridge University Press:  03 March 2011

Hongzhou Gu
Affiliation:
Department of Chemistry, University of Science and Technology of China, Hefei, Anhui 230026, People's Republic of China
Yunle Gu
Affiliation:
Department of Chemistry, University of Science and Technology of China, Hefei, Anhui 230026, People's Republic of China
Zhefeng Li
Affiliation:
Department of Chemistry, University of Science and Technology of China, Hefei, Anhui 230026, People's Republic of China
Yongcheng Ying
Affiliation:
Department of Chemistry, University of Science and Technology of China, Hefei, Anhui 230026, People's Republic of China
Yitai Qian*
Affiliation:
Structure Research Laboratory and Department of Chemistry, University of Science and Technology of China, Hefei, Anhui 230026, People's Republic of China
*
a)Address all correspondence to this author. e-mail: [email protected]
Get access

Abstract

Nanoscale hollow spheres of amorphous phosphorus nitride (P3N5) were synthesized by reacting PCl3 with NaN3 at 150–250 °C. Transmission electron microscope images show that the hollow spheres have a diameter of 150–350 nm, and the thickness of the shell is 20 nm. A very small amount of curly films were also found in the sample prepared at 150 °C. The infrared spectrum indicates a high degree of purity. X-ray photoelectron spectroscopy indicates the presence of P and N, with a molar ratio of 1:1.62 for P:N. Ultraviolet-visible absorption spectroscopy shows an absorption band at 265–315 nm. Under photoluminescent excitation at 230 nm, the P3N5 emits ultraviolet light at 305 nm. With a band gap of 4.28 eV, the products may be a wide gap semiconductor. A possible mechanism and the influence of temperature on the formation of the hollow spheres are also discussed.

Type
Articles
Copyright
Copyright © Materials Research Society 2003

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.Kroto, H.W., Heath, J.R., O'Brien, S.C., Curl, R.F., and Smalley, R.E., Nature 318, 162 (1985).Google Scholar
2.Iijima, S., Nature 354, 56 (1991).Google Scholar
3.Terrones, M., Hsu, W.K., Kroto, H.W., and Walton, D.R.M., Top. Curr. Chem. 199, 189 (1999).Google Scholar
4.Tenne, R., Hornyonfer, M., and Feldman, Y., Chem. Mater. 10, 3225 (1998).Google Scholar
5.Afanasiev, P., Geantet, C., Thomazeau, C., and Jouget, B., Chem. Commun. 1001 (2000).CrossRefGoogle Scholar
6.Kroll, P. and Schnick, W., Chem. Eur. J. 8, 3530 (2002).Google Scholar
7.Schnick, W., Lucke, J., and Krumeich, F., Chem. Mater. 8, 281 (1996).Google Scholar
8.Schnick, W. and Lucke, J., Solid State Ionics 38, 271 (1990).Google Scholar
9.Baldus, H.P., Schnick, W., Lucke, J., Wannagat, U., and Bogedain, G., Chem. Mater. 5, 845 (1993).Google Scholar
10.Schnick, W., Angew. Chem. Int. Ed. Engl. 32, 806 (1993).Google Scholar
11.Schnick, W., Stud. Surf. Sci. Catal. 84, 2221 (1994).Google Scholar
12.Meng, Z., Peng, Y., Yang, Z., and Qian, Y., Chem. Lett. 1252 (2000).CrossRefGoogle Scholar
13.Veprek, S., Iabal, Z., Brunner, J., and Scharli, M., Philos. Mag. B 43, 527 (1981).Google Scholar
14.Cremer, J., Joerchel, E., and Harnish, H. (Hoechst AG), Patient No. DE-A 2516915 (1977).Google Scholar
15.Horstmann, S., Irran, E., and Schnick, W., Z. Anorg. Allg. Chem. 624, 620 (1998).Google Scholar
16.Dake, L.S., Baer, D.R., and Friedrich, D.M., J. Vac. Sci. Technol. A 7, 1634 (1989).Google Scholar
17.Efros, A.L., Rosen, M., Kuno, M., Nirmal, M., Norris, D.J., and Bawendi, M., Phys. Rev. B 54, 4843 (1996).Google Scholar
18.Nirmal, M., Norris, D.J., Huno, M., Bawendi, M.G., Efros, A., and Rosen, M., Phys. Rev. Lett. 75, 3728 (1995).Google Scholar
19.Norris, D.J. and Bawendi, M.G., J. Chem. Phys. 103, 5260 (1995).Google Scholar
20.Tang, K., Hu, J., Lu, Q., Xie, Y., Zhu, J., and Qian, Y., Adv. Mater. 11, 653 (1999).Google Scholar
21.Hu, J.Q., Deng, B., Zhang, W.X., Tang, K.B., and Qian, Y.T., Chem. Phys. Lett. 351, 229 (2002).Google Scholar