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硫化锌纳米颗粒中锰(II)的光谱学与动力学

Spectroscopy and dynamics of Mn(2+) in ZnS nanoparticles.

作者信息

Kim Mee Rahn, Chung Jae Hun, Jang Du-Jeon

机构信息

School of Chemistry, Seoul National University, NS60, Seoul, 151-742, Korea.

出版信息

Phys Chem Chem Phys. 2009 Feb 14;11(6):1003-6. doi: 10.1039/b813452a. Epub 2008 Nov 28.

Abstract

Both spectra of transient absorption (lambda(max) = 390 nm) and luminescence (lambda(max) = 590 nm) for the (4)T(1) state of Mn(2+) in ZnS nanoparticles shift to long wavelengths by 40 nm and broaden by 1.7 times as the state becomes banded. The (4)T(1) band of capping Mn(2+) in ZnS nanoparticles decays on the time scale of 0.35 mus, which is much shorter than either the decay time of the (4)T(1) state (2000 micros) for lattice-bound isolated Mn(2+) or that (180 micros) for surface-bound isolated Mn(2+) in ZnS nanoparticles.

摘要

随着ZnS纳米颗粒中Mn(2+)的(4)T(1)态变为带状,其瞬态吸收光谱(λmax = 390 nm)和发光光谱(λmax = 590 nm)均向长波长方向移动40 nm,且展宽了1.7倍。ZnS纳米颗粒中封端Mn(2+)的(4)T(1)带在0.35微秒的时间尺度上衰减,这比晶格束缚的孤立Mn(2+)的(4)T(1)态的衰减时间(2000微秒)或ZnS纳米颗粒中表面束缚的孤立Mn(2+)的衰减时间(180微秒)都要短得多。

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