Strong photoluminescence characteristics of sulforhodamine B attached on photonic crystal

Byoung-Ju Kim, K. Kang
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Abstract

The optical properties of sulforhodamine B (SRH) impregnated in photonic crystal by two step synthetic processes including a urethane bond formation between a 3-isocyanatopropyl triethoxysilane (ICPTES, -N=C=O) and a SRH with elevated temperature in pyridine and hydrolysis-condensation reactions between synthesized ICPTES/SRH (ICPSRH) and tetraethoxyorthosilicate (TEOS) in NH4OH. The monodisperse silica spheres impregnated the ICPSRH (ICPSRHS) are fabricated. The reduction of the absorption peak at 2270 cm-1 representing asymmetric stretching vibration of –N=C=O indicates the progress of the reaction and new absorption peak at 1712 cm-1 characterizing –C=O stretching vibration indicates the formation of urethane bond. The UV-visible absorption spectra show the broadened spectral line width by intermolecular interaction. The photoluminescence (PL) peak of the SRH in methanol shows a hypsochromic shift with the increase the excitation wavelength. However, the PL peak for the ICPSRH exhibits a bathochromic shift as the excitation wavelength increases. The PL peak for the ICPSRH shows no hypsochromic or bathochromic shift. The PL peaks for SRH in methanol, ICPSRH and ICPSRHS are at 568, 598 and 572 nm, respectively. The main cause of the PL peak shift is due to the intermolecular interaction.
光子晶体上的强光致发光特性
研究了3-异氰基三乙氧基硅烷(ICPTES, -N=C=O)与SRH在吡啶中形成聚氨酯键以及合成的ICPTES/SRH (ICPSRH)与四乙氧基硅酸盐(TEOS)在NH4OH中水解缩合反应两步法制备光子晶体中的硫代丹B (SRH)的光学性质。制备了浸渍ICPSRH的单分散硅球(ICPSRHS)。2270 cm-1处-N =C=O的不对称伸缩振动吸收峰的减小表明反应的进行,1712 cm-1处-C =O伸缩振动吸收峰的出现表明氨基甲酸乙酯键的形成。紫外-可见吸收光谱显示出分子间相互作用使谱线宽度变宽。随着激发波长的增加,SRH在甲醇中的光致发光峰出现了次色移。然而,随着激发波长的增加,ICPSRH的PL峰呈现出色移。ICPSRH的PL峰没有出现色移和色移。SRH在甲醇、ICPSRH和ICPSRHS中的PL峰分别在568、598和572 nm处。分子间的相互作用是引起PL峰位移的主要原因。
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