Surface-enhanced resonance-Raman scattering: An informative probe of surfaces

被引:52
作者
Rodger, C [1 ]
Smith, WE [1 ]
Dent, G [1 ]
Edmondson, M [1 ]
机构
[1] ZENECA SPECIAL,MANCHESTER M9 8ZS,LANCS,ENGLAND
来源
JOURNAL OF THE CHEMICAL SOCIETY-DALTON TRANSACTIONS | 1996年 / 05期
关键词
D O I
10.1039/dt9960000791
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
Surface-enhanced resonance-Raman scattering (SERRS) experiments using a citrate-coated silver colloid have been performed. Transmission electron microscopy showed that the colloid consists of nearly mondisperse hexagonal particles with a maximum dimension of 36 nm. For maximum sensitivity, SERRS requires the controlled aggregation of the colloid. The nature of the aggregate formed is dependent on the method of aggregation. The effect of poly-L-lysine on the aggregation procedure was characterised using transmission and scanning electron microscopy. With SERRS, sensitivities down to 6.87 x 10(-18) mol dm(-3) were obtained using rhodamine dye. This corresponds to less than 200 molecules in the beam at any one time and suggests a sensitivity equal to or greater than that of fluorescence. A comparison of the use of SERRS with surface-enhanced Raman scattering (SERS) to follow adsorbate reactivity on a surface at less than monolayer coverage was obtained by studying metal complex formation using a preresonant Schiff base (SERRS) and 2-hydroxy-1-naphthaldehyde excited off resonance (SERS). In the former case, complex formation on the surface at well below monolayer coverage was observed and differences between the surface and the bulk complex characterised. In the latter complex formation was again observed but the bands were broad and problems of contamination, photodecomposition and selectivity evident.
引用
收藏
页码:791 / 799
页数:9
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