Micro-heterogeneous oxygen response in luminescence sensor films

被引:48
作者
Bedlek-Anslow, JM
Hubner, JP
Carroll, BF
Schanze, KS [1 ]
机构
[1] Univ Florida, Dept Chem, Gainesville, FL 32611 USA
[2] Univ Florida, Dept Aerosp Engn Mech & Engn Sci, Gainesville, FL 32611 USA
关键词
D O I
10.1021/la0011679
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
A fluorescence microscopy technique has been developed that allows investigation of the luminescence properties of working film-based O-2 sensors with spatial resolution of < 5 <mu>m The new technique has been applied to investigate the properties of two sensor formulations that differ widely in their Stern-Volmer (SV) luminescence intensity response to variation in air pressure (P-air). One sensor is based on platinum(II) meso-tebrakis(pentafluorophenyl)porphyrin (PtTFPP) dispersed in poly(dimethylsiloxane) (PDMS) while the other consists of tris(4,7-diphenyl-1,10-phenanthroline)ruthenium(II) dichloride (Rudpp) dispersed in the same binder. The PtTFPP/PDMS sensor features a strong SV response that is spatially homogeneous on length scales ranging from 5 trm to several millimeters. By contrast, the Rudpp/PDMS sensor features a poor SV response. Moreover, the microscopy studies reveal that the SV response of the Rudpp sensor is spatially heterogeneous, even on length scales < 5 <mu>m. The difference in performance of the two sensor formulations is clearly due to the different solubility of the luminescent dyes in the polymer matrix. PtTFPP is compatible with the nonpolar PDMS matrix and thus disperses well in the binder, while the more polar Rudpp dye is less soluble in the PDMS and consequently microphase separation occurs in the sensor film. The results have broad implications in the formulation of oxygen sensor films for application as "pressure sensitive paints" (PSP).
引用
收藏
页码:9137 / 9141
页数:5
相关论文
共 27 条
[1]   DETERMINATION OF OXYGEN CONCENTRATIONS BY LUMINESCENCE QUENCHING OF A POLYMER-IMMOBILIZED TRANSITION-METAL COMPLEX [J].
BACON, JR ;
DEMAS, JN .
ANALYTICAL CHEMISTRY, 1987, 59 (23) :2780-2785
[2]  
Bout DAV, 1997, ACCOUNTS CHEM RES, V30, P204
[3]   PHOTOPHYSICS AND PHOTOCHEMISTRY OF OXYGEN SENSORS BASED ON LUMINESCENT TRANSITION-METAL COMPLEXES [J].
CARRAWAY, ER ;
DEMAS, JN ;
DEGRAFF, BA ;
BACON, JR .
ANALYTICAL CHEMISTRY, 1991, 63 (04) :337-342
[4]   LUMINESCENCE QUENCHING MECHANISM FOR MICROHETEROGENEOUS SYSTEMS [J].
CARRAWAY, ER ;
DEMAS, JN ;
DEGRAFF, BA .
ANALYTICAL CHEMISTRY, 1991, 63 (04) :332-336
[5]   APPLICATIONS OF HIGHLY LUMINESCENT TRANSITION-METAL COMPLEXES IN POLYMER SYSTEMS [J].
DEMAS, JN ;
DEGRAFF, BA .
MAKROMOLEKULARE CHEMIE-MACROMOLECULAR SYMPOSIA, 1992, 59 :35-51
[6]   Oxygen sensors based on luminescence quenching [J].
Demas, JN ;
DeGraff, BA ;
Coleman, PB .
ANALYTICAL CHEMISTRY, 1999, 71 (23) :793A-800A
[7]   LUMINESCENCE-BASED SENSORS - MICROHETEROGENEOUS AND TEMPERATURE EFFECTS [J].
DEMAS, JN ;
DEGRAFF, BA .
SENSORS AND ACTUATORS B-CHEMICAL, 1993, 11 (1-3) :35-41
[8]   MODELING OF LUMINESCENCE QUENCHING-BASED SENSORS - COMPARISON OF MULTISITE AND NONLINEAR GAS SOLUBILITY MODELS [J].
DEMAS, JN ;
DEGRAFF, BA ;
XU, WY .
ANALYTICAL CHEMISTRY, 1995, 67 (08) :1377-1380
[9]   Excited state interactions in electropolymerized thin films of Ru-II, Os-II, and Zn-II polypyridyl complexes [J].
Devenney, M ;
Worl, LA ;
Gould, S ;
Guadalupe, A ;
Sullivan, BP ;
Caspar, JV ;
Leasure, RL ;
Gardner, JR ;
Meyer, TJ .
JOURNAL OF PHYSICAL CHEMISTRY A, 1997, 101 (25) :4535-4540
[10]   EFFECTS OF POLYMER MATRICES ON THE TIME-RESOLVED LUMINESCENCE OF A RUTHENIUM COMPLEX QUENCHED BY OXYGEN [J].
DRAXLER, S ;
LIPPITSCH, ME ;
KLIMANT, I ;
KRAUS, H ;
WOLFBEIS, OS .
JOURNAL OF PHYSICAL CHEMISTRY, 1995, 99 (10) :3162-3167