Chemisorption and chemical reaction effects on the resistivity of ultrathin gold films at the liquid-solid interface

被引:59
作者
Zhang, YM
Terrill, RH
Bohn, PW
机构
[1] Univ Illinois, Dept Chem, Beckman Inst, Urbana, IL 61801 USA
[2] Univ Illinois, Mat Res Lab, Urbana, IL 61801 USA
关键词
D O I
10.1021/ac980571y
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Ultrathin gold films, with thicknesses between the onset of conductivity (d similar to 5 mn) and the electron mean free path (d similar to 80 nm), display surface-sensitive resistivities, which have been exploited to follow the adsorption and desorption of molecular monolayers at the metal-solution interface with high precision. For nominal Au film thicknesses (d similar to 40 nm), strongly chemisorbed thiolate monolayers increase the resistivity of the thin Au films by similar to 4%, but weakly adsorbed species, such as pyridine or phenolate at open circuit, induce no observable change in the Au film resistance. Resistivity measurements implemented with a high-stability current source and high precision digital voltmeter sampling at 1 Hz resulted in 3 sigma uncertainties in alkanethiolate coverage of 1.4 x 10(-4) monolayer, Surface plasmon resonance measurements, performed simultaneously with resistivity measurementsi indicate that changes in resistivity vary monotonically with coverage with three distinct regions: a low-coverage region of heightened adsorbate mobility, an intermediate-coverage region with generally linear behavior, and a chain length-dependent saturation region at high coverages. Resistivity measurements were also capable of reproducibly following the chemical state of the Au surface through a complex set of redox manipulations, demonstrating the versatility of this simple measurement.
引用
收藏
页码:119 / 125
页数:7
相关论文
共 73 条
[51]  
Raether H., 1988, SURFACE PLASMONS SMO, V111
[52]  
RAUH M, 1995, APPL PHYS A-MATER, V61, P587, DOI 10.1007/BF01542868
[53]   IN-SITU STM AND IR STUDIES OF PHENOXIDE ELECTROOXIDATION ON AU(111) ELECTRODE SURFACES [J].
RICHARD, KM ;
GEWIRTH, AA .
JOURNAL OF PHYSICAL CHEMISTRY, 1995, 99 (32) :12288-12293
[54]   THIOAROMATIC MONOLAYERS ON GOLD - A NEW FAMILY OF SELF-ASSEMBLING MONOLAYERS [J].
SABATANI, E ;
COHENBOULAKIA, J ;
BRUENING, M ;
RUBINSTEIN, I .
LANGMUIR, 1993, 9 (11) :2974-2981
[55]   ORGANIZED SELF-ASSEMBLING MONOLAYERS ON ELECTRODES .2. MONOLAYER-BASED ULTRAMICROELECTRODES FOR THE STUDY OF VERY RAPID ELECTRODE-KINETICS [J].
SABATANI, E ;
RUBINSTEIN, I .
JOURNAL OF PHYSICAL CHEMISTRY, 1987, 91 (27) :6663-6669
[56]  
SCHAD R, 1992, PHYS REV B, V45, P430
[57]   THE MEAN FREE PATH OF ELECTRONS IN METALS [J].
SONDHEIMER, EH .
ADVANCES IN PHYSICS, 1952, 1 (01) :1-42
[58]   REAL-TIME ANALYSIS OF CHEMICAL-REACTIONS OCCURRING AT A SURFACE-CONFINED ORGANIC MONOLAYER [J].
SUN, L ;
THOMAS, RC ;
CROOKS, RM ;
RICCO, AJ .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1991, 113 (22) :8550-8552
[59]  
TANNER B, 1995, INTRO PHYSICS ELECT, P37
[60]   UV PHOTOPATTERNING OF ALKANETHIOLATE MONOLAYERS SELF-ASSEMBLED ON GOLD AND SILVER [J].
TARLOV, MJ ;
BURGESS, DRF ;
GILLEN, G .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1993, 115 (12) :5305-5306