An energy-transfer cataluminescence reaction on nanosized catalysts and its application to chemical sensors

被引:48
作者
Zhang, ZY
Xu, K
Baeyens, WRG
Zhang, XR [1 ]
机构
[1] Tsing Hua Univ, Dept Chem, Minist Educ, Key Lab Atom & Mol Nanosci, Beijing 100084, Peoples R China
[2] State Univ Ghent, Fac Pharmaceut Sci, B-9000 Ghent, Belgium
基金
中国国家自然科学基金;
关键词
cataluminescence; energy-transfer; chemical sensors;
D O I
10.1016/j.aca.2004.12.025
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
When reductive gases pass over the surface of nanosized catalysts, a kind of chemiluminescence named cataluminescence (CTL) can be generated due to the production of excited intermediates. Here we report the observation of an energy transfer process between excited intermediates and the nanosized catalysts. The CTL is quenched when introducing Ho3+, Co2+ and Cu2+ into the catalyst, while new intensive CTL peaks appear when the catalyst is doped with Eu3+ or Tb3+. Further study indicates that the new CTL peak on Eu3+- or Tb3+-doped catalyst originates from the luminescence of the doped ions, excited by the energy transferred from excited intermediates produced during the reaction. Based on this novel energy-transfer CTL (ETCTL), an ethanol sensor is developed with Eu3+-doped nanosized ZrO2 that is linear to ethanol concentrations from 45 to 550 ppm, with the whole linear range lower than the lower limit of the previous CTL sensor. The ETCTL from Eu3+-doped in nanosized ZrO2 shows 72 times higher sensitivity than the CTL from excited intermediates in the sensor. High selectivity and stability are also obtained for this sensor. The results also indicate that the main factor limiting the sensitivity of CTL sensor on pure catalyst may be the inevitable energy quenching of excited intermediates with the catalyst, which is artfully utilized in the present work by the introduction of Eu3+, that effectively absorbs this part of energy and transfers it into light energy. (c) 2004 Elsevier B.V. All rights reserved.
引用
收藏
页码:145 / 152
页数:8
相关论文
共 35 条
[1]   Semiconductor clusters, nanocrystals, and quantum dots [J].
Alivisatos, AP .
SCIENCE, 1996, 271 (5251) :933-937
[2]   UNIVERSAL SULFUR DETECTION BY CHEMI-LUMINESCENCE [J].
BENNER, RL ;
STEDMAN, DH .
ANALYTICAL CHEMISTRY, 1989, 61 (11) :1268-1271
[3]  
Buchez Jr. M., 1998, SCIENCE, V281, P2013
[4]   Quantum dot bioconjugates for ultrasensitive nonisotopic detection [J].
Chan, WCW ;
Nie, SM .
SCIENCE, 1998, 281 (5385) :2016-2018
[5]   Fluorescence resonance energy transfer between quantum dot donors and dye-labeled protein acceptors [J].
Clapp, AR ;
Medintz, IL ;
Mauro, JM ;
Fisher, BR ;
Bawendi, MG ;
Mattoussi, H .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2004, 126 (01) :301-310
[6]   Nanowire nanosensors for highly sensitive and selective detection of biological and chemical species [J].
Cui, Y ;
Wei, QQ ;
Park, HK ;
Lieber, CM .
SCIENCE, 2001, 293 (5533) :1289-1292
[7]   Electrochemistry and electrogenerated chemiluminescence from silicon nanocrystal quantum dots [J].
Ding, ZF ;
Quinn, BM ;
Haram, SK ;
Pell, LE ;
Korgel, BA ;
Bard, AJ .
SCIENCE, 2002, 296 (5571) :1293-1297
[8]   Chemiluminescence of systems containing lanthanide ions [J].
Elbanowski, M ;
Makowska, B ;
Staninski, K ;
Kaczmarek, M .
JOURNAL OF PHOTOCHEMISTRY AND PHOTOBIOLOGY A-CHEMISTRY, 2000, 130 (2-3) :75-81
[9]   Hydrogen sensors and switches from electrodeposited palladium mesowire arrays [J].
Favier, F ;
Walter, EC ;
Zach, MP ;
Benter, T ;
Penner, RM .
SCIENCE, 2001, 293 (5538) :2227-2231
[10]   CATALYTIC OXIDATION OF COKE ON ALUMINOSILICATES [J].
GOLDSTEIN, MS .
INDUSTRIAL & ENGINEERING CHEMISTRY PROCESS DESIGN AND DEVELOPMENT, 1966, 5 (02) :189-+