Selective sensing of isoprene by Ti-doped ZnO for breath diagnostics

被引:114
作者
Guntner, A. T. [1 ]
Pineau, N. J. [1 ]
Chie, D. [1 ]
Krumeich, F. [1 ]
Pratsinis, S. E. [1 ]
机构
[1] ETH, Particle Technol Lab, Inst Proc Engn, Dept Mech & Proc Engn, Sonneggstr 3, CH-8092 Zurich, Switzerland
基金
瑞士国家科学基金会;
关键词
FLAME SPRAY-PYROLYSIS; GAS SENSORS; NANOCRYSTALLINE TIO2; EXHALED ISOPRENE; NANOPARTICLES; TEMPERATURE; ACETONE; FILMS; FERROMAGNETISM; NANOSTRUCTURES;
D O I
10.1039/c6tb01335j
中图分类号
TB3 [工程材料学]; R318.08 [生物材料学];
学科分类号
0805 ; 080501 ; 080502 ;
摘要
Exhaled isoprene could enable non-invasive monitoring of cholesterol-lowering therapies. Here, we report an isoprene-selective sensor at high relative humidity (RH) for the first time (to our knowledge). It is made of nanostructured, chemo-resistive Ti-doped ZnO particles (10-20 nm crystal size) produced by flame spray pyrolysis (FSP) and directly deposited in one step onto compact sensor substrates forming highly porous films. The constituent particles consist of stable Ti-doped ZnO solid solutions for Ti levels up to 10 mol% apparently by substitutional incorporation of Ti4+ into the ZnO wurtzite lattice and dominant presence at the particle surface. These Ti4+ point defects strongly enhance the isoprene sensitivity (>15 times higher than pure ZnO) and turn ZnO isoprene-selective, while also improving its thermal stability. In situ infrared spectroscopy confirms that Ti4+ intensifies the surface interaction of Ti-doped ZnO with isoprene by providing additional sites for chemisorbed hydroxyl species. In fact, at an optimal Ti content of 2.5 mol%, this sensor shows superior isoprene responses compared to acetone, NH3 and ethanol at 90% RH. Most notably, breath-relevant isoprene concentrations can be detected accurately down to 5 ppb with high (>10) signal-to-noise ratio. As a result, an inexpensive isoprene detector has been developed that could be easily incorporated into a portable breath analyzer for noninvasive monitoring of metabolic disorders (e.g. cholesterol).
引用
收藏
页码:5358 / 5366
页数:9
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