Cluster secondary ion mass spectrometry microscope mode mass spectrometry imaging

被引:14
|
作者
Kiss, Andras [1 ]
Smith, Donald F. [1 ]
Jungmann, Julia H. [1 ]
Heeren, Ron M. A. [1 ]
机构
[1] FOM Inst AMOLF, NL-1098 XG Amsterdam, Netherlands
关键词
PIXEL READOUT CHIP; SIMS; TISSUE; TIME; BOMBARDMENT; SYSTEM; QUANTIFICATION; LOCALIZATION; MEDIPIX2; WORKING;
D O I
10.1002/rcm.6719
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
RATIONALEMicroscope mode imaging for secondary ion mass spectrometry is a technique with the promise of simultaneous high spatial resolution and high-speed imaging of biomolecules from complex surfaces. Technological developments such as new position-sensitive detectors, in combination with polyatomic primary ion sources, are required to exploit the full potential of microscope mode mass spectrometry imaging, i.e. to efficiently push the limits of ultra-high spatial resolution, sample throughput and sensitivity. METHODSIn this work, a C-60 primary source was combined with a commercial mass microscope for microscope mode secondary ion mass spectrometry imaging. The detector setup is a pixelated detector from the Medipix/Timepix family with high-voltage post-acceleration capabilities. The system's mass spectral and imaging performance is tested with various benchmark samples and thin tissue sections. RESULTSThe high secondary ion yield (with respect to 'traditional' monatomic primary ion sources) of the C-60 primary ion source and the increased sensitivity of the high voltage detector setup improve microscope mode secondary ion mass spectrometry imaging. The analysis time and the signal-to-noise ratio are improved compared with other microscope mode imaging systems, all at high spatial resolution. CONCLUSIONSWe have demonstrated the unique capabilities of a C-60 ion microscope with a Timepix detector for high spatial resolution microscope mode secondary ion mass spectrometry imaging. Copyright (c) 2013 John Wiley & Sons, Ltd.
引用
收藏
页码:2745 / 2750
页数:6
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