Molecular secondary ion mass spectrometry with a liquid metal ion primary source
Molecular secondary ion mass spectrometry with a liquid metal ion primary source
复制标题
使用液态金属离子主源进行分子二次离子质谱分析
DOI:
10.1021/ac00259a031
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发表时间:
1983
影响因子:
7.4
通讯作者:
L. Swanson
中科院分区:
文献类型:
--
作者:
D. Barofsky;U. Giessmann;A. Bell;L. Swanson
The use of Ga, In, SiAu, and Bi liquid metal Ion (LMI) emitters as primary sources In matrix assisted molecular secondary ion mass spectrometry (SIMS) was investigated. The prin-cipal observations were a very high molecular Ion abundance from the glycerol solution of every test compound (10-50 times that attainable with Ar fast atom bombardment), a strong increasing dependence of molecular Ion signal on primary beam current density up to a saturation level at~ 10~® A cm-2, a strong Increasing dependence of molecular Ion abundance on atomic number of the bombarding element, a secondary Ion energy spread of~ 3 eV, and a statistical fluctuation of~ 3-10% In the secondary Ion signals. No essential, qualitative differences were observed between LMI/SI MS mass spectra and those of other soft Ionization techniques. Applications In SIMS analyses, fundamental in-vestigations of secondary ion processes, and, possibly, localized molecular analysis of biological tissue coupled with Ion microscopy are Indicated.Beginning with the introduction of field desorption mass spectrometry in 1969 (1), revolutionary advances have taken place in the mass spectrometric analysis of thermally labile, high molecular weight organic compounds. Relatively recently, secondary ion mass spectrometry (SIMS) employing either atomic ion (2-4) or neutral atom (5, 6) primary beams has contributed significantly to this progress. Some of the major developments in molecular SIMS have been brought about through the use of primary beams with