Visualizing mass transport in desorption electrospray ionization using time-of-flight secondary ion mass spectrometry: a look at the geometric configuration of the spray

被引:2
作者
Muramoto, Shin [1 ]
机构
[1] NIST, Gaithersburg, MD 20899 USA
关键词
EXPLOSIVES; MECHANISMS; MOLECULES; SURFACES; DESI; INSTRUMENTATION; CHEMISTRY; FORENSICS; SAMPLES; DRUGS;
D O I
10.1039/c4an01481b
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Time-of-flight secondary ion mass spectrometry (ToF-SIMS) was used to visualize the transport of analyte molecules desorbed onto a silicon wafer collection substrate by desorption electrospray ionization (DESI). The effect of spray incidence angle, tip height, and probe distance on the concentration and the spatial distribution of desorbed analyte molecules were investigated with the objective of identifying DESI operational parameters that provide more reproducible results by achieving steady ion transmission and minimized material loss. An incidence angle between 25 and 35 with respect to the plane of the surface provided the best compromise between maximizing ambient MS signal and achieving the best reliability. Glancing incidence angles provided higher ambient MS signals through a tighter dispersion of the secondary droplet plume, but run-to-run variability of as much as 40%. On the other hand, steeper incidence angles led to a widening of the lateral dispersion of the secondary droplets and decreased analyte desorption. For all incidence angles, shorter probe distances were preferred since the resulting tighter dispersion of the secondary droplets produced higher ion transmission and therefore higher ambient MS signals. Tip height was found to correlate with the spot size (footprint) of the spray on the surface; changing the tip height from (1 to 2 to 3) mm changed the diameter of the spray impact area from (1.3, 1.8, to 2.1) mm, respectively. For shorter probe to MS inlet distances, larger tip heights increased the ambient MS signal due to increased analyte desorption while maintaining a tighter dispersion of the secondary droplet plume. Equally important to optimizing instrument configuration was the understanding that the deposition of a sample onto the surface resulted in a coffee ring, where the diameter was larger than the spot size of the spray. Higher tip heights may be preferred for a more consistent analyte response since all or a large fraction of the analyte could be sampled to reduce variability in ambient MS response. The study showed that ToF-SIMS can be used as a unique tool for characterizing the transport of desorbed analyte molecules for DESI, and potentially offers insight into new interface designs for improved transmission of analyte into the mass spectrometer.
引用
收藏
页码:5868 / 5878
页数:11
相关论文
共 50 条
[31]   The in vivo absorbed constituents and metabolites of Danshen decoction in rats identified by HPLC with electrospray ionization tandem ion trap and time-of-flight mass spectrometry [J].
Zhao, Xin ;
Yang, Dong-Hui ;
Xu, Feng ;
Huang, Shuai ;
Zhang, Lei ;
Liu, Guang-Xue ;
Cai, Shao-Qing .
BIOMEDICAL CHROMATOGRAPHY, 2015, 29 (02) :285-304
[32]   Rapid and specific detection of urea nitrate and ammonium nitrate by electrospray ionization time-of-flight mass spectrometry using infusion with crown ethers [J].
de Perre, Chloe ;
Prado, Adelheid ;
McCord, Bruce R. .
RAPID COMMUNICATIONS IN MASS SPECTROMETRY, 2012, 26 (02) :154-162
[33]   Femtogram Detection and Quantitation of Residues Using Laser Ionization Orthogonal Time-of-Flight Mass Spectrometry [J].
Yu, Quan ;
Cao, Zhiyu ;
Li, Lingfeng ;
Yan, Bin ;
Hang, Wei ;
He, Jian ;
Huang, Benli .
ANALYTICAL CHEMISTRY, 2009, 81 (20) :8623-8626
[34]   Fragmentation Study of the C Ring in Flavone and Isoflavone Aglycones by Electrospray Ion Trap Time-of-Flight Mass Spectrometry [J].
Xu Ying ;
Dong Jing ;
Wang Hong ;
Wan Le-Ren ;
Hashi Yuki ;
Chen Shi-Zhong .
CHEMICAL JOURNAL OF CHINESE UNIVERSITIES-CHINESE, 2009, 30 (01) :46-50
[35]   Ion-plasma treatment of reed switch contacts: A study by time-of-flight secondary ion mass spectrometry [J].
Tolstoguzov, A. B. ;
Drozdov, M. N. ;
Zeltser, I. A. ;
Arushanov, K. A. ;
Teodoro, Orlando M. N. D. .
JOURNAL OF ANALYTICAL CHEMISTRY, 2014, 69 (13) :1245-1251
[36]   Potential of desorption electrospray ionization and paper spray ionization with high-resolution mass spectrometry for the screening of sports doping agents in urine [J].
Bressan, Claudia ;
Sero, Raquel ;
Alechaga, Elida ;
Monfort, Nuria ;
Moyano, Encarnacion ;
Ventura, Rosa .
ANALYTICAL METHODS, 2023, 15 (04) :462-471
[37]   Salt Effects on Ion Formation in Desorption Mass Spectrometry: An Investigation into the Role of Alkali Chlorides on Peak Suppression in Time-of-Flight-Secondary Ion Mass Spectrometry [J].
Piwowar, Alan M. ;
Lockyer, Nick P. ;
Vickerman, John C. .
ANALYTICAL CHEMISTRY, 2009, 81 (03) :1040-1048
[38]   Direct analysis of alkaloids in natural Cinchona bark and commercial extracts using time-of-flight secondary ion mass spectrometry [J].
Ateacha, Derick N. ;
Koch, Ulrike ;
Engelhard, Carsten .
ANALYTICAL METHODS, 2018, 10 (09) :950-958
[39]   Synthesis of tellurium nanosheet for use in matrix assisted laser desorption/ionization time-of-flight mass spectrometry of small molecules [J].
Chen, Ya-Shun ;
Ding, Jun ;
He, Xiao-Mei ;
Xu, Jing ;
Feng, Yu-Qi .
MICROCHIMICA ACTA, 2018, 185 (08)
[40]   Identification of Fleeting Electrochemical Reaction Intermediates Using Desorption Electrospray Ionization Mass Spectrometry [J].
Brown, Timothy A. ;
Chen, Hao ;
Zare, Richard N. .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2015, 137 (23) :7274-7277