Matrix enrichment by black phosphorus improves ionization and reproducibility of mass spectrometry of intact cells, peptides, and amino acids.

Intact (whole) cell matrix-assisted laser desorption/ionization mass spectrometry (MALDI-TOF MS) is an established method for biotyping in clinical microbiology as well as for revealing phenotypic shifts in cultured eukaryotic cells. Intact cell MALDI-TOF MS has recently been introduced as a quality control tool for long-term cultures of pluripotent stem cells. Despite the potential this method holds for revealing minute changes in cells, there is still a need for improving the ionization efficiency or peak reproducibility. Here we report for the first time that supplementation by fine particles of black phosphorus to the standard MALDI matrices, such as sinapinic and α-cyano-4-hydroxycinnamic acids enhance intensities of mass spectra of particular amino acids and peptides, presumably by interactions with aromatic groups within the molecules. In addition, the particles of black phosphorus induce the formation of small and regularly dispersed crystals of sinapinic acid and α-cyano-4-hydroxycinnamic acid with the analyte on a steel MALDI target plate. Patterns of mass spectra recorded from intact cells using black phosphorus-enriched matrix were more reproducible and contained peaks of higher intensities when compared to matrix without black phosphorus supplementation. In summary, enrichment of common organic matrices by black phosphorus can improve discrimination data analysis by enhancing peak intensity and reproducibility of mass spectra acquired from intact cells.

Laser Ablation Generation of Bismuth Selenide Clusters from Mixtures of Elements, Crystalline Bi2Se3, or Thin Films: Laser Desorption Ionization (LDI) and Surface Assisted LDI Time-of-Flight Mass Spectrometry using Graphene and Nanodiamonds.

A bismuth-selenium system from mixtures of the powdered elements in various molar ratios and from Bi2Se3 crystals and/or thin films was studied using laser desorption ionization and surface assisted laser desorption ionization. The BimSen clusters were observed in both positive and negative ion modes, but the mass spectra were more intense, and also a higher number of clusters was formed in the positive ion mode than in the negative mode. The BiSen+ (n = 1-8), Bi2Sen+ (n = 1-5), and Bi3Sen+ (n = 1-6) clusters were detected. Similarly, in the negative ion mode, BiSen- (n = 2-9) and Bi2Sen- (n = 1-2) clusters were observed. In addition, the formation of Bim+ (m = 1-5), Sen+ (n = 1-8), and Sen- (n = 1-7) clusters was also observed. In total, 33 clusters were generated, and 4 new bismuth selenide clusters that have not been reported before (namely, BiSe7+/-, BiSe8+/-, BiSe9-, and Bi2Se5+) were detected. The formation of similar clusters was also observed from bismuth-selenium mixtures and from crystalline Bi2Se3. Furthermore, the Bi2Se3 thin films prepared from a magnetron sputtering technique were also examined via laser desorption ionization. The generation of clusters from the surface of graphene and nanodiamonds was also studied, but no remarkable difference with comparison to the metal surface was observed.

Amorphous Ge-Bi-Se Thin Films: A Mass Spectrometric Study.

The Ge-Bi-Se thin films of varied compositions (Ge content 0-32.1 at. %, Bi content 0-45.7 at. %, Se content 54.3-67.9 at. %) have been prepared by rf magnetron (co)-sputtering technique. The present study was undertaken in order to investigate the clusters generated during the interaction of laser pulses with Ge-Bi-Se thin films using laser ablation time-of-flight mass spectrometry. The stoichiometry of the clusters was determined in order to understand the individual species present in the plasma plume. Laser ablation of Ge-Bi-Se thin films accompanied by ionization produces about 20 positively and/or negatively charged unary, binary and ternary (Gex+, Biy+, Sez+/-, GexSez+/-, BiySez+/- and GexBiySez-) clusters. Furthermore, we performed the laser ablation experiments of Ge:Bi:Se elemental mixtures and the results were compared with laser ablation time-of-flight mass spectrometry analysis of thin films. Moreover, to understand the geometry of the generated clusters, we calculated structures of some selected binary and ternary clusters using density functional theory. The generated clusters and their calculated possible geometries can give important structural information, as well as help to understand the processes present in the plasma processes exploited for thin films deposition.

Laser ablation synthesis of carbon-phosphides from graphene/nanodiamond-phosphorus composite precursors: Laser desorption ionisation time-of-flight mass spectrometry.

RATIONALE: Carbon-phosphides are new and promising strategic materials with applications e.g. in optoelectronics. However, their chemistry and methods of synthesis are not completely understood, and only a limited number of C-P clusters have been detected up to now. Laser ablation synthesis (LAS) or laser desorption ionisation (LDI) has great potential to generate Cm Pn clusters in the gas phase and to act as the basis for the development of new technology. METHODS: The LAS of carbon phosphides using mixtures of nano-carbon sources (graphene, nanodiamonds) with phosphorus allotropes (red, black, and phosphorene) was examined. Since phosphorene is not commercially available, it was synthesised. A reflectron time-of-flight mass spectrometer was used to produce and identify the C-P clusters. A transmission electron microscope was used to characterise the prepared composites. RESULTS: LDI of various carbon-phosphorus composites generated a range of carbon-phosphides. From graphene-red phosphorus, Cm P+ (m = 3-47), Cm P2 + (m = 2-44), Cm P3 + (m = 1-42), Cm P4 + (m = 1-39), Cm P5 + (m = 1-37), Cm P6 + (m = 1-34), Cm P7 + (m = 1-31), Cm P8 + (m = 1-29), Cm P9 + (m = 1-26), Cm P10 + (m = 1-24), Cm P11 + (m = 1-21), and Cm P12 + (m = 1-19) clusters were detected, while nanodiamond composites with red/black phosphorus and with phosphorene yielded C24 P5 + 2n + (n = 0-28), C24 P5 + 2n + (n = 0-16), and C24 P5 + 2n + (n = 0-14) clusters, respectively. In total, over 300 new carbon-phosphide clusters were generated. CONCLUSIONS: The novel series of carbon-phosphide clusters generated from graphene or nanodiamond composites with red/black phosphorus or with phosphorene demonstrated rich carbon-phosphide chemistry that might inspire the development of novel nano-materials with specific properties.