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A novel direct sampling ionization scheme for ambient mass spectrometry is presented. Desorption and ionization is achieved by a quasi-continuous laser induced plasma in air. Since there are no solid or liquid electrodes involved the ion source does not suffer from chemical interferences or fatigue originating from erosive burning or from electrode consumption. A laser plasma was ignited under ambient conditions in front of a modified TOF MS atmospheric pressure interface, using a high repetition rate DPSS laser operating at 532 nm and 26 kHz and an aspherical lens with a focal length of 8 mm. Emission spectroscopy (40-1100 nm) and time resolved studies on specific plasma parameters revealed insight into the physical and chemical plasma properties. Plasma ignition can be performed in rare gases and under ambient conditions. The hot plasma zone was kept at a certain distance from the sample region. Thus, effective collisional cooling seemed to prevent thermal fragmentation. Every single spark generates a shockwave, providing new reactive species, which expands concentrically from the hot region. Under ambient conditions primary charge carriers (ions and electrons) as well as VUV radiation initialize reaction cascades equivalent to other ambient ionization methods, such as DART or DBD. Mass spectra of polar/nonpolar hydrocarbons, sugars, pharmaceuticals and natural biomolecules in food were observed. Comprehensive emission spectroscopic measurements and time resolved electron current studies revealed insight into some plasma properties, such as the emitted high energetic radiation and the time evolution of the expanding plume.
Only a few years after the invention of the laser, the concept of laser microprobe mass spectrometry (LMMS), a technique which employed intense laser radiation for ion generation, was introduced. In these early studies at excessive irradiation microplasma formation could be observed to be an effective channel for ion formation. However, this plasma generation in vacuum led to undesired distortions of the mass analyzers and, thus, was discarded as an analytical ion source.
Under ambient conditions, the surrounding air effectively cools the plasma cloud, making the plasma more controllable. The resulting laser induced plasma is nowadays commonly used in laser induced breakdown spectroscopy (LIBS) applications as excitation source for optical emission spectroscopy experiments. However, little effort has been made to introduce a LIBS plasma as a promising ion source for ambient mass spectrometry. The main hindrance is the transient character of laser induced plasmas that typically only has a lifetime on the order of several microseconds. This drastically reduces the duty cycle of these plasma sources. After these microseconds, the generated ions recombinate to uncharged
atoms and even newly bound molecules, making them inaccessible to mass-to-charge analyzers. The advent of high repetition lasers together with the ever growing knowledge about manipulation of charged species at atmospheric pressures allow overcoming these obstacles. This presentation will introduce an ionization scheme using a laser induced plasma as the primary ion source. We believe that this novel ionization strategy will pave the way for future applications in ambient mass spectrometry.
Recently, a novel ionization scheme for ambient MS has been introduced. It is based on a quasi-continuous laser induced plasma (LIP), ignited in front of the MS inlet. This setup comprises the advantages of an ambient probe, electro neutrality, a sufficient duty cycle, a ubiquitous plasma medium, low power consumption, the absence of solvents and high sensitivity. To assess its future applicability for the detection of volatile organic compounds, plasma properties and operating conditions are investigated to understand the processes, that lead to the unexpected formation of intact molecular ions. Comprehensive studies include optical Emission spectroscopy, shadowgraphic shockwave visualization and time-of-flight mass spectrometry.