This topical issue of the journal Analytical and Bioanalytical Chemistry (ABC) is devoted to Photo Ionisation in Mass Spectrometry. Some of the publications presented in this special issue are based on contributions to a full-day scientific lecture session entitled Light and Molecular Ions—Photo Ionisation in Mass Spectrometry organised in the framework of the 2012 Analytica Conference in Munich. All twenty-one publications, including this introductory editorial, focus on this topic. As guest editor I am happy to introduce you to the content of the issue. Approximately 40 years after the beginning of the now 100year-long history of mass spectrometry [1], photo ionisation was invented—the first photo ions being observed in the fifties of the last century [2–4]. Vacuum UV (VUV) lamps were used for single-photon ionisation (SPI) of gaseous analytes. An overview of the physical fundamentals of photo ionisation in the gas phase is available in the literature [5]. The generation of sufficiently intense light in the required photon energy band has always been a challenge, and sometimes still is. The discovery of the laser effect and the technological realisation of pulsed high-power lasers started a new era in photo ionisation. Nearly coincidentally with the invention of the laser, the first laser desorption/ionisation (LDI) mass spectrometric experiments were reported; in these, ruby laser pulses were used for formation of ions from different solid materials [6]. The first observation of laser-induced gasphase photo ionisation, by a process later named multi photon ionisation (MPI), was reported in 1970 [7]. Following this pioneering work, application of resonance-enhanced multi photon ionisation to mass spectral analysis of organic molecules was introduced in 1978 [8]. With the invention of the third harmonic generation (THG) gas cell setups for production of VUV laser pulses in 1973 [9], a laser-based VUV light source also became available for SPI mass spectrometry [10]. A large variety of widely used analytical methods and technologies evolved from these initial studies on ionisation by either photon–molecule or laser pulse–surface interactions. A schematic time-of-flight mass spectrometer and some photo ionisation (PI) techniques used in analytical mass spectrometry are depicted in Fig. 1. Other PI techniques are given as acronyms only, and there is no claim to completeness. Onemeasure of the acceptance and applicability of scientific methods and technology is the annual number of publications, as recorded by, e.g., the ISI Web of Knowledge/Science. Figure 2 shows the development of the “photo ionisation mass spectrometry” field, measured by use of this bibliographical tool in the time range 1996–2012. It is obvious that laserdesorption-based techniques are by far the most commonly used. Laser desorption/ionisation (LDI), laser ablation (LA), and laser desorption (LD) and, in particular, matrix-assisted laser desorption/ionisation (MALDI) in conjunction with mass spectrometry dominate the numbers of applications, stimulated by the readily applicability ofMALDImass spectrometry to the life sciences (lipids, proteomics etc.). However, the intention of this special issue is to show the variety of methods and approaches of photo ionisation-based techniques. Although the most dominant application of PIMS, MALDI-MS [11] is already covered by a very large variety of monographs and books. Therefore, only a limited number of articles on MALDI are included in this special issue. These articles cover an important fundamental Published in the topical collection Photo Ionisation in Mass Spectrometry with guest editor Ralf Zimmermann.
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