Abstract

The development of Static or Molecular secondary ion mass spectrometry (SIMS) is reviewed with particular reference to the journey made by the Manchester group and its collaborators. The earliest studies focussed on the application of static SIMS to single crystal surface studies. These studies successfully demonstrated that static SIMS delivered information on the delicate adsorbate state that mirrored that obtained by other surface science techniques. Subsequent application of the technique to studying the state and reactivity of bimetallic surfaces stimulated by collaboration with the Ertl group, demonstrated that static SIMS could be applied to the investigation of quite complex surface chemistry. This success stimulated the application of the technique to surface chemistry studies of much more complex systems such as polymers, ice mimics of polar stratospheric clouds, aerosols, culminating in biological systems. The need to enhance ion yields of the larger biological molecules led to the development and introduction of polyatomic primary ion beams, most notably based on C 60 buckminsterfullerene. This type of ion beam has transformed molecular analysis by SIMS. Not only have the yields of larger molecular ions been greatly increased, the bombardment induced damage that necessitated the static limit has been dramatically reduced such that for many materials the static limit requirement can be abandoned. A completely new analytical regime has opened up so that molecular depth profiling and 3D chemical imaging is possible. To fully realise the new capabilities for biological analysis a new generation of ToF-SIMS instrument is being developed that overcomes the compromises of pulsed beam instruments and that enables high mass resolution, high spatial resolution and high duty cycle to be attained simultaneously.

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