Electronic excitation by lasers or electron beams can modify the properties of materials. The changes are not just due to heat, nor do they result from the well-known collision dynamics of much radiation damage. Everyday examples of modi®cation by electronic excitation include photography, and photochromics (such as sunglasses) which change colour. In the last few years it has become clear that excitation can offer novel types of modi®cation, with better-controlled changes. The ®eld has evolved through a mix of basic science, of new laser and electron beam tools, and of new needs from microelectronics, photonics and nanotechnology. Underlying this development are some common themes which integrate the basic science and its applications. These include especially the ideas of energy localisation and charge localisation. There are detailed comparisons of experiment and theory for halides, but there is a wealth of information for other materials. From this, we identify ways to connect understanding to technological needs, like selective removal of material, controlled changes, altering the balance between process steps, and possibilities of quantum control. The ®eld is reviewed in full in our recent book [N. Itoh, A.M. Stoneham, Materials Modi®cation

The design and fabrication of materials that exhibit both semiconducting and magnetic properties for spintronics and quantum computing has proven difficult. Important starting points are high-purity thin films as well as fundamental theoretical understanding of the magnetism. Here we show that small molecules have great potential in this area, due to ease of insertion of localised spins in organic frameworks and both chemical and structural purity. In particular, we demonstrate that archetypal molecular semiconductors, namely the metal phthalocyanines (Pc), can be readily fabricated as thin film quantum antiferromagnets, important precursors to a solid state quantum computer. Their magnetic state can be switched via fabrication steps which modify the film structure, offering practical routes into information processing. Theoretical calculations show that a new mechanism, which is the molecular analogue of the interactions between magnetic ions in metals, is responsible for the magnetic states. Our combination of theory and experiments opens the field of organic thin film magnetic engineering

Magnetism is not usually expected in simple sp oxides like MgO or in carbons like graphite. Yet basic intrinsic defects in these systems can be magnetic in ways that seem to be shared by more complex oxides. A second puzzle comes from reports of possible room temperature ferromagnetism in simple oxides, where experiments are not always in agreement. This paper discusses what determines whether point defects like cation vacancies in oxides have magnetic or non-magnetic ground states. It also discusses the possible connections between point defect ground states and oxide ferromagnetism. The connectivity issue raises questions about possible diffuse states in nanocrystalline oxides, several possibilities being outlined. These ideas raise the further possibility that the magnetism might be written in these oxides at the nanoscale, perhaps using atomic force microscopy.