International
Tables for Crystallography Volume F Crystallography of biological macromolecules Edited by M. G. Rossmann and E. Arnold © International Union of Crystallography 2006 |
International Tables for Crystallography (2006). Vol. F. ch. 6.2, pp. 136-137
Section 6.2.1.4.2. Image plates
a
Life Sciences Division M888, University of California, Los Alamos National Laboratory, Los Alamos, NM 8745, USA, and bSmall Angle Scattering Facility, Australian Nuclear Science & Technology Organisation, Physics Division, PMB 1 Menai NSW 2234, Australia |
The principles underlying the operation of an image plate (IP) are presented in detail in Chapter 7.2 . Briefly, the important difference between an IP for X-ray and neutron detection is the presence of a converter (either Gd2O3 or 6Li). The role of the converter is to capture an incoming neutron and create an event within the IP that mimics the detection of an X-ray photon. For example, neutron capture in Gd produces conversion electrons that exit the Gd2O3 grains, enter neighbouring photostimulated luminescence (PSL) material and create colour centres to form a latent image (Niimura et al., 1994; Takahashi et al., 1996). A neutron IP may have a virtually unlimited area and a shape limited only by the requirement to locate the detection event in a suitable coordinate system. With a neutron-detection efficiency of up to 80% at ~1–2 Å, a dynamic quantum efficiency of ~25–30% can be obtained. The dynamic range is intrinsically 1:105. The spatial resolution is primarily limited by scattering processes of the readout laser beam, and measured line spread functions are typically 150–200 µm. The γ sensitivity is high and may restrict the application to instruments with low ambient γ background.
Neutron IPs are integrating devices well suited to data-acquisition techniques with long accumulation times, such as Laue diffraction (Niimura et al., 1997) and small-angle scattering. On-line readout is a distinct advantage (Cipriani et al., 1997).
References
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