10 years of the Medipix2 Collaboration

Campbell, M.

doi:10.1016/j.nima.2010.06.106

Cited by 77 publications

(49 citation statements)

References 147 publications

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“…Charge coupled device (CCD) detectors enjoy a modicum of success, though they suffer from reduced sensitivity alongside a slew of other issues [7]. A costly but overall relatively problem-free detector came about with the development of the direct-detection photon counting detector systems such as the linear position sensitive MYTHEN detector [156], the 2D PILATUS detector [44], its upcoming successor, the EIGER detector [88], and the Medipix and PIXcel detectors [19]. The required corrections for these detectors will be discussed in section 3.3.…”

Section: The Push For Better Datamentioning

confidence: 99%

Everything SAXS: small-angle scattering pattern collection and correction

Pauw

2013

J. Phys.: Condens. Matter

159

136

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Section: The Push For Better Datamentioning

confidence: 99%

Everything SAXS: small-angle scattering pattern collection and correction

Pauw

2013

J. Phys.: Condens. Matter

159

136

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“…The detectors have been developed by the Medipix collaboration hosted by CERN. 36 A single chip contains 256 × 256 pixels (pixel size = 55 μm × 55 μm) and it is possible to build chip arrays of 2 × 2n (n = 1,2. . . )…”

Section: A the Medipix/timepix Detectorsmentioning

confidence: 99%

Microscope mode secondary ion mass spectrometry imaging with a Timepix detector

Kiss

Jungmann

Smith

et al. 2013

Review of Scientific Instruments

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In-vacuum active pixel detectors enable high sensitivity, highly parallel time-and space-resolved detection of ions from complex surfaces. For the first time, a Timepix detector assembly was combined with a secondary ion mass spectrometer for microscope mode secondary ion mass spectrometry (SIMS) imaging. Time resolved images from various benchmark samples demonstrate the imaging capabilities of the detector system. The main advantages of the active pixel detector are the higher signal-to-noise ratio and parallel acquisition of arrival time and position. Microscope mode SIMS imaging of biomolecules is demonstrated from tissue sections with the Timepix detector.

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“…For example, liquid-metal-jet anode electron-impact X-ray micro-sources [44] are today available as valid high brilliance alternatives to rotating anodes; scatterless hybrid metal-single-crystal slits have been proposed with success for small-angle X-ray scattering and high-resolution X-ray diffraction [45]; direct-detection photon counting detector systems such as the PIxeL apparATUs (PILATUS) series of detectors [46], the EIGER detector [47] or the Medipix and PIXcel detectors [48] are definitively a better choice in terms of dynamic range or pixel size. …”

Section: A Laboratory Set Up: the Xmi-l@b For Saxs/waxs Or Gisaxs/giwmentioning

confidence: 99%

X-ray Diffraction: A Powerful Technique for the Multiple-Length-Scale Structural Analysis of Nanomaterials

et al. 2016

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During recent decades innovative nanomaterials have been extensively studied, aiming at both investigating the structure-property relationship and discovering new properties, in order to achieve relevant improvements in current state-of-the art materials. Lately, controlled growth and/or assembly of nanostructures into hierarchical and complex architectures have played a key role in engineering novel functionalized materials. Since the structural characterization of such materials is a fundamental step, here we discuss X-ray scattering/diffraction techniques to analyze inorganic nanomaterials under different conditions: dispersed in solutions, dried in powders, embedded in matrix, and deposited onto surfaces or underneath them.

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10 years of the Medipix2 Collaboration

Cited by 77 publications

References 147 publications

Everything SAXS: small-angle scattering pattern collection and correction

Everything SAXS: small-angle scattering pattern collection and correction

Microscope mode secondary ion mass spectrometry imaging with a Timepix detector

X-ray Diffraction: A Powerful Technique for the Multiple-Length-Scale Structural Analysis of Nanomaterials

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