1. Field of the Invention
The present invention is a high performance room-temperature semiconductor x-ray and gamma ray radiation detector and method of manufacture thereof. Although the invention will be described in connection with a semi-insulating CdxZn1-xTe (0≦x≦1) radiation detector, the invention is applicable to any II-VI compound with semi-insulating properties. As such, the invention is applicable to any nonlinear or electro-optical device or application where semi-insulating or high resistivity semiconductor material is required. The 0≦x≦1 concentration, or mole fraction range, encompasses CdZnTe with any Zn percentage including CdTe (x=1) and ZnTe (x=0).
2. Description of the Prior Art
With reference to
In use, detector 1 is typically bonded to a carrier or substrate 12 that includes a suitable pattern of conductors (not shown) that facilitate the acquisition of radiation event signals from segmented electrodes 8. More specifically, segmented electrodes 8 of detector 1 are bonded to electrode pads 14 of substrate 12, that match the geometry of segmented electrodes 8 of detector 1, via bonding bumps 16. Each bonding bump 16 can be, without limitation, an In bump, a low-temperature solder bump, a bump of conductive adhesive, and the like.
Segmented electrodes 8 can be pixels, strips, grids, steering grids, bars or rings of arbitrary size and geometry. Segmented electrodes 8 can be biased or unbiased relative to each other, to side electrode 6 and/or continuous electrode 4.
An exemplary embodiment of detector 1 includes 256 equal sized electrodes, like segmented electrodes 8, arranged in a 16×16 two-dimensional array that is surrounded by a side electrode, like side electrode 6, thereby defining a 257th electrode.
Detector 1 is operated by applying one or more voltages between continuous electrode 4 and segmented electrodes 8 that cause charge carriers (electrons and holes) generated by radiation events in the volume of substrate 2 to drift toward continuous electrode 4 and segmented electrodes 8. Segmented electrodes 8 are coupled to appropriate readout circuitry via substrate 12 to convert the charge or current generated in each segmented electrode 8 from the motion of the generated charge carriers to an electronic signal tailored by the readout circuitry for further processing. Desirably, side electrode 6 is biased to optimize the electric field distribution in the volume substrate 2 and, as a result, optimize the performance of detector 1.
Problems encountered with prior art detector 1 include unacceptably low breakdown voltages between pairs of segmented electrodes 8 and/or between continuous electrode 4 and one or more segmented electrodes 8, with or without side electrode 6 present. Another problem with prior art detector 1 is that unacceptably high levels of leakage current may flow during operation thereby adversely effecting the performance of detector 1.
It would, therefore, be desirable to provide an improved detector that overcomes at least the above the problems and perhaps others.
The present invention is a high performance room-temperature semiconductor x-ray and gamma ray radiation detector and method of manufacture thereof. The present invention provides a detector having excellent performance and long-term stability.
A detector in accordance with the present invention can include on a side surface thereof a passivation layer that exhibits very low side-surface leakage current, very high side surface breakdown voltage, excellent physical and chemical stability, and excellent long-term stability under continuous biasing conditions.
The detector can include between the segmented electrodes a passivation layer that exhibits very low surface leakage current, very high surface breakdown voltage, excellent physical and chemical stability, and excellent long-term stability under continuous biasing conditions.
The detector can include conductive electrodes. Also or alternatively, the detector can include insulator-conductor electrodes with superior current blocking properties that enable the detector to exhibit very low bulk leakage current, very high bulk breakdown voltage, excellent physical and chemical stability, and excellent long-term stability under continuous biasing conditions.
The detector can exhibit superior adhesion properties of the electrodes to the detector surface thereby eliminating electrode delamination due to surface contamination.
The detector can be formed with thin, highly electrically insulating layers.
The detector can be fabricated utilizing a unique combination of the following thin film deposition and surface modification techniques:
The detector includes a crystalline substrate formed of a II-VI compound and a first electrode covering a substantial portion of one surface of the substrate. A plurality of second, segmented electrodes is provided in spaced relation on a surface of the substrate opposite the first electrode. A passivation layer is disposed between the second electrodes on the surface of the substrate opposite the first electrode.
The passivation layer can be an oxide film having a thickness that enables a tunneling current to flow therethrough. The thickness of the passivation layer can be #250 Angstroms, desirably #100 Angstroms and more desirably #25 Angstroms. The passivation layer can also be disposed between the substrate and each second electrode.
The passivation layer can include a first insulating film formed of native oxides of the II-VI compound and a second insulating film overlaying the first film. The second insulating film can either be a nitride film, an oxynitride film or an oxide film.
The passivation layer can also cover at least part of a side surface of the substrate. A side electrode can be disposed on the passivation layer covering the at least part of the side surface of the substrate.
The passivation layer can also be disposed between the first electrode and the one surface of the substrate.
A method of forming the detector includes (a) forming a passivation layer on a crystalline substrate formed of a II-VI compound; (b) forming an array of apertures in the passivation layer on a first surface of the substrate; (c) depositing conductive material in each aperture and over the passivation layer on the first surface of the substrate; and (d) selectively removing the conductive material deposited over the passivation layer on the first surface of the substrate, whereupon the conductive material remains in each aperture of the passivation layer and the conductive material in each aperture of the passivation layer is separated from the conductive material in each other aperture of the passivation layer on the first surface of the substrate.
In the method, the conductive material deposited in each aperture can contact at least one of the first surface of the substrate and a thin oxide layer over the first surface of the substrate.
The method can further include removing at least part of the passivation layer from a second surface of the substrate opposite the first surface thereby exposing at least a portion of the second surface of the substrate and depositing conductive material on the exposed portion of the second surface of the substrate.
The method can further include depositing conductive material over the passivation layer on a side surface of the substrate.
The passivation layer can include a first insulating film formed of native oxides of the II-VI compound and a second insulating film overlaying the first film. Step (b) can include forming the array of apertures in the second film and step (c) can include depositing the conductive material on the exposed surface of the first film in each aperture.
At least a part of the second film can be removed from a second surface of the substrate opposite the first surface thereby exposing at least a portion of a surface of the first film on the second surface of the substrate. Conductive material can then be deposited on the exposed surface of the first film on the second surface of the substrate. Desirably, the first film has a thickness that enables a tunneling current to flow therethrough. The thickness of the first film can be #250 Angstroms, desirably #100 Angstroms and more desirably #25 Angstroms.
The present invention will be described with reference to
With reference to
Substrate 2 can be etched utilizing any suitable wet or dry etching technique. Examples of suitable wet chemical etching solutions include a bromine methanol solution or a bromine ethanol solution. During etching of substrate 2, a thin, slightly oxidized amorphous Te film 20 typically forms on substrate 2.
With reference to
An electrically insulating film 24 (500 to 5000 Angstrom), such as a nitride (AlN, Si3N4 or similar), oxynitride or oxide film, is deposited atop of film 22 to protect it from damage during further processing and during operation of detector 1′. Desirably, insulating film 24 is deposited by pulsed DC reactive sputtering under conditions to provide a highly electrically insulating, low-stress film.
Either one of film 22 and film 24 can be omitted from a top surface 30 of substrate 2 and/or around a side surface 28 of substrate 2 if the other film is deemed sufficient. For example, film 24 can be omitted on one or both of top surface 30 and around side surface 28 of substrate 2 whereupon film 22 is the sole insulating film. Alternatively, film 22 can be omitted on one or both of top surface 30 and around side surface 28 of substrate 2 whereupon film 24 is the sole insulating film. In yet another alternative, any combination of film 22 and/or film 24 can be utilized on top surface 30, side surface 28 and/or bottom surface 32 of substrate 2 as desired. For purpose of describing the present invention, films 22 and 24 will be described as being deposited on substrate 2. However, this is not to be construed as limiting the invention.
With reference to
With reference to
Generally, a positive photoresist is one where each portion of the photoresist that is exposed to light, such as ultraviolet (UV) light, becomes soluble to a photoresist developer and the portion of the photoresist that is unexposed remains insoluble to the photoresist developer. A negative resist is one where each portion of the photoresist that is exposed to light becomes insoluble to the photoresist developer and the portion of the photoresist that is unexposed is soluble to the photoresist developer.
Next, UV/Ozone oxidation is applied to the top surface 30 of substrate 2 exposed in each aperture 34 to remove trace residues of photoresist therefrom. During UV/Ozone oxidation, a thin oxide layer 35 (shown in phantom) forms on the top surface 30 exposed in each aperture 34. If desired, thin oxide layer 35 can be removed utilizing any suitable etching technique, such as, without limitation, atomic hydrogen etching, desirably done in-situ in an electrode deposition chamber, such as a sputtering chamber, to avoid re-oxidation of the surface due to contact with ambient air.
With reference to
With reference to
Detector 1′ shown in
In an alternative configuration of detector 1′, a side electrode 40 (shown in phantom in
With reference to
Provided film 22 is not too thick (e.g., #250 Angstroms, desirably #100 Angstroms, and more desirably #25 Angstroms) electrical current can flow between substrate 2 and continuous electrode 4 and/or between substrate 2 and each segmented electrode 8 by way of so-called tunneling current. If desired, the embodiment of detector 1′ shown in
The present invention has been described with reference to the preferred embodiments. Obvious modifications and alterations will occur to others upon reading and understanding the preceding detailed description. For example, while the present invention has been described with reference to segmented electrodes on top surface 30 of substrate 2, it is envisioned that the foregoing technique can be adapted and modified as necessary in order to form segmented electrodes on top surface 30 and bottom surface 32 of substrate 2. It is intended that the invention be construed as including all such modifications and alterations insofar as they come within the scope of the appended claims or the equivalents thereof.
Filing Document | Filing Date | Country | Kind | 371c Date |
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PCT/US06/18779 | 5/16/2006 | WO | 00 | 1/9/2008 |
Number | Date | Country | |
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60681381 | May 2005 | US |