TY - GEN
T1 - Fabrication and characterization of an indium tin oxide acoustoelectric hydrophone
AU - Ingram, Pier
AU - Greenlee, Charles L.
AU - Wang, Zhaohui
AU - Olafsson, Ragnar
AU - Norwood, Robert A.
AU - Witte, Russell S.
PY - 2010
Y1 - 2010
N2 - Clinical ultrasound (US) imaging and therapy require a precise knowledge of the intensity distribution of the acoustic field. Although piezoelectric hydrophones are most common, these devices are limited in terms of, for example, type of materials, cost, and performance at high frequency and pressure. As an alternative to conventional acoustic detectors, we describe acoustoelectric hydrophones, developed using photolithographic fabrication techniques, where the induced voltage (phase and amplitude) is proportional to both the US pressure and bias current injected through the device. In this study a number of different hydrophone designs were created using indium tin oxide (ITO). A constriction of the current path within the hydrophone created a localized "sensitivity zone" of high current density. The width of this zone ranged from 30 to 1000 μm, with a thickness of 100 nm. A raster scan of the US transducer produced a map of the acoustic field. Hydrophones were evaluated by mapping the pressure field of a 2.25 MHz single element transducer, and their performance was compared to a commercial capsule hydrophone. Focal spot sizes at -6 dB were as low as 1.75 mm, comparing well with the commercial hydrophone measurement of 1.80 mm. Maximum sensitivity was 2 nV/Pa and up to the 2nd harmonic was detected. We expect improved performance with future devices as we optimize the design. Acoustoelectric hydrophones are potentially cheaper and more robust than the piezoelectric models currently in clinical use, potentially providing more choice of materials and designs for monitoring therapy or producing arrays for imaging.
AB - Clinical ultrasound (US) imaging and therapy require a precise knowledge of the intensity distribution of the acoustic field. Although piezoelectric hydrophones are most common, these devices are limited in terms of, for example, type of materials, cost, and performance at high frequency and pressure. As an alternative to conventional acoustic detectors, we describe acoustoelectric hydrophones, developed using photolithographic fabrication techniques, where the induced voltage (phase and amplitude) is proportional to both the US pressure and bias current injected through the device. In this study a number of different hydrophone designs were created using indium tin oxide (ITO). A constriction of the current path within the hydrophone created a localized "sensitivity zone" of high current density. The width of this zone ranged from 30 to 1000 μm, with a thickness of 100 nm. A raster scan of the US transducer produced a map of the acoustic field. Hydrophones were evaluated by mapping the pressure field of a 2.25 MHz single element transducer, and their performance was compared to a commercial capsule hydrophone. Focal spot sizes at -6 dB were as low as 1.75 mm, comparing well with the commercial hydrophone measurement of 1.80 mm. Maximum sensitivity was 2 nV/Pa and up to the 2nd harmonic was detected. We expect improved performance with future devices as we optimize the design. Acoustoelectric hydrophones are potentially cheaper and more robust than the piezoelectric models currently in clinical use, potentially providing more choice of materials and designs for monitoring therapy or producing arrays for imaging.
KW - HIFU
KW - ITO
KW - MEMS
KW - acoustic detector arrays
KW - acoustoelectric
KW - high frequency ultrasound
KW - hydrophone
KW - photolithography
KW - ultrasound imaging arrays
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UR - http://www.scopus.com/inward/citedby.url?scp=77956848727&partnerID=8YFLogxK
U2 - 10.1117/12.845631
DO - 10.1117/12.845631
M3 - Conference contribution
AN - SCOPUS:77956848727
SN - 9780819480309
T3 - Progress in Biomedical Optics and Imaging - Proceedings of SPIE
BT - Medical Imaging 2010 - Ultrasonic Imaging, Tomography, and Therapy
T2 - Medical Imaging 2010 - Ultrasonic Imaging, Tomography, and Therapy
Y2 - 14 February 2010 through 15 February 2010
ER -