J. L. Jackel
Bell Labs
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Featured researches published by J. L. Jackel.
Applied Physics Letters | 1982
J. L. Jackel; C. E. Rice; J.J. Veselka
We describe the fabrication and characterization of optical waveguides formed in LiNbO3 by proton exchange in benzoic acid melts at 200–250 °C. Proton exchange, in LiNbO3 the replacement of lithium ions with protons, takes place when the substrate is immersed in the molten acid. We observe a surface increase in the refractive index of 0.12, for the extraordinary polarization only, with a step function index profile. This is the highest index increase obtainable to date for LiNbO3. Measured diffusion rates for x‐cut crystals are 1.37 μm2/h at T = 249 °C and 0.37 μm2/h at T = 217 °C, so that very deep guides can be formed in short times. Diffusion is somewhat slower in the z direction. The process as described is not useful for y‐cut crystals, since it damgaes this surface. Losses, measured on x‐cut samples, were <0.5 dB/cm. All measurements were made at 0.633 μm.
Applied Physics Letters | 1981
J. L. Jackel; V. Ramaswamy; S. P. Lyman
We describe a means of eliminating undesired surface guiding in titanium‐diffused strip waveguides on LiNbO3. Surface guiding for light of the extraordinary polarization, normally produced when the crystal is diffused in dry argon or oxygen, can be eliminated entirely by adding water vapor to the diffusion gases. Infrared absorption measurements show that hydrogen enters crystals diffused in a wet atmosphere. Although the mechanism for the prevention of surface guiding is not fully understood, we suggest that the presence of excess hydrogen reduces lithium mobility.
Applied Physics Letters | 1982
Gerardo Beni; Susan Hackwood; J. L. Jackel
We introduce a new electrowetting effect, continuous electrowetting (CEW), and show its advantages for applications to displays and other electro‐optic devices. We demonstrate experimentally, by using CEW, fast and reversible electrowetting flow on the theoretically predicted scale of ∼10 cm/s for ∼1‐V driving voltage.
Applied Optics | 1983
J. L. Jackel; Susan Hackwood; J. J. Veselka; Gerardo Beni
Construction and characterization of an optical switch, based on electrowetting and suitable for use with multimode fibers are described. With a 50-μm core, 0.23-N.A. input and output fibers, the measured fiber-to-fiber insertion loss at λ = 0.633 μm was 0.5 ± 0.1 dB for one channel and 2.0 ± 0.2 dB for the other, with cross talk of −22.8 ± 0.5 and <−51 dB, respectively. Response time is ≈20 msec with driving power of ≈25 μW and a voltage requirement of ≤1.0 V. The switch has been tested for over 107 cycles with no observable degradation.
Applied Physics Letters | 1981
J. L. Jackel; R. E. Howard; E. L. Hu; S. P. Lyman
We describe the reactive ion etching of LiNbO3 in gas mixtures containing CCl2F2, CF4, O2, and Ar. The effects of gas composition and pressure, in the range 1–10‐μm total pressure are discussed. Because it is possible to replicate fine features (∼2000 A) with control of etch profiles, we expect the process to be used for three‐dimensional patterning of LiNbO3 for electro‐optic and acoustic‐optic devices.
Processing of Guided Wave Optoelectronic Materials I | 1984
J. L. Jackel; Catherine E Rice
We describe fabrication conditions which produce proton exchanged waveguides with long and short term index stability. We present also the surface index change and effective diffusion coefficients associated with exchange in melts of varying concentration, from pure benzoic acid to mixtures containing up to 4 Mole % lithium benzoate. Infrared absorption measurements supporting our explanation for the causes of index instability are presented.
Ferroelectrics | 1983
J. L. Jackel; C. E. Rice; J.J. Veselka
Abstract This paper reviews the recently described process of proton exchange in LiNbO3 and reports some current results. Only results directly applicable to integrated optics will be described, although other applications are possible, and much of the work is interesting from a more fundamental point of view.
The International Journal of Robotics Research | 1983
Gerardo Beni; Susan Hackwood; Lawrence A. Hornak; J. L. Jackel
Dynamic sensing is discussed in detail. We have initiated a systematics of robotic sensor design by formulating the general problems and addressing the specific question of how to arrange the sensing elements. We have derived a general relationship between the number and speed of the sensing elements as a function of their response and processing times. We have thus constructed afiber-optic sensor for the fingers of a Unimation Puma 500 robot. The sensor consists of three linear arrays ( each with 12 sensing elements), attached to the edges of the robot fingers in a U shape. The elements are composed of parallel, equally spaced, collimated light beams that pass from finger to finger. Each linear array can be scanned dynamically to provide a 12 X 18 = 256-pixel cov erage of a 2 X 3-cm area.
Applied Physics Letters | 1980
J. L. Jackel
Waveguides with large Δne have been fabricated in x‐cut LiNbO3 using ion exchange in a TlNO3 melt. The exchange was carried out at ∼240 °C, producing surface index increases of Δne ≅0.12–0.13. No increase in Δn0 was seen. A simple index profile resulting in the best fit to the observed mode structure is a step‐index profile. Analysis of the diffusion process shows that such a profile can be produced by ion exchange in which self‐diffusion coefficients of the two counterdiffusing species are concentration dependent. This provides the first direct evidence that ion exchange occurs in LiNbO3.
Applied Physics Letters | 1982
J. L. Jackel; C. E. Rice
Optical waveguides fabricated in LiNbO3 by what has previously been described as silver‐lithium or thallium‐lithium ion exchange in the molten nitrates AgNO3 or TlNO3 have not generally been reproducible. We show that the large increases of the extraordinary index (Δne = 0.12), which are observed intermittently, result not from introduction of the heavy ions, Ag+ or Tl+, but from hydrogen‐lithium exchange, which occurs when hydrogen is present as an impurity in the melts.