4.6 Article

Enhancement of second-order optical nonlinearities and nanoscale periodic domain patterning in ferroelectric boron-substituted aluminum nitride thin films

Journal

OPTICAL MATERIALS EXPRESS
Volume 13, Issue 6, Pages 1522-1534

Publisher

Optica Publishing Group
DOI: 10.1364/OME.488459

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This study investigates the viability of ferroelectric Al1-xBxN as a large bandgap nonlinear optical material for ultraviolet light generation. An enhancement in the nonlinear coefficients is observed with increasing B concentration, along with a change in bandgap. A periodically poled, quasi-phase-matched ferroelectric domain pattern is demonstrated.
The discovery and development of CMOS-compatible, nonlinear optical materials is essential to produce integrated photonic devices with advanced functionalities. AlN is a strong candidate for on-chip device demonstration due to its intrinsic second-order optical nonlinearities, large bandgap, and well-established fabrication techniques. However, AlN is not easily phase matched for the largest coefficient d33; the coefficients that could potentially be dispersion phase-matched, d31 and d15, have weak nonlinearities. This work investigates ferroelectric Al1-xBxN (x = 0 to 0.11) for viability as a large bandgap nonlinear optical material with unique suitability towards ultraviolet light generation using second harmonic generation. The linear and nonlinear optical properties are characterized accounting for material anisotropy. With increasing B concentration, a large enhancement from near negligible values to d31 = 0.9 & PLUSMN; 0.1 pm/V and d15= 1.2 & PLUSMN; 0.1 pm/V is observed. This compares favorably to other large bandgap materials like & beta;-Ba(BO2)2, where the largest nonlinear coefficient is d22 & SIM;2.3 pm/V at 800 nm. This is accompanied by a change in the bandgap from 6.1 eV to 5.8 eV as B substitution goes from 0 to 11%. A periodically poled, quasi-phase-matched ferroelectric domain pattern with 400 nm domain size and a wall roughness of <16 nm is demonstrated.

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