Lithium niobate (LiNbO3) is a synthetic salt consisting of niobium, lithium, and oxygen. Its single crystals are an important material for optical waveguides, mobile phones, piezoelectric sensors, optical modulators and various other linear and non-linear optical applications.[6] Lithium niobate is sometimes referred to by the brand name linobate.[7]
After a crystal is grown, it is sliced into wafers of different orientation. Common orientations are Z-cut, X-cut, Y-cut, and cuts with rotated angles of the previous axes.[9]
Thin films
Thin-film lithium niobate (e.g. for optical wave guides) can be transferred to or grown on sapphire and other substrates, using the smart cut (ion slicing) process[10][11] or MOCVD process.[12] The technology is known as lithium niobate on insulator (LNOI).[13]
Nanoparticles
Nanoparticles of lithium niobate and niobium pentoxide can be produced at low temperature.[14] The complete protocol implies a LiH induced reduction of NbCl5 followed by in situ spontaneous oxidation into low-valence niobium nano-oxides. These niobium oxides are exposed to air atmosphere resulting in pure Nb2O5. Finally, the stable Nb2O5 is converted into lithium niobate LiNbO3 nanoparticles during the controlled hydrolysis of the LiH excess.[15] Spherical nanoparticles of lithium niobate with a diameter of approximately 10 nm can be prepared by impregnating a mesoporous silica matrix with a mixture of an aqueous solution of LiNO3 and NH4NbO(C2O4)2 followed by 10 min heating in an infrared furnace.[16]
In the past few years lithium niobate is finding applications as a kind of electrostatic tweezers, an approach known as optoelectronic tweezers as the effect requires light excitation to take place.[20][21] This effect allows for fine manipulation of micrometer-scale particles with high flexibility since the tweezing action is constrained to the illuminated area. The effect is based on the very high electric fields generated during light exposure (1–100 kV/cm) within the illuminated spot. These intense fields are also finding applications in biophysics and biotechnology, as they can influence living organisms in a variety of ways.[22] For example, iron-doped lithium niobate excited with visible light has been shown to produce cell death in tumoral cell cultures.[23]
Periodically poled lithium niobate (PPLN)
Periodically poled lithium niobate (PPLN) is a domain-engineered lithium niobate crystal, used mainly for achieving quasi-phase-matching in nonlinear optics. The ferroelectric domains point alternatively to the +c and the −c direction, with a period of typically between 5 and 35 μm. The shorter periods of this range are used for second-harmonic generation, while the longer ones for optical parametric oscillation. Periodic poling can be achieved by electrical poling with periodically structured electrode. Controlled heating of the crystal can be used to fine-tune phase matching in the medium due to a slight variation of the dispersion with temperature.
Periodic poling uses the largest value of lithium niobate's nonlinear tensor, d33 = 27 pm/V. Quasi-phase-matching gives maximum efficiencies that are 2/π (64%) of the full d33, about 17 pm/V.[24]
However, due to its low photorefractive damage threshold, PPLN only finds limited applications, namely, at very low power levels. MgO-doped lithium niobate is fabricated by periodically poled method. Periodically poled MgO-doped lithium niobate (PPMgOLN) therefore expands the application to medium power level.
Sellmeier equations
The Sellmeier equations for the extraordinary index are used to find the poling period and approximate temperature for quasi-phase-matching. Jundt[27] gives
valid from 20 to 250 °C for wavelengths from 0.4 to 5 micrometers, whereas for longer wavelengths,[28]
which is valid for T = 25 to 180 °C, for wavelengths λ between 2.8 and 4.8 micrometers.
In these equations f = (T − 24.5)(T + 570.82), λ is in micrometers, and T is in °C.
More generally for ordinary and extraordinary index for MgO-doped LiNbO3:
with:
Parameters
5% MgO-doped CLN
1% MgO-doped SLN
ne
no
ne
a1
5.756
5.653
5.078
a2
0.0983
0.1185
0.0964
a3
0.2020
0.2091
0.2065
a4
189.32
89.61
61.16
a5
12.52
10.85
10.55
a6
1.32×10−2
1.97×10−2
1.59×10−2
b1
2.860×10−6
7.941×10−7
4.677×10−7
b2
4.700×10−8
3.134×10−8
7.822×10−8
b3
6.113×10−8
−4.641×10−9
−2.653×10−8
b4
1.516×10−4
−2.188×10−6
1.096×10−4
for congruent LiNbO3 (CLN) and stochiometric LiNbO3 (SLN).[29]
^Wilkinson, A. P.; Cheetham, A. K.; Jarman, R. H. (1993). "The defect structure of congruently melting lithium niobate". Journal of Applied Physics. 74 (5): 3080–3083. Bibcode:1993JAP....74.3080W. doi:10.1063/1.354572.
^Aufray M, Menuel S, Fort Y, Eschbach J, Rouxel D, Vincent B (2009). "New Synthesis of Nanosized Niobium Oxides and Lithium Niobate Particles and Their Characterization by XPS Analysis". Journal of Nanoscience and Nanotechnology. 9 (8): 4780–4789. CiteSeerX10.1.1.465.1919. doi:10.1166/jnn.2009.1087. PMID19928149.
^Carrascosa, M.; García-Cabañes, A.; Jubera, M.; Ramiro, J. B.; Agulló-López, F. (2015). "LiNbO3: A photovoltaic substrate for massive parallel manipulation and patterning of nano-objects". Applied Physics Reviews. 2 (4). AIP Publishing: 040605. Bibcode:2015ApPRv...2d0605C. doi:10.1063/1.4929374. hdl:10486/669584. ISSN1931-9401.
^Ferraro, P.; Grilli, S. (2006). "Modulating the thickness of the resist pattern for controlling size and depth of submicron reversed domains in lithium niobate". Applied Physics Letters. 89 (13): 133111. Bibcode:2006ApPhL..89m3111F. doi:10.1063/1.2357928.
^Deng, L. H.; Gao, X. M.; Cao, Z. S.; Chen, W. D.; Yuan, Y.Q.; Zhang, W. J.; Gong, Z. B. (2006). "Improvement to Sellmeier equation for periodically poled LiNbO3 crystal using mid-infrared difference-frequency generation". Optics Communications. 268 (1): 110–114. Bibcode:2006OptCo.268..110D. doi:10.1016/j.optcom.2006.06.082.
