Vanadium and magnesium co-doped LiNbO 3 (LN) crystals were grown, and their photorefractive properties were studied in the visible spectral region. At 488 nm the shortest response time of 80 ms was achieved for an LN crystal co-doped with 0.1 mol% V 2 O 5 and 6.0 mol% MgO, which is the more rapid than other reported doped LN crystals in the same wavelength region. The sensitivity of this crystal reaches 17 cm J −1 with an adequate diffraction efficiency of 4.0%. A schematic diagram for energy level is proposed and discussed. Through the analysis of defect structure and absorption spectra, we found that the change of the vanadium ions occupancy from Li sites to Nb sites is responsible for significant shortening the response time. The rapid response of vanadium and magnesium co-doped LN crystal can play an excellent role in the field of dynamic holography and practical holographic 3D-storage applications.

We mainly investigated the effect of the valence state of photorefractive resistant elements on the photorefractive properties of codoped crystals, taking the Zn and Mo codoped LiNbO3 (LN:Mo,Zn) crystal as an example. Especially, the response time and photorefractive sensitivity of 7.2 mol% Zn and 0.5 mol% Mo codoped with LiNbO3 (LN:Mo,Zn7.2) crystal are 0.65 s and 4.35 cm/J at 442 nm, respectively. The photorefractive properties of the LN:Mo,Zn crystal are similar to the Mg and Mo codoped LiNbO3 crystal, which are better than the Zr and Mo codoped LiNbO3 crystal. The results show that the valence state of photorefractive resistant ions is an important factor for the photorefractive properties of codoped crystals and that the LN:Mo,Zn7.2 crystal is another potential material with fast response to holographic storage.

A series of mono-, double-, and tri-doped LiNbO3 crystals with vanadium were grown by Czochralski method, and their photorefractive properties were investigated. The response time for 0.1 mol% vanadium, 4.0 mol% zirconium, and 0.03 wt.% iron co-doped lithium niobate crystal at 488 nm was shortened to 0.53 s, which is three orders of magnitude shorter than the mono-iron-doped lithium niobate, with a maintained high diffraction efficiency of 57% and an excellent sensitivity of 9.2 cm/J. The Ultraviolet-visible (UV-Vis) and OH− absorption spectra were studied for all crystals tested. The defect structure is discussed, and a defect energy level diagram is proposed. The results show that vanadium, zirconium, and iron co-doped lithium niobate crystals with fast response and a moderately large diffraction efficiency can become another good candidate material for 3D-holographic storage and dynamic holography applications.

The authors wish to make the following corrections to this paper [...]

We grew a series of co-doped LiNbO 3 crystals with fixed 1.5 mol % ZrO 2 and various MgO concentrations (1.0, 3.0, 4.0, 6.0 mol %), and investigated their optical properties and defect structures. By 3.0 mol % MgO co-doping, the optical damage resistance at 532 nm reached 6.5 × 10 6 W/cm 2 , while the phase-matching temperature for doubling 1064 nm was only 29.3 • C-close to room temperature-which was conducive to realizing the 90 • phase matching at room temperature by slightly modulating the incident angle of the fundamental beam. Notably, we found that the phase-matching temperature increased linearly with the increase of MgO doping, and this linear dependence helped us to grow the high-quality crystal for room temperature 90 • phase matching. Moreover, the defect analysis indicated that the linear tuning of phase-matching temperature might be attributed to Mg + Li + Zr − Nb neutral pairs in crystals.