Open Access Article
Tao Wanga,
Jian Zhangab,
Na Zhang
a,
Siyuan Wanga,
Baiyi Wua,
Zhitai Jia
*ab and
Xutang Tao
*ab
aState Key Laboratory of Crystal Materials, Shandong University, Jinan, 250100, China. E-mail: z.jia@sdu.edu.cn; txt@sdu.edu.cn
bKey Laboratory of Functional Crystal Materials and Device, Ministry of Education, Jinan 250100, China
First published on 22nd July 2019
Single crystal fibers (SCFs), especially ytterbium (Yb) doped crystal fibers, have great potential in the field of high-power lasers. Colorless Yb:YAG single crystal fibers were fabricated using a laser heated pedestal growth (LHPG) method with a diameter fluctuation of less than 2% and a length to diameter ratio greater than 320
:
1. An abnormal color issue exists with respect to Yb:YAG crystals. The origin of coloration was studied via density functional theory, single-crystal X-ray diffraction, XPS and Raman spectroscopy and it was confirmed that the cyan coloration of Yb:YAG crystals is due to oxygen vacancies. Yb:YAG SCFs prepared via the LHPG method could avoid this type of defect due to the large specific surface area and melt convection caused by surface tension. The fundamental properties of the cyan Yb:YAG crystal source rod and colorless Yb:YAG SCFs were systematically investigated. The colorless Yb:YAG SCFs have higher infrared transmittance and thermal conductivity. The distributions of Yb3+ along the radial and axial directions were also measured. Meanwhile we demonstrated the propagation loss and a fiber laser using the colorless Yb:YAG SCFs, obtaining a minimum loss coefficient of 0.008 dB cm−1 and a maximum continuous-wave (CW) output power of 3.62 W. The colorless Yb:YAG SCFs with good thermal conductivity, low propagation loss, wide transparency and uniform ion distribution show promise for acting as the host material in single-mode lasers.
Yttrium aluminium garnet (YAG) belongs to a cubic system, with the unit cell parameter a = 12.0089 Å. YAG crystals have good physical and chemical stabilities and have been widely used in solid-state lasers.18 At the same time, YAG crystals can achieve high doping concentrations because of the similar sizes of yttrium atoms and rare-earth atoms. Compared to traditional silica fibers, YAG crystal fibers have a lower Brillouin gain coefficient, a higher laser damage threshold and higher thermal conductivity. The theoretical single-mode output of a YAG SCF laser is more than 100 times that of a glass fiber laser.19–23
Yb-doped YAG crystals are an excellent laser medium. Yb3+ ions have a simple electronic structure, with only one excited state (2F5/2) above the ground state (2F7/2), avoiding thermal effects due to up-conversion and excited state absorption. Moreover, the theoretical segregation coefficient of Yb3+ is close to 1, which is beneficial for miniaturizing devices. Compared to Nd3+, Yb3+ is well suited for IR InGaAs diode laser pumping between 900 and 980 nm. Meanwhile, the close absorption (900–980 nm) and emission wavelengths (980–1100 nm) lead to a low thermal load (11% relative to 30% in Nd3+-doped laser hosts), thereby significantly improving the slope efficiency, which reaches almost 90% theoretically.24–26 Therefore, Yb:YAG crystals are considered to be the most promising fiber material for 1 μm band lasers.27–30 A continuous-wave output power of 251 W obtained by a Yb:YAG SCF laser is also reported to be a record in the field of crystal fiber lasers.31
However, it is interesting to find that commercial Yb:YAG crystals are usually different shades of cyan, and the color always deepens with an increase in the crystal size. This color issue relating to Yb:YAG crystals should be the primary problem to be solved, especially if they are going to be used in high-power lasers. Usually, most commercial Yb:YAG crystals are grown via the Czochralski method. An inert or reductive atmosphere may be the cause of the discoloration.32,33 This color issue has puzzled people for a long time, but the origin of the coloration of Yb:YAG crystals has never been systematically justified.
In this work, we have successfully fabricated colorless and transparent Yb:YAG SCFs using Yb:YAG bulk crystals with a cyan color in both oxygen-rich and inert atmospheres via a LHPG method. Besides, we have designed an experimental scheme to seek the origins of the coloration. Some optical and thermal properties of cyan Yb:YAG crystal source rods and colorless YAG SCFs were also compared. The second part of this paper relates to the fundamental characteristics of Yb:YAG SCFs, including diameter fluctuations, crystal quality, propagation loss and ion distribution. A Yb:YAG fiber laser is also reported in this paper.
:
1, converting to a diameter ratio of 3
:
1. Therefore, some SCFs need to be grown twice to obtain finer examples. Compared with other crystal growth methods, there is no crucible in the LHPG method, which greatly improves the purity of the raw materials. At the same time, non-crucible growth conditions enrich the growing atmosphere. We can use not only inert atmospheres but also air or even oxygen atmospheres during crystal growth.
As shown in Fig. 2, the Yb:YAG crystal source rods are cyan, however, after processing via the LHPG method, colorless and transparent crystal fibers were obtained without any post-processing. In this paper, we obtained Φ2.0 × 50 mm3 Yb:YAG SCFs with a pulling ratio of 3
:
1; these were then grown twice, obtaining Φ0.8 × 260 mm3 and Φ0.6 × 150 mm3 Yb:YAG SCFs with pulling ratios of 5
:
1 and 9
:
1, and a length-to-diameter ratio greater than 320
:
1.
The RT optical transmission spectra of the Yb:YAG crystal source rod and as-grown Yb:YAG SCFs were obtained using a PE IR SPECTRUM ASCII PEDS 1.60 Fourier transform infrared (FTIR) spectrometer over the wavenumber range of 450–7800 cm−1.
The RT Raman spectra of the Yb:YAG crystal source rod and as-grown Yb:YAG SCFs were recorded using a Horiba Jobin Yvon LabRAM HR Raman spectrometer equipped with a liquid N2 cooled Ge detector. A solid laser power of 150 mW at 532 nm was used for excitation.
The thermal conductivities were measured using the Thermal Transport Option (P670B) of a Quantum Design Physical Property Measurement System (PPMS) from 4–400 K with a liquid nitrogen cooling system. The cooling and heating rates selected in the experiment were 6 °C min−1 and 0.5 °C min−1, respectively.
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| Fig. 3 The optimized Yb:YAG crystal structure. The red, green, purple, and blue spheres represent O, Yb, Al, and Y atoms, respectively. | ||
The experimental apparatus used for the laser experiments is depicted in Fig. 5. A Yb:YAG SCF was pumped using a fiber-coupled 940 nm semiconductor laser with a 200 μm core diameter and a NA of 0.22. The magnification ratio of the focusing system is 1
:
1. The pump beam was focused to a 200 μm diameter, with the focal point located on the input side of the SCF. The input mirror (IM) is a concave mirror, which was coated for high transmission (T > 98%) at the pump wavelength (940–976 nm) and high reflectivity (R > 99%) from 1020 to 1060 nm. The output mirror (OM) was plated with 1020–1070 nm partially reflective films with transmittances of 3%, 10% and 30%, respectively. The IM was placed as close as possible to the input side of the SCF, so as to provide as much feedback as possible at the lasing wavelength. The resonant cavity consisted of a flat-concave short cavity structure with a length of 11 mm. In order to reduce the thermal effects of the crystal, the SCF was placed in a copper block and the temperature was set to 15 °C. Spectral detection was performed using an AQ6370D spectrum analyzer and the scanning interval was set to 1020 nm to 1080 nm to facilitate observations. Φ0.6 × 10 mm3 Yb:YAG SCFs (2 at% doping) were applied in the laser experiments.
| a (Å) | b (Å) | c (Å) | V (Å3) | |
|---|---|---|---|---|
| Yb:YAG source rod | 12.03 | 12.03 | 12.03 | 1743 |
| As-grown Yb:YAG SCFs | 12.05 | 12.05 | 12.05 | 1749 |
Fig. 8 shows simulated absorption spectra and refractive indices under different defect conditions. From the simulation results in Fig. 8(a), we can find that YAG crystals with oxygen vacancies show obvious absorption in the region of 300–650 nm, which is consistent with the measured absorption spectrum of the discolored Yb:YAG crystal. Fig. 8(b) shows that the Yb:YAG crystal is predicted to possess a higher refractive index in the presence of oxygen vacancies. The Fresnel reflection is positively correlated with differences in the refractive indices at the interface. Therefore, a higher refractive index caused by oxygen vacancies in the Yb:YAG crystal will increase the reflectance at the interface, resulting in greater optical loss. In the measured infrared transmission spectra shown in Fig. 7(b), the transmittance of the discolored sample is lower compared with a colorless sample of the same thickness, which is consistent with the simulation results.
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| Fig. 8 Calculated (a) absorption spectra and (b) refractive index values under different defect conditions. | ||
Raman spectra of the source rod and the as-grown SCFs under an inert atmosphere are shown in Fig. 9. By comparison, we found that the intensity of the Raman peak at 546 cm−1 has decreased for the cyan source rod sample and the Raman peak at 1100 cm−1 has disappeared. These two peaks are considered to be attributed to the υ2 mode of AlO4 units and Yb–O vibrations, respectively.38 These data indicate that the formation of oxygen vacancies in Yb:YAG is related to Yb3+.
The specific heat (Cv) values of the Yb:YAG crystal source rod and the colorless Yb:YAG SCFs grown under an inert atmosphere as a function of temperature are shown in Fig. 10. As can be seen, the specific heat of the Yb:YAG SCF increases from 0.679 J g−1 K−1 at 30 °C to 0.973 J g−1 K−1 at 295 °C. The specific heat of the source rod is 1.0653 J g−1 K−1 at 30 °C; as the temperature increases, it increases to 1.3723 J g−1 K−1 at 295 °C. Lattice thermal vibration is considered to be one of the important factors affecting the specific heat of crystalline materials. The formation of oxygen vacancies will increase the lattice distortion, which is considered to cause abnormal fluctuations in the specific heat of the source rod.
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| Fig. 10 Thermal properties: (left) specific heat and (right) thermal conductivity as a function of temperature. | ||
The thermal conductivity (κ) of the crystals can be calculated using the following formula:
![]() | (1) |
denote the specific heat of the crystal, the mean free path of phonons and the average speed of phonons, respectively. Thermal conductivity versus temperature plots (4–383 K) of the source rod and as-grown Yb:YAG SCFs under an inert atmosphere are shown in Fig. 10. The thermal conductivity of the Yb:YAG SCF along the 〈111〉 direction reaches a maximum of 34.5 W m−1 K−1 at 40 K. As the temperature increases, the thermal conductivity gradually approaches 7.1 W m−1 K−1 (at 100 °C). The thermal conductivity of the cyan source rod was significantly lower than that of the colorless crystal fiber at the same temperatures, especially in low temperature environments. The thermal conductivity at low temperatures is mainly determined by the mean free path of phonons. However, the presence of defects, impurities, and grain boundaries will greatly reduce the mean free path of phonons, which explains why the cyan source rod has lower thermal conductivity. The lower thermal conductivity will reduce the thermal management abilities of the fiber laser and increase thermal effects inside the fiber, thus affecting the laser power and beam quality.
![]() | (2) |
Table 2 lists the free energy values of the system under different conditions and the oxygen vacancy formation energies. The formation energy of an oxygen vacancy is 6.51 eV in a YAG crystal. As the Yb3+ content increases to 4% and 8%, the formation energies of oxygen vacancies decrease to 6.48 eV and 6.06 eV, respectively. We speculate that this is related to the valence state of Yb3+. When Yb3+ is converted to Yb2+, a negative electric center is formed, which induces positive electric vacancies around it. Therefore, choosing an appropriate doping concentration is also an effective way to avoid defects.
| Type | Etot/eV | Evac/eV |
|---|---|---|
| 4O2 | −33.63 | |
| Y24Al40O96, without oxygen vacancies | −1303.06 | |
| Y24Al40O88, with 8 oxygen vacancies in dispersed states | −1217.32 | 6.51 |
| Y23Yb1Al40O96, without oxygen vacancies | −1298.68 | |
| Y23Yb1Al40O88, with 8 oxygen vacancies | −1213.20 | 6.48 |
| Y22Yb2Al40O96, without oxygen vacancies | −1290.45 | |
| Y22Yb2Al40O88, with 8 oxygen vacancies | −1208.27 | 6.07 |
Movement instability (fiber or source rod) and power fluctuations of the carbon dioxide laser are the main reasons for diameter fluctuations in fibers, especially for micron-sized single crystal fibers.
Through the adjustment of growth parameters and the optimization of the laser, the diameter stability of the SCFs has been obviously improved. The diameter fluctuations of two YAG SCFs are shown in Fig. 11. The average diameters of the two samples are 0.6089 mm and 0.8352 mm, respectively. At the same time, the data indicates that the diameter ranges (the difference between the maximum and minimum diameters) of the two YAG SCFs are 0.02 mm and 0.03 mm, representing excellent diameter control of better than ±2%, which is beneficial for the fabrication of cladding and related devices.
The quality of the as-grown Yb:YAG SCFs was characterized via HRXRD and Laue back-reflection measurements. The rocking curve of the (111) diffraction plane is shown in Fig. 12. The diffraction peak presents a symmetric shape without splitting. The full width at half maximum (FWHM) is estimated to be 72.2′′. Laue back-reflection measurements are broadly applied to investigate the crystallinity and orientation of an as-grown crystal. As can be apparently seen from Fig. 13, the characteristic Laue back-reflection patterns at different positions along the crystal fiber are uniform, clear, and bright. The above results demonstrate that the crystalline quality of the Yb:YAG SCFs is high enough, which furnishes the basis for assessing their intrinsic physical properties.
![]() | (3) |
In order to achieve single-mode laser output, a fiber must maintain a mutant refractive index profile, which means that the refractive index of the core must be uniform. For doped crystals, it is necessary to ensure the uniformity of rare earth ion distribution. We determined the elemental compositions of the source rod and crystal fibers via X-ray fluorescence (XRF). As shown in Table 3, the concentrations of Yb3+ in the source rod and the as-grown SCF were measured to be 2.36 and 2.35, respectively. The calculated segregation coefficient of Yb3+ is close to 1.
| Al (mass%) | Y (mass%) | Yb (mass%) | Yb/Y (at%) | |
|---|---|---|---|---|
| Source rod | 21.2 | 75.3 | 3.46 | 2.36 |
| As-grown SCF | 25.5 | 72.1 | 3.31 | 2.35 |
The concentrations of Yb3+ along the radial and axial directions are shown in Fig. 15. We found that Yb3+ is uniformly distributed in both the radial and axial directions without significant ion-rich regions, which is a key factor for achieving single-mode lasers.
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| Fig. 15 The radial distribution of Yb3+. The inset shows the distribution of Yb3+ along the axial direction. | ||
![]() | (4) |
| Sample | L (cm) | Pin (W) | Pout (W) | Pout/Pin (without subtraction of the reflection loss) | Pout/Pin (with subtraction of the reflection loss) | Reflection loss | αdB |
|---|---|---|---|---|---|---|---|
| Fiber 1 | 0.8 | 1.034 | 0.914 | 88.39% | 99.76% | 11.37% | 0.013 dB cm−1 |
| Fiber 2 | 1.8 | 1.034 | 0.911 | 88.10% | 99.47% | 11.37% | 0.013 dB cm−1 |
| Fiber 1 | 0.8 | 2.003 | 1.763 | 88.02% | 99.72% | 11.7% | 0.015 dB cm−1 |
| Fiber 2 | 1.8 | 2.003 | 1.756 | 87.67% | 99.37% | 11.7% | 0.015 dB cm−1 |
| Fiber 1 | 0.8 | 3.016 | 2.637 | 87.43% | 99.84% | 12.41% | 0.008 dB cm−1 |
| Fiber 2 | 1.8 | 3.016 | 2.631 | 87.23% | 99.64% | 12.41% | 0.008 dB cm−1 |
| Fiber 1 | 0.8 | 4.005 | 3.490 | 87.14% | 99.78% | 12.64% | 0.012 dB cm−1 |
| Fiber 2 | 1.8 | 4.005 | 3.479 | 86.87% | 99.51% | 12.64% | 0.012 dB cm−1 |
:
1 were successfully grown in both aerobic and anaerobic environments via a LHPG method. The diameter fluctuation is less than 2%, indicating that the crystal growth process is stable and the crystal fibers are relatively uniform. By means of single crystal X-ray diffraction, XPS and Raman spectroscopy, we found that the colorless Yb:YAG SCFs possess larger unit cell parameters, fewer oxygen vacancies and more obvious AlO4 and Yb–O vibrations than the cyan Yb:YAG crystal source rod. Therefore, we conclude that the discoloration of Yb:YAG crystals is caused by oxygen vacancies, and the formation energy of oxygen vacancies decreases as the Yb3+ content increases. We believe that the large specific surface area of the grown Yb:YAG SCFs, the low Yb3+ doping concentration and the surface tension convection of the LHPG method are the main factors in avoiding defects.
At the same time, some optical and thermal properties of the cyan Yb:YAG crystal source rod and colorless Yb:YAG SCFs were measured. The discolored Yb:YAG crystal, with discoloration caused by oxygen vacancies, has lower infrared transmittance and thermal conductivity, which will reduce the laser output and the beam quality dramatically. Meanwhile, the as-grown SCFs were confirmed to be of high quality from rocking curve and Laue back-reflection measurements, and the propagation attenuation coefficient is around 0.01 dB cm−1. Through EPMA measurements, we found that Yb3+ is uniformly distributed in the YAG SCFs, which is necessary for achieving single-mode lasers. Based on this, we carried out laser experiments under different conditions and achieved a maximum continuous-wave (CW) output power of 3.62 W with a slope efficiency of 28.2%. In conclusion, all properties, including the small diameter fluctuation, good crystal quality, good thermal conductivity and uniform ion distribution, prove that the colorless Yb:YAG SCFs are a promising host material for single-mode lasers.
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