Multiphonon-coupling yellow laser in Yb:La2CaB10O19 crystal.

Yellow lasers at 590 nm have many extensive applications in our daily life, but extremely difficult to attain by traditional solid-state laser technology, owing to the absence of highly-efficient transition channels at this spectral range. In this work, we proposed a cooperative lasing mechanism to obtain the yellow light emission, with multiphonon-assisted electronic transitions and phase-matched frequency-doubling. Based on the predictable configurational coordinate model, we can calculate the multiphonon-assisted emission step-by-step. Using Yb3+-doped La2CaB10O19 crystal as an example, it is capable of producing yellow laser at 581-590 nm, with a maximum output power of 4.83 W and a high slope efficiency of 31.6%. To the best of our knowledge, it represents the highest power of solid-state yellow laser realized in one single crystal pumped by a laser diode. This power scaling can be assigned to the amplified phonon-assisted emission beyond the fluorescence spectrum, and optimized crystal angle for phase-matching condition. Such a compact, low-cost, and high-power laser device, provides an alternative candidate for the spectral "yellow-gap" where no practical solid-state laser exists at present.

Influence of Cation-Size Effects of Alkaline Earth (Ae) Metals on Dimensionality and Optical Anisotropy Regulation in K4AeP2S8 Thiophosphates.

Cationic substitution demonstrates significant potential for regulating structural dimensionality and physicochemical performance owing to the cation-size effect. Leveraging this characteristic, this study synthesized a new family of K4AeP2S8 (Ae = alkaline earth elements: Mg, Ca, Sr, and Ba) thiophosphates, involving the substitution of Ae2+ cations. The synthesized compounds crystallized in distinct space groups, monoclinic P2/c (Ae = Mg) versus orthorhombic Ibam (Ae = Ca, Sr, and Ba), exhibiting intriguing dimensionality transformations from zero-dimensional (0D) [Mg2P4S16]8- clusters in K4MgP2S8 to 1D ∞[AeP2S8]4- chains in other K4AeP2S8 thiophosphates owing to the varying ionic radii of Ae2+ cations, Ae-S bond lengths, and coordination numbers of AeSn (Mg: n = 6 versus other: n = 8). Experimental investigations revealed that K4AeP2S8 thiophosphates featured wide optical bandgaps (3.37-3.64 eV), and their optical absorptions were predominantly influenced by the S 3p and P 3s orbitals, with negligible contributions from the K and Ae cations. Notably, within the K4AeP2S8 series, birefringence (Δn) increased from K4MgP2S8 (Δn = 0.034) to other K4AeP2S8 (Δn = 0.050-0.079) compounds, suggesting that infinite 1D chains more significantly influence Δn origins than 0D clusters, thus offering a feasible approach for enhancing optical anisotropy and exploring potential new birefringent materials.

Intracavity frequency-doubled yellow laser in an electron-phonon-coupled Nd:YVO4 crystal.

An approach to obtain a yellow laser is demonstrated for the first time to our knowledge by the employment of an Nd3+-doped YVO4 crystal and a LBO frequency-doubling crystal. Differing from the previous stimulated self-Raman radiation of Nd:YVO4, a direct 1176 nm lasing, without a high-intensity intracavity 1064 nm laser, was realized by utilizing an electron-phonon coupling effect and amplifying the thermally activated vibronic transitions. Combining with intracavity frequency-doubling, a yellow laser at 588 nm was obtained. At the pump power of 14.3 W, the output power of the yellow laser was 1.17 W, corresponding to a diode-to-visible efficiency of 8.2%. Moreover, for the first time, the yellow laser at 584 nm with output power of 164 mW was realized by tuning the filter, indicating the great potential of such an electron-phonon coupling laser for a wavelength extension in the yellow regime.

Flexible Anionic Groups-Activated Structure Dissymmetry for Strong Nonlinearity in Ln2 Ae3 MIV 3 S12 Family.

Structural dissymmetry and strong second-harmonic generation (SHG) responses are key conditions for nonlinear optical (NLO) crystals, and targeted combinatorial screening of suitable anionic groups has become extremely effective. Herein, optimal combination of flexible SnSn (n = 5, 6) groups and highly electropositive cations (lanthanides (Ln3+ ) and alkaline earth (Ae2+ : Sr, Ca) metals) affords the successful synthesis of 12 NLO thiostannates including Ln2 Sr3 Sn3 S12 (Pmc21 ) and Ln2 Ca3 Sn3 S12 (P-62m); whereas 17 rigid GeS4 or SiS4 tetrahedra-constructed Ln2 Ae3 Ge3 S12 and Ln2 Ae3 Si3 S12 crystallize in the centrosymmetric (CS) Pnma. This unprecedented CS to noncentrosymmetric (NCS) structural transformation (Pnma to P-62m to Pmc21 ) in the Ln2 Ae3 MIV 3 S12 family indicates that chemical substitution of the tetrahedral GeS4 /SiS4 units with SnSn breaks the original symmetry to form the requisite NCS structures. Remarkably, strong polarization anisotropy and hyperpolarizability of the Sn(4+) S5 unit afford huge performance improvement from the nonphase-matching (NPM) SHG response (1.4 × AgGaS2 and Δn = 0.008) of La2 Ca3 Sn3 S12 to the strong phase-matching (PM) SHG effect (3.0 × AgGaS2 and Δn = 0.086) of La2 Sr3 Sn3 S12 . Therefore, Sn(4+) S5 is proven to be a promising "NLO-active unit." This study verifies that the coupling of flexible SnSn building blocks into structures opens a feasible path for designing targeted NCS crystals with strong nonlinearity and optical anisotropy.

Noncentrosymmetric Na6Pb3P4S16 and Centrosymmetric K2MIIP2S6 (MII = Mg and Zn) Displaying Multiple Membered-Ring Configurations and Strong Optical Anisotropy.

Three thiophosphates including noncentrosymmetric Na6Pb3P4S16 and centrosymmetric K2MIIP2S6 (MII = Mg and Zn) were successfully synthesized in vacuum-sealed silica tubes. Note that interesting multiple six membered-rings (6-MRs) including 6-NaS6-MRs and 6-KSn-MRs (n = 6 and 7) formed by A+-centered polyhedra were discovered in the structures of title thiophosphates and these MR-composed three-dimensional (3D) tunnels show great possibility to facilitate the filling of various structural blocks (such as zero-dimensional (0D) Pb3S10 trimers or one-dimensional (1D) (MIISn)n chains). Na6Pb3P4S16 exhibits the strongest nonlinear optical (NLO) response (5.4 × AgGaS2) with phase-matching (PM) behavior among the known Pb-based PM NLO sulfides, which is much larger than that of Pb3P2S8 (3.5 × AgGaS2); it was verified that such large second harmonic generation (SHG) response in Na6Pb3P4S16 can be attributed to the huge contribution of stereochemically active PbS4 units based on the SHG-density and dipole-moment calculations. Moreover, title thiophosphates show large birefringences (Δn = 0.102-0.21), which indicates that incorporation of [P2S6] dimers or polarized PbS4 units into structures provides positive benefits for the onset of strong optical anisotropy.

Monolithic 591-nm laser with cooperative multiphonon-coupling and nonlinear frequency-doubling.

Stable and miniaturized orange lasers at 591 nm are in urgent demand for ophthalmology and dermatological treatment. However, at present, traditional dye lasers and nonlinear sum-frequency lasers are limited by their complex setup and high cost, whereas semiconductor laser diodes (LDs) emitting in the yellow-orange range suffer from low output power. Here, we propose a new, to the best of our knowledge, route to create self-frequency-doubling (SFD) orange laser with a combination of multiphonon-assisted lasing and nonlinear frequency-doubling in one crystal. Using Yb3+-doped YCa4O(BO3)3 (Yb:YCOB) crystal, we first realize a widely tunable laser beyond the fluorescence spectrum in the wavelength range of 1175-1248 nm. Then, by selecting the laser polarization and crystal angle to satisfy phase-matching conditions, we obtained a directly diode-pumped orange laser at 591.8 nm with 3.07-W output power and an optical-to-optical conversion efficiency of 13%. This work represents a new step forward for portable high-power solid-state orange lasers and provides an intriguing platform for electron-phonon coupled lasing.

Phonon engineering in Yb:La2CaB10O19 crystal for extended lasing beyond the fluorescence spectrum.

Since the first invention of the laser in 1960, direct lasing outside the fluorescence spectrum is deemed impossible owing to the "zero-gain" cross-section. However, when electron-phonon coupling meets laser oscillation, an energy modulation by the quantized phonon can tailor the electronic transitions, thus directly creating some unprecedented lasers with extended wavelengths by phonon engineering. Here, we demonstrate a broadband lasing (1000-1280 nm) in a Yb-doped La2CaB10O19 (Yb:LCB) crystal, far beyond its spontaneous fluorescence spectrum. Numerical calculations and in situ Raman verify that such a substantial laser emission is devoted to the multiphonon coupling to lattice vibrations of a dangling "quasi-free-oxygen" site, with the increasing phonon numbers step-by-step (n = 1-6). This new structural motif provides more alternative candidates with strong-coupling laser materials. Moreover, the quantitative relations between phonon density distribution and laser wavelength extension are discussed. These results give rise to the search for on-demand lasers in the darkness and pave a reliable guideline to study those intriguing electron-phonon-photon coupled systems for integrated photonic applications.

Deciphering the vibronic lasing performances in an electron-phonon-photon coupling system.

Coupling between electronic motions and the lattice vibrations, phonons could broaden the spectral bandwidth of the fluorescence spectroscopy by the energy transferring, which was recognized from the beginning of last century and successfully applied in many vibronic lasers. However, the laser performances under electron-phonon coupling were mainly prejudged by the experimental spectroscopy. The multiphonon participated lasing mechanism is still elusive and should be in-depth investigated. Here, a direct quantitative relationship between the laser performance and phonon participating dynamic process was derived in theory. With a transition metal doped alexandrite (Cr3+:BeAl2O4) crystal, the multiphonon coupled laser performance was manifested in experiments. Associated with the Huang-Rhys factor calculations and hypothesis, the multiphonon participated lasing mechanism with phonon numbers from 2 to 5 was discovered and identified. This work provides not only a credible model for understanding the multiphonon participated lasing, but should also boost the study of laser physics in the electron-phonon-photon coupled systems.

Investigation of crystal field effects for the spectral broadening of Yb3+-doped Lu x Y2-x O3 sesquioxide crystals.

The investigation of crystal field effects is significant for elucidating the spectral characteristics of Yb3+-doped sesquioxide crystals for ultrafast laser generation. The narrow spectra of Yb3+-doped single sesquioxide crystals limit the generation of ultrafast lasers; in this study, the Y3+ ions were introduced into Lu2O3 single crystals by the employment of ion replacement to broaden the spectra. To analyze the spectral broadening, the responsible crystal field parameters (CFPs) were calculated. The conversion of the host dominant ion and the distortion of the ligand affected the values and signs of the CFPs, and further determined the energy level splitting and fluorescence spectra. A linear relationship expressed by the semi-empirical equations for Yb3+-doped sesquioxide crystals was produced, which could be used for high throughput spectral prediction. Opposite variations of high- and low-frequency vibrational energies and the influence of the electron-phonon coupling on the spectra were also achieved. The redshift from the crystal field and the blueshift from the electron-phonon coupling make the optimal spectral broadening appear when x = 1.19 in the Yb:Lu x Y2-x O3 crystals. The results of these analyses could provide some key clues for the development of Yb3+-doped crystals for the generation and amplification of ultrafast lasers.

Anion-Centered Polyhedron Strategy for Strengthening Photon Emission Induced by Electron-Phonon Coupling.

Electron-phonon coupling emerges as a growing frontier in the heart of condensed matter from physical symmetry to the electronic quantum state, but its quantitative strength dependence on the chemical structure has not been assessed. Here, we originally proposed the anion-centered polyhedron (ACP) strategy for elaborating the electron-phonon coupling interaction in rare-earth (RE) materials comprising three chemical factors, RE-O bond length, the effective charge of the coordinated atom, and structural dimensionality. Using Gd3+ cation with 4f7 configuration as a fluorescence probe, we found that the "free-O"-centered polyhedron is the most crucial motif in strengthening the phonon-assisted energy transfer and photon emission. The temperature-dependent Huang-Rhys S factors were calculated to identify the electron-phonon coupling intensity based on the fluorescence spectrum quantitatively. Finally, beyond conventional wisdom, a series of structural criteria were presented, serving as useful guidelines for discovering strongly coupled rare-earth optical materials. Our study breaks the long-time "blind"-searching diagram and provides reliable principles for many functional materials associated with electron-phonon coupling, such as superconductors, multiferroics, and phosphors.

Compact acousto-optical Q-switched Yb:ScBO3 laser with giant pulse energy.

In this Letter, a continuous-wave Yb:ScBO3 laser was enhanced with a maximum output power of 1.63 W and a slope efficiency of 48.97%, pumped by a continuous-wave 965 nm diode laser. Subsequently, the first, to the best of our knowledge, acousto-optically Q-switched Yb:ScBO3 laser was realized with an output wavelength of 1022 nm and repetition rates ranging from 0.04 to 1 kHz. The characteristics of pulsed lasers modulated by a commercial acousto-optic Q switcher were comprehensively demonstrated. With a low repetition rate of 0.05 kHz, the pulsed laser was generated under an absorbed pump power of 2.62 W, having an average output power of 0.44 W and giant pulse energy of 8.80 mJ. The pulse width and peak power were 80.71 ns and 109 kW, respectively. The findings manifest that the Yb:ScBO3 crystal is a gain medium with great potential for Q-switched laser generation with high pulse energy.

Diode-pumped continuous-wave laser of a self-frequency-doubling Yb:La2CaB10O19 crystal.

We report the first, to the best of our knowledge, laser operation of acentric Yb3+-doped La2CaB10O19 (Yb:LCB) crystal since its discovery in 1998. The polarized absorption and emission cross-section spectra of Yb:LCB were calculated at room temperature. Using a fiber-coupled 976 nm laser diode (LD) as the pump source, we realized effective dual-wavelength laser generation at around 1030 and 1040 nm. The highest slope efficiency of 50.1% was obtained in the Y-cut Yb:LCB crystal. In addition, via resonant cavity design on a phase-matching crystal, a compact self-frequency-doubling (SFD) green laser at 521 nm was also realized in a single Yb:LCB crystal with an output power of 152 mW. These results promote Yb:LCB as a competitive multifunctional laser crystal, especially for highly integrated microchip laser devices ranging from the visible to the near-infrared regime.

Mid-infrared pulsed nanosecond difference frequency generation of oxide LGN crystal up to 5.7 µm.

We demonstrate the tunable difference frequency generation (DFG) of an oxide La3Ga5.5Nb0.5O14 (LGN) crystal pumped by near-infrared lasers with nanosecond pulses for the first time to our knowledge. The type I and II phase-matching conditions of DFG were calculated in the mid-infrared region. With the processed LGN crystals, tunable lasers in the wavelength range from 4.4 to 5.7 µm and 4.56 to 5.6 µm were achieved under type II and I phase-matching conditions, respectively, with the maximum output energy of 13.1 µJ, which agreed well with the theoretical calculation. This work provides the kind of promising mid-infrared nonlinear crystals for the pumping of nanosecond pulsed lasers as well as a tunable mid-infrared laser source at a wavelength over 5 µm in further photonic applications.

Few-cycle pulses tunable from 3 to 7 µm via intrapulse difference-frequency generation in oxide LGN crystals.

An ultrashort mid-infrared (IR) source beyond 5 µm is crucial for a plethora of existing and emerging applications in spectroscopy, medical diagnostics, and high-field physics. Nonlinear generation of such sources from well-developed near-IR lasers, however, remains a challenge due to the limitation of mid-IR crystals. Based on oxide La3Ga5.5Nb0.5O14 (LGN) crystals, here we report the generation of femtosecond pulses tunable from 3 to 7 µm by intrapulse difference-frequency generation of 7.5 fs, 800 nm pulses. The efficiency and bandwidth dependences on pump polarization and crystal length are studied for both Type-I and Type-II phase-matching configurations. Maximum pulse energy of ∼10nJ is generated at 5.2 µm with a conversion efficiency of ∼0.14%. Because of the few-cycle pump pulse duration, the generated mid-IR pulses are as short as about three cycles. These results, to the best of our knowledge, represent the first experimental demonstration of LGN in generating mid-IR ultrashort pulses.

High-efficiency Er-doped yttrium gallium garnet laser resonantly pumped by a laser diode at 1.47 µm.

The spectroscopic and laser properties of an Er3+-doped yttrium gallium garnet crystal, Y3Ga5O12 (YGG), are studied. The stimulated emission cross section is 1.4×10-21cm2 at 1.65 µm. A continuous-wave laser resonantly pumped by a laser diode at 1.47 µm is demonstrated, delivering a maximum output power of 3.34 W. Benefiting from the low phonon energy of the YGG host, the corresponding slope efficiency is as high as ∼42%. To the best of our knowledge, this is the highest slope efficiency from the laser-diode resonantly pumped Er lasers at room temperature in the 1.6 µm spectral range.

Power scaling of the self-frequency-doubled quasi-two-level Yb:YCOB laser with a 30% slope efficiency.

The lab-on-chip integration of photonic devices has been attracting increasing attention recently. Multifunctional materials provide natural platforms for the desirable performance by the coupling of different functionalities. The insufficient coupling efficiency of the laser and nonlinear processes in self-frequency-doubled (SFD) lasers is the limiting factor for the output power and further practical applications. Here we demonstrate a SFD Yb3+-doped calcium yttrium oxoborate (Yb:YCOB) crystal laser with an unprecedented slope efficiency of 30% and output power of 6.2 W at 513 nm. The successful realization of this laser operating in a quasi-two-level configuration is based on enhanced coupling of the laser and frequency-doubling processes using a monolithic configuration, benefiting from an ultimately small laser quantum defect, the anisotropic gain cross sections, and the high effective nonlinearity of the monoclinic YCOB outside the principal planes. Solid-state lasers in the spectral range around 510 nm are scarce, and the results not only present a significant advancement in the field of SFD lasers, but also pave the way for future applications of such green lasers, especially in areas such as medical treatment, daily life, and scientific investigations.

Kerr-lens mode-locked Pr3+:LuLiF4 laser.

We demonstrate the Kerr-lens mode-locked Pr3+:LuLiF4 (Pr:LLF) laser pumped by a blue laser diode (LD). By theoretical calculation of the group velocity dispersion in the laser gain, the compensation was employed for the realization of the continuous-wave mode-locked laser at the wavelength of 604 nm with the pulse width of 1.1 ps which, to the best of our knowledge, is the shortest pulse width in the Pr3+ ion doped crystal lasers pumped with LDs. It can be believed that the present Pr:LLF laser should provide some inspiration for the development of the blue LD pumped visible lasers, especially in the mode-locking laser operation.

Demonstration of a White Laser with V2 C MXene-Based Quantum Dots.

Multicolor photoluminescence over the full visible color spectrum is critical in many modern science and techniques, such as full-color lighting, displays, biological and chemical monitoring, multiband communication, etc., but the ultimate white lasing especially on the nanoscale is still a challenge due to its exacting requirements in the balance of the gain and optical feedback at different wavelengths. Recently, 2D transition metal carbides (MXenes) have emerged, with some superior chemical, physical, and environmental properties distinguishing them from traditional 2D materials. Here, a white laser with V2 C MXene quantum dots (MQDs) is originally demonstrated by constructing a broadband nonlinear random scattering system with enhanced gain. The excitation-dependent photoluminescence of V2 C MQDs is enhanced by passivation and characterized, and their localized nonlinear random scattering is realized by the generation of excitation-power-dependent solvent bubbles. With the optimized excitation, the blue, green, yellow, and red light is amplified and simultaneously lased. This work not only provides a kind of promising material for white lasers, but also a design strategy of novel photonics for further applications.

High-efficiency 3 µm Er:YGG crystal lasers.

By balancing energy transfer and thermal effects, we demonstrate efficient erbium-doped yttrium gallium garnet (Er:YGG) crystal lasers at a wavelength of 2.82-2.92 µm for the first time, to the best of our knowledge. Associated with the influence of doping concentration on energy transfer and thermal effects, the Er3+ doping concentration was optimized to be 10 at.%, and with the optimized crystal, the maximum continuous-wave output power was 1.38 W, corresponding to the slope efficiency of 35.4% approaching the theoretical quantum limits. The thermal effects during the laser process were discussed. We believe that this work should be helpful for optimizing the erbium-doped gain for the 3 µm laser and the development of 3 µm lasers.

Validation of the angular quasi-phase-matching theory for the biaxial optical class using PPRKTP.

We report the first experimental validation of angular quasi-phase-matching (AQPM) theory in a biaxial crystal by performing second-harmonic generation (SHG) in the periodically-poled Rb-doped KTiOPO4 (PPRKTP) crystal cut as a sphere. Both AQPM and birefringence phase-matching (BPM) angles were measured thanks to a Kappa circle.