Pulsed Laser Research Articles

Defining the Treatment Window: Early Versus Late Pulsed Dye Laser Therapy for Posttraumatic and Surgical Scars in Asian Patients

ABSTRACTObjectivesThis retrospective study evaluates the effectiveness of pulsed dye laser (PDL) treatment in early versus late treatment groups for traumatic or postoperative scars. The study aims to determine the threshold between early and late treatment. Additionally, it investigates factors that may influence wound healing outcomes.MethodsThe medical records of 147 patients who underwent PDL treatment at our institution between January 2018 and December 2022 were retrospectively reviewed. Inclusion criteria were patients receiving PDL treatment for traumatic or postoperative scars. Out of these patients, we selected those who were willing to receive telephone interviews or re‐visit at a scheduled time. Eventually, 52 participants were included in our study. A standardized questionnaire was administered to all participants during telephone interviews, encompassing inquiries regarding their medical history, treatment experiences, and the patient component of the Patient and Observer Scar Assessment Scale. Among the enrolled patients, 38 were contacted and interviewed via telephone, while the remaining 14 patients attended follow‐up visits where photographs of their current skin condition were captured. The pretreatment and latest follow‐up photographs obtained from the clinical database were independently scored in a blinded manner by two dermatologist reviewers using both the Vancouver Scar Scale and the Manchester Scar Scale.ResultsAmong the 52 patients, 43 (82.7%) were successfully treated with good response. The correlation coefficients between week‐to‐treatment initiation and posttreatment MSS and VSS among patients with good response were 0.50 (p < 0.001) and 0.46 (p = 0.002), respectively. Given these findings, we established a treatment initiation threshold of 10 weeks, distinguishing patients into early and late treatment groups. The early treatment group showed borderline significantly lower posttreatment MSS and VSS scores than the late treatment group (MSS: 7.5 ± 2.1 vs. 9.3 ± 2.5, p = 0.011; VSS: 2.8 ± 2.0 vs. 4.5 ± 2.3, p = 0.011). Furthermore, both MSS and VSS of posttreatment showed significantly greater improvement in the early treatment group (4.4 ± 1.6 vs. 3.2 ± 1.9; p = 0.03 and 3.8 ± 1.8 vs. 2.8 ± 1.4; p = 0.04).ConclusionsEarly intervention using a PDL within 10 weeks post‐injury achieved better outcomes in treating traumatic and postoperative scars based on both clinical and patient opinions.

Investigating the properties of n-type Nb2O5 thin film semiconductor under pulsed laser deposition: number of laser pulses impact

Investigating the properties of n-type Nb2O5 thin film semiconductor under pulsed laser deposition: number of laser pulses impact

Interfacial local activation strategy tailoring selective zinc deposition pattern for stable zinc anodes

"Tip effect" triggered by uneven zinc deposition accelerates the growth of Zn dendrites. The unfavorable interfacial activity gradient aggravates zinc deposition at the tips, which is the root cause of zinc dendrites. This study reports an interfacial local activation strategy to reconfigure the interfacial activity gradient of zinc anode to promote more stable operation of zinc batteries. A locally activated zinc anode (Zn-ILA) is proposed as the proof-of-concept zinc anode by constructing high-active microchannels to induce preferential zinc deposition, while the remaining low-active region is accompanied by zinc epitaxial growth, thus achieving bottom-up zinc deposition at the anode interface. A fabrication method based on nanosecond pulsed laser is used to modify the zinc anode by creating high-active microchannels through thermal impingement. Additionally, low-active regions covered by dense ZnO nanoparticles are also formed due to the plasma effect. The laser-induced cross-scale oxide layers help improve the corrosion resistance at the full zinc anode interface. The proposed interfacial local activation strategy enables ordered selective deposition at the Zn-ILA interface owing to the activity gradient, as well as stabilizes the long-term operation of symmetric and full cells. The effectiveness of Zn-ILA is also validated in large-area pouch batteries, showing great potential for large-scale energy storage systems.

Epitaxial growth and characterization of copper gallate (CuGa2O4) thin films by pulsed laser deposition

High-quality crystalline copper gallate (CuGa2O4) thin films were grown on c-plane sapphire substrates using the pulsed laser deposition (PLD) technique by optimizing the growth parameters (i.e., temperature, oxygen chamber pressure, and laser energy density). The obtained XRD patterns validated that the preferred orientation of the crystalline CuGa2O4 thin film is along the [111] direction, and the crystallinity of the films improved with increasing substrate temperature while maintaining a constant O2 pressure, as assessed by measuring the full width at half maximum (FWHM) of the prominent (222) plane. Reducing the oxygen pressure leads to the emergence of β-Ga2O3 peaks rather than the CuGa2O4 peaks due to the incomplete oxidation of copper (Cu). Subsequent XRD phi (φ) scans revealed a sixfold rotational symmetry of CuGa2O4 and a 30° epitaxial relationship between the film and the sapphire substrate. X-ray photoelectron spectroscopy (XPS) spectra confirmed the presence of Cu1+, Cu2+, and Ga3+ oxidation states in the films. Increasing laser energy density resulted in the complete oxidation of Cu and an increase in the film thickness from 51.8 nm to 183.4 nm. The direct bandgap of CuGa2O4 films was determined to be approximately 4.50 eV by analyzing the UV–Vis absorbance spectra using the Tauc equation. The refractive index was found to be approximately 2.05 ± 0.01 based on the spectroscopic ellipsometry data. While the impact of increasing laser energy density was negligible on the parameters such as crystal structure, rotational symmetry, oxidation states of gallium (Ga), oxygen (O), bandgap, and refractive index of CuGa2O4 thin film, notable alterations in the oxidation state of Cu and film thickness were observed. The surface roughness (Rrms) measured from AFM images showed a strong correlation with the values derived from ellipsometry analysis.

Ultrafast Synthesis of Transition Metal Phosphides in Air via Pulsed Laser Shock.

Transition metal phosphide nanoparticles (TMP NPs) represent a promising class of nanomaterials in the field of energy; however, a universal, time-saving, energy-efficient, and scalable synthesis method is currently lacking. Here, a facile synthesis approach is first introduced using a pulsed laser shock (PLS) process mediated by metal-organic frameworks, free of any inert gas protection, enabling the synthesis of diverse TMP NPs. Additionally, through thermodynamic calculations and experimental validation, the phase selection and competition behavior between phosphorus and oxygen have been elucidated, dictated by the redox potential and electronegativity. The resulting composites exhibit a balanced performance and extended durability. When employed as electrocatalysts for overall water splitting, the as-constructed electrolyzer achieves a low cell voltage of 1.54 V at a current density of 10 mA cm-2. This laser method for phosphide synthesis provides clear guidelines and holds potential for the preparation of nanomaterials applicable in catalysis, energy storage, biosensors, and other fields.

Periodic Domain Inversion in Single Crystal Barium Titanate‐on‐Insulator Thin Film

AbstractExperimentally achieving the first‐ever electric field periodic poling of single crystal barium titanate oxide (BTO, or BaTiO3) thin film on‐insulator is reported. Owing to the outstanding optical nonlinearities of BTO, this result is a key step toward achieving quasi‐phase‐matching (QPM). First, the BTO thin film is grown on a dysprosium scandate substrate using pulsed laser deposition with a thin layer of strontium ruthenate later serving as the bottom electrode for poling. The characterization of the BTO thin film using x‐ray diffraction (XRD) and piezo‐response force microscopy to demonstrate single crystal, single domain growth of the film that enables the desired periodic poling, are presented. To investigate the poling quality, both non‐destructive piezo force response microscopy and destructive etching‐assisted scanning electron microscopy (SEM) are applied, and it is shown that high quality, uniform, and intransient poling with 50% duty cycle and periods ranging from 2 µm to 10 µm is achieved. The successful realization of periodic poling in BTO thin film unlocks the potential for highly efficient nonlinear processes under QPM that seemed far‐fetched with prior polycrystalline BTO thin films which predominantly relied on efficiency‐limited random or non‐phase matching conditions and is a key step toward integration of BTO photonic devices.

Au/ZnO nanocomposites based on simple laser ablation method for water treatment

A binary heterostructure of Au/ZnO nanocomposite is prepared in a novel way based on successive pulsed laser ablation of the two targets in an aqueous solution with varied pulse time. The development of the method allows generating a noble metal (Au) and metal oxide (ZnO) one after one to produce a novel heterostructure with a tunable shell applicable as a catalytic degradable material. The nanocomposite samples are tested to study their optical, morphological, and structural properties. The photocatalytic degradation study demonstrates a significant decrease in the absorbance intensity of Rohdamin B (RhB) dye as the irradiation time increases. It indicates a reduction in dye concentration with a remarkable improvement in contact time. Besides, the degradation percentage against pH value is investigated. It reveals an increasing trend as the pH value rises with a maximum percentage at pH 10. The study is also concerned with the influence of the initial concentration of RhB dye on the degradation efficiency of the nanocomposite. Higher initial concentrations of the dye lead to a decrease in the degradation efficiency of the catalysts. Finally, the kinetic analysis of RhB photodegradation reveals that the Langmuir-Hinshelwood first-order kinetic model accurately describes RhB's adsorption onto the nanocomposites.

An insight in to microwave induced defects and its impact on nonlinear process in NiO nanostructures under femtosecond and continuous wave laser excitation.

This work demonstrates the impact of microwave (MW) irradiation on third-order nonlinear optical (NLO) processes in chemically deposited NiO nanostructure films. The optical nonlinearity of the NiO nanostructure films was studied using third-harmonic generation (THG) measurements in the pulsed femtosecond laser regime and the Z-scan technique in the continuous wave laser regime. In the ultrafast pulsed regime, THG measurements revealed a significant increase in the THG signal of MW-irradiated NiO nanostructures due to photoexcitation and relaxation processes, resulting from an enhancement in defect concentration. This increase in defect density upon MW irradiation was quantified by PL and XPS studies. Under continuous wave laser irradiation, the Z-scan technique showed an enhanced absorption coefficient of ∼10-1 m W-1 and a nonlinear refractive index of ∼10-7 m2 W-1. The high NLO values in both pulsed and continuous laser regimes indicate that MW-irradiated NiO nanostructure films hold promise for optoelectronic device applications.

Effect of substrate temperature on the growth mechanism of FeSe superconducting films

Abstract Among all the iron-based superconductors (IBSs), Fe-chalcogenides (Fe-Ch) possess the advan tages of simple structure, non-toxicity, low anisotropy and the potential for high-field applications.One of the most effective methods for preparing Fe-Ch films is pulsed laser deposition (PLD). However, high quality film growth is challenged by the significant volatility difference between the iron
and chalcogens (S, Se, Te), which affects stoichiometric transfer from target to substrate and subsequently impacts superconductivity. Currently, there is limited research on the correlation between the growth mechanism and preparation conditions of Fe-Ch films, particularly in explaining chalcogen volatility during deposition. Technically, PLD offers various adjustable parameters, among
which the substrate temperature (Ts) is the most critical one affecting film quality. It governs particle behavior on the substrate including adsorption, diffusion, bonding reactions, crystallization processes while also strongly affecting volatilization rates. In this study, we fabricated a series of FeSe films using PLD at different Ts ranging from 25 ℃ to 750 ℃.We reveal in detail the impact of
competitive processes between Se volatilization and reactive crystallization of Fe/Se on film quality. The optimal film was obtained at Ts=500 ℃ with a composition ratio of Fe1.01Se. We also investigate the correlations between Ts and film crystallinity, surface morphology, along with their influence on superconductivity. Additionally, the pinning mechanism in FeSe film grown at the
optimal Ts was briefly analyzed. Our results provide reliable experimental evidence regarding the growth mechanism of FeSe films while revealing comprehensive insights into how Ts affects both film quality and performance.

Laser-synthesized TiN-based nanoparticles as novel efficient electrostatic nanosorbent for environmental water cleaning

Abstract Dyes used in industries such as textile, paper, and leather are known to be harmful to both human health and aquatic ecosystems, which makes critically important the search of effective and sustainable methods for their removal from wastewater in order to mitigate the detrimental pollution effects. Here, we show that titanium nitride nanoparticles (TiN NPs) synthesized by scalable methods of pulsed laser ablation in liquid ambient (water, acetone and acetonitrile) can serve as extremely efficient sorbents for water decontamination from dye molecules (methylene blue, crystal violet, and malachite green). Our tests show that adsorption of TiN NPs is associated with the electrostatic effect due to a strong negative charge of laser-synthesized TiN NPs and the presence of pores in the NPs. Comprehensive characterization using scanning and transmission electron microscopy, along with Raman spectroscopy, evidenced that the appearance of surface charge is related to the formation of under-stoichiometric TiN (TiN1-x), associated with the predominance of nitrogen vacancies. This study identifies an optimal configuration of vacancy defects that maximizes dye adsorption, with TiN NPs synthesized in water exhibiting superior performance, achieving a dye sorption capacity of 136.5 mg/g at room temperature for methylene blue, which corresponds to best earlier reported values for nanomaterials. This study not only extends the utility of TiN NPs to environmental remediation but also highlights the critical influence of synthesis conditions on their functional properties, offering a pathway towards the design of more effective materials for pollution control.

Numerical simulation of heat transfer properties of skin tissue acted on repetitive laser irradiation

Pulsed laser has been widely used in the clinical treatment of various diseases and injuries due to its unique advantages in the process of interaction with skin tissue. In order to ensure the therapeutic effect and patient safety, it is necessary to accurately monitor the time-space response of the whole-field temperature of the target tissue irradiated by pulsed laser. A research strategy to explore the thermal response and incidental thermal damage of skin tissue induced by repeated pulses laser has been proposed in present work. A theoretical model involved variable physical properties was first proposed, in which the dual-phase lag (DPL) equation and Henrique burn equation were employed to evaluate the tissue temperature and thermal damage induced by repeated pulse laser irradiation. With the help of finite difference method, the governing equation with variable physical properties was then numerical solved to obtain the time-space distribution of tissue temperature, and the evolution process of the thermal damage was further calculated. The effects of laser input parameters and variable physical parameters on the laser penetration depth, temperature distribution and burn degree of the irradiated tissue were analyzed.

Effect of RF acetylene plasma on the composition and dynamics of a titanium plasma plume in a plasma enhanced pulsed laser deposition system

We report the effect of radio frequency (RF) acetylene plasma on the dynamics and composition of titanium (Ti) plasma plume in a plasma-enhanced pulsed laser deposition (PEPLD) system. The titanium target, mounted inside a capacitively coupled RF discharge, was ablated by using a nanosecond Nd:YAG pulsed laser at 1064 nm with a power density of 2.65 GW/cm2. The experiments were performed at different operating pressures of acetylene. Fast imaging and optical emission spectroscopy were employed to study the physics behind the pulsed laser deposition in both (PLD) and PEPLD systems. A nonlinear dependence of the plasma plume evolution was observed over a range of pressure. Different expansion regimes correspond to the pressure of the experiments. The plume expansion velocity ranges between 6 × 103 m/s and 30 × 103 m/s. Emission spectra reveal the presence of C II and Ti II lines depending on the experimental conditions. The presence of background RF plasma leads to substantial enhancement of the emission intensity of the C II spectral lines. In addition, with increasing RF power and background pressure, the intensities of the C II spectral lines increase; whereas the intensities of the Ti II spectral lines decrease with the increase in RF power. Plasma temperature was estimated from the Ti II lines using the Boltzmann plot method, whereas the electron density was estimated from the Stark-broadened Ti II line at 454.9 nm. The calculated densities and temperatures lie between 1017–1018 cm−3 and 0.8–2.0 eV, respectively. These results show the effects of the different backgrounds (either neutral or RF plasma) on the propagation of the laser-produced plasma (LPP), which we propose to be useful in the thin film deposition process using PLD.

One-step pulsed laser deposition of carbon/metal oxynitride composites for supercapacitor application

Abstract Advanced material composite of nanocarbons and metal-based materials provides a synergistic effect to obtain excellent electrochemical charge-storage performance and other properties. Herein, 3D porous carbon-metal oxynitride nanocomposites with tunable carbon/metal and oxygen/nitrogen ratio are synthesized uniquely by simultaneous ablation from two different targets by single-step pulsed laser deposition at room temperature. Co-ablation of titanium and vanadium nitride targets together with graphite allowed us to synthesize carbon-metal oxynitride porous nanocomposite and exploit them as a binder-free thin film supercapacitor electrode in aqueous electrolyte. We show that the elemental composition ratio and hence the structural properties can be tuned by selecting target configuration and by manipulating the ablation position. We investigate how this tuning capability impacts their charge-storage performances. We anticipate the utilization of as-synthesized various composites in a single PLD production run as next-generation active materials for flexible energy storage and optoelectronic applications.

Multiwavelength highly transient stimulated Raman scattering on dual Raman modes in Sr(MoO4)0.8(WO4)0.2 and Sr(MoO4)0.4(WO4)0.6.

For the first time to our knowledge, multiwavelength, highly transient, single-pass stimulated Raman scattering with a low wavelength spacing on dual (stretching and bending) Raman modes in Sr(MoO4)0.8(WO4)0.2 and Sr(MoO4)0.4(WO4)0.6 solid solutions in a range of 1000-1300 nm (transparence window of biological tissue) under ultrafast chirped pulse laser pumping is comparatively investigated in the interests of multicolor two-photon imaging of a living tissue. For both the solid solutions, the optimum range (1-5 ps) of chirped pump pulse durations for multiwavelength Raman conversion on dual Raman modes was wider than for SrMoO4 (2-3 ps) due to the higher integral cross section of the bending Raman mode. Higher efficient SRS conversion took place at negative chirping of the pump pulse with its stretching from 0.25 ps up to 5 ps due to the compensation of a positive chirp caused by nonlinear phase modulation with total Raman conversion efficiency of up to 36% for Sr(MoO4)0.8(WO4)0.2 and 49% for Sr(MoO4)0.4(WO4)0.6. The highest number (five) of Stokes components in the desired range (1000-1300 nm) was observed in the optimum Sr(MoO4)0.4(WO4)0.6 solid solution, which has the Raman modes with comparable intensities.

High power deep ultraviolet radiation generation from short pulse laser induced electron–hole pair production in a wide bandgap semiconductor

High power deep ultraviolet radiation generation from short pulse laser induced electron–hole pair production in a wide bandgap semiconductor

Kinetic Study of OH Radical Reactions with Cyclopentenone Derivatives.

We investigated the reactions of the hydroxyl radical (OH) with cyclopentenone derivatives and cyclopentanone in a quasi-static reaction cell at 4 Torr across a 300-500 K temperature range. The OH radicals were generated using pulsed laser photolysis of hydrogen peroxide vapors, and the ketone reactants were introduced in excess. The relative concentrations of the radicals were monitored as a function of reaction time using laser-induced fluorescence. At room temperature, the reaction rate coefficients were measured to be 1.2(±0.1) × 10-11 cm3 s-1 for reaction with 2-cyclopenten-1-one (R1); 1.7(±0.2) × 10-11 cm3 s-1 for reaction with 2-methyl-2-cyclopenten-1-one (R2); and 4.4(±0. 7) × 10-12 cm3 s-1 for reaction with 3-methyl-2-cyclopenten-1-one (R3). Over the experimental temperature range, the rate coefficients can be fitted with the modified Arrhenius expressions k1(T) = 1.2 × 10-11 (T/300)0.26 exp (6.7 kJ mol-1/R {1/T - 1/300}) cm3 s-1, k2(T) = 1.7 × 10-11 (T/300)6.4 exp (27.6 kJ mol-1/R {1/T - 1/300}) cm3 s-1, k3(T) = 4.4 × 10-12 (T/300)17.8 exp (57.8 kJ mol-1/R {1/T - 1/300}) cm3 s-1. In the cases of 2-cyclopenten-1-one and 2-methyl-2-cyclopenten-1-one, the temperature dependence of the rate coefficients is similar to that calculated or measured for noncyclic conjugated ketones. We also found that the reaction with 3-methyl-2-cyclopenten-1-one was slower, with rate coefficients similar to those measured for the reaction with the saturated cyclic ketone cyclopentanone. To discuss the experimental data, we use potential energy surfaces (PES) calculated at the CCSD(T)/cc-pVTZ//M06-2X/6-311+G** level of theory. RRKM-based Master equation calculations were also performed to infer the most likely reaction products over a wide range of temperatures and pressures. We suggest that both abstraction and addition mechanisms contribute to the overall OH removal, forming radical products stabilized by resonance. We also discuss the relevance for combustion and atmospheric chemistry.

All-fiber GHz few-cycle pulse generation at 2 µm.

We demonstrate an all-fiber GHz mode-locked laser system with few-cycle duration operating at 2 µm. Based on a dispersion-managed mode-locked oscillator, a multi-stage fiber amplifier, and a nonlinear pulse compressor, the laser system can deliver watt-level few-cycle pulses at a fundamental repetition rate of 1.041 GHz. This 2-µm pulsed laser offers outstanding performance metrics, including a pulse duration of 33 fs (corresponding to ∼5 optical cycles) and an average power of 4.17 W. Moreover, the all-fiber laser system exhibits excellent power stability, and the integrated relative intensity noise (RIN) is only 0.052% (10 Hz-1 MHz). It is anticipated that this new, to the best of our knowledge, laser source is promising for frontier applications, including coherent supercontinuum generation, nonlinear frequency conversion, and laser-material interaction.

Diagnostic study on laser-produced metal hydride plasmas

The characteristics of laser-produced metal hydride plasmas have been investigated in this work. The charge state and velocity of ions were determined by employing a time-of-flight technique in conjunction with an electrostatic deflection method. The ion velocities were found to be supersonic with values in the range of 104 to 105 m/s. The proportion of hydrogen ions was found to be lower than that of titanium ions. The ion emission behavior was studied by using a Faraday cup. When the total integrated space was taken into account, the ns pulsed laser was capable of producing hydrogen ion currents greater than one hundred mA. In order to understand the plasma generation process, we performed a comparative analysis between laser-generated plasma and arc plasma, and also investigated the effect of laser power density on the composition and velocity of the ions, the ablation properties of metal hydrides, and the maintainability of hydrogen ion emission.

Optical and thermoplasmonic properties of core (AuxAg1- x)- shell (Au) nanostructures

The optical and thermoplasmonic properties of bimetallic nanoparticles (NPs) offer a wide range of possibilities for designing functional materials and innovative nanotechnological devices. Their exploration is generating increasing interest in experimental and theoretical scientific research. The combination of noble metals such as gold (Au) and silver (Ag) within the same nanostructure, in the form of an alloy or core/shell arrangement, presents several advantages and potential applications. In this paper, the finite element method (FEM) is used to study the optical response and nanoscale heat generation capability of bimetallic core/shell nanospheres composed of a mixed alloy (AuxAg1−x)-core and an Au-shell. First, we studied the surface plasmon resonance (SPR) properties by generating absorption spectra. Our results show that the position and amplitude of the SPR peak of these nanospheres are strongly influenced by the fractions of Au and Ag metals composing the core, as well as by the Au-shell thickness. In particular, the SPR-peak position can be adjusted between 535nm and 1085nm depending on the composition and structure of these NPs. Secondly, we studied the ability of these NPs to convert absorbed light into heat when exposed to either a continuous wave (cw) laser or a femtosecond pulsed (fs-pulsed) laser. The results demonstrate the ability to control the temperature generated by these NPs based on the core composition, Au-shell thickness, illumination intensity, and the type of illumination (cw or fs-pulsed). In particular, under fs-pulsed illumination, the internal temperature of the NPs is significantly higher than under cw illumination. These findings are crucial for the use of these alloy-core and Au-shell nanoparticles in various thermoplasmonic applications.

High responsivity and detectivity β-Ga2O3 solar-blind photodetectors optimized by oxygen vacancy engineering

Solar-blind photodetectors (SBPDs) are core essential components for many critical applications such as precision guidance, fire warning, and space communications. Ultra-wide bandgap semiconductor β-Ga2O3 is considered to be an ideal material for the fabrication of SBPDs. However, synthetizing β-Ga2O3 with high quality factor while simultaneously in situ modulation of electronic and optoelectronic properties to enhance performance has been challenging. Here, pulsed laser deposition (PLD) technology is used to synthesize high-quality β-Ga2O3 thin films on a sapphire substrate. The oxygen vacancy engineered β-Ga2O3 films can achieve in situ precise control of their surface morphology, optical parameters, and optoelectronic properties by simply adjusting the oxygen pressure. Meanwhile, the optimal thickness of the β-Ga2O3 film for the developing high-performance SBPD is ∼221 nm, determined by fitting and analyzing the optical parameters measured by the ellipsometry. Subsequently, the influence of oxygen pressure on the performance of β-Ga2O3 SBPD is thoroughly explored, considering the optimization of electrode size and deposition time. When the oxygen pressure is set to 15 Pa, the β-Ga2O3-based SBPD achieves highly competitive responsivity (R) and detectivity (D*) at 250 nm, with values of 1080 A·W−1 and 1.4 × 1016 cm·W−1·Hz1/2, respectively. Additionally, the noise component of the β-Ga2O3 SBPD is further studied to calibrated the traditional device performance results. This work introduces a simple and straightforward approach to in situ tuning of the optoelectronic properties of β-Ga2O3, which is important for advancing β-Ga2O3 film growth technology and fabricating high-performance photodetectors.