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This study developed a novel frequency-doubled Fabry–Perot cavity method based on a femtosecond laser of 1030 nm, 190 fs, 1 mJ, and 1 kHz. The time interval (60–1000 ps) and attenuation ratio (0.5–0.9) between adjacent sub-pulses of the 515 nm pulse train were able to be easily adjusted, while the efficiency was up to 50% and remained unchanged. Extremely high-quality low-spatial-frequency LIPSS (LSFL) was efficiently fabricated on an indium tin oxide (ITO) film using a pulse train with a time interval of 150 ps and attenuation ratio of 0.9 focused with a cylindrical lens. Compared with the LSFL induced by the primary Gaussian pulse, the uniformity of the LSFL period was enhanced from 481 ± 41 nm to 435 ± 8 nm, the divergence of structural orientation angle was reduced from 15.6° to 3.7°, and the depth was enhanced from 74.21 ± 14.35 nm to 150.6 ± 8.63 nm. The average line edge roughness and line height roughness were only 7.34 nm and 2.06 nm, respectively. The depths and roughness values were close to or exceeded those of resist lines made by the interference lithography. Compared with the common Fabry–Perot cavity, the laser energy efficiency of the pulse trains and manufacturing efficiency were enhanced by factors of 19 and 25. A very colorful "lotus" pattern with a size of 30×28 mm2 was demonstrated, which was covered with high-quality LSFLs fabricated by a pulse train with optimized laser parameters. Pulse trains can efficiently enhance and prolong the excitation of surface plasmon polaritons, inhibit deposition particles, depress ablation residual heat and thermal shock waves, and eliminate high-spatial-frequency LIPSS formed on LSFL, therefore, producing extremely high-quality LSFL on ITO films. [ABSTRACT FROM AUTHOR]

Using low-density solar energy in the environment and converting it into chemical energy that can drive the degradation of organic pollutants is considered to be a very promising strategy for solving the problem of environmental pollution. The efficacy of photocatalytic destruction of organic contaminants is nonetheless constrained by the high composite rate of photogenic carriers, insufficient light absorption and utilization impact, and sluggish charge transfer rate. In this work, we created a new type of heterojunction photocatalyst with a spherical Bi2Se3/Bi2O3@Bi core–shell structure and investigated its degrading properties of organic pollutants in the environment. Interestingly, benefiting from the fast electron transfer capability of the Bi0 electron bridge, the charge separation and transfer efficiency between Bi2Se3 and Bi2O3 is greatly improved. In this photocatalyst, Bi2Se3 not only has a photothermal effect to speed up the process of photocatalytic reaction, but also has fast electrical conductivity of topological materials at the surface, which speeds up the transmission efficiency of photogenic carriers. As expected, the removal performance of the Bi2Se3/Bi2O3@Bi photocatalyst to atrazine is 4.2 and 5.7 times higher than that of the original Bi2Se3 and Bi2O3. Meanwhile, the best samples Bi2Se3/Bi2O3@Bi showed 98.7%, 97.8%, 69.4%, 90.6%, 91.2%, 77.2%, 97.7%, and 98.9% removal of ATZ, 2,4-DCP, SMZ, KP, CIP, CBZ, OTC-HCl, and RhB, and 56.8%, 59.1%, 34.6%, 34.5%, 37.1%, 73.9%, and 78.4% mineralization. Through characterization such as XPS and electrochemical workstations, it is proved that the photocatalytic properties of Bi2Se3/Bi2O3@Bi catalysts are far superior to other materials, and a suitable photocatalytic mechanism is proposed. A novel form of bismuth-based compound photocatalyst is anticipated to be produced as a result of this research in order to address the increasingly critical problem of environmental water pollution in addition to presenting fresh avenues for the creation of adaptable nanomaterials for additional environmental applications. [ABSTRACT FROM AUTHOR]