The photocurrent conversions of transition metal dichalcogenide nanosheets are unprecedentedly impressive, making them great candidates for visible range photodetectors. Here we demonstrate a method for fabricating micron-thick, flexible films consisting of a variety of highly separated transition metal dichalcogenide nanosheets for excellent band-selective photodetection. Our method is based on the non-destructive modification of transition metal dichalcogenide sheets with amine-terminated polymers. The universal interaction between amine and transition metal resulted in scalable, stable and high concentration dispersions of a single to a few layers of numerous transition metal dichalcogenides. Our MoSe2 and MoS2 composites are highly photoconductive even at bending radii as low as 200 μm on illumination of near infrared and visible light, respectively. More interestingly, simple solution mixing of MoSe2 and MoS2 gives rise to blended composite films in which the photodetection properties were controllable. The MoS2/MoSe2 (5:5) film showed broad range photodetection suitable for both visible and near infrared spectra.

Application of a multilayer Molybdenum Disulfide (MoS2) thin film as a saturable absorber was experimentally demonstrated by realizing a stable and robust passive mode-locked fiber laser via the evanescent field interaction between the light and the film. The MoS2 film was grown by chemical vapor deposition, and was then transferred to a side polished fiber by a lift-off method. Intensity-dependent optical transmission through the MoS2 thin film on side polished fiber was experimentally observed showing efficient saturable absorption characteristics. Using erbium doped fiber as an optical gain medium, we built an all-fiber ring cavity, where the MoS2 film on the side polished fiber was inserted as a saturable absorber. Stable dissipative soliton pulse trains were successfully generated in the normal dispersion regime with a spectral bandwidth of 23.2 nm and the pulse width of 4.98 ps. By adjusting the total dispersion in the cavity, we also obtained soliton pulses with a width of 637 fs in the anomalous dispersion regime near the lasing wavelength λ = 1.55 μm. Detailed and systematic experimental comparisons were made for stable mode locking of an all-fiber laser cavity in both the normal and anomalous regimes.

A new extraordinary application of deoxyribonucleic acid (DNA) thin-solid-film was experimentally explored in the field of ultrafast nonlinear photonics. Optical transmission was investigated in both linear and nonlinear regimes for two types of DNA thin-solid-films made from DNA in aqueous solution and DNA-cetyltrimethylammonium chloride (CTMA) in an organic solvent. Z-scan measurements revealed a high third-order nonlinearity with n2 exceeding 10−9 at a wavelength of 1570 nm, for a nonlinarity about five orders of magnitude larger than that of silica. We also demonstrated ultrafast saturable absorption (SA) with a modulation depth of 0.43%. DNA thin solid films were successfully deposited on a side-polished optical fiber, providing an efficient evanescent wave interaction. We built an organic-inorganic hybrid all-fiber ring laser using DNA film as an ultrafast SA and using Erbium-doped fiber as an efficient optical gain medium. Stable transform-limited femtosecond soliton pulses were generated with full width half maxima of 417 fs for DNA and 323 fs for DNA-CTMA thin-solid-film SAs. The average output power was 4.20 mW for DNA and 5.46 mW for DNA-CTMA. Detailed conditions for DNA solid film preparation, dispersion control in the laser cavity and subsequent characteristics of soliton pulses are discussed, to confirm unique nonlinear optical applications of DNA thin-solid-film.