Two-dimensional (2D) Sn-based perovskites are a kind of non-toxic environment-friendly luminescent material. However, the research on the luminescence mechanism of this type of perovskite is still very controversial, which greatly limits the further improvement and application of the luminescence performance. At present, the focus of controversy is defects and phonon scattering rates. In this work, we combine the organic cation control engineering with temperature-dependent transient absorption spectroscopy to systematically study the interband exciton relaxation pathways in layered A₂SnI₄ (A = PEA⁺, BA⁺, HA⁺, and OA⁺) structures. It is revealed that exciton-phonon scattering and exciton-defect scattering have different effects on exciton relaxation. Our study further confirms that the deformation potential scattering by charged defects, not by the non-polar optical phonons, dominates the excitons interband relaxation, which is largely different from the Pb-based perovskites. These results enhance the understanding of the origin of the non-radiative pathway in Sn-based perovskite materials.

A comparative research on saturable absorption (SA) behavior dependence on wavelength and pulse duration was performed for graphene polymer composites. Free-standing graphene-polyvinyl alcohol (PVA) composite films were fabricated by using solution cast method in combination of liquid phase exfoliation. SA responses were observed by using an open-aperture Z-scan technique for 340 fs pulses at 1030 nm and 515 nm from a mode-locked fiber laser, and 6 ns pulses at 1064 nm and 532 nm from a Q-switched Nd:YAG laser. The graphene films possess better SA property, i.e., larger SA coefficient and figure of merit (FOM), and lower saturation intensity I_s, for ns pulses than that for fs pulses at the similar near infrared (NIR) wavelength. For fs pulses, the films show better SA response at 1030 nm than that at 515 nm. By employing slow and fast SA modelling, the excited state and ground state absorption cross sections were estimated to be ~10⁻¹⁷ cm², and the ratio was ~0.6 at NIR for both fs and ns pulses.

Novel donor–acceptor blends composed of black phosphorus (BP) and C ₆₀ are embedded into a transparent poly(methylmethacrylate) (PMMA) matrix to form a BP:C ₆₀ /PMMA film. In contrast to C ₆₀ , BP and BP:C ₆₀ blends, annealed BP:C ₆₀ blends show a significantly enhanced optical limiting response.

Nonlinear scattering, originating from laser induced solvent micro-bubbles and/or micro-plasmas, is regarded as the principal mechanism for nonlinear optical (NLO) response of graphene dispersions at ns timescale. In this work, we report the significant enhancement of NLO response of graphene dispersions by decreasing the atmospheric pressure, which has strong influence on the formation and growth of micro-bubbles and/or micro-plasmas. A modified open-aperture Z-scan apparatus in combination with a vacuum system was used to study the effect of vacuum pressure on the NLO property of graphene dispersions prepared by liquid-phase exfoliation technique. We show that the atmospheric pressure can be utilized to control and tune the nonlinear responses of the graphene dispersions for ns laser pulses at both 532 nm and 1064 nm. The lower the vacuum pressure was, the larger the NLO response was. In contrast, the NLO property of fullerene was found to be independent of the pressure change, due to its nature of nonlinear absorption. This work affords a simple method to distinguish the nonlinear scattering and absorption mechanisms for NLO nanomaterials.

Highly soluble polyacrylonitrile (PAN)-covalently grafted MoS ₂ nanosheets (MoS ₂ –PAN) were synthesized in situ . This material shows superior optical limiting response in the visible and near-infrared ranges.