Optical limiting is an important application of nonlinear optics, useful for the protection of human eyes, optical elements, and optical sensors from intense laser pulses. An optical limiter is such a device that strongly attenuates high intensity light and potentially damaging light such as focused laser beams, whilst allowing for the high transmission of ambient light. Optical limiting properties of carbon nanotube suspensions, solubilized carbon nanotubes, small molecules doped carbon nanotubes and polymer/carbon nanotube composites have been reviewed. The optical limiting responses of carbon nanotube suspensions are shown to be dominated by nonlinear scattering as a result of thermally induced solvent-bubble formation and sublimation of the nanotubes, while the solubilized carbon nanotubes optically limit through nonlinear absorption mechanism and exhibit significant solution-concentration-dependent optical limiting responses. In the former case the optical limiting results are independent of nanotube concentrations at the same linear transmittance as that of the solubilized systems. Many efforts have been invested into the research of polymer/carbon nanotube composites in an attempt to allow for the fabrication of films required for the use of nanotubes in a real optical limiting application. The higher carbon nanotube content samples block the incident light more effectively at higher incident energy densities or intensities. The optical limiting mechanism of these composite materials is quite complicated. Besides nonlinear scattering contribution to the optical limiting, there may also be other contributions e.g., nonlinear absorption, nonlinear refraction, electronic absorption and others to the optical limiting. Further improvements in the optical limiting efficiency of the composites and in the dispersion and alignment properties of carbon nanotubes in the polymer matrix could be realized by variation of both nanostructured guest and polymer host, and by ex situ alignment and other methods. It would be very desirable, from the practical application point of view, if one can design broadband optical limiting chromophores that would function in a multimechanistic fashion.

The emergence of aggregation-induced emission (AIE) has opened up a new avenue for scientists. There is a great demand for the development of a new generation chemiluminescence resonance energy transfer (CRET) acceptors with AIE characteristics due to the aggregation-caused chemiluminescence (CL) quenching effect commonly observed in the conventional fluorophore CL acceptors at high concentrations. However, the systematical studies involving in AIE-amplified CL are still scarce. Herein, it is the first report that the gold nanocluster aggregates (a type of well-defined AIE molecules) are used to study their influence on the bis(2,4,6-trichlorophenyl) oxalate (TCPO)-H2O2 CL reaction. Interestingly, the AIE molecules in the diluted solution are unable to boost the CL signal of the TCPO-H2O2 system, but their aggregates display a strongly enhanced CL emission compared to their counterparts of fluorophore molecules, thanks to the unique AIE effect of gold nanoclusters. In comparison to rhodamine B with the aid of an imidazole catalyst, the detection limit of the gold nanocluster aggregate-amplified CL probe for H2O2 (S/N = 3) is low in the absence of any catalyst. Finally, the other two typical AIE molecules, Au(I)-thiolate complexes and 9,10-bis[4-(3-sulfonatopropoxyl)-styryl]anthracene (BSPSA), are investigated to verify the generality of the AIE molecule-amplified CL emissions. These results demonstrate effective access to highly fluorescent AIE molecules with practical applications in avoiding the aggregation-induced CL quenching at high concentrations, which can be expected to provide a novel and sensitive platform for the CL amplified detection.

Phthalocyanines (Pcs) usually exhibit stronger optical limiting response that can be used to protect human eyes, optical elements, and sensors from intense laser pulses. New unsymmetrically substituted metal-free phthalocyanine-covalently functionalized multiwalled carbon nanotubes (PcH 2 -MWNTs), in which the wt % of MWNTs in the resulting product was found to be 35%, were synthesized. A considerably quenching of the fluorescence intensity was found in the photoluminescence spectrum of PcH 2 -MWNTs. This observation suggests a quenching of the singlet excited PcH 2 by the covalently linked MWNTs. This material exhibits strong scattering at higher intensities, which evidently comes from the MWNT counterpart. The nonlinear response of tBu 3 NH 2 PcH 2 is due to reverse saturable absorption (RSA), while that of PcH 2 -MWNTs is due to both RSA and nonlinear scattering, which could be two conflicted mechanisms for optical limiting, giving rise to suppression of the whole nonlinear response of PcH 2 -MWNTs.

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