Compositing gold nanoparticles into conjugated molecules have been developed to be one of the most important approaches to increase stability, since degradation of conjugated materials is now one of the biggest bottle-necks to be conquered before industrialization application. Big-size colloidal gold nanoparticles with strong surface plasma resonance are designed to composite with conjugated molecules, in order to realize effective fluorescence enhancement and stabilization. The uniform composition film of hydrophilic colloidal gold nanoparticles (particle diameter of 30 nm) and hydrophobic carbazole functionalized fluorene trimers has been obtained by direct mixing of their aqueous and THF solutions, which is determined by AFM. By the comparison of composition based on fluorene trimers with similar structures, we have found that peripheral carbazole group and molecular size of fluorene trimers play an important role in the balance of incompatible solubility, which is regarded as increasing solubility of fluorene trimers in mixed solvent, connecting AuNP and peripheral carbazole groups, and restraining aggregate of gold nanoparticle. This allows facile hydrophilic gold nanoparticle to disperse uniformly in hydrophobic-conjugated host. Our investigations show that fluorescence intensity of composition film is enhanced by 4 folds, and heat treatment (200°C for 4h) for the composition film does not induce the degradation of conjugated backbone without the appearance of low-energy emission band, demonstrating the prominent potency of gold nanoparticles in enhanced fluorescence and stability of conjugated molecules and polymers.
Organic light-emitting diodes （OLEDs） have been extensively studied since the first efficient device based on small molecular luminescent materials was reported by Tang. Organic electroluminescent material, one of the centerpieces of OLEDs, has been the focus of studies by many material scientists. To obtain high luminosity and to keep material costs low, a few remarkable design concepts have been developed. Aggregation-induced emission （AIE） materials were invented to overcome the common fluorescence-quenching problem, and cross-dipole stacking of fluorescent molecules was shown to be an effective method to get high solid-state luminescence. To exceed the limit of internal quantum efficiency of conventional fluorescent materials, phosphorescent materials were successfully applied in highly efficient electroluminescent devices. Most recently, delayed flu- orescent materials via reverse-intersystem crossing （RISC） from triplet to singlet and the ＂hot exciton＂ materials based on hy- bridized local and charge-transfer （HLCT） states were developed to he a new generation of low-cost luminescent materials as efficient as phosphorescent materials. In terms of the device-fabrication process, solution-processible small molecular lumi- nescent materials possess the advantages of high purity （vs. polymers） and low procession cost （vs. vacuum deposition）, which are garnering them increasing attention. Herein, we review the progress of the development of small-molecule luminescent materials with different design concepts and features, and also briefly examine future development tendencies of luminescent materials.
