Realization of solid-state red fluorescence and concentration-induced multicolor emission from N,B co-doped carbon dots

As a new type of luminescent material,carbon dots(CDs)have attracted increased attention for their superior optical properties in recent years.However,solidstate fluorescent CDs,especially with red emission,are still a major challenge.Here,CDs with solid-state red emission were synthesized by co-doping of N and B using the one-step microwave method.The CD powder exhibits excitation-independent solid-state red fluorescence without any dispersion matrices,with optimum solid-state fluorescence wavelength of 623 nm.The hydrogen bonding interaction in CDs is helpful for solid-state fluorescence of CDs.The IG/ID value of CDs reaches up to 3.49,suggesting their very high graphitization degree,which is responsible for their red emission.In addition,CDs show the concentration-induced multicolor emission,which is attributed to the decreased energy gap in the high concentrated CD solution.To exploit their concentration-dependent emission,CDs with changing ratio in matrices are applied as a color-converting layer on ultraviolet chip to fabricate multicolor light-emitting diodes with light coordinates of(0.33,0.38),(0.41,0.48),(0.49,0.44),and(0.67,0.33),which belong to green,yellow,orange,and red light,respectively.

Multicolor upconversion reversible modulations in YNbO_(4):Er^(3+)/Tm^(3+)/Yb^(3+) photochromic materials

Photochromic materials with multicolor upconversion reversible modulations are attractive in optical switching devices.Herein,the fabricated YNbO_(4):Er^(3+)/Tm^(3+)/Yb^(3+) materials exhibit excellent photochromism and multicolor upconversion properties from green,red to near infrared(NIR) emissions with increasing Yb concentrations.Reversible multiband upconversion modulations are achieved by alternating light(365 and 405 nm) or thermal stimuli.After 365 nm irradiation,the luminescence color changes from yellow to red,the luminescent photoswitching contrast reaches up to 86.21%(green),82.12%(red) and 77.38%(NIR) in the Y_(0.83)Er_(0.01)Tm_(0.01)NbO_(4):0.15 Yb sample.Besides,the upconversion emission intensity before and after photochromic reaction shows remarkable change in a wide temperature range of 298-718 K.These results indicate that the Er^(3+)/Tm^(3+)/Yb^(3+) tri-doped YNbO_(4) materials can be a good candidate in optical switching and data storage applications.

Design and achieving of multicolor upconversion emission based on rare-earth doped tellurite glasses

yD3＋/Tm3＋ co-doped and yD3＋/Ho3＋/Tm3＋ tri-doped tellurite glasses were synthesized by fusing the mixture of TeO2, PbF2, AIF3, BaF2, Yb2O3, Tm203 and H0203 in a cortmdum crucible at 850 ℃ for 20 min. The synthesized glasses were characterized by upconversion emission spectra under the excitation of 980 nm laser, and the emission colors were investigated according to the CIE-1931 standards. The results indicated that yD3＋/Tm3＋ co-doped tellurite glass exhibited blue upconversion emission with favor- able color coordinates of （0.20, 0.07）. Yb3＋, HO3＋ and Tm3＋ tri-doped tellurite glasses presented white upconversion luminescence under a single 980 nm laser excitation. Moreover, a very wide range of emission colors could be tuned by altering Ho3＋ concentration. Combining the contribution of adjusting Ho3＋ concentration and pump power, near equal energy white light was obtained.

Aggregation-induced emission luminogens and tunable multicolor polymer networks modulated by dynamic covalent chemistry

Aggregation-induced emission(AIE) based luminescent materials are generating intensive interest due to their unique fluorescence in the aggregation state. Herein we report a strategy of dynamic covalent chemistry(DCC) controlled AIE luminogens for the regulation of multicolor emission in reversible covalent polymer networks. Tetraphenylethene derived ring-chain tautomers were prepared, and the emission was readily controlled through multimode, such as changing the solvent, adding the base, and dynamic covalent reactions with amines. Moreover, the construction of dynamic covalent cross-linked luminescent hydrogels with tunable fluorescent, self-healing, and mechanical properties, was realized. The combination of AIE and aggregation-caused quenching(ACQ) fluorophores in the polymer network further enabled the realization of a multicolor modulator, including white emission, in both solution and gel states. The strategies and results presented should find utility in dynamic assemblies, polymer networks, chemical sensing, and responsive materials.

Sandwich-like QDs/MOFs films for selective sensing and multicolor emitting

A novel type sandwich-like composite films composed of ZIF-8 and CdTe QDs were successfully constructed through facile layer-by-layer assembly strategy and their potential applications were also explored.Based on the limitation effects of the aperture of ZIF-8,CdTe QDs/ZIF-8 fluorescent composite films exhibit obvious selective optical response toward hydrogen peroxide and folic acid.Furthermore,tunable colorful light emission composite films in the red-green region are obtained through incorporating two different sized QDs and ZIF-8 films into one composite films.