White light, which contains polychromic visible components, affects the rhythm of organisms and has the potential for advanced applications of lighting, display, and communication. Compared with traditional incandescent bulbs and inorganic diodes, pure organic materials are superior in terms of better compatibility, flexibility, structural diversity, and environmental friendliness. In the past few years, polychromic emission has been obtained based on organic aggregates, which provides a platform to achieve white-light emission. Several white-light emitters are sporadically reported, but the underlying mechanistic picture is still not fully established. Based on these considerations, we will focus on the single-component and multicomponent strategies to achieve efficient white-light emission from pure organic aggregates. Thereinto, single-component strategy is introduced from four parts: dual fluorescence, fluorescence and phosphorescence, dual phosphorescence with anti-Kasha’s behavior, and clusteroluminescence. Meanwhile, doping, supramolecular assembly, and cocrystallization are summarized as strategies for multicomponent systems. Beyond the construction strategies of white-light emitters, their advanced representative applications, such as organic light-emitting diodes, white luminescent dyes, circularly polarized luminescence, and encryption, are also prospected. It is expected that this review will draw a comprehensive picture of white-light emission from organic aggregates as well as their emerging applications.

Broadband Raman spectroscopy (detection bandwidth >1000 cm ^{- 1}) is a valuable and widely used tool for understanding samples via label-free measurements of their molecular vibrations. Two important Raman spectral regions are the chemically specific “fingerprint” (200 to 1800 cm ^{- 1}) and “low-frequency” or “terahertz” (THz) (<200 cm ^{- 1}; <6 THz) regions, which mostly contain intramolecular and intermolecular vibrations, respectively. These two regions are highly complementary; broadband simultaneous measurement of both regions can provide a big picture comprising information about molecular structures and interactions. Although techniques for acquiring broadband Raman spectra covering both regions have been demonstrated, these methods tend to have spectral acquisition rates <10 spectra / s, prohibiting high-speed applications, such as Raman imaging or vibrational detection of transient phenomena. Here, we demonstrate a single-laser method for ultrafast (24,000 spectra / s) broadband Raman spectroscopy covering both THz and fingerprint regions. This is achieved by simultaneous detection of Sagnac-enhanced impulsive stimulated Raman scattering (SE-ISRS; THz-sensitive) and Fourier-transform coherent anti-Stokes Raman scattering (FT-CARS; fingerprint-sensitive). With dual-detection impulsive vibrational spectroscopy, the SE-ISRS signal shows a >500 × enhancement of <6.5 THz sensitivity compared with that of FT-CARS, and the FT-CARS signal shows a >10 × enhancement of fingerprint sensitivity above 1000 cm ^{- 1} compared with that of SE-ISRS.