Owing to the unique mechanism of photoelectron storage and release, long persistent phosphorescence, also called long persistent luminescence or long lasting afterglow/phosphorescence, plays a pivotal role in the areas of spectroscopy, photochemistry, photonics and materials science. In recent years, more research has focused on the manipulation of the morphology, operational wavebands and persistent duration of long persistent phosphors (LPPs). These desired achievements stimulated the growing interest in designing bio-labels, photocatalysts, optical sensors, detectors and photonic devices. In this review, we present multidisciplinary research on synthetic methods, afterglow mechanisms, characterization techniques, materials system, and applications of LPPs. First, we introduce the recent developments in LPPs for the synthesis of nanoparticles from the aspects of particle sizes, monodispersity and homogeneity based on the urgent application of bio-imaging. In the later sections, we present the possible mechanisms, which involve the variation of trap distribution during the trapping and de-trapping process, complicated photo-ionization reaction of trap site levels and impurity centers together with their corresponding migration kinetics of carriers. Meanwhile, we emphasize the characterization techniques of defects, used to qualitatively or quantitatively describe the types, concentrations and depths of the traps. This review article also highlights the recent advances in suggested LPPs materials with a focus on the LPPs' hosts and optically active centers as well as their control, tuning and intrinsic links. We further discuss the classification of LPPs based on the different emission and excitation wavebands from the ultraviolet to the near-infrared region along with an overview of the activation mode of afterglow. Afterwards, we provide an exhibition of new products towards diverse application fields, including solar energy utilization, bio-imaging, diagnosis, and photocatalysts. Finally, we summarize the current achievements, discuss the problems and provide suggestions for potential future directions in the aforementioned parts.

We show that permanent optical waveguides can be formed in various bulk glasses by photoinduced refractive index change with an ultrashort pulse laser. The waveguides were fabricated by focusing the laser beam through an microscope objective and translating the sample parallel to the axis of the laser beam. From the observations of intensity distributions in the output of guided light by a CCD camera, we demonstrated that permanent optical waveguides can be successfully formed in various glasses. In addition, from the analysis of a near-field pattern, it was confirmed that single mode waveguides of the graded index type can be formed by a writing technique using the ultrashort pulse laser.

Low-dimensional (LD) materials demonstrate intriguing optical properties, which lead to applications in diverse fields, such as photonics, biomedicine and energy. Due to modulation of electronic structure by the reduced structural dimensionality, LD versions of metal, semiconductor and topological insulators (TIs) at the same time bear distinct nonlinear optical (NLO) properties as compared with their bulk counterparts. Their interaction with short pulse laser excitation exhibits a strong nonlinear character manifested by NLO absorption, giving rise to optical limiting or saturated absorption associated with excited state absorption and Pauli blocking in different materials. In particular, the saturable absorption of these emerging LD materials including two-dimensional semiconductors as well as colloidal TI nanoparticles has recently been utilized for Q-switching and mode-locking ultra-short pulse generation across the visible, near infrared and middle infrared wavelength regions. Beside the large operation bandwidth, these ultrafast photonics applications are especially benefit from the high recovery rate as well as the facile processibility of these LD materials. The prominent NLO response of these LD materials have also provided new avenues for the development of novel NLO and photonics devices for all-optical control as well as optical circuits beyond ultrafast lasers.

Compact near‐infrared (NIR) light sources with broad emission band are essential to enable NIR spectroscopy compatible with portable devices, and phosphor‐converted light emitting diodes (pc‐LEDs) are efficient, low‐cost, and compact light sources. However, it is more challenging to develop highly efficient and thermally stable broadband NIR phosphors than conventional phosphors for white LEDs. Here, a series of solid solution phosphors with broadband NIR emission designed by cationic substitution in Cr3+ activated garnet Gd3Sc2Ga3O12 are reported. The internal quantum efficiency of Cr3+ emission can be significantly improved to nearly 100% via the substitution of ScO6 with smaller AlO6 octahedrons, which is attributed to the reduction of antisite defects. Moreover, the phosphor with optimized composition shows highly thermally stable emission, which renders the as‐fabricated pc‐LED with high‐power (750.8 mW) NIR emission covering the wavelength range of 700–1000 nm. The results could advance the development of NIR pc‐LEDs as high‐performance light sources for miniature NIR spectrometers.

Broadband infrared luminescence from bismuth-doped germanium oxide glasses prepared by a conventional melting-quenching technique was discovered. The absorption spectrum of the glasses covered a wide range from the visible to the near-infrared wavelength regions and consisted of five broad peaks below 370, 500, 700, 800, and 1000 nm. The fluorescence spectrum exhibited broadband characteristics (FWHM) greater than 300 nm with a maximum at 1300 nm pumped by an 808-nm laser. The fluorescence lifetime at room temperature decreased with increasing Bi2O3 concentration in the glass. Codoping of aluminum and bismuth was indispensable for the broadband infrared luminescence in GeO2:Bi, Al glass.

We report near infrared broadband emission of bismuth-doped barium-aluminum-borate glasses. The broadband emission covers 1.3microm window in optical telecommunication systems. And it possesses wide full width at half maximum (FWHM) of ~200nm and long lifetime as long as 350micros. The luminescent properties are quite sensitive to glass compositions and excitation wavelengths. Based on energy matching conditions, we suggest that the infrared emission may be ascribed to 3P1? 3P0 transition of Bi+. The broad infrared emission characteristics of this material indicate that it might be a promising candidate for broadband optical fiber amplifiers and tunable lasers.

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Ultra‐broadband luminescent sources that emit light over an extremely wide wavelength range are of great interest in the fields of photonics, medical treatment, and precision measurement. Extensive research has been conducted on materials doped with rare‐earth and transition‐metal ions, but the goal of fabricating an ultra‐broadband emitter has not been attained. We present a facile method to realize this kind of novel light source by stabilizing “active” centers (bismuth) in a “tolerant” host (nanoporous silica glass). The obtained highly transparent materials, in which, unusually, multiple bismuth centers (Bi+, Bi2+, and Bi3+) can be stabilized, emit in an ultra‐broadband wavelength range from blue‐green, orange, red, and white to the near‐infrared region. This tunable luminescence covers the spectral range of the traditional three primary colors (RGB) and also the telecommunications windows.