Undoped ZnO, Ce-doped ZnO, and (Li, Ce)-codoped ZnO nanophosphors were prepared by a sol-gel process. The effects of the additional doping with Li ions on the crystal structure, particle morphology, and luminescence properties of Ce-doped ZnO were investigated by X-ray diffraction, scanning electron microscopy, X-ray photoelectron spectroscopy, electron paramagnetic resonance spectroscopy and photoluminescence spectroscopy. The results indicate that the obtained samples are single phase, and a nanorod shaped morphology is observed for (Li, Ce)-codoping. Under excitation with 325 nm light, Ce-doped ZnO phosphors show an ultraviolet emission, a green emission, and a blue emission caused by Zn interstitials. The spectrum of the sample codoped with a proper Li concentration features two additional emissions that can be attributed to the Ce3+ ions. With the increase of the Li doping concentration, the Ce3+ blue luminescence of (Li, Ce)-codoped ZnO is obviously enhanced, which results not only from the increase of the Ce3+ ion concentration itself but also from the energy transfer from the ZnO host material to the Ce3+ ions. This enhancement reaches a maximum at a Li content of 0.02, and then decreases sharply due to the concentration quench. These nanophosphors may promise for application to the visible-light-emitting devices.

Organic materials exhibit efficient light absorption and low‐temperature, large‐scale processability, and have stimulated enormous research efforts for next‐generation optoelectronics. While, high‐performance organic devices with fast speed and high responsivity still face intractable challenges, due to their intrinsic limitations including finite carrier mobility and high exciton binding energy. Here an ultrafast and highly sensitive broadband phototransistor is demonstrated by integrating high‐quality pentacene single crystal with monolayer graphene. Encouragingly, the −3 dB bandwidth can reach up to 26 kHz, which is a record‐speed for such sensitized organic phototransistors. Enormous absorption, long exciton diffusion length of pentacene crystal, and efficient interfacial charge transfer enable a high responsivity of >10⁵ A W⁻¹ and specific detectivity of >10¹¹ Jones. Moreover, self‐powered weak‐light detection is realized using a simple asymmetric configuration, and the obvious zero‐bias photoresponses can be displayed even under 750 nW cm⁻² light intensity. Excellent response speed and photoresponsivity enable high‐speed image sensor capability in UV‐Vis ranges. The results offer a practical strategy for constructing high‐performance self‐powered organic hybrid photodetectors, with strong applicability in wireless, weak‐light detection, and video‐frame‐rate imaging applications.

Lanthanide materials have great applications in optical communication, biological fluorescence imaging, laser, and so on, due to their narrow emission bandwidths, large Stokes’ shifts, long emission lifetimes, and excellent photo-stability. However, the photon absorption cross-section of lanthanide ions is generally small, and the luminescence efficiency is relatively low. The effective improvement of the lanthanide-doped materials has been a challenge in the implementation of many applications. The local surface plasmon resonance (LSPR) effect of plasmonic nanoparticles (NPs) can improve the luminescence in different aspects: excitation enhancement induced by enhanced local field, emission enhancement induced by increased radiative decay, and quenching induced by increased non-radiative decay. In addition, plasmonic NPs can also regulate the energy transfer between two close lanthanide ions. In this review, the properties of the nanocomposite systems of lanthanide material and plasmonic NPs are presented, respectively. The mechanism of lanthanide materials regulated by plasmonic NPs and the scientific and technological discoveries of the luminescence technology are elaborated. Due to the large gap between the reported enhancement and the theoretical enhancement, some new strategies applied in lanthanide materials and related development in the plasmonic enhancing luminescence are presented.

Organic single crystals (OSCs) have attracted increasing interest in advanced optoelectronic devices, in particular for flexible and wearable devices, due to their high carrier mobility and intrinsic mechanical flexibility.

Organic light-emitting diodes (OLEDs) are widely recognized as the forefront technology for displays and lighting technology. Now, the global OLED market is nearly mature, driven by the rising demand for superior displays in smartphones. In recent years, numerous strategies have been introduced and demonstrated to optimize the hole injection layer to further enhance the efficiency of OLEDs. In this paper, different methods of optimizing the hole injection layer were elucidated, including using a suitable hole injection material to minimize the hole injection barrier and match the energy level with the emission layer, exploring new preparation methods to optimize the structure of hole injection layer, and so on. Meanwhile, this article can help people to understand the current research progress and the challenges still faced in relation to the hole injection layer in OLEDs, providing future research directions to enhance the properties of OLEDs.