High-efficiency narrowband emission is always in the central role of organic optoelectronic display applications. However, the development of organic afterglow materials with sufficient color purity and high quantum efficiency for hyperafterglow is still great challenging due to the large structural relaxation and severe non-radiative decay of triplet excitons. Here we demonstrate a simple yet efficient strategy to achieve hyperafterglow emission through sensitizing and stabilizing isolated fluorescence chromophores by integrating multi-resonance fluorescence chromophores into afterglow host in a single-component copolymer. Bright multicolor hyperafterglow with maximum photoluminescent efficiencies of 88.9%, minimum full-width at half-maximums (FWHMs) of 38 nm and ultralong lifetimes of 1.64 s under ambient conditions are achieved. With this facilely designed polymer, a large-area hyperafterglow display panel was fabricated. By virtue of narrow emission band and high luminescent efficiency, the hyperafterglow presents a significant technological advance in developing highly efficient organic afterglow materials and extends the domain to new applications.

Graphene is a new type of carbon material with a flexible, two-dimensional structure. Due to the excellent stability of its lattice structure and its mechanical flexibility, graphene-based materials can be applied in flexible humidity sensors. At present, the application of graphene-based flexible humidity sensors in the fields of medical care and environmental monitoring is attracting widespread attention. In this review, the basic properties of graphene oxide (GO) and reduced graphene oxide (rGO) as moisture-sensitive materials and methods for their preparation were introduced. Moreover, three methods for improving the performance of moisture-sensitive materials were discussed. The working principle of different types of graphene-based humidity sensors were introduced. The progress in the research on graphene-based flexible humidity sensors in four respects: Human respiration, skin moisture, human sweat, and environmental humidity were discussed. Finally, the future research, following the development trends and challenges, to develop the potential of integrated, graphene-based flexible humidity sensors were discussed.

The development of stimuli-responsive materials with afterglow emission is highly desirable but remains a formidable challenge in a single-component material system. Herein, we propose a strategy to achieve photoactivated afterglow emission in a variety of amorphous copolymers through self-doping, endowed by the synergetic effect of self-host-induced guest sensitization and thermal-processed polymer rigidification for boosting the generation and stabilization of triplet excitons. Upon continuous ultraviolet illumination for regulating the oxygen concentration, a photoactivated afterglow showing increased lifetimes from 0.34 to 867.4 ms is realized. These afterglow emissions can be naturally or quickly deactivated to the pristine state under ambient conditions or heating treatment. Interestingly, programmable and reusable afterglow patterns, conceptual pulse-width indicators, and “excitation-time lock” Morse code are successfully established using stimuli-responsive afterglow polymers as recorded media. These findings offer an avenue to construct a single-component polymeric system with photoactivated organic afterglow features and demonstrate the superiority of stimuli-responsive materials for remarkable applications.

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