Self-quenching in the aggregation state is overcome, and tunable solid-state photoluminescence of carbon-dot powder is achieved. Furthermore, based on the controllable optical property in organic solvents, a novel concept, i.e., constructing dual-fluorescence morphologies from single luminescent species, is presented to realize white-light emission.

Carbon dots (CDs) have been studied for years as one of the most promising fluorescent nanomaterials. However, CDs with red or solid-state fluorescence are rarely reported. Herein, through a one-pot solvothermal treatment, hydrophobic CDs (H-CDs) with blue dispersed emission and red aggregation-induced emission are obtained. When water is introduced, the hydrophobic interaction leads to aggregation of the H-CDs. The formation of H-CD clusters induces the turning off of the blue emission, as the carbonized cores suffer from π-π stacking interactions, and the turning on of the red fluorescence, due to restriction of the surfaces’ intramolecular rotation around disulfide bonds, which conforms to the aggregation-induced-emission phenomenon. This on-off fluorescence of the H-CDs is reversible when the H-CD powder is completely dissolved. Moreover, the H-CD solution dispersed in filter paper is nearly colorless. Finally, we develop a reversible two switch-mode luminescence ink for advanced anti-counterfeiting and dual-encryption.

Carbon dots (CDs) have attracted attention in metal‐free afterglow materials, but most CDs were heteroatom‐containing and the afterglow emissions are still limited to the short‐wavelength region. A universal approach to activate the room‐temperature phosphorescence (RTP) of both heteroatom‐free and heteroatom‐containing CDs was developed by one‐step heat treatment of CDs and boric acid (BA). The introduction of an electron‐withdrawing boron atom in composites can greatly reduce the energy gap between the singlet and triplet state; the formed glassy state can effectively protect the excited triplet states of CDs from nonradiative deactivation. A universal host for embedding CDs to achieve long‐lifetime and multi‐color (blue, green, green‐yellow and orange) RTP via a low cost, quick and facile process was developed. Based on their distinctive RTP performances, the applications of these CD‐based RTP materials in information encryption and decryption are also proposed and demonstrated.

Enhancing solar energy conversion is imperative and maximizing solar energy capture remains significant. Here, nanotechnology toward engineering hybrid photosystem involving biological photosynthetic chloroplasts and dualemissive carbon dots (CDs) is employed for improved photosynthesis by harnessing more effective light. Specifically, the as-prepared CDs show strong absorption in ultraviolet (UV) light region and exhibit intense blue and red light in water, which exactly match the absorption spectrum of chloroplasts. After coating the CDs on the surface of extracted chloroplasts, the hybrid photosystem produces 2.8 times more adenosine triphosphate (ATP) than chloroplasts themselves in vitro. Moreover, CD-induced enhancement of photosynthesis in living plant is proved as well, showing a maximum increase of 25% in electron transport rates over the leaves without CDs, demonstrating the effective nanobionics engineering of plant performance in vivo. This is the first report on employing the unique dual-emission trait of nanoparticles, especially the red emission, to augment photoabsorption of both extracted chloroplasts and intact leaves for enhanced photosynthetic properties. This work provides a promising strategy for engineering biological photosynthetic system with dual-emissive CDs to enhance solar energy conversion both in vivo and in vitro, and promotes the development in the field of nanobionic.

Compared to fluorescence imaging with short-lived emissive probes, the use of phosphorescent probes conveys the advantage of long signal persistance in time and this permits one to discriminate against interference from autofluorescence. However, the realization of room temperature phosphorescence (RTP) probes that feature ultralong emission lifetimes in aqueous solution is still a challenge. Here, we present a rational strategy for realizing ultralong RTP in air-saturated aqueous media from carbon dot-based silica composites (CDs@SiO2) which feature emission lifetimes as long as 1.64 s. The excellent phosphorescence properties, their small size, and their water solubility make CDs@SiO2 a promising material for biological imaging application. We demonstrate their use as efficient reporters both in plant tissue and in animal cells where strong autofluorescence poses a severe challenge for conventional, short-lifetime probes.