Secret information recorded by traditional single-encrypted invisible inks is easily cracked because the inks can switch only between “NONE” and “TRUTH”. Developing double-encrypted systems makes the information reversibly switchable between “FALSE” and “TRUTH”, which is helpful to ensure the safety of the secret information during transport. Here, we prepared heat-developed invisible inks by hydrochromic molecules donor–acceptor Stenhouse adducts (DASAs) and oxazolidines (OXs) and promoted the invisible inks from single to double encryption. DASAs coordinate with water molecules and form stable colorless cyclic DASA·xH2O molecules, which lose coordinated water molecules after heating and switch to colored linear DASAs. In contrast, OXs are colored with water and are colorless after heating. Single-encrypted secrecy was realized by DASA invisible inks. The information is invisible under the encrypted state and becomes bright purple after heating. Vapor treating re-encrypted the information in ∼5 min. Furthermore, the single-encryption was promoted to double-encryption by a DASA/OX invisible inks system. Heating and vapor treating switch the information between the “FALSE” and “TRUTH” reversibly. The DASA/OX invisible ink system is applied for secrecy of texts, graphic images, and quick response (QR) codes.

Light is not the only stimulus that can induce linear-to-cyclic isomerization of donor-acceptor Stenhouse adducts (DASAs). Here we demonstrate the water-induced linear-to-cyclic isomerization of DASAs. The mechanism of the water-induced linear-to-cyclic isomerization of DASAs is investigated by density functional theory (DFT) calculations. Water molecules coordinate with DASAs and stabilize the intermediates and cyclic isomers, which favors cyclization thermodynamically. Moreover, the linear-to-cyclic isomerization is reversible. Heating removes the coordinated H 2 O molecules, which further triggers cyclic-to-linear isomerization. DASAs have been applied in information hiding/displaying and color switching under water vapor and heating control.

Conventional photosensitizers (PSs) often show poor tumor retention and are rapidly cleared from the bloodstream, which is one of the key hindrances to guarantee precise and efficient photodynamic therapy (PDT) in vivo. In this work, a photosensitizer assembly nanosystem that sharply enhances tumor retention up to ≈10 days is present. The PSs are synthesized by meso‐substituting anthracene onto a BODIPY scaffold (AN‐BDP), which then self‐assembles into stable nanoparticles (AN‐BDP NPs) with amphiphilic block copolymers due to the strong intermolecular π–π interaction of the anthracene. Additionally, the incorporated anthracene excites the PSs, producing singlet oxygen under red‐light irradiation. Although AN‐BDP NPs can completely suppress regular test size tumors (≈100 mm3) by one‐time radiation, only 12% tumor growth inhibition rate is observed in the case of large‐size tumors (≈350 mm3) under the same conditions. Due to the long‐time tumor retention, AN‐BDP NPs allow single‐dose injection and three‐time light treatments, resulting in an inhibition rate over 90%, much more efficient than single‐time radiation of conventional clinically used PSs including chlorin‐e6 (Ce6) and porphyrin with poor tumor retention. The results reveal the importance of long tumor retention time of PSs for efficient PDT, which can accelerate the clinical development of nanophotosensitizers.

Rewritable paper is meaningful to the recyclable and sustainable utilization of environmental resources and thus has been extensively investigated for several decades. In this work, we demonstrated an efficient and convenient strategy to fabricate rewritable paper based on reversible hydrochromism of donor−acceptor Stenhouse adducts (DASAs). The kinetics and efficiency of isomerization could be well-controlled by adjusting the surrounding temperature and humidity. Monocolored rewritable paper was prepared by coating cyclic DASA• xH 2 O on the paper surface. Writing, printing, stamping and patterning were realized on the rewritable paper. The information could be controllably erased by treatment in a humid atmosphere. More importantly, the rewritable paper was upgraded to multicolored by combination of two DASA materials. The color of chirography was switched by controlling the writing speed.

One key limitation of artificial skin-like materials is the shortened service life caused by mechanical damages during practical applications. The ability to self-heal can effectively extend the material service life, reduce the maintenance cost, and ensure safety. Therefore, it is important and necessary to fabricate materials with simultaneously mechanical and electrical self-healing behavior in a facile and convenient way. Herein, we report a stretchable and conductive self-healing elastomer based on intermolecular networks between poly(acrylic acid) (PAA) and reduced graphene oxide (rGO) through a facile and convenient postreduction and one-pot method. The introduction of rGO provides the PAA-GO elastomers with good mechanical stability and electrical properties. Moreover, this material exhibited both electrical and mechanical self-healing properties. After cutting, the elastomers self-healed quickly (∼30 s) and efficiently (∼95%) at room temperature. The elastomers were accurate and reliable in detecting external strain even after healing. The elastomers were further applied for strain sensors, which were attached directly to human skin to monitor external movements, including finger bending and wrist twisting.

Conventional photocages only respond to short wavelength light, which is a significant obstacle to developing efficient phototherapy in vivo. The development of photocages activated by near-infrared (NIR) light at wavelengths from 700 to 950 nm is important for in vivo studies but remains challenging. Herein, we describe the synthesis of a photocage based on a ruthenium (Ru) complex with NIR light-triggered photocleavage reaction. The commercial anticancer drug, tetrahydrocurcumin (THC), was coordinated to the Ru II center to create the Ru-based photocage that is readily responsive to NIR light at 760 nm. The photocage inherited the anticancer properties of THC. As a proof-of-concept, we further engineered a self-assembled photocage-based nanoparticle system with amphiphilic block copolymers. Upon exposure to NIR light at 760 nm, the Ru complex-based photocages were released from the polymeric nanoparticles and efficiently inhibited tumor proliferation in vivo.

We demonstrated that introducing hydrogen bonds is a promising strategy to fabricate high performance and stable organic solar cells.

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