Developing novel long-lived room-temperature polymer phosphorescence (RTPP) materials could significantly expand their application scope. Herein, a series of RTPP materials based on eight simple vanilla derivatives for security ink application are reported. Attributed to strong mutual hydrogen bonding with polyvinyl alcohol (PVA) matrix, vanilla-doped PVA films exhibit ultralong phosphorescence emission under ambient conditions observed by naked eyes, where methyl vanillate shows the longest emission time up to 7 s. Impressively, when vanilla-doped PVA materials are utilized as invisible security inks, and the inks not only present excellent luminescent emission stability under ambient conditions but also maintain perfect reversibility between room temperature and 65°C for multiple cycles. Owing to the unique RTPP performance, an advanced anticounterfeiting data encoding/reading strategy based on handwriting technology and complex pattern steganography is developed.

Solar-driven photocatalytic regeneration of cofactors, including reduced nicotinamide adenine dinucleotide (NADH), reduced nicotinamide adenine dinucleotide phosphate (NADPH), and reduced flavin adenine dinucleotide (FADH₂), could ensure the sustainable energy supply of enzymatic reactions catalyzed by oxidoreductases for the efficient synthesis of chemicals. However, the elevation of cofactor regeneration efficiency is severely hindered by the inefficient utilization of electrons transferred on the surface of photocatalysts. Inspired by the phenomenon of ferredoxin-NADP⁺ reductase (FNR) anchoring on thylakoid membrane, herein, a homogeneous catalyst of rhodium (Rh) complex, [Cp\astRh(bpy)H₂O]²⁺, was anchored on polymeric carbon nitride (PCN) mediated by a tannic acid/polyethyleneimine (TA/PEI) adhesive layer, acquiring PCN@TA/PEI-Rh core@shell photocatalyst. Illuminated by visible light, electrons were excited from the PCN core, then transferred through the TA/PEI shell, and finally captured by the surface-anchored Rh for instant utilization during the regeneration of NADH. The TA/PEI-Rh shell could facilitate the electron transfer from the PCN core and, more importantly, achieved ~1.3-fold elevation of electron utilization efficiency compared with PCN. Accordingly, the PCN@TA/PEI-Rh afforded the NADH regeneration efficiency of 37.8% after 20 min reaction under LED light (405 nm) illumination, over 1.5 times higher than PCN with free Rh. Coupling of the NADH regeneration system with formate dehydrogenase achieved continuous production of formate from carbon dioxide (CO₂). Our study may provide a generic and effective strategy to elevate the catalytic efficiency of a photocatalyst through intensifying the electron utilization.

The developing flexible electronic equipment are greatly affected by the rapid accumulation of heat, which is urgent to be solved by thermally conductive polymer composite films. However, the interfacial thermal resistance (ITR) and the phonon scattering at the interfaces are the main bottlenecks limiting the rapid and efficient improvement of thermal conductivity coefficients (\lambda) of the polymer composite films. Moreover, few researches were focused on characterizing ITR and phonon scattering in thermally conductive polymer composite films. In this paper, graphene oxide (GO) was aminated (NH₂-GO) and reduced (NH₂-rGO), then NH₂-rGO/polyimide (NH₂-rGO/PI) thermally conductive composite films were fabricated. Raman spectroscopy was utilized to innovatively characterize phonon scattering and ITR at the interfaces in NH₂-rGO/PI thermally conductive composite films, revealing the interfacial thermal conduction mechanism, proving that the amination optimized the interfaces between NH₂-rGO and PI, reduced phonon scattering and ITR, and ultimately improved the interfacial thermal conduction. The in-plane \lambda ({\lambda }_{\parallel }) and through-plane \lambda ({\lambda }_{\perp }) of 15 wt% NH₂-rGO/PI thermally conductive composite films at room temperature were, respectively, 7.13 W/mK and 0.74 W/mK, 8.2 times {\lambda }_{\parallel } (0.87 W/mK) and 3.5 times {\lambda }_{\perp } (0.21 W/mK) of pure PI film, also significantly higher than {\lambda }_{\parallel } (5.50 W/mK) and {\lambda }_{\perp } (0.62 W/mK) of 15 wt% rGO/PI thermally conductive composite films. Calculation based on the effective medium theory model proved that ITR was reduced via the amination of rGO. Infrared thermal imaging and finite element simulation showed that NH₂-rGO/PI thermally conductive composite films obtained excellent heat dissipation and efficient thermal management capabilities on the light-emitting diodes bulbs, 5G high-power chips, and other electronic equipment, which are easy to generate heat severely.

Highly sensitive ethanol sensors have been widely utilized in environmental protection, industrial monitoring, and drink-driving tests. In this work, a fully self-powered ethanol detector operating at room temperature has been developed based on a triboelectric nanogenerator (TENG). The gas-sensitive oxide semiconductor is selected as the sensory component for the ethanol detection, while the resistance change of the oxide semiconductor can well match the “linear” region of the load characteristic curve of TENG. Hence, the output signal of TENG can directly reveal the concentration change of ethanol gas. An accelerator gearbox is applied to support the operation of the TENG, and the concentration change of ethanol gas can be visualized on the Liquid Crystal Display. This fully self-powered ethanol detector has excellent durability, low fabrication cost, and high selectivity of 5 ppm. Therefore, the ethanol detector based on TENG not only provides a different approach for the gas detection but also further demonstrates the application potential of TENG for various sensory devices.

Energy collection ways using solar energy, wave, wind, or mechanical energy have attracted widespread attention for small self-powered electronic devices with low power consumption, such as sensors, wearable devices, electronic skin, and implantable devices. Among them, triboelectric nanogenerator (TENG) operated by coupling effect of triboelectrification and electrostatic induction has gradually gained prominence due to its advantages such as low cost, lightweight, high degree of freedom in material selection, large power, and high applicability. The device with a single energy exchange mechanism is limited by its conversion efficiency and work environment and cannot achieve the maximum conversion of energy. Thus, this article reviews the research status of different types of hybrid generators based on TENG in recent years. Hybrid energy generators will improve the output performance though the integration of different energy exchange methods, which have an excellent application prospect. From the perspective of energy complementation, it can be divided into harvesting mechanical energy by various principles, combining with harvesters of other clean energy, and converting mechanical energy or various energy sources into hydrogen energy. For integrating multitype energy harvesters, mechanism of single device and structural design of integrated units for different application scenarios are summarized. The expanding energy harvesting efficiency of the hybrid TENG makes the scheme of self-charging unit to power intelligent mobile electronic feasible and has practical significance for the development of self-powered sensor network.

Organic semiconductors with bipolar transporting character are highly attractive as they offer the possibility to achieve high optoelectronic performance in simple device structures. However, the continual efforts in preparing bipolar materials are focusing on donor-acceptor (D-A) architectures by introducing both electron-donating and electron-withdrawing units into one molecule in static molecular design principles. Here, we report a dynamic approach to construct bipolar materials using only electron-donating carbazoles connected by N-P=X resonance linkages in a donor-resonance-donor (D-r-D) structure. By facilitating the stimuli-responsive resonance variation, these D-r-D molecules exhibit extraordinary bipolar properties by positively charging one donor of carbazole in enantiotropic N⁺=P-X^- canonical forms for electron transport without the involvement of any acceptors. With thus realized efficient and balanced charge transport, blue and deep-blue phosphorescent organic light emitting diodes hosted by these D-r-D molecules show high external quantum efficiencies up to 16.2% and 18.3% in vacuum-deposited and spin-coated devices, respectively. These results via the D-r-D molecular design strategy represent an important concept advance in constructing bipolar organic optoelectronic semiconductors dynamically for high-performance device applications.

Eco-friendly printing is important for mass manufacturing of thin-film photovoltaic (PV) devices to preserve human safety and the environment and to reduce energy consumption and capital expense. However, it is challenging for perovskite PVs due to the lack of eco-friendly solvents for ambient fast printing. In this study, we demonstrate for the first time an eco-friendly printing concept for high-performance perovskite solar cells. Both the perovskite and charge transport layers were fabricated from eco-friendly solvents via scalable fast blade coating under ambient conditions. The perovskite dynamic crystallization during blade coating investigated using in situ grazing incidence wide-angle X-ray scattering (GIWAXS) reveals a long sol-gel window prior to phase transformation and a strong interaction between the precursors and the eco-friendly solvents. The insights enable the achievement of high quality coatings for both the perovskite and charge transport layers by controlling film formation during scalable coating. The excellent optoelectronic properties of these coatings translate to a power conversion efficiency of 18.26% for eco-friendly printed solar cells, which is on par with the conventional devices fabricated via spin coating from toxic solvents under inert atmosphere. The eco-friendly printing paradigm presented in this work paves the way for future green and high-throughput fabrication on an industrial scale for perovskite PVs.

Electronic skin (e-skin) with skin-like flexibility and tactile sensation will promote the great advancements in the fields of wearable equipment. Thus, the multifunction and high robustness are two important requirements for sensing capability of the e-skin. Here, a fully organic self-powered e-skin (FOSE-skin) based on the triboelectric nanogenerator (TENG) is developed. FOSE-skin based on TENG can be fully self-healed within 10 hours after being sheared by employing the self-healing polymer as a triboelectric layer and ionic liquid with the temperature sensitivity as an electrode. FOSE-skin based on TENG has the multifunctional and highly robust sensing capability and can sense the pressure and temperature simultaneously. The sensing capability of the FOSE-skin based on TENG can be highly robust with no changes after self-healing. FOSE-skin based on TENG can be employed to detect the arm swing, the temperature change of flowing water, and the motion trajectory. This work provides a new idea for solving the issues of monofunctional and low robust sensing capability for FOSE-skin based on TENG, which can further promote the application of wearable electronics in soft robotics and bionic prosthetics.

Emotion recognition has been used widely in various applications such as mental health monitoring and emotional management. Usually, emotion recognition is regarded as a text classification task. Emotion recognition is a more complex problem, and the relations of emotions expressed in a text are nonnegligible. In this paper, a hierarchical model with label embedding is proposed for contextual emotion recognition. Especially, a hierarchical model is utilized to learn the emotional representation of a given sentence based on its contextual information. To give emotion correlation-based recognition, a label embedding matrix is trained by joint learning, which contributes to the final prediction. Comparison experiments are conducted on Chinese emotional corpus RenCECps, and the experimental results indicate that our approach has a satisfying performance in textual emotion recognition task.

Hydrogen energy, with environment amicable, renewable, efficiency, and cost-effective advantages, is the future mainstream substitution of fossil-based fuel. However, the extremely low volumetric density gives rise to the main challenge in hydrogen storage, and therefore, exploring effective storage techniques is key hurdles that need to be crossed to accomplish the sustainable hydrogen economy. Hydrogen physically or chemically stored into nanomaterials in the solid-state is a desirable prospect for effective large-scale hydrogen storage, which has exhibited great potentials for applications in both reversible onboard storage and regenerable off-board storage applications. Its attractive points include safe, compact, light, reversibility, and efficiently produce sufficient pure hydrogen fuel under the mild condition. This review comprehensively gathers the state-of-art solid-state hydrogen storage technologies using nanostructured materials, involving nanoporous carbon materials, metal-organic frameworks, covalent organic frameworks, porous aromatic frameworks, nanoporous organic polymers, and nanoscale hydrides. It describes significant advances achieved so far, and main barriers need to be surmounted to approach practical applications, as well as offers a perspective for sustainable energy research.