Covalent organic frameworks (COFs) have served as a family of porous crystalline molecules for various promising applications. However, controllable synthesis of COFs with uniform morphology is paramount yet still remains quite challenging. Herein, we report self-templated synthesis of uniform and unique hollow spheres based on highly conjugated three-dimensional (3D) COFs with diameters of 500–700 nm. A detailed time-dependent study reveals the continuous transformation from initial nano sphere-like particles into uniform hollow spherical structures with Ostwald ripening mechanism. Particularly, the resulting 3D COF (3D-Sp-COF) is prone to transport ions more efficiently and the lithium-ion transference number (t+) of 3D-Sp-COF reaches 0.7, which even overwhelms most typical PEO-based polymer electrolytes. Inspiringly, the hollow spherical structures show enhanced capacitance performance with a specific capacitance of 251 F g−1 at 0.5 A g−1, which compares favorably with the vast majority of two-dimensional COFs and other porous electrode materials.

Artificial intelligent skins hold the potential to revolutionize artificial intelligence, health monitoring, soft robotics, biomedicine, flexible, and wearable electronics. Present artificial skins can be characterized into electronic skins ( e-skins) that convert external stimuli into electrical signals and photonic skins ( p-skins) that convert deformations into intuitive optical feedback. Merging both electronic and photonic functions in a single skin is highly desirable, but challenging and remains yet unexplored. We report herein a brand-new type of artificial intelligent skin, an optoelectronic skin ( o-skin), which combines the advantages of both e-skins and p-skins in a single skin device based on one-dimensional photonic crystal-based hydrogels. Taking advantage of its anisotropic characteristics, the resulting o-skin can easily distinguish vector stimuli such as stress type and movement direction to meet the needs of multi-dimensional perception. Furthermore, the o-skin also demonstrates advanced functions such as full-color displays and intelligent response to the environment in the form of self-adaptive camouflage. This work represents a substantial advance in using the molecular engineering strategy to achieve artificial intelligent skins with multiple anisotropic responses that can be integrated on the skin of a soft body to endow superior functions, just like the natural organisms that inspire us.

Narrow‐bandgap small molecular acceptors (SMAs) with absorption extending into the near‐infrared spectral region such as ITIC derivatives are widely investigated, while the development of their wide‐bandgap counterparts remains largely unexplored. Wide‐bandgap non‐fullerene acceptors (NFAs) are highly desirable and beneficial for constructing efficient device layouts such as ternary blend and tandem solar cells that require multiple light‐harvesting materials with different regions of absorption. In this contribution, the design and synthesis of two wide‐bandgap SMAs (IDT‐TBA and IDDT‐TBA), consisting of a weak electron‐withdrawing moiety (1,3‐diethyl‐2‐thiobarbituric acid, TBA) is presented. Compared to ITIC, this molecular design strategy results in energetically down‐shifted HOMO levels and hence much enlarged bandgaps of 1.91 eV for IDT‐TBA and 1.78 eV for IDDT‐TBA, respectively. Further photovoltaic performance evaluation demonstrates power conversion efficiencies (PCEs) of 6.5% for IDT‐TBA and 7.5% for IDDT‐TBA, respectively, when using PBDB‐T as the electron donor polymer. In addition, time‐delayed collection field (TDCF) experiments suggest that both IDT‐TBA and IDDT‐TBA based cells exhibit field‐independent charge generation with external charge generation efficiencies exceeding 90%, implying negligible geminate recombination losses. The results demonstrate that TBA units are promising and attractive building blocks as weak electron‐withdrawing acceptors to construct wide‐bandgap high‐efficiency SMAs for efficient organic photovoltaic devices.

Human–machine interfaces (HMIs) enable users to interact with machines, thus playing a significant role in artificial intelligence, virtual reality, and the metaverse. Conventional HMIs are based on bulky and rigid electronic devices, seriously limiting their ductility, damage reconfiguration, and multifunctionality. In terms of replacing conventional HMIs, artificial bionic skins with good ductility, self-reparation, and multisensory ability are promising candidates. Still, they in their present form require innovations in mechanical and sensory properties, especially damage recovery and environmental stability, which seriously affect the service life and result in tons of electric waste. Herein, we present a new type of artificial bionic skin with excellent mechanical performance (>13,000% strain), high environmental stability (−80 to 80 °C), and multiple sensory properties toward strain, stress, temperature, solvent, and bioelectricity. Besides, this new type of artificial bionic skin also exhibits effective reconfiguration ability after damage and recyclability. The as-prepared artificial bionic skin was used as an interactive HMI to collect and distinguish the different sensory stimuli. The electronics assembled by HMI with artificial bionic skin can adhere compliantly on the human body for wireless motion capturing and sensing via Bluetooth, Wi-Fi, and the Internet. With simple programming, complex human motions can be mimicked in real-time by robots.