Bingxiang Li

Abstract Flexible conductive materials with intrinsic structural characteristics are currently in the spotlight of both fundamental science and advanced technological applications due to their functional preponderances such as the remarkable conductivity, excellent mechanical properties, and tunable physical and chemical properties, and so on. Typically, conductive hydrogel fibers (CHFs) are promising candidates owing to their unique characteristics including light weight, high length‐to‐diameter ratio, high deformability, and so on. Herein, a comprehensive overview of the cutting‐edge advances the CHFs involving the architectural features, function characteristics, fabrication strategies, applications, and perspectives in flexible electronics are provided. The fundamental design principles and fabrication strategies are systematically introduced including the discontinuous fabrication (the capillary polymerization and the draw spinning) and the continuous fabrication (the wet spinning, the microfluidic spinning, 3D printing, and the electrospinning). In addition, their potential applications are crucially emphasized such as flexible energy harvesting devices, flexible energy storage devices, flexible smart sensors, and flexible biomedical electronics. This review concludes with a perspective on the challenges and opportunities of such attractive CHFs, allowing for better understanding of the fundamentals and the development of advanced conductive hydrogel materials.

Self-assembled architectures of soft matter have fascinated scientists for centuries due to their unique physical properties originated from controllable orientational and/or positional orders, and diverse optic and photonic applications. If one could know how to design, fabricate, and manipulate these optical microstructures in soft matter systems, such as liquid crystals (LCs), that would open new opportunities in both scientific research and practical applications, such as the interaction between light and soft matter, the intrinsic assembly of the topological patterns, and the multidimensional control of the light (polarization, phase, spatial distribution, propagation direction). Here, we summarize recent progresses in self-assembled optical architectures in typical thermotropic LCs and bio-based lyotropic LCs. After briefly introducing the basic definitions and properties of the materials, we present the manipulation schemes of various LC microstructures, especially the topological and topographic configurations. This work further illustrates external-stimuli-enabled dynamic controllability of self-assembled optical structures of these soft materials, and demonstrates several emerging applications. Lastly, we discuss the challenges and opportunities of these materials towards soft matter photonics, and envision future perspectives in this field.

Abstract Circularly polarized luminescent (CPL) materials have received significant attention in the field of fundamental science recently. These materials offer substantial advancement of technological applications, such as optical data storage, displays, and quantum communication. Various strategies have been proposed in self‐assembled materials consisting of inorganic, organic, and hybrid systems, particularly in the chiral orientationally ordered soft matter systems (e.g., chiral liquid crystals (LCs) and LC polymers). However, developing scientific approaches to achieve the pronounced and steerable circularly polarized light emission remains challenging. Herein, we present a comprehensive review on the recent development of CPL materials based on chiral LCs, including thermotropic LCs (cholesteric LCs and bent‐core LCs), lyotropic LCs (nanocellulose LCs and polyacetylene‐based LCs), and LC polymers (cholesteric LC‐based polymers, helical nanofibers, and helical network). In addition, the fundamental mechanisms, design principles, and potential applications based on these chiral LCs and LC polymers in soft matter systems are systematically reviewed. This review summarizes with a prospect on the latent challenges, which can strengthen our understanding of the basic principles of CPL in chiral orientationally ordered soft matter systems and provide a new insight into the progress in several fields, such as chemistry, materials science, optics, electronics, and biology.

Abstract Long‐lived room‐temperature phosphorescence (RTP) of organic materials holds a significant potential for optical information. Circularly polarized organic ultralong room‐temperature phosphorescence (CP‐OURTP) with extremely high dissymmetry factor ( g lum ) values is even highly demanded and considerably challenging. Here, an effective strategy is introduced to realize CP‐OURTP with an emission decay time of 735 ms and a g lum value up to 1.49, which exceeds two orders of magnitude larger than previous records, through a system composed of RTP polymers and chiral helical superstructures. The system exhibits excellent stability under multiple cycles of photoirradiation and thermal treatment, and is further employed for information encryption based on optical multiplexing. The results are anticipated to lay the foundation for the development of CP‐OURTP materials in advanced photonic applications.

Abstract Visible‐light‐driven molecular switches endowing reversible modulation of the functionalities of self‐organized soft materials are currently highly sought after for fundamental scientific studies and technological applications. Reported herein are the design and synthesis of two novel halogen bond donor based chiral molecular switches that exhibit reversible photoisomerization upon exposure to visible light of different wavelengths. These chiral molecular switches induce photoresponsive helical superstructures, that is, cholesteric liquid crystals, when doped into the commercially available room‐temperature achiral liquid crystal host 5CB, which also acts as a halogen‐bond acceptor. The induced helical superstructure containing the molecular switch with terminal iodo atoms exhibits visible‐light‐driven reversible unwinding, that is, a cholesteric–nematic phase transition. Interestingly, the molecular switch with terminal bromo atoms confers reversible handedness inversion to the helical superstructure upon irradiation with visible light of different wavelengths. This visible‐light‐driven, reversible handedness inversion, enabled by a halogen bond donor molecular switch, is unprecedented.