Publications by authors named "Honglong Hu"

Article Synopsis
  • Sterically hindered diarylethenes with intrinsic chirality have potential for regulating chiral signals and controlling liquid crystals using light, as they can change properties through unique phototransformations.
  • Traditional methods for creating these chiral structures face challenges like limited separation efficiency and production scale, requiring advanced techniques like chiral HPLC.
  • This study introduces a new enantioselective olefination method to create intrinsic chiral diarylethenes directly from prochiral compounds, yielding high enantioselectivity and allowing for effective photoregulation in liquid crystals with excellent stability and minimal disorder.
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Liquid crystal (LC) distributed feedback (DFB) lasers hold significant potential for integrated photonics applications. However, limitations in wavelength spacing for wavelength switching, device size, and compatibility with other technologies have impeded advancements of the LC DFB laser in integration and responsiveness. Herein, we propose a thin-film multi-wavelength DFB laser array utilizing high-resolution patterned programmable nematic LC polymers, enabling rapid switching with high-resolution wavelength spacing between wavelength division multiplexing channels while maintaining a stable single longitudinal mode (SLM) for each laser.

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The development of ultra-long room-temperature phosphorescence (UL-RTP) in processable amorphous organic materials is highly desirable for applications in flexible displays, anti-counterfeiting, and bio-imaging. However, achieving efficient UL-RTP from amorphous materials remains a challenging task, especially with activation by visible light and a bright afterglow. Here we report a general and rational molecular-design strategy to enable efficient visible-light-excited UL-RTP by multi-esterification of a rigid large-plane phosphorescence core.

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Dynamic chiral superstructures are of vital importance for understanding the organization and function of chirality in biological systems. However, achieving high conversion efficiency for photoswitches in nanoconfined architectures remains challenging but fascinating. Herein, we report a series of dynamic chiral photoswitches based on supramolecular metallacages through the coordination-driven self-assembly of dithienylethene (DTE) units and octahedral zinc ions, thereby successfully achieving an ultrahigh photoconversion yield of 91.

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The spontaneous formation of self-assembly monolayer (SAM) on various substrates represents an effective strategy for interfacial engineering of optoelectronic devices. Hole-selective SAM is becoming popular among high-performance inverted perovskite solar cells (PSCs), but the presence of strong acidic anchors (such as -POH) in state-of-the-art SAM is detrimental to device stability. Herein, we report for the first time that acidity-weakened boric acid can function as an alternative anchor to construct efficient SAM-based hole-selective contact (HSC) for PSCs.

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Halide diffusion across the charge-transporting layer followed by a reaction with metal electrode represents a critical factor limiting the long-term stability of perovskite solar cells (PSCs). In this work, a supramolecular strategy with surface anion complexation is reported for enhancing the light and thermal stability of perovskite films, as well as devices. Calix[4]pyrrole (C[4]P) is demonstrated as a unique anion-binding agent for stabilizing the structure of perovskite by anchoring surface halides, which increases the activation energy for halide migration, thus effectively suppressing the halide-metal electrode reactions.

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Manual intervention in the self-organization of soft matter to obtain a desired superstructure is a complex but significant project. Specifically, optical components made fully or partially from reconfigurable and stimuli-responsive soft materials, referred to as soft photonics, are poised to form versatile platforms in various areas; however, a limited scale, narrow spectral adaptability, and poor stability are still formidable challenges. Herein, a facile way is developed to program the optical jigsaw puzzle of nematic liquid crystals via pixelated holographic surface reliefs, leading to an era of manufacturing for programmable soft materials with tailored functions.

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Article Synopsis
  • Researchers are tackling the challenge of actively controlling various optical properties like wavelength and polarization in real time, which has been difficult due to the lack of suitable materials.
  • They introduce a novel photo-modulated soft helix with a unique structure that enables reversible changes in pitch length based on light intensity, adding an extra degree of control over its optical properties.
  • This innovation paves the way for better manipulation of absorbance and chirality, potentially enhancing applications in fields such as biophotonics and creating advanced optical devices with improved performance.
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Dynamic electric field frequency actuated helical and spiral structures enable a plethora of attributes for advanced photonics and engineering in the contemporary era. Nevertheless, leveraging the frequency responsiveness of adaptive devices and systems within a broad dynamic range and maintaining restrained high-frequency induced heating remain challenging. Herein, we establish a frequency-actuated heliconical soft architecture that is quite distinct from that of common frequency-responsive soft materials.

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Dynamic and multi-dimensional manipulation of laser emission with light allows for optical coding, computing, and imaging photonic chips. However, the coupling balance between photonic resonance and transmission is a formidable challenge due to the uncontrollable chiral microcavity with photo-reversibility, which is limited to the multi-freedom of the laser with sustainable and repeatable output beams. Herein, a helical superstructure system with a unique intrinsic chiral photoswitch is developed for resolving the always pendent problems on organized defects in the microcavity.

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