SinoGreenTech Academic Portal
Open AccessDOI: 10.1007/s40843-025-3742-5Original Research

Function block combination in light-driven cholesteric liquid crystal elastomer actuator

Peking University

Read Executive PreviewQuick FAQ
Function block combination in light-driven cholesteric liquid crystal elastomer actuator
Graphical Abstract / Figure
Published In
SCIENCE CHINA Materials
Published:January 15, 2026Edition:Vol. 69, Issue 5 • pp. 100-112Citation:Shuoning Zhang et al. (2026), SCIENCE CHINA Materials
Impact Factor3.5 (Q2 Scopus)
Source Journal中国科学: 材料

Key Takeaways & Executive Findings

  • • • The newly synthesized diselenide bond molecule (DSeAc) exhibits excellent bond exchange ability due to the lower bond energy between selenium atoms, enabling seamless bonding of LCE matrices under mild conditions. • • The function block combination strategy integrates a CLCE film and an NLCE actuator into a monolithic film, allowing tailored functional characteristics for diverse applications. • • The approach addresses the challenge of combining the mechanical advantages of NLCEs with the optical properties of CLCEs, overcoming limitations of high-voltage actuation in previous systems. • • The resulting material shows potential in information storage, anti-counterfeiting, and biomimetics, with the ability to induce deformation in CLCEs through the actuation of the NLCE matrix.

Abstract

Nematic liquid crystal elastomers (NLCEs) exhibit excellent mechanical properties and diverse deformation modes, while cholesteric liquid crystal elastomers (CLCEs) as photonic crystals (PCs) possess superior optical performance and intelligent response characteristics. Combining these two elastomers into a monolithic material is a challenging yet promising endeavor. Here, we designed and synthesized a new diselenide-bonded molecule (DSeAc), whose lower bond energy between selenium atoms endows it with excellent bond exchange ability. Consequently, two LCE matrices containing DSeAc molecules can achieve seamless bonding under mild conditions via dynamic diselenide bond exchange. By integrating a CLCE film and an NLCE actuator into a monolithic film, we enable the integration of two functional components, whose functional characteristics can be tailored as required. This function block combination strategy offers a promising pathway for developing smart materials with complex functions, showing great potential in information storage, anti-counterfeiting, and biomimetics.

1. Introduction

Photonic crystals (PCs) with stimuli-responsive characteristics have attracted significant research interest for applications in information storage, anti-counterfeiting, and intelligent bionics. Cholesteric liquid crystal elastomers (CLCEs), as one-dimensional PCs, combine the properties of PCs and LCEs, with reflection color tunable by mechanical deformation. However, integrating CLCEs with actuators typically requires high-voltage driving, posing safety risks and limiting practical deployment. The challenge lies in selecting an appropriate matrix material with multiple actuation modes to induce controlled deformation in CLCEs.

Liquid crystal elastomers (LCEs) are promising soft actuators due to their unique mesogenic anisotropy, enabling stimuli-responsive contraction upon heating above the isotropic temperature. By incorporating photothermal or other responsive materials, LCEs can be actuated by various stimuli. This work introduces a novel function block combination strategy using a diselenide-bonded molecule (DSeAc) to seamlessly bond a CLCE film and an NLCE actuator into a monolithic material. This approach enables the integration of optical and mechanical functionalities, overcoming the limitations of previous high-voltage systems and paving the way for advanced smart materials.

SinoTechIntel Interactive Document Reader
Page 1–5 of Preview
100%
Download Full PDF

Loading authentic research manuscript (Pages 1–5)...

Cite This Research Paper
Shuoning Zhang, Jiale Liu, Jianying Zhang, Chang Sun, Yunxiao Ren, Lanying Zhang, Wei Hu, Huai Yang (2026). Function block combination in light-driven cholesteric liquid crystal elastomer actuator. SCIENCE CHINA Materials. https://doi.org/10.1007/s40843-025-3742-5
SinoGreenTech Academic & Legal Disclaimer

Research & Educational Purpose Only: The translations, structured abstracts, analytical annotations, and data reports provided by SinoGreenTechare intended exclusively for academic research, internal corporate R&D, and educational benchmarking. They do not constitute formal engineering, chemical safety, legal, or professional advice.

Copyright & Intellectual Property Notice: Original copyright of the underlying source articles and experimental data remains with the respective authors, institutions, and original publishing journals. SinoGreenTech claims intellectual property only over its proprietary translations, analytical syntheses, and AEO structured enhancements in accordance with international fair use and academic citation principles.

Frequently Asked Questions

What is the bond energy of the diselenide bond in DSeAc and how does it facilitate bonding under mild conditions?

The diselenide bond in DSeAc has a lower bond energy compared to typical covalent bonds, enabling efficient bond exchange at mild temperatures. This allows seamless bonding of LCE matrices without harsh conditions, as demonstrated in the study.

How does the function block combination strategy achieve tailored functional characteristics?

By integrating a CLCE film and an NLCE actuator into a monolithic film, the strategy allows independent optimization of each component. The CLCE provides photonic properties, while the NLCE offers mechanical actuation, enabling tailored responses for specific applications.

What are the potential applications of this material in information storage and anti-counterfeiting?

The material's ability to change structural color in response to mechanical deformation makes it suitable for information storage and anti-counterfeiting. The integration of CLCE and NLCE allows dynamic color changes that can be controlled by light-driven actuation, offering secure and reversible encoding.

How does this approach compare to previous methods that used dielectric elastomers for CLCE actuation?

Previous methods required high voltages to actuate dielectric elastomers, posing safety risks. This work uses light-driven NLCE actuators, which are safer and allow remote and precise control. The diselenide bonding enables seamless integration without compromising the performance of either component.

What are the scalability and manufacturing considerations for this function block combination strategy?

The synthesis of DSeAc and the bonding process are relatively straightforward, potentially allowing scalability. However, further optimization of the bonding conditions and film fabrication is needed to ensure uniformity and reproducibility for industrial production.

Related Chinese Research & Cross-Citations

Research Citation2026
Ammonium Vanadate Cathodes in Aqueous Zinc-Ion Batteries: Design Strategies and Research Progress

Ammonium Vanadate Cathodes in Aqueous Zinc-Ion Batteries: Design Strategies and Research Progress

Aqueous zinc-ion batteries (AZIBs) offer a compelling combination of high safety, environmental compatibility, and abundant zinc resources, positioning them as viable candidates for grid-scale energy storage. Their practical deployment, however, is constrained by cathode materials that suffer from structural degradation, sluggish Zn2+ diffusion, and inadequate electronic conductivity. Ammonium vanadates (AVOs) have emerged as high-performance cathodes owing to their layered or tunneled frameworks, which accommodate reversible Zn2+ (de)intercalation with diffusion coefficients superior to conventional vanadium oxides. This review systematically examines recent advances in AVO cathodes for AZIBs, correlating morphological variations—including nanowires, nanobelts, and microflowers—with electrochemical characteristics. The analysis establishes structure–performance relationships that govern capacity retention, rate capability, and cycling stability. Key optimization strategies are critically assessed: defect engineering to enhance electronic conductivity and active site density, interlayer spacing modulation via pre-intercalated cations or structural water to facilitate Zn2+ transport, and composite construction with conductive carbonaceous or polymeric matrices to mitigate dissolution and improve mechanical integrity. Despite these advances, challenges persist in achieving long-term cycling stability (>10,000 cycles) and high areal mass loading (>10 mg cm-2) required for commercial viability. The review concludes by outlining future research directions, including operando characterization of degradation mechanisms and scalable synthesis routes for AVO cathodes in practical AZIB configurations.

Examine Full Data & PDF
Research Citation2026
Microenvironment-responsive therapeutic platforms: Innovations for spinal cord injury repair

Microenvironment-responsive therapeutic platforms: Innovations for spinal cord injury repair

Spinal cord injury (SCI) remains a formidable clinical challenge due to the complex, dynamic lesion microenvironment that impedes axonal regeneration and functional recovery. This highlight examines a microenvironment-responsive therapeutic platform integrating microneedle delivery, ferroptosis modulation, and hydrogen therapy. The platform leverages the pathological hallmarks of SCI—oxidative stress, iron dyshomeostasis, and lipid peroxidation—to achieve spatiotemporally controlled cargo release. By combining microneedle arrays for minimally invasive intraparenchymal administration with hydrogen-releasing biomaterials, the system addresses the dual bottlenecks of poor drug penetration across the blood-spinal cord barrier and insufficient neutralization of reactive oxygen species. Ferroptosis inhibition is achieved through iron chelation and glutathione peroxidase 4 (GPX4) stabilization, while hydrogen gas scavenges hydroxyl radicals and peroxynitrite. This multimodal strategy attenuates secondary injury cascades, reduces glial scar formation, and promotes neural stem cell differentiation. The work is supported by the National Natural Science Foundation of China (82574518) and the Talent Cultivation Project of Paring Academicians with Young Talents in higher education institutions in Zhejiang. The authors declare no conflict of interest. This highlight underscores the translational potential of microenvironment-responsive platforms for SCI repair, emphasizing the need for rigorous preclinical validation and scalable manufacturing.

Examine Full Data & PDF
Research Citation2026
Dual-Site Adsorption over Phosphorus-Doped Copper Oxide for Efficient CO2 Electroreduction to Ethylene

Dual-Site Adsorption over Phosphorus-Doped Copper Oxide for Efficient CO2 Electroreduction to Ethylene

Electroreduction of CO2 to ethylene offers a promising route for renewable electricity storage, yet achieving high ethylene selectivity at industrial current densities remains challenging due to the large energy barrier for C–C coupling. Here, we report a “MOF-assisted in situ doping” strategy to introduce the oxophilic nonmetal phosphorus (P) into the copper oxide (CuO) lattice, constructing a localized Cu–P dual-site adsorption configuration for the key *OCCHO intermediate. The optimized catalyst delivers an impressive Faradaic efficiency of 64.6% for ethylene with a partial current density of 646 mA cm-2. Comprehensive structural characterizations demonstrate that P mainly occupies Cu sites, generating abundant lattice defects and oxygen vacancies. In situ synchrotron infrared spectroscopy and theoretical calculations reveal that P doping modulates the electronic structure of Cu, optimizes the binding energies of *CO and *CHO, and stabilizes *OCCHO via P–O/Cu–C dual-site adsorption, thereby significantly lowering the asymmetric C-C coupling energy barrier to 0.74 eV. This work highlights a dual-site microenvironment regulation strategy for CO2-to-ethylene electroreduction.

Examine Full Data & PDF
Research Citation2026
Hydrophilic Single-Atom Interface Unlocks Low-Potential CO Removal on Pt in PEMFCs

Hydrophilic Single-Atom Interface Unlocks Low-Potential CO Removal on Pt in PEMFCs

Proton exchange membrane fuel cells (PEMFCs) fed with reformate hydrogen suffer severe anode poisoning by trace CO, necessitating high CO electrooxidation potentials that degrade performance and durability. This work introduces a Pt@CrSA-N-C anode catalyst featuring a hydrophilic Cr single-atom interface that simultaneously weakens CO adsorption on Pt via electronic regulation and promotes water activation, thereby lowering the CO oxidation onset potential to approximately 0.13 V vs. RHE. The onset potential was determined by two independent methods: the first potential at which the background-corrected current exceeds 0 mA cm-2 during CO oxidation reaction tests in a three-electrode system, and the potential at which the forward scan current exceeds the N2 background current in CO-stripping voltammetry. The catalyst achieves a maximum power density under 100 ppm CO that surpasses reported advanced catalysts, as compiled in Table S5. Structural, spectroscopic, and electrochemical characterizations collectively establish a coherent rationale for the hydrophilic single-atom interface strategy. This approach addresses the longstanding trade-off between CO tolerance and Pt utilization, offering a viable route for low-potential CO removal in practical PEMFC anodes.

Examine Full Data & PDF
Research Citation2026
An Ionoelastomer-Based Bioinspired Wearable Electronics with Tele-Perception and Tactile Sensation for Machine Learning-Assisted Rehabilitation Management

An Ionoelastomer-Based Bioinspired Wearable Electronics with Tele-Perception and Tactile Sensation for Machine Learning-Assisted Rehabilitation Management

Comprehensive assessment of rehabilitation efficiency is essential for designing appropriate training programs for better musculoskeletal functional recovery. Existing contact-receptor-dependent rehabilitation assessment systems mostly focus on assessing the restoration of muscle function by evaluating grip strength or joint flexion angle; however, parameters reflecting neuromuscular synergistic function are always overlooked. Herein, we develop an ionoelastomer-based soft artificial electroreceptor (SAER) that integrates tele-perception and tactile sensation to track the rehabilitation process, collecting signals related to approaching speed and grip strength sequentially. The SAER uses polyurethane ionoelastomer incorporated with quasi-solid conductive salt as the electric field receptor, and is integrated on a rehabilitation-training ball after assembly to establish an untethered detection device; this enables the remote capture of hand approaching parameter within a 9 cm range, followed by the quantification of grip strength when contacting and grasping. Furthermore, a data-driven assessment system is established by integrating machine learning, which accurately classifies rehabilitation efficiency into six levels; it supports for rehabilitation evaluation and training programs adjustment. Overall, the SAER-based rehabilitation management system establishes a paradigm that synergistically evaluating parameters corresponding to neuromuscular functional restoration and holds strong potential for home-based active rehabilitation for minimizing dependence on frequent clinical supervision.

Examine Full Data & PDF
Research Citation2026
Microwave-Absorbing Materials with Strong Environmental Adaptability for Corrosion Protection, Anti-Icing, and Thermal Management

Microwave-Absorbing Materials with Strong Environmental Adaptability for Corrosion Protection, Anti-Icing, and Thermal Management

Microwave-absorbing materials (MAMs) deployed on naval vessels, aerospace vehicles, and critical electronic systems face coupled electromagnetic, marine salt-spray corrosion, and extreme-temperature loads that legacy single-function absorbers cannot withstand. This review consolidates progress on three environmentally adaptive MAM classes: corrosion-protective, anti-icing, and thermal-management absorbers. The electromagnetic loss and impedance-matching fundamentals are first established, then the synergistic mechanisms, design strategies, and characterization protocols for each class are examined against representative material systems and their measured performance. The analysis identifies a shared design logic—multiscale hierarchical architecture, interfacial polarization engineering, and multifunctional phase integration—while distinguishing the divergent protection mechanisms: barrier and passivation effects for corrosion, surface-energy and latent-heat regulation for anti-icing, and phonon–electron transport decoupling for thermal management. Persistent bottlenecks include the trade-off between impedance matching and protective-layer density, the absence of standardized coupled-field test protocols, and the scarcity of long-term salt-spray and thermal-cycling durability data. Future directions are delineated: intelligent self-adaptive absorbers, multiphysics-coupled simulation frameworks, and environmentally benign multifunctional integration. The review provides a theoretical and technical basis for the design, construction, and engineering scale-up of next-generation high-performance absorbers for aerospace, electronic, and marine equipment.

Examine Full Data & PDF