Triple energy conversion cascade in a densely charged redox active covalent organic actuator
Development of efficient actuators and understanding of their mechanisms are crucial for progress in areas such as soft robotics and artificial muscles. Here, we report a self-standing film of an ionic covalent organic framework ( V 2+ –TG ) composed of cationic guanidinium and viologen linkers, whi...
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Published in | Nature communications Vol. 16; no. 1; pp. 5083 - 12 |
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Main Authors | , , , , , , , , , , , , |
Format | Journal Article |
Language | English |
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London
Nature Publishing Group UK
31.05.2025
Nature Publishing Group Nature Portfolio |
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Abstract | Development of efficient actuators and understanding of their mechanisms are crucial for progress in areas such as soft robotics and artificial muscles. Here, we report a self-standing film of an ionic covalent organic framework (
V
2+
–TG
) composed of cationic guanidinium and viologen linkers, which shows an instantaneous and reversible photoactuation. Upon UV light exposure, the film deflects by 100 ° in less than 3 s, through a triple energy conversion cascade, where light is first converted into chemical energy via intramolecular charge transfer, then to thermal energy, and finally into mechanical energy, causing the film to bend. The localized heat induces water molecule elimination, creating a hydrogen bonding gradient between the two surfaces of the film, triggering the bending. Actuation property of the film is modulated by varying film thickness, light intensity, and humidity. The film also demonstrates practical potential for applications like lifting payloads, heating, and surface deicing where ice accumulation poses operational risks.
The development of efficient actuators and the understanding of their mechanisms is crucial for improving their application. Here, the authors develop a self-standing film of an ionic covalent organic framework which undergoes a reversible photoactuation following a triple energy conversion cascade in a short time. |
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AbstractList | Development of efficient actuators and understanding of their mechanisms are crucial for progress in areas such as soft robotics and artificial muscles. Here, we report a self-standing film of an ionic covalent organic framework (
V
2+
–TG
) composed of cationic guanidinium and viologen linkers, which shows an instantaneous and reversible photoactuation. Upon UV light exposure, the film deflects by 100 ° in less than 3 s, through a triple energy conversion cascade, where light is first converted into chemical energy via intramolecular charge transfer, then to thermal energy, and finally into mechanical energy, causing the film to bend. The localized heat induces water molecule elimination, creating a hydrogen bonding gradient between the two surfaces of the film, triggering the bending. Actuation property of the film is modulated by varying film thickness, light intensity, and humidity. The film also demonstrates practical potential for applications like lifting payloads, heating, and surface deicing where ice accumulation poses operational risks.
The development of efficient actuators and the understanding of their mechanisms is crucial for improving their application. Here, the authors develop a self-standing film of an ionic covalent organic framework which undergoes a reversible photoactuation following a triple energy conversion cascade in a short time. Development of efficient actuators and understanding of their mechanisms are crucial for progress in areas such as soft robotics and artificial muscles. Here, we report a self-standing film of an ionic covalent organic framework (V2+-TG) composed of cationic guanidinium and viologen linkers, which shows an instantaneous and reversible photoactuation. Upon UV light exposure, the film deflects by 100 ° in less than 3 s, through a triple energy conversion cascade, where light is first converted into chemical energy via intramolecular charge transfer, then to thermal energy, and finally into mechanical energy, causing the film to bend. The localized heat induces water molecule elimination, creating a hydrogen bonding gradient between the two surfaces of the film, triggering the bending. Actuation property of the film is modulated by varying film thickness, light intensity, and humidity. The film also demonstrates practical potential for applications like lifting payloads, heating, and surface deicing where ice accumulation poses operational risks.Development of efficient actuators and understanding of their mechanisms are crucial for progress in areas such as soft robotics and artificial muscles. Here, we report a self-standing film of an ionic covalent organic framework (V2+-TG) composed of cationic guanidinium and viologen linkers, which shows an instantaneous and reversible photoactuation. Upon UV light exposure, the film deflects by 100 ° in less than 3 s, through a triple energy conversion cascade, where light is first converted into chemical energy via intramolecular charge transfer, then to thermal energy, and finally into mechanical energy, causing the film to bend. The localized heat induces water molecule elimination, creating a hydrogen bonding gradient between the two surfaces of the film, triggering the bending. Actuation property of the film is modulated by varying film thickness, light intensity, and humidity. The film also demonstrates practical potential for applications like lifting payloads, heating, and surface deicing where ice accumulation poses operational risks. Development of efficient actuators and understanding of their mechanisms are crucial for progress in areas such as soft robotics and artificial muscles. Here, we report a self-standing film of an ionic covalent organic framework (V -TG) composed of cationic guanidinium and viologen linkers, which shows an instantaneous and reversible photoactuation. Upon UV light exposure, the film deflects by 100 ° in less than 3 s, through a triple energy conversion cascade, where light is first converted into chemical energy via intramolecular charge transfer, then to thermal energy, and finally into mechanical energy, causing the film to bend. The localized heat induces water molecule elimination, creating a hydrogen bonding gradient between the two surfaces of the film, triggering the bending. Actuation property of the film is modulated by varying film thickness, light intensity, and humidity. The film also demonstrates practical potential for applications like lifting payloads, heating, and surface deicing where ice accumulation poses operational risks. Abstract Development of efficient actuators and understanding of their mechanisms are crucial for progress in areas such as soft robotics and artificial muscles. Here, we report a self-standing film of an ionic covalent organic framework (V 2+ –TG) composed of cationic guanidinium and viologen linkers, which shows an instantaneous and reversible photoactuation. Upon UV light exposure, the film deflects by 100 ° in less than 3 s, through a triple energy conversion cascade, where light is first converted into chemical energy via intramolecular charge transfer, then to thermal energy, and finally into mechanical energy, causing the film to bend. The localized heat induces water molecule elimination, creating a hydrogen bonding gradient between the two surfaces of the film, triggering the bending. Actuation property of the film is modulated by varying film thickness, light intensity, and humidity. The film also demonstrates practical potential for applications like lifting payloads, heating, and surface deicing where ice accumulation poses operational risks. Development of efficient actuators and understanding of their mechanisms are crucial for progress in areas such as soft robotics and artificial muscles. Here, we report a self-standing film of an ionic covalent organic framework (V2+–TG) composed of cationic guanidinium and viologen linkers, which shows an instantaneous and reversible photoactuation. Upon UV light exposure, the film deflects by 100 ° in less than 3 s, through a triple energy conversion cascade, where light is first converted into chemical energy via intramolecular charge transfer, then to thermal energy, and finally into mechanical energy, causing the film to bend. The localized heat induces water molecule elimination, creating a hydrogen bonding gradient between the two surfaces of the film, triggering the bending. Actuation property of the film is modulated by varying film thickness, light intensity, and humidity. The film also demonstrates practical potential for applications like lifting payloads, heating, and surface deicing where ice accumulation poses operational risks.The development of efficient actuators and the understanding of their mechanisms is crucial for improving their application. Here, the authors develop a self-standing film of an ionic covalent organic framework which undergoes a reversible photoactuation following a triple energy conversion cascade in a short time. |
ArticleNumber | 5083 |
Author | Duncan, Connor M. Trabolsi, Ali Das, Gobinda El-Roz, Mohamad Gándara, Felipe Nour, Hany F. Olson, Mark A. Prakasam, Thirumurugan Hamoud, Houeida Issa Varghese, Sabu Martinez, Jose Ignacio Benyettou, Farah Garai, Bikash |
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Title | Triple energy conversion cascade in a densely charged redox active covalent organic actuator |
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