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 inNature communications Vol. 16; no. 1; pp. 5083 - 12
Main Authors Garai, Bikash, Das, Gobinda, Duncan, Connor M., Nour, Hany F., Benyettou, Farah, Prakasam, Thirumurugan, Varghese, Sabu, Hamoud, Houeida Issa, El-Roz, Mohamad, Martinez, Jose Ignacio, Gándara, Felipe, Olson, Mark A., Trabolsi, Ali
Format Journal Article
LanguageEnglish
Published London Nature Publishing Group UK 31.05.2025
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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.
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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K Ciepluch (60257_CR44) 2012; 9
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Snippet Development of efficient actuators and understanding of their mechanisms are crucial for progress in areas such as soft robotics and artificial muscles. Here,...
Abstract Development of efficient actuators and understanding of their mechanisms are crucial for progress in areas such as soft robotics and artificial...
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Actuation
Actuators
Artificial muscles
Charge transfer
Chemical energy
Covalence
Deicers
Deicing
Energy charge
Energy conversion
Film thickness
Humanities and Social Sciences
Hydrogen bonding
Ice accumulation
Light intensity
Luminous intensity
multidisciplinary
Muscles
Payloads
Robotics
Science
Science (multidisciplinary)
Thermal energy
Ultraviolet radiation
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Title Triple energy conversion cascade in a densely charged redox active covalent organic actuator
URI https://link.springer.com/article/10.1038/s41467-025-60257-8
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