Table 1.
Activation mechanism | Typical materials | Fabrication methods | Response speeda | Advantages | Limitations | |
---|---|---|---|---|---|---|
Mechanical actuation | Elastomers, polymers, papers, metals | DIW, SLA, PolyJet, DLP, TPL, SLS, machining | Fast | Mature fabrication and advanced design methods; easy mechanical control; marginal sensitivity to surrounding environment; stable reconfigurability | Difficult to deploy or modulate remotely; response depends on specific loading conditions (such as uniaxial loading) | |
Heat transfer | Phase change | Polymers, metals, polymer-filler composites, LCEs, SMPs, hydrogels | DIW, DLP, TPL, microfabrication, machining | Slow to medium | Remote activation by temperature; thermal expansion is universal and can be modelled systematically; phase-changing materials have substantial thermal expandability and programmable anisotropy; SMPs can be willfully deformed after fabrication and achieve nearly full shape recovery | Limited to specific temperatures and environments (for example, cannot operate when temperature cannot be changed); may require large temperature change and long heating or cooling time |
Shape memory | ||||||
Chemomechanical transformation | Swelling | Hydrogels, hydrogel-filler composites, polymers, multi-material composites | DIW, DLP, microfabrication, machining | Slow to medium | Large, programmable structural changes; easy activation by wetting | Transformation speed limited by mass transport; require large environmental changes |
Chemistry | Hydrogels | DLP, TPL, microfabrication, machining | Medium to fast | Chemical activation is useful for biomedical applications; autonomous feedback can be achieved via chemical reactions | Require specific reactions and relevant materials synthesis to respond to different chemical cues | |
Electrochemistry | Electrochemically active materials (such as conjugated polymers, battery electrode materials) | Machining, microfabrication, TPL | Slow to medium | Structure and property retention upon stimulus removal; continuous control of transformation; potential to simultaneously store energy | Typically require two electrodes, a liquid or gel electrolyte, and a power source; 3D structuring methods are not fully developed | |
Electromagnetic interactions | Magnetic field | Polymers with embedded magnetic particles | DIW, DLP, microfabrication | Fast | Fast, remote activation (typically <1 s); complex, reversible, and programmable structural changes | Require strong magnetic fields (typically >0.1 T); mostly soft materials |
Electric field | Ionic hydrogels, dielectric elastomers, piezoelectric composites | DLP, moulding, machining, microfabrication | Medium to fast | Dielectric elastomers integrate into electronic control circuits for autonomous devices; piezoelectric materials can measure strain | Require additional electrodes and electronic control | |
Light | Polymers with light-absorbing nanoparticles, azobenzene-containing liquid crystal polymers | DIW, microfabrication, machining | Medium to fast | Fast, remote activation and active manipulation; independent control of shape changes by different polarizations and wavelengths | Limited 3D patterning methods; cannot function without a light source and sufficient transmission |
DIW, direct ink writing; DLP, digital light processing; LCE, liquid crystal elastomer; SLS, selective laser sintering; SMP, shape memory polymer; TPL, two-photon lithography. aResponse speed is compared in relative terms between representative responsive materials with similar dimensions; the demonstrated response speed of specific responsive architected materials examples depends on both the activation mechanism and the architecture’s geometry and feature sizes. Illustration in row 1 adapted with permission from ref.24, Wiley. Illustration in row 5 adapted from ref.96, Springer Nature Limited. Illustration in row 7 adapted from ref.14, Springer Nature Limited. Illustration in row 9 adapted from ref.147, Springer Nature Limited.