Volumetric additive manufacturing (VAM) is an emerging approach to photo polymerbased 3D printing that produces complex 3D structures in a single step, rather than from layer-by-layer assembly. [1] This paradigm holds promise because it overcomes many of the drawbacks of layerbased fabrication, such as long build times and rough surfaces. VAM also augurs a broadening of the materials available for photopolymer 3D printing, having fewer constraints on viscosity and reactivity compared to layerwise printing. Indeed, though VAM has been demonstrated with extremely soft hydrogels, [2,3] it has relied until now almost exclusively on acrylate-based chemistry. [4] This is natural, because the oxygen inhibition of acrylate polymerization provides the threshold behavior required for VAM. However, acrylate chemistry is in general limiting due to the brittle and glassy properties of the resulting materials. Accordingly, extensive efforts have been made to identify and target specific soft, elastic acrylate formulations. [5-9] Introducing alternative crosslinking chemistries to the VAM realm, as well as AM more broadly, is highly desirable as an alternative method to gain access to a wider range of mechanical, thermal, and optical performance. [10-14] Thiol-ene-based polymers are one class of materials that have drawn significant attention owing to their controllable, tunable mechanical properties. [15-17] This is generally attributed to more uniform molecular networks in thiol-ene materials, resulting from the step-growth mechanism of the polymerization reaction. [18,19] Thiol-ene materials have already shown promise for applications including use in adhesives, electronics, and as biomaterials. [20,21] This work expands the versatility of volumetric AM by introducing a new class of VAM-compatible thiol-ene resins. We demonstrate the formulation of thiol-ene resins with the nonlinear threshold-type kinetics required for VAM and show bulk-equivalent performance in the resulting 3D printed parts, confirming the advantage of the layerless whole-part process. In our volumetric AM system, a 3D distribution of light energy is delivered to the resin vat by superimposing exposures from multiple angles, a method termed computed axial litho graphy (CAL) (Figure 1a). [2] The exposures are a sequence of projections calculated from 3D CAD models using algorithms from computed Volumetric additive manufacturing (VAM) forms complete 3D objects in a single photocuring operation without layering defects, enabling 3D printed polymer parts with mechanical properties similar to their bulk material counterparts. This study presents the first report of VAM-printed thiol-ene resins. With well-ordered molecular networks, thiol-ene chemistry accesses polymer materials with a wide range of mechanical properties, moving VAM beyond the limitations of commonly used acrylate formulations. Since free-radical thiol-ene polymerization is not inhibited by oxygen, the nonlinear threshold response required in VAM is introduced by incorporating 2,2,6,6-tetrameth...

Glass is increasingly desired as a material for manufacturing complex microscopic geometries, from the micro-optics in compact consumer products to microfluidic systems for chemical synthesis and biological analyses. As the size, geometric, surface roughness, and mechanical strength requirements of glass evolve, conventional processing methods are challenged. We introduce microscale computed axial lithography (micro-CAL) of fused silica components, by tomographically illuminating a photopolymer-silica nanocomposite that is then sintered. We fabricated three-dimensional microfluidics with internal diameters of 150 micrometers, free-form micro-optical elements with a surface roughness of 6 nanometers, and complex high-strength trusses and lattice structures with minimum feature sizes of 50 micrometers. As a high-speed, layer-free digital light manufacturing process, micro-CAL can process nanocomposites with high solids content and high geometric freedom, enabling new device structures and applications.

Flexible electronic skin with features that include sensing, processing, and responding to stimuli have transformed human–robot interactions. However, more advanced capabilities, such as human‐like self‐protection modalities with a sense of pain, sign of injury, and healing, are more challenging. Herein, a novel, flexible, and robust diffusive memristor based on a copolymer of chlorotrifluoroethylene and vinylidene fluoride (FK‐800) as an artificial nociceptor (pain sensor) is reported. Devices composed of Ag/FK‐800/Pt have outstanding switching endurance >106 cycles, orders of magnitude higher than any other two‐terminal polymer/organic memristors in literature (typically 102–103 cycles). In situ conductive atomic force microscopy is employed to dynamically switch individual filaments, which demonstrates that conductive filaments correlate with polymer grain boundaries and FK‐800 has superior morphological stability under repeated switching cycles. It is hypothesized that the high thermal stability and high elasticity of FK‐800 contribute to the stability under local Joule heating associated with electrical switching. To mimic biological nociceptors, four signature nociceptive characteristics are demonstrated: threshold triggering, no adaptation, relaxation, and sensitization. Lastly, by integrating a triboelectric generator (artificial mechanoreceptor), memristor (artificial nociceptor), and light emitting diode (artificial bruise), the first bioinspired injury response system capable of sensing pain, showing signs of injury, and healing, is demonstrated.

Shape memory polymers (SMPs) are stimuli responsive materials with programmable recovery from a deformed state. SMP behavior is often impacted by manufacturing features like layering that can impart anisotropic responses....

Volumetric additive manufacturing (VAM) enables rapid printing into a wide range of materials, offering significant advantages over other printing technologies, with a lack of inherent layering of particular note. However, VAM suffers from striations, similar in appearance to layers, and similarly limiting applications due to mechanical and refractive index inhomogeneity, surface roughness, etc. We hypothesize that these striations are caused by a self-written waveguide effect, driven by the gelation material nonlinearity upon which VAM relies, and that they are not a direct recording of non-uniform patterning beams. We demonstrate a simple and effective method of mitigating striations via a uniform optical exposure added to the end of any VAM printing process. We show this step to additionally shorten the period from initial gelation to print completion, mitigating the problem of partially gelled parts sinking before print completion, and expanding the range of resins printable in any VAM printer.

We present a general approach to isolate chemical reaction mechanism as an independently controllable variable across chemically distinct systems. Modern approaches to reduce the computational expense of molecular dynamics simulations often group multiple atoms into a single “coarse-grained” interaction site, which leads to a loss of chemical resolution. In this work we convert this shortcoming into a feature and use identical coarse-grained models to represent molecules that share nonreactive characteristics but react by different mechanisms. As a proof of concept, we use this approach to simulate and investigate distinct, yet similar, trifunctional isocyanurate resin formulations that polymerize by either chain- or step-growth. Because the underlying molecular mechanics of these models are identical, all emergent differences are a function of the reaction mechanism only. We find that the microscopic morphologies resemble related all-atom simulations and that simulated mechanical testing reasonably agrees with experiment.

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202100700dramatically reduced after deposition from the nozzle, thus allowing for ink composition flexibility to encompass a wide range of mechanical properties. [11,12] However, materials with poor hysteretic recovery or low yield stresses can limit spatial precision for complex print patterns (e.g., spanning gaps). To address these difficulties, recent published methods utilized various mechanisms to aid in filament shape retention while maintaining desired material properties. For example, embedded printing methods enable freeform printing within support-bath material that provides buoyant forces to stabilize the deposited filaments. [10] Other approaches include the use of multimaterial 3D printing for fine compositional tuning within printed materials in which scaffolding material can be precisely deposited, or manipulating an electromagnetic field to control the placement of inks doped with ferromagnetic particles. [13,14] On-demand UV curing has further improved spatial resolution of DIW by rapidly modifying ink rheology, typically through the addition of acrylate functional groups and a photoinitiator. [15][16][17] Past attempts with rapid UV curing, however, have resulted in brittle and rigid mechanical properties due to high concentrations of low-molecular-weight monomers in the ink formulations. [15] Additionally, on-demand UV curing has reduced interfacial strength between filaments resulting in anisotropic mechanical properties depending on print orientation. [15,18] This occurs as a result of uncontrolled rapid UV kinetics reaching gelation to rapidly to enable subsequent interfilament bonding, or, the formulation is too sensitive to UV light upon exiting the nozzle. Dual-curing efforts have shown promise in controlling the extent of UV-curable components to allow sufficient stiffening when printing while accessing mechanical properties inherent to tough epoxies. [15,[19][20][21] Here we expand this dual-curing approach to a urethanegrafted acrylate polymer (UGAP) in order to exploit the rheological flexibility provided by on-demand curing. Elastomeric mechanical properties provided by combinations of urethane and acrylate components and leaching of solid filler [22][23][24] produce a material that accesses previously unattainable structures often required for application spaces such as soft robotics, functional materials, and biomedical devices. [25][26][27][28]