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Undercooling metals relies on frustration of liquid–solid transition mainly by an increase in activation energy. Passivating oxide layers are a way to isolate the core from heterogenous nucleants (physical barrier) while also raising the activation energy (thermodynamic/kinetic barrier) needed for solidification. The latter is due to composition gradients (speciation) that establishes a sharp chemical potential gradient across the thin (0.7–5 nm) oxide shell, slowing homogeneous nucleation. When this speciation is properly tuned, the oxide layer presents a previously unaccounted for interfacial tension in the overall energy landscape of the relaxing material. We demonstrate that 1) the integrity of the passivation oxide is critical in stabilizing undercooled particle, a key tenet in developing heat‐free solders, 2) inductive effects play a critical role in undercooling, and 3) the magnitude of the influence of the passivating oxide can be larger than size effects in undercooling. [ABSTRACT FROM AUTHOR]

Undercooling metals relies on frustration of liquid–solid transition mainly by an increase in activation energy. Passivating oxide layers are a way to isolate the core from heterogenous nucleants (physical barrier) while also raising the activation energy (thermodynamic/kinetic barrier) needed for solidification. The latter is due to composition gradients (speciation) that establishes a sharp chemical potential gradient across the thin (0.7–5 nm) oxide shell, slowing homogeneous nucleation. When this speciation is properly tuned, the oxide layer presents a previously unaccounted for interfacial tension in the overall energy landscape of the relaxing material. We demonstrate that 1) the integrity of the passivation oxide is critical in stabilizing undercooled particle, a key tenet in developing heat‐free solders, 2) inductive effects play a critical role in undercooling, and 3) the magnitude of the influence of the passivating oxide can be larger than size effects in undercooling. [ABSTRACT FROM AUTHOR]

Paper-based platforms for biological studies have received significant attention given that cellulose is ubiquitous, biocompatible, and can be readily organized into tunable fibrous structures. In the latter form, effect of complexity in surface morphologies (roughness, porosity and fiber organization) on cell-substrate interaction has not been thoroughly explored. We infer that altering the properties of a fibrous material should lead to significant changes in cellular microenvironment and direct the deposition of structurally analogous extracellular matrix (fiber-fiber templating) like collagen. Here, we elucidate the effect of varying paper roughness and surface chemistry on NIH/3T3 fibroblasts via organization of excreted collagen. Collagen intensity was found to increase linearly with paper porosity, indicating a 3D culture platform. The intensity, however, decays over time due to biodegradation of the substrate. Stability can be improved by introducing fluorinated alkyl silanes to yield hydrophobic paper. This process concomitantly transforms the substrate to a 2D-like scaffold where collagen is predominantly assembled on the surface, thus changing the cellular microenvironment. Altering surface energy also led to fluctuations in collagen intensity and organization over time for smooth (calendered) paper substrates. We infer that the increased roughness improves collagen adsorption through capillary driven petal effect. In general, the influence of the substrate simultaneously affects its ability to host collagen and guide orientation. These findings offer insights into the effects of secondary structures and chemistry of fibrous polymeric materials on cell culture, which we propose as vital parameters when using paper-based platforms. Unlabelled Image • Collagen secreted from NIH/3T3 fibroblast cells increases linearly with paper porosity. • Paper transitions from 3D to 2D cell culture scaffold when rendered hydrophobic. • Hydrophobic paper relies on capillary driven petal effect for collagen adsorption. [ABSTRACT FROM AUTHOR]

Abstract: A facile method is reported for rapid, room‐temperature synthesis of block copolymers (BCP) of complex morphology and hence nontraditional spherical assembly. The use of solvated electrons generates radical anions on olefinic monomers, and with a felicitous choice of monomer pairs, this species will propagate bimechanistically (via radical and the anion) to form BCPs. Molecular weight of the obtained BCP range from Mw = 97 000–404 000 g mol−1 (polydispersity index, PDI = 1.4–3.0) depending on monomer pairs. The composition of the blocks can be controlled by changing monomer ratio, with the caveat that yield is affected. Detailed characterization by 2D nuclear magnetic resonance spectroscopy, differential scanning calorimetry (DSC), and analysis of the mechanisms involved indicate the structure of obtained block copolymers to be at least a triblock with a complex central unit. Evaluating trends in the Hammett parameter segregates monomer pairs into “armed and disarmed” groups with respect to radical or anionic polymerization akin to oligosaccharides synthesis. [ABSTRACT FROM AUTHOR]

Block copolymers (BCPs) self-assemble into intricate nanostructures that enhance a multitude of advanced applications in semiconductor processing, membrane science, nanopatterned coatings, nanocomposites, and battery research. Kinetics and thermodynamics of self-assembly are crucial considerations in controlling the nanostructure of BCP thin films. The equilibrium structure is governed by a molecular architecture and the chemistry of its repeat units. An enormous library of materials has been synthesized and they naturally produce a rich equilibrium phase diagram. Non-equilibrium phases could potentially broaden the structural diversity of BCPs and relax the synthetic burden of creating new molecules. Furthermore, the reliance on synthesis could be complicated by the scalability and the materials compatibility. Non-equilibrium phases in BCPs, however, are less explored, likely due to the challenges in stabilizing the metastable structures. Over the past few decades, a variety of processing techniques were introduced that influence the phase transformation of BCPs to achieve a wide range of morphologies. Nonetheless, there is a knowledge gap on how different processive pathways can induce and control the non-equilibrium phases in BCP thin films. In this review, we focus on different solvent-induced and thermally induced processive pathways, and their potential to control the non-equilibrium phases with regards to their unique aspects and advantages. Furthermore, we elucidate the limitations of these pathways and discuss the potential avenues for future investigations. [ABSTRACT FROM AUTHOR]

Cover Picture: Stabilization of Undercooled Metals via Passivating Oxide Layers (Angew. Engineering composition across a thin surface oxide layer of a metal particle, and stabilizing it with appropriate ligands, leads to a sharp surface stress that frustrates solidification. Engineering composition across a thin surface oxide layer of a metal particle, and stabilizing it with appropriate ligands, leads to a sharp surface stress that frustrates solidification. [Extracted from the article]

Energy landscape, inductive effect, metastability, phase transformation, stable undercooling Es bildet sich ein unterkühltes flüssiges Metallteilchen, was ein neues Konzept für das gezielte Engineering der Energielandschaft eines Materials unter Verwendung einer dünnen Oberflächenschicht aufzeigt, wie Martin Thuo et al. in ihrem Forschungsartikel auf S. 5993 beschreiben. Keywords: energy landscape; inductive effect; metastability; phase transformation; stable undercooling EN energy landscape inductive effect metastability phase transformation stable undercooling 5633 5633 1 03/03/21 20210308 NES 210308 B Kühle Frustration b . [Extracted from the article]

In article number 1903687, Martin Thuo and co-workers describe a unique heat-free approach for the fabrication of conductive metallic interconnects on diverse types of substrates. This method hinges on undercooled metal particles fabricated by encapsulating molten metal in thin shells to enable solidification. Heat-free solder, interconnects, liquid metal, multimaterial manufacturing, undercooled. [Extracted from the article]

Exploiting interfacial excess (Γ), Laplace pressure jump (ΔP), surface work, and coupling them to surface reactivity have led to the synthesis of undercooled metal particles. Metastability is maintained by a core–shell particle architecture. Fracture of the thin shell leads to solidification with concomitant sintering. Applying Scherer's constitutive model for load‐driven viscous sintering on the undercooled particles implies that they can form conductive traces. Combining metastability to eliminate heat and robustness of viscous sintering, an array of conductive metallic traces can be prepared, leading to plethora of devices on various flexible and/or heat sensitive substrates. Besides mechanical sintering, chemical sintering can be performed, which negates the need of either heat or load. In the latter, connectivity is hypothesized to occur via a Frenkel's theory of sintering type mechanism. This work reports heat‐free, ambient fabrication of metallic conductive interconnects and traces on all types of substrates. [ABSTRACT FROM AUTHOR]

The demand for rapid diagnostic in developing countries has recently increased, in part due to growing populations, emerging diseases, and rise in healthcare cost. Use of low-cost lateral flow/dipstick devices, especially paper-based ones, has increased. In most of the developing world, however, biomedical waste management systems either do not exist or are poor, as such, used devices either get incinerated or dumped alongside household trash. The plastic casing that is often used to hold the test strip, while useful before the test, also slows the biodegradation of the used contaminated devices. We demonstrate that by replacing the plastic casing with paper encasements, we promote biodegradation of these devices while reducing its total weight, making their transport and packaging more compact and more environmentally friendly—hence qualifying this simple modification as green engineering. The ability to use paper casing has the added advantage that devices can be readily assembled locally with ease and without need for sophisticated manufacturing tools as needed with the plastic casings. [ABSTRACT FROM AUTHOR]