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Folding the Energy Storage: Beyond the Limit of Areal Energy Density of Micro-Supercapacitors
Despite the ever-growing interest in micro-supercapacitors (MSCs) as a promising power source for microelectronics, their low areal energy density has plagued practical applications. Herein, accordion foldable MSCs (af-MSCs) are presented as a cell architectural strategy in contrast to traditional material-driven approaches. The constituent unit cells of an in-plane MSC array are compactly stacked in a confined device footprint via accordion folding. Decoupling the energy storage (MSC cells) and folding section (electrical interconnection between the cells) in the MSC array, in combination with neutral plane-controlled flexible hydrophobic cellulose nanofiber (CNF) substrates, enables the realization of the af-MSCs. The af-MSCs achieve high areal integration density with a fill factor of 81.1% and on-demand (in-series/in-parallel) cell configurations owing to the microscale direct-ink-writing of rheology-tuned MSC cell components on the CNF substrates. The af-MSC with a miniaturized footprint (22.75 mm(2)) achieves exceptional areal electrochemical performances (areal energy density of 89.2 mu Wh cm(-2)), which exceed those of previously reported in-plane MSCs
Bioadhesives based on multifunctional biopolymers for biomedical applications
With the recent advancement in emerging biomedical engineering fields, such as tissue engineering, regenerative medicine, and wearable medical devices, there is a growing need to develop adhesives that can function not only as tissue sealants for surgery and wound closure, but also attach various biomaterials and devices. These "bioadhesives" should allow refined control of cohesive and adhesive properties, while significantly improving the biocompatibility and biodegradability. For this reason, bioadhesives are being developed using a wide range of natural biopolymers with proven biocompatibility that can also impart multifunctionality either using their innate properties and/ or obtained via various chemical modifications. In this review, state-of-the-art bioadhesives made from multifunctional biopolymers are introduced. [GRAPHICS]
Electrical Transport Properties Driven by Unique Bonding Configuration in ?-GeSe
Group IV monochalcogenides have recently shown great potential for their thermoelectric, ferroelectric, and other intriguing properties. The electrical properties of group IV monochalcogenides exhibit a strong dependence on the chalcogen type. For example, GeTe exhibits high doping concentration, whereas S/Se-based chalcogenides are semiconduc-tors with sizable bandgaps. Here, we investigate the electrical and thermoelectric properties of gamma-GeSe, a recently identified polymorph of GeSe. gamma-GeSe exhibits high electrical conductivity (similar to 106 S/m) and a relatively low Seebeck coefficient (9.4 mu V/K at room temperature) owing to its high p-doping level (5 x 1021 cm-3), which is in stark contrast to other known GeSe polymorphs. Elemental analysis and first-principles calculations confirm that the abundant formation of Ge vacancies leads to the high p -doping concentration. The magnetoresistance measurements also reveal weak antilocalization because of spin-orbit coupling in the crystal. Our results demonstrate that gamma-GeSe is a unique polymorph in which the modified local bonding configuration leads to substantially different physical properties
A machine learning approach to discover migration modes and transition dynamics of heterogeneous dendritic cells
Dendritic cell (DC) migration is crucial for mounting immune responses. Immature DCs (imDCs) reportedly sense infections, while mature DCs (mDCs) move quickly to lymph nodes to deliver antigens to T cells. However, their highly heterogeneous and complex innate motility remains elusive. Here, we used an unsupervised machine learning (ML) approach to analyze long-term, two-dimensional migration trajectories of Granulocyte-macrophage colony-stimulating factor (GMCSF)-derived bone marrow-derived DCs (BMDCs). We discovered three migratory modes independent of the cell state: slow-diffusive (SD), slow-persistent (SP), and fast-persistent (FP). Remarkably, imDCs more frequently changed their modes, predominantly following a unicyclic SD -> FP -> SP -> SD transition, whereas mDCs showed no transition directionality. We report that DC migration exhibits a history-dependent mode transition and maturation-dependent motility changes are emergent properties of the dynamic switching of the three migratory modes. Our ML-based investigation provides new insights into studying complex cellular migratory behavior
Buried Guanidinium Passivator with Favorable Binding Energy for Perovskite Solar Cells
Rational design and modification of the buried interface toward high performance perovskite solar cells (PSCs) are highly desired and challenging. Here, we demonstrate a series of guanidinium passivators with multiamine substitutions to shed light on the effective passivation geometry at the SnO2/perovskite heterojunction interface. Comparative theoretical and experimental studies reveal that the binding geometry of the highly polarized imine moiety in guanidinium passivators dominates its energeti-cally favorable passivation on the SnO2 surface, which decreases the trap density to 1.11 x 1016 cm-3 with reduced interior/interface nonradiative recombination in the unsymmetrical aminoguanidine hydrochloride (Agu) platform. Consequently, the PSCs with buried Agu passivator deliver a champion power conversion efficiency (PCE) of 24.4% with an advanced open-circuit voltage (VOC) of 1.197 V and prolonged lifetime over 90% of the initial PCE after 900 h in ambient conditions
Human atlastins are sufficient to drive the fusion of liposomes with a physiological lipid composition
The dynamin-like GTPase atlastin is believed to be the minimal machinery required for homotypic endoplasmic reticulum (ER) membrane fusion, mainly because Drosophila atlastin is sufficient to drive liposome fusion. However, it remains unclear whether mammalian atlastins, including the three human atlastins, are sufficient to induce liposome fusion, raising doubts about their major roles in mammalian cells. Here, we show that all human atlastins are sufficient to induce fusion when reconstituted into liposomes with a lipid composition mimicking that of the ER. Although the fusogenic activity of ATL1, which is predominantly expressed in neuronal cells, was weaker than that of ATL2 or ATL3, the addition of M1-spastin, a neuron-specific factor, markedly increased ATL1-mediated liposome fusion. Although we observed efficient fusion between ER microsomes isolated from cultured, non-neuronal cells that predominantly express ATL2-1, an autoinhibited isoform of ATL2, ATL2-1 failed to support liposome fusion by itself as reported previously, indicating that cellular factors enable ATL2-1 to mediate ER fusion in vivo. Atlastins regulate the structure and function of the endoplasmic reticulum (ER). In this study, using reconstituted proteoliposomes with a lipid composition mimicking that of the ER, Jang et al. show that all human atlastins are sufficient to drive membrane fusion
All-natural water-resistant paper coated by chitosan nanowhiskers through hydrophilic-to-hydrophobic self-assembly
Although chitosan-coated hydrostable papers are promising alternatives to non-degradable plastic-coated papers, an acidic chitosan solution is not eco-friendly. Therefore, we developed a non-acidic aqueous coating technique for preparing all-natural water-resistant papers using chitosan nanowhiskers (CSWs). As the CSWs disperse in water after synthesis, they form a hydrophobic layer on the paper after the coating process owing to the hydrophilic-to-hydrophobic self-assembly. Quantum simulations reveal that the repulsion between protonated amine groups contributes to water dispersibility; however, their interfibrillar interaction after coating is hardly dissociated by water. Together with soybean oil, the CSW- and oil-coated papers (C/O-papers) exhibit significantly higher water contact angles (95.8??) and absorption (6.0%) than control paper (21.9?? and 91.9%, respectively). Moreover, the C/O-papers had a 16.0- and 9.1-fold higher mechanical modulus and strength (1498.5 and 31.0 MPa, respectively) than control paper (93.8 and 3.4 MPa, respectively) under wet conditions. Therefore, bio-renewable water-resistant paper has great potential for preparing disposable materials
Intestinal Peyer's Patches: Structure, Function, and In Vitro Modeling
Backgound:Considering the important role of the Peyer's patches (PPs) in gut immune balance, understanding of the detailed mechanisms that control and regulate the antigens in PPs can facilitate the development of immune therapeutic strategies against the gut inflammatory diseases.Methods:In this review, we summarize the unique structure and function of intestinal PPs and current technologies to establish in vitro intestinal PP system focusing on M cell within the follicle-associated epithelium and IgA(+) B cell models for studying mucosal immune networks. Furthermore, multidisciplinary approaches to establish more physiologically relevant PP model were proposed.Results:PPs are surrounded by follicle-associated epithelium containing microfold (M) cells, which serve as special gateways for luminal antigen transport across the gut epithelium. The transported antigens are processed by immune cells within PPs and then, antigen-specific mucosal immune response or mucosal tolerance is initiated, depending on the response of underlying mucosal immune cells. So far, there is no high fidelity (patho)physiological model of PPs; however, there have been several efforts to recapitulate the key steps of mucosal immunity in PPs such as antigen transport through M cells and mucosal IgA responses.Conclusion:Current in vitro PP models are not sufficient to recapitulate how mucosal immune system works in PPs. Advanced three-dimensional cell culture technologies would enable to recapitulate the function of PPs, and bridge the gap between animal models and human
Controlling the formation energy of perovskite phase via surface polarity of substrate for efficient pure-blue light-emitting diodes
Quasi-two-dimensional (quasi-2D) perovskites are composed of self-organized multiple-quantum-well structures. Imbalanced crystallization during the solution-processed deposition results in the formation of different 2D phases, which are affected by the surface polarity of substrates. Herein, we investigate the influence of the surface polarity of the underlying hole injection layer (HIL) on the crystallization dynamics of each 2D phase and the luminescence properties of resulting quasi-2D perovskite films. Incorporating L-dopa involving hydroxyl groups into the HIL gives the substrate a higher surface polarity, allowing the decrease in the critical free energy of nucleation. This HIL ensures the formation of dense nuclei involving a small-sized nucleus, which enables the quasi-2D perovskite film to entail a lower-n-dominated phase distribution. The modulated phase distribution eventually induces a hypsochromically shifted luminescence spectrum. Furthermore, by controlling the ratio of L-phenylalanine and L-dopa, efficient perovskite light-emitting diodes (PeLEDs) having well-matched electronic structure and pure-blue perovskite emitter are realized with a maximum external quantum efficiency of 5.57% at 472 nm. This work provides a facile approach to achieving efficient pure-blue PeLEDs