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Visualizing the network of a solvent‐swollen polymer gel remains problematic. To address this challenge, open transmission electron microscopy (TEM) was applied to thin gel films permeated by a nonvolatile ionic liquid. The targeted physical gels were prepared by cooling concentrated solutions of poly(ethylene glycol) in 1‐ethyl‐3‐methyl imidazolium ethyl sulfate [EMIM][EtSO4]. During the cooling, gelation occurred by a frustrated crystallization of the dissolved polymer, leading to a percolated, solvent‐permeated semicrystalline network in which nanoscale polymer crystals acted as crosslinks. Crystalline features ranging from ~5 to ~200 nm were observed, with the visible network strands dominantly consisting of long curvilinear crystallites of ~15–20 nm diameter. Nascent spherulites irregularly decorated the network, creating a complex structural hierarchy that complicated analyses. Lacking diffraction contrast, TEM did not visualize the many disordered, fully solvated PEG chains present in the voids between crystals. Recognizing that a network's three dimensionality is ambiguous when assessed through two‐dimensional microscopy projections, a small gel region was studied by TEM tomography, revealing a nearly isotropic three‐dimensional arrangement of the curvilinear crystallites, which displayed remarkably uniform cylindrical cross sections.

As a class of semiconductor nanocrystals that exhibit high photoluminescence quantum yield (PLQY) at tunable wavelengths, perovskite nanocrystals (PNCs) are attractive candidates for optoelectronic and light‐emitting devices. However, attempts to optimize PNC integration into such applications suffer from PNC instability and loss of PL over time. Here, we describe the impact of organic and polymeric N‐oxides when used in conjunction with PNCs, whereby a significant increase in PNC quantum yield is observed in solution, and stable PL emission is obtained in polymeric nanocomposites. Specifically, when using aliphatic N‐oxides in ligand exchange with CsPbBr3PNCs in solution, a substantial boost in PNC brightness is observed (~40% or more PLQY increase), followed by an alteration of the perovskite chemistry. When N‐oxide substituents are positioned pendent to a poly(n‐butyl methacrylate) backbone, the optically clear flexible nanocomposite films obtained have bright PL emission and maintain optical clarity for months. X‐ray diffraction is useful for characterizing the PNC crystalline structure following exposure to aliphatic N‐oxides, while electron microscopy (EM) and small‐angle X‐ray scattering (SAXS) measurements of the PNC‐polymer nanocomposites show this polymeric N‐oxide platform to cleanly disperse PNCs in flexible polymer films.

We describe a fully open‐sourced Python package to process raw X‐ray scattering data using a GANESHA SAXSLAB facility, and review in this manuscript the connection of X‐ray scattering theories with the open‐sourced package. This package affords researchers more flexibility in analyzing and visualizing X‐ray scattering and reflectivity data from what is now a commonplace facility at many universities and research laboratories engaged in polymer research. We briefly review the applications of X‐ray scattering and diffraction, followed by the scattering theories. A pedagogical introduction to processing X‐ray scattering data is provided using the modules in the Python package. We compare conventions to visualize and interpret transmission and grazing‐incidence scattering data using self‐assembled lamellar morphology of bottlebrush copolymers as an example, then describe how area detectors measure specular and off‐specular reflectivity. Examples of in‐house reflectivity and grazing incidence scattering for the metrological examination of a grating are provided, where the full pitch and pitch height of a line pattern is measured easily without needing to simulate the full scattering intensity profile.

Star block copolymers (s-BCPs) have potential applications as novel surfactants or amphiphiles for emulsification, compatibilization, chemical transformations, and separations. s-BCPs have chain architectures where three or more linear diblock copolymer arms comprised of two chemically distinct linear polymers, e.g., solvophobic and solvophilic chains, are covalently joined at one point. The chemical composition of each of the subunit polymer chains comprising the arms, their molecular weights, and the number of arms can be varied to tailor the surface and interfacial activity of these architecturally unique molecules. This makes identification of the optimal s-BCP design nontrivial as the total number of plausible s-BCP architectures is experimentally or computationally intractable. In this work, we use molecular dynamics (MD) simulations coupled with a reinforcement learning-based Monte Carlo tree search (MCTS) to identify s-BCP designs that minimize the interfacial tension between polar and nonpolar solvents. We first validate the MCTS approach for the design of small- and medium-sized s-BCPs and then use it to efficiently identify sequences of copolymer blocks for large-sized s-BCPs. The structural origins of interfacial tension in these systems are also identified by using the configurations obtained from MD simulations. Chemical insights into the arrangement of copolymer blocks that promote lower interfacial tension were mined using machine learning (ML) techniques. Overall, this work provides an efficient approach to solve design problems via fusion of simulations and ML and provides important groundwork for future experimental investigation of s-BCPs for various applications.

Relativistic jets are observed from accreting and cataclysmic transients throughout the Universe, and have a profound impact on their surroundings1,2. Despite their importance, their launch mechanism is not known. For accreting neutron stars, the speed of their compact jets can reveal whether the jets are powered by magnetic fields anchored in the accretion flow3or in the star itself4,5, but so far no such measurements exist. These objects can show bright explosions on their surface due to unstable thermonuclear burning of recently accreted material, called type-I X-ray bursts6, during which the mass-accretion rate increases7–9. Here, we report on bright flares in the jet emission for a few minutes after each X-ray burst, attributed to the increased accretion rate. With these flares, we measure the speed of a neutron star compact jet to be v=0.38−0.08+0.11c, much slower than those from black holes at similar luminosities. This discovery provides a powerful new tool in which we can determine the role that individual system properties have on the jet speed, revealing the dominant jet launching mechanism.

Structured liquids stabilized by interfacial assemblies enable spatial control over chemical systems. To prescribe a lifetime for structured liquids requires that the interfacially trapped material eventually reverts to molecularly dissolved species. Here, we show that poly(acrylic acid) fueled with carbodiimide segregates to an oil-water interface and forms assemblies of aggregates, solidifying the interface. When the fuel is consumed, the assembly dissipates into soluble polymer chains, destroying any out-of-equilibrium structure imparted to the liquid. We exploit this phenomenon to control liquid compartment temporal stability. Using interfacial rheology, we identify crossover points in the interfacial storage and loss moduli at times commensurate with the fuel concentration, evidencing transitions from solid-like to liquid-like assemblies that cause compartmentalized liquids to burst. These solid-like assemblies demonstrate reduced permeability to dye, showing the potential of this system for timed partitioning or release of chemical species. This work opens a pathway to time- and shape-programmable chemical systems.

The self-assembly of high-χ low-Nblock copolymers (BCPs) can give patterns with sub-10 nm full pitch, serving as a promising alternative to photolithographic methods. In this work, we synthesized poly(solketal methacrylate)-block-polystyrene copolymers, PSM-b-PS, with various volume ratios of the two blocks. After hydrolysis of the PSM block into poly(glycerol monomethacrylate), PGM, the BCPs had both lamellar and cylindrical microdomain morphologies in the bulk phase and in thin films. In addition to our previously developed solid-state hydrolysis strategy involving trifluoroacetic acid vapor, we developed a new photoinduced solid-state hydrolysis using photoacid generators, PAGs, embedded within the polymer films. After exposure to UV followed by a postexposure baking or solvent vapor annealing, the BCPs transitioned from the disordered, phase-mixed state into laterally ordered cylindrical patterns. In comparison to linear BCPs that rely on a random copolymer layer to modify interfacial interactions with the substrate to promote an orientation of the microdomains normal to the interface, we found that the microdomains in bottlebrush multiblock copolymers oriented normal to the interface absent substrate modification due to the chain architecture.

The liquid–liquid interface provides a promising platform to construct supramolecular polymers and materials with advanced functions. However, supramolecular polymerization at the interface usually requires monomers with different or even orthogonal solubilities, which significantly limit the number of usable monomers. Here, we report a new strategy to construct supramolecular polymer networks at the oil–water interface using a water-soluble catechol–iron complex and an oil-soluble diend-functionalized polymer. Owing to the dynamic catechol–iron coordination bond and imine bond, the resulting supramolecular polymer networks demonstrate excellent dynamic features and responsiveness to different stimuli including the pH, redox, competing ligands, and temperature. With a supramolecular polymer network serving as a building block, emulsions and 2D films can be generated that have potential applications in encapsulation, release, and molecular separation.

Cellulose, often considered a highly promising substitute for petroleum-based plastics, offers several compelling advantages, including abundant availability, cost-effectiveness, environmental friendliness, and biodegradability. However, its inherent highly crystalline structure and extensive hydrogen-bonded network pose challenges for processing and recycling. In this study, we introduce the concept of cellulose vitrimers (CVs), wherein dynamic bonds are incorporated to reconfigure the hydrogen-bonded network, resulting in a mechanically robust, highly transparent material. CVs exhibit exceptional malleability, thermal stability, and noteworthy resistance to water and solvents. Due to the dynamic bond disassociation, CVs can be effectively chemically recycled using a well-established “dissolution-and-reforming” process. Moreover, CVs have proven successful as flexible substrate materials for organic solar cells, outperforming traditional petroleum-based polyethylene naphthalate (PEN). Given these advantages, CVs have the potential to replace conventional petroleum-based materials as recyclable and environmentally friendly alternatives, particularly within the realm of electronic devices and displays.

Formation damage due to fines migration after water breakthrough during oil and gas production results in significant well productivity decline. A recent study derived an analytical model for fines migration during commingled water-oil production in homogeneous reservoirs. Yet, reservoir heterogeneity highly affects well productivity. This paper develops an analytical model for layer-cake reservoirs. We develop a novel methodology of characterising productivity decline by the function of impedance versus water-cut, two quantities that are commonly measured throughout the production life of the well. The methodology is based on a new analytical model for inflow performance in layer-cake reservoirs under fines migration. The new model integrates pseudo phase-permeability functions for water-oil flow with equations for fines release and induced permeability damage. The analytical model reveals linear well impedance growth versus water-cut increase, where the slope is determined by a modified form of the mobility ratio which includes the extent of formation damage. This linear form is shown to arise when the formation damage factor is constant, regardless of the reservoir permeability distribution. The model is validated by comparison with production histories of five wells from three fields, which exhibit good agreement with the linear trend predicted by the new model. The explicit formulae allow for prediction of productivity at abandonment, determining the optimal well stimulation time, as well as reconstructing skin values during the early stages of production to better estimate the influences of other formation damage factors, like those induced during drilling and completion.

Reversible Pickering emulsions, achieved by switchable, interfacially active colloidal particles, that enable on-demand emulsification/demulsification or phase inversion, hold substantial promise for biphasic catalysis, emulsion polymerization, cutting fluids, and crude oil pipeline transportation. However, particles with such a responsive behavior usually require complex chemical syntheses and surface modifications, limiting their extensive use. Herein, we report a simple route to generate emulsions that can be controlled and reversibly undergo phase inversion. The emulsions are prepared and stabilized by the interfacial assembly of polyoxometalate (POM)–polymer, where their electrostatic interaction at the interface is dynamic. The wettability of the POMs that dictates the emulsion type can be readily regulated by tuning the number of polymer chains bound to POMs, which, in turn, can be controlled by varying the concentrations of both components and the water/oil ratio. In addition, the number of polymer chains anchored to the POMs can be varied by controlling the number of negative charges on the POMs through an in situ redox reaction. As such, a reversible inversion of the emulsions can be triggered by switching between exposure to ultraviolet light and the introduction of oxygen. Combining the functions of POM itself, a cyclic interfacial catalysis system was realized. Inversion of the emulsion also affords a pathway to high-internal-phase emulsions. The diversity of the POMs, the polymers, and the responsive switching groups open numerous new, simple strategies for designing a wide range of responsive soft matter for cargo loading, controlled release, and delivery in biomedical and engineering applications without time-consuming particle syntheses.

Bottlebrush polymer surfactants (BPSs), formed by the interfacial interactions between bottlebrush polymers (BPs) with poly(acrylic acid) side chains dissolved in an aqueous phase and amine-functionalized ligands dissolved in the oil phase, assemble and bind strongly to the fluid–fluid interface. The ratio between NBB(backbone degree of polymerization) and NSC(side chain degree of polymerization) defines the initial assembly kinetics, interface packing efficiency, and stress relaxation. The equilibrium interfacial tension (γ) increases when NBB< NSC, but decreases when NBB≫ NSC, correlating to a pronounced change in the effective shape of the BPs from being spherical to worm-like structures. The apparent surface coverage (ASC), i.e., the interfacial packing efficiency, decreases as NBBincreases. The dripping-to-jetting transition of an injected polymer solution, as well as fluorescence recovery after photobleaching experiments, revealed faster initial assembly kinetics for BPs with higher NBB. Euler buckling of BPS assemblies with different NBBvalues was used to characterize the stress relaxation behavior and bending modulus. The stress relaxation behavior was directly related to the ASC, reflecting the strong influence of macromolecular shape on packing efficiency. The bending modulus of BPSs decreases for NBB< NSC, but increased when NBB≫ NSC, showing the effect of molecular architecture and multisite anchoring. All-liquid printed constructs with lower NBBBPs yielded more stable structured liquids, underscoring the importance of macromolecular packing efficiency at fluid interfaces. Overall, this work elucidates fundamental relationships between nanoscopic structures and macroscopic properties associated with various bottlebrush polymer architectures, which translate to the stabilization of all-fluidic printed constructs.

The direct 3D printing of ultralight architectures with ultralow-concentration 2D nanomaterial inks is necessary yet challenging. Here, we describe an emulsion-based ink for direct printing using 2D nanomaterials, i.e., MXene and graphene oxide (GO). The electrostatic interactions between the ligands in the oil phase and the 2D nanomaterials in the aqueous phase help form sheet-like surfactants at the interface. The interactions between the anchored ligands among different droplets dictate the rheological characteristics of inks, enabling a gel-like behavior ideally suitable for 3D printing at ultralow concentrations of 2D nanomaterials. The 3D printed foams possess lightweight structures with densities of 2.8 mg cm–3(GO-based) and 4.1 mg cm–3(MXene-based), and the latter integrates outstanding electrical conductivity, electromagnetic shielding performance, and thermal insulation comparable to air. This work describes a general approach for direct-printing ultralight porous structures that take advantage of the inherent properties of 2D building blocks.

Nanoparticle surfactant (NPS) offers a powerful strategy to generate all-liquid constructs that integrate the inherent properties of the NPs into 3D architectures. Here, using the co-assembly of fluorescent polymeric nanoparticles and amine-functionalized polyhedral oligomeric silsesquioxane, the assembly and jamming behavior of a new type of NPS at the oil–water interface is uncovered. Unlike “solid” inorganic nanoparticles, “soft” polymeric nanoparticles can reorganize when jammed, leading to a relaxation and deformation of the interfacial assemblies, for example, the 3D printed sugar-coated haw stick-like liquid tubules. With NPS serving as emulsifiers, stable Pickering emulsions are prepared that can be converted into robust colloidosomes with pH responsiveness, showing numerous potential applications for encapsulation and controlled release.

The objectives of this investigation were to experimentally examine the cage motion and ball-cage contact forces for an angular contact ball bearing (ACBB) operating under various load and speed combinations. In order to achieve the objectives, a Counter Rotating Angular Contact Ball Bearing Test Rig (CRACTR) was designed and developed such that both the races of an ACBB can be rotated simultaneously in opposite directions, providing valuable insights into the ball-cage interaction. Five proximity probes were used concurrently to measure the in-plane (radial) and out-of-plane (axial) motion for three commercially available cage designs. Two load cells were used to measure the contact forces between the balls and cage pocket. The experimental results demonstrate that high inner race speeds and high axial loads develop the smallest and most circular cage whirl motions. Additionally, cage radius, cage pocket clearance, cage pocket area and cage inertia were the prominent factors affecting the magnitude of cage whirl. Experimental results also indicate that contact forces between the ball and cage pocket increase linearly with the increased race speeds. Ball-cage contact force was shown to be different for the three cages and was primarily governed by the cage pocket area and the cage radius. Results from this investigation can be utilized to predict the correlation between the ball-cage contact forces and the race speeds, and identify the key parameters governing the stable cage motion during bearing operation.

Amyotrophic lateral sclerosis, or motor neuron disease, is an uncommon progressive neurological disorder. Professionals working in the perioperative field may encounter patients with amyotrophic lateral sclerosis only rarely. The relevant published literature on amyotrophic lateral sclerosis is broad in scope, but a contemporary review focused on the perioperative period is absent. This structured narrative review seeks to provide a summary of the contemporary management of patients and then focuses on eliciting if there are perioperative management considerations specific to amyotrophic lateral sclerosis that can be optimised. A comprehensive structured narrative literature review, including grey literature searching, indicated worsening ventilatory failure is of prime concern but that patients may present with a broad range of neurological symptoms, and that cardiovascular and cognitive dysfunction specific to amyotrophic lateral sclerosis may exist and be occult. Exacerbation of neuromuscular weakness during the perioperative period is multifaceted and requires the application of a high standard of the core principles of surgical and anaesthetic management of neuromuscular disease. Standard perioperative approaches require rigorous attention and potential exists for significant alteration. There is a potential high risk of postoperative increased morbidity from neurological decline and mortality from pulmonary complications. A meticulous approach to planning preoperative assessment, shared decision-making, intraoperative and postoperative care is required.

The relaxation and aging of an assembly of spherical nanoparticles (NPs) at a water–oil interface are characterized in situ by grazing incidence X-ray photon correlation spectroscopy. The dynamics of the interfacial assembly is measured while the interface saturates with NPs. Weak attractions between NPs lead to gel-like structures in the assembly, where the in-plane ordering is inhibited by the broad size distribution of the NPs. Structural rearrangements on the length scale of the NP–NP center-to-center distances proceed by intermittent fluctuations instead of continuous cooperative motions. The coexistence of rapid and slow NP populations is confirmed, as commonly observed in soft glass-forming materials. Dynamics are increasingly slowed as the NPs initially segregate to the locally clustered interface. The structural relaxation of the NPs in these localized clusters is 5 orders of magnitude slower than that of free particles in the bulk. When the interface is nearly saturated, the time for relaxation increases suddenly due to the onset of local jamming, and the dynamics slow exponentially afterward until the system reaches collective jamming by cooperative rearrangements. This investigation provides insights into structural relaxations near the glass transition and the evolution of the structure and dynamics of the assemblies as they transition from an isotropic liquid to a dense disordered film.

Obtaining homogeneous blends of two covalently cross-linked polymers by mechanical mixing is not possible due to their permanent network topologies. Here, we demonstrate an effective route to prepare polymer blends from the common cross-linked epoxidized natural rubber (ENR) and epoxy resin vitrimer (EV) by mechanical mixing. Interfacial exchange reactions between these two networks occur by a dynamic transesterification. The as-prepared ENR–EV blends show excellent mechanical strength, extensibility, and thermal stability. Moreover, they also show typical vitrimeric properties, including self-healing, welding, and reprocessability. This work demonstrates a large-scale preparation of vitrimeric materials with high performance and versatility from commercially available polymers and affords a promising strategy to recycle both waste rubbers and resins.

The paper presents a strength-failure mechanism for colloidal detachment by breakage and permeability decline in reservoir rocks. The current theory for permeability decline due to colloidal detachment, including microscale mobilisation mechanisms, mathematical and laboratory modelling, and upscaling to natural reservoirs, is developed only for detrital particleswith detachment that occurs against electrostatic attraction. We establish a theory for detachment of widely spread authigenic particlesdue to breakage of the particle-rock bonds, by integrating beam theory of particle deformation, failure criteria, and creeping flow. Explicit expressions for stress maxima in the beam yield a graphical technique to determine the failure regime. The core-scale model for fines detachment by breakage has a form of maximum retention concentration of the fines, expressing rock capacity to produce breakable fines. This closes the governing system for authigenic fines transport in rocks. Matching of the lab coreflood data by the analytical model for 1D flow exhibits two-population particle behaviour, attributed to simultaneous detachment and migration of authigenic and detrital fines. High agreement between the laboratory and modelling data for 16 corefloods validates the theory. The work is concluded by geo-energy applications to (i) clay breakage in geological faults, (ii) typical reservoir conditions for kaolinite breakage, (iii) well productivity damage due to authigenic fines migration, and (iv) feasibility of fines breakage in various geo-energy extraction technologies.

A Gibbs monolayer of jammed, or nearly jammed, spherical nanoparticles was imaged at a liquid surface in real time by in-situscanning electron microscopy performed at the single-particle level. At nanoparticle areal fractions above that for the onset of two-dimensional crystallization, structural reorganizations of the mobile polymer-coated particles were visualized after a stepwise areal compression. When the compression was small, slow shearing near dislocations and reconfigured nanoparticle bonding were observed at crystal grain boundaries. At larger scales, domains grew as they rotated into registry by correlated but highly intermittent motions. Simultaneously, the areal density in the middle of the monolayer increased. When the compression was large, the jammed monolayers exhibited out-of-plane deformations such as wrinkles and bumps. Due to their large interfacial binding energy, few (if any) of the two-dimensionally mobile nanoparticles returned to the liquid subphase. Compressed long enough (several hours or more), monolayers transformed into solid nanoparticle films, as evidenced by their cracking and localized rupturing upon subsequent areal expansion. These observations provide mechanistic insights into the dynamics of a simple model system that undergoes jamming/unjamming in response to mechanical stress.

Organic photovoltaics (OPVs) have the advantages of being lightweight, mechanically flexible, and solution-processable over large areas, and for decades, they have been the focus of the academic and industrial communities. Recent progress in the design of high-performance organic semiconductors and device optimization has promoted solar cell efficiencies of up to 19%, showing great promise for commercialization. Optimally designed OPVs are achieved using a bicontinuous interpenetrating network of donor and acceptor materials in between two charge-collecting electrodes. Charge extraction and transport between metal electrodes and organic semiconductors are crucial to device operation. The energy-level mismatch when metal electrodes and organic semiconductors are in contact usually induces additional energy barriers and resultant inefficient charge transport and collection, leading to charge carrier recombination at the interface and inferior device performance. To align energy levels at the interface, interlayer materials and their integration into devices have emerged as a widely used strategy to promote the performance of solar cell devices. Interlayer materials have the ability to modify the work functions (WFs) of metal electrodes, holding the potential to enhance the built-in electrostatic field (Vbi) of the devices and suppress the charge recombination loss, which is beneficial to improving the open circuit voltage (VOC), short circuit current density (JSC), and fill factor (FF) of the solar cells.

The severe acute respiratory syndrome coronavirus (SARS-CoV-2) pandemic has disrupted normal health care utilization patterns worldwide, including decreasing emergency department (ED) visits for various medical emergencies. We examined whether this pattern was present in febrile pediatric oncology patients. In this single-center cohort study, we conducted a retrospective chart review of ED visits of febrile pediatric oncology patients during the first 4 months of the global SARS-CoV-2 pandemic and compared those data to the same time periods in the previous 2 years. During the first 5 months of the pandemic, 25 pediatric oncology patients with fever visited our ED; 65 children visited during the same time period in 2018; and 60 visited in 2019. Compared with 2018 and 2019, encounters for 2020 were decreased by 62% and 58%, respectively. A significantly higher percentage of febrile pediatric oncology patients (84%) were admitted to our hospital during the pandemic compared the previous years (58%). Of concern is the possibility that fear of exposure to coronavirus disease-19 (COVID-19) at our health care facility prompted caregivers of pediatric oncology patients to avoid seeking care for their child with fever. Consistent communication with families about the life-threatening nature of fever should be prioritized among pediatric oncology providers.

Chemical systems may be maintained far from equilibrium by sequestering otherwise reactive species into different microenvironments. It remains a significant challenge to control the amount of chemical energy stored in such systems and to utilize it on demand to perform useful work. Here, we show that redox-active molecules compartmentalized in multiphasic structured-liquid devices can be charged and discharged to power a load on an external circuit. The two liquid phases of these devices feature charge-complementary polyelectrolytes that serve a dual purpose: they generate an ionically conductive coacervate membrane at the liquid–liquid interface, providing structural support; they also mitigate active-material crossover between phases via ion pairing with the oppositely charged anolyte and catholyte active materials. Structured-liquid batteries enabled by this design were rechargeable over hundreds of hours. We envision that these devices may be integrated with soft electronics to enable functional circuits for smart textiles, medical implants, and wearables.

Water-walking insects can harness capillary forces by changing their body posture to climb or descend the meniscus between the surface of water and a solid object. Controlling surface tension in this manner is necessary for predation, escape and survival. Inspired by this behaviour, we demonstrate autonomous, aqueous-based synthetic systems that overcome the meniscus barrier and shuttle cargo subsurface to and from a landing site and a targeted drop-off site. We change the sign of the contact angle of a coacervate sac containing an aqueous phase or of a hydrogel droplet hanging from the surface by controlling the normal force acting on the sac or droplet. The cyclic buoyancy-induced cargo shuttling occurs continuously, as long as the supply of reactants diffusing to the sac or droplet from the surrounding aqueous phase is not exhausted. These findings may lead to potential applications in autonomously driven reaction or delivery systems and micro-/milli-robotics.

The benefits of excess PbI2on perovskite crystal nucleation and growth are countered by the photoinstability of interfacial PbI2in perovskite solar cells (PSCs). Here we report a simple chemical polishing strategy to rip PbI2crystals off the perovskite surface to decouple these two opposing effects. The chemical polishing results in a favorable perovskite surface exhibiting enhanced luminescence, prolonged carrier lifetimes, suppressed ion migration, and better energy level alignment. These desired benefits translate into increased photovoltages and fill factors, leading to high-performance mesostructured formamidinium lead iodide-based PSCs with a champion efficiency of 24.50%. As the interfacial ion migration paths and photodegradation triggers, dominated by PbI2crystals, were eliminated, the hysteresis of the PSCs was suppressed and the device stability under illumination or humidity stress was significantly improved. Moreover, this new surface polishing strategy can be universally applicable to other typical perovskite compositions.

Conductive ionenes were synthesized by integrating the electron donor dialkoxynaphthalene (DAN) with the electron acceptor naphthalene diimide (NDI) using the Menshutkin reaction. The crystallinity and morphology of the films of these polymers can be optimized by varying the DAN-to-NDI ratio. These ionenes show strong charge transfer from DAN to NDI, though absent conjugated backbones, affording self-doping polymers with enhanced π–π interactions and excellent electronic properties. This is the first example where an electron donor can dope the electron acceptor in nonconjugated polymers, opening a new avenue for designing efficient interlayer materials. These ionenes markedly modify the electrode interface and promote efficient interfacial self-doping to boost the performance of fullerene-based, non-fullerene-based, and ternary organic solar cells, affording high power conversion efficiencies over a wide range of interlayer thicknesses, from ∼8 to ∼40 nm, with a maximum efficiency of 17.05%.

With the recent development of non-fullerene acceptors, power conversion efficiencies of bulk-heterojunction organic solar cells have exceeded 18%. The morphology of the BHJ active layer, including packing, ordering, orientation, and phase behavior of the donor(s) and acceptor(s), plays critical roles in determining the device performance. We characterized the morphology of active layers consisting of mixtures of a PTB7/PTB7-Th (donor) and ITIC (acceptor) using grazing incidence wide-angle X-ray scattering, resonant soft X-ray scattering, and solid-state nuclear magnetic resonance (ssNMR) to correlate the morphology with device performance. PTB7-Th/ITIC shows a better device performance than that of PTB7/ITIC due to a smaller π–π stacking distance and smaller domain size of the phase separated morphology. One of PTB7/ITIC samples, processed from mixed solvents (chlorobenzene/benzene = 1:1 by volume), shows a possible partial miscibility and smaller domain size as revealed by ssNMR T1ρrelaxation times, which is detrimental to device performance. ssNMR results showed that ITIC could crystallize into different forms depending on processing conditions, which may have implications on the manufacturing of devices using it as an ingredient, as well as its long-term stability in service.

Most patients who undergo curative-intent resection for pancreatic cancer are malnourished. This correlates with poor outcomes. There are no guidelines for the nutritional management of these patients. We aimed to establish current UK practice by surveying all hepatopancreatobiliary (HPB) units. Questions covered: dietetic service, nutrition risk screening (RS), micronutrients, prehabilitation, nutritional support, pancreatic exocrine replacement therapy (PERT), and details of follow-up. Twenty-six units (83.9%) responded. Twenty-three (88.5%) provide a specialist HPB dietetic service. Twelve (52.2%) cover the entire treatment pathway. Thirteen (50.0%) routinely perform RS, eleven (42.3%) check micronutrients, and fourteen (53.8%) provide a prehabilitation programme. Twelve units (46.2%) allow nutritional supplements within 48 h of surgery, and eight (30.8%) do not allow this until at least 72 h. The use of PERT and acid-suppressing agents is highly variable. Seventeen units (65.4%) routinely provide dietitian follow-up. Practice is highly variable; robust studies are required so consensus guidelines can be formulated.

Host–guest molecular recognition at the liquid–liquid interface endows the interface with unique properties, including stimuli-responsiveness and self-regulation, due to the dynamic and reversible nature of non-covalent interactions. Increasing research efforts have been put into the preparation of supramolecular interfacial systems such as films and microcapsules by integrating functional components (e.g., colloidal particles, polymers) at the interface, providing tremendous opportunities in the areas of encapsulation, delivery vehicles, and biphasic reaction systems. In this review, we summarize recent progress in supramolecular interfacial systems assembled by host–guest chemistry, and provide an overview of the fabrication process, functions, and promising applications of the resultant constructs.

Successfully interfacing enzymes and biomachinery with polymers affords on-demand modification and/or programmable degradation during the manufacture, utilization and disposal of plastics, but requires controlled biocatalysis in solid matrices with macromolecular substrates1–7. Embedding enzyme microparticles speeds up polyester degradation, but compromises host properties and unintentionally accelerates the formation of microplastics with partial polymer degradation6,8,9. Here we show that by nanoscopically dispersing enzymes with deep active sites, semi-crystalline polyesters can be degraded primarily via chain-end-mediated processive depolymerization with programmable latency and material integrity, akin to polyadenylation-induced messenger RNA decay10. It is also feasible to achieve processivity with enzymes that have surface-exposed active sites by engineering enzyme–protectant–polymer complexes. Poly(caprolactone) and poly(lactic acid) containing less than 2 weight per cent enzymes are depolymerized in days, with up to 98 per cent polymer-to-small-molecule conversion in standard soil composts and household tap water, completely eliminating current needs to separate and landfill their products in compost facilities. Furthermore, oxidases embedded in polyolefins retain their activities. However, hydrocarbon polymers do not closely associate with enzymes, as their polyester counterparts do, and the reactive radicals that are generated cannot chemically modify the macromolecular host. This study provides molecular guidance towards enzyme–polymer pairing and the selection of enzyme protectants to modulate substrate selectivity and optimize biocatalytic pathways. The results also highlight the need for in-depth research in solid-state enzymology, especially in multi-step enzymatic cascades, to tackle chemically dormant substrates without creating secondary environmental contamination and/or biosafety concerns.

Using host–guest chemistries in a biphasic system, a novel supramolecular nanoparticle surfactant (s-NPS) with redox-responsiveness is presented to structure liquids. The in situ assembly/jamming and disassembly/unjamming of s-NPSs at the oil–water interface are reversibly controlled by a switchable redox process, imparting a nanoscale redox-responsiveness, affecting the assemblies on all length scales. “Smart” all-liquid constructs including structured emulsions and programmable liquid devices are easily prepared, showing promising applications in responsive delivery, release, and reaction systems.

Protein-based electronic biomaterials represent an attractive alternative to traditional metallic and semiconductor materials due to their environmentally benign production and purification. However, major challenges hindering further development of these materials include (1) limitations associated with processing proteins in organic solvents and (2) difficulties in forming higher-order structures or scaffolds with multilength scale control. This paper addresses both challenges, resulting in the formation of one-dimensional bundles composed of electrically conductive protein nanowires harvested from the microbes Geobacter sulfurreducensand Escherichia coli. Processing these bionanowires from common organic solvents, such as hexane, cyclohexane, and DMF, enabled the production of multilength scale structures composed of distinctly visible pili. Transmission electron microscopy revealed striking images of bundled protein nanowires up to 10 μm in length and with widths ranging from 50–500 nm (representing assembly of tens to hundreds of nanowires). Conductive atomic force microscopy confirmed the presence of an appreciable nanowire conductivity in their bundled state. These results greatly expand the possibilities for fabricating a diverse array of protein nanowire-based electronic device architectures.

Typical organization of science and mathematics K12 education divides subjects into discrete courses. However, science and engineering are highly interdisciplinary fields. To better equip students to engage in the interdisciplinary nature of real-world STEM research and practice, projects can be used to highlight the interconnectivity of core subjects. Here, we present an exploratory, guided inquiry classroom research project. This work details student-led experiments combining physics and chemistry principles to fabricate silicone bouncy balls and analyze resulting mechanochemical relationships in these elastomeric materials. In this project, students embodied researchers to uncover foundational relationships among chemistry, physics, and mathematics. To do this, students used silicone kits to design an array of polymer formulations resulting in bouncy balls of varying stiffnesses. Students aimed to answer a physics-based research question using chemistry and mathematics. The resulting data was used to discuss the effect of polymer chemistry on the behavior of the bouncy balls. This exercise serves to combine hands-on fabrication methods with quantitative analysis, using experimental methods of varying costs and complexities that can be tailored to instructor time and budget. The project presented here is appropriate for upper-level high school students or first-year undergraduates. The pedagogical goal of the work is to empower students to realize and use connections between chemistry, physics, polymer science, and engineering to understand the process of material design and selection.

The phase behavior of poly(ethylene oxide) (PEO) in aqueous salt solutions has been studied many times but rarely for solution conditions relevant to the hydration process of cement, where PEO's interactions with surrounding ions modulate its application as both plasticizer and strength‐building additive. Here, the conformation, that is, coil size, of PEO was examined in aqueous solutions in the presence of sodium‐, calcium‐ and aluminum‐containing salts. Ion‐induced conformational changes for a model linear PEO were mostly unremarkable and consistent with past reports. However, trends for aluminum‐containing ions, which predominantly occur in water at neutral and basic pH as the monovalent hydroxo‐aluminate anion Al(OH)4−, were different: either present as the sodium or calcium salt, PEO's hydrodynamic radius determined by dynamic light scattering was approximately 30% larger than determined by intrinsic viscosity. The intrinsic viscosity was similar to that measured in the presence of simpler monovalent anions. We hypothesize that aluminum containing ions weakly couple the model polymer's hydroxyl end groups (present at just one chain end), creating polymeric aggregates sensitive to disruption by shearing. Supporting our argument, the hydrodynamic radius determined by dynamic light scattering dropped to the intrinsic viscosity value after hydroxyl groups were converted to methoxy groups. Weak coupling between the complex aluminum ions and the hydroxyl end group of the PEO chain results in a significant difference between the radii measured by the intrinsic viscosity and dynamic light scattering (DLS). The coupling is stable in the DLS's quiescent conditions but broken by the shear forces exerted during the intrinsic viscosity measurement.

The interfacial assembly of polystyrene-b-poly(2-vinylpyridine) (PS-b-P2VP) diblock copolymer and carboxylated carbon quantum dots (c-CQDs) at the water/oil interface and the morphology of the resultant assemblies, transferred to a solid substrate, were investigated as a function of pH and the molecular weight of PS-b-P2VP. As expected, the interfacial assembly of PS-b-P2VP and c-CQDs decreased the interfacial tension between the water and toluene. The assembly of the PS-b-P2VP is strongly dependent on pH, that is, the extent of protonation of the P2VP block and, in the presence of the c-CQDs, the extent of interactions between the P2VP block and the c-CQDs. The behavior of the P2VP block also influences the state of the PS block, with the entanglement of the PS block increasing with decreasing pH, since the extension of the PVP block into the aqueous phase increases the packing density of the PS block at the interface. This is reflected in the modulus of the assemblies at the interface where marked changes are observed. The interactions between the CQDs and PS-b-P2VP are found to be sufficiently strong to show the potential of manipulating the structure of the interface with the BCP micelles.

This paper describes a correlation between charge extraction and energy-level alignment at the interface of polymeric hole transport layers and perovskite active layers. By tailoring the composition of the conjugated backbone of the hole transport material, energy levels between perovskites and hole transport layers are varied. Matching the band alignment at perovskite/hole transport interfaces dramatically improved charge extraction and thus device performance. Time-resolved microwave conductivity measurements, performed to elucidate hole transfer kinetics, suggest that hole transport layer energy levels greatly influence hole extraction efficiency at this interface, a finding that agrees well with device performance metrics. Furthermore, photoluminescence, Mott–Schottky, and space charge limited current measurements support that energy-level alignment between the hole transport layer and perovskite active layer enables more efficient hole extraction and transport at the device interface. The insight surrounding hole extraction in inverted perovskite devices will help design effective hole transport materials, which, in turn, facilitates the production of more efficient solar cells.

The assembly and binding of nanoparticles at the interfaces of aqueous two-phase systems enable the three-dimensional (3D) printing of all-aqueous naturally occurring materials. When a dispersion of cellulose nanocrystals (CNCs) in an aqueous solution of polyethylene glycol (PEG) is brought into contact with chitosan dissolved in an aqueous solution of dextran, the CNCs and chitosan diffuse to the interface between the two immiscible aqueous solutions, electrostatically interact, and form a solid, membranous layer sufficiently rapidly to 3D print tubules of one liquid in the other. The diameter, length, spatial arrangement, and stability of the printed tubules can be broadly controlled. Adsorption and directional diffusion of ionic species across the membranous layer make heavy metal ion removal possible. The results present a platform for fabricating and developing all-aqueous compartmentalized systems where function can be independently coupled to the inherent functionality of the nanoparticles or ligands.

We report a “one-step” method for preparing conductive thin films with cylindrical microdomains oriented normal to the surface over large areas using the supramolecular assembly of poly(styrene-block-4-vinylpyridine) (PS19-b-P4VP5) and 5,10,15,20-tetrakis(4-hydroxyphenyl)-21H,23H-porphine (HOTPP). HOTPP interacts with the P4VP block by hydrogen bonding between the hydroxyl group of HOTPP and pyridine ring of PS19-b-P4VP5, forming cylindrical P4VP(HOTPP) domains having an average diameter of ∼17 nm in a PS matrix. Dynamic light scattering, contact angle, and in situgrazing incidence small-angle X-ray scattering measurements show a morphological transition from spherical micelles in solution to cylindrical microdomains oriented normal to the substrate surface during the drying process. From the dependence of current on voltage, an average current of ∼4.0 nA is found to pass through a single microdomain, pointing to a promising route for organic semiconductor device applications.

We designed and synthesized a series of fused-ring electron acceptors (FREAs) based on naphthalene-fused octacyclic cores end-capped by 3-(1,1-dicyanomethylene)-5,6-difluoro-1- indanone (NOICs) using a bottom-up approach. The NOIC series shares the same end groups and side chains, as well as similar fused-ring cores. The butterfly effects, arising from different methoxy positions in the starting materials, impact the design of the final FREAs, as well as their molecular packing, optical and electronic properties, charge transport, film morphology, and performance of organic solar cells. The binary-blend devices based on this NOIC series show power conversion efficiencies varying from 7.15% to 14.1%, due to the different intrinsic properties of the NOIC series, morphologies of blend films, and voltage losses of devices.

Producing artificial multicellular structures to process multistep cascade reactions and mimic the fundamental aspects of living systems is an outstanding challenge. Highly biocompatible, artificial systems consisting of all-aqueous, compartmentalized multicellular systems have yet to be realized. Here, a rapid multilevel compartmentalization of an all-aqueous system where a 3D sheet of subcolloidosomes encloses a mother colloidosome by interfacial phase separation is demonstrated. These spatially organized multicellular structures are termed “blastosomes” since they are similar to blastula in appearance. The barrier to nanoparticle assembly at the water–water interface is overcome using oppositely charged polyelectrolytes that form a coacervate–nanoparticle–composite network. The conditions required to trigger interfacial phase separation and form blastosomes are quantified in a mapped state diagram. We show a versatile model for constructing artificial multicellular spheroids in all-aqueous systems. The rapid interfacial assembly of charged particles and polyelectrolytes can lock in nonequilibrium shapes of water, which also enables top-down technologies, such as 3D printing and microfluidics, to program flexible compartmentalized structures.

Jammed packings of bidisperse nanospheres were assembled on a nonvolatile liquid surface and visualized to the single-particle scale by using an in situscanning electron microscopy method. The PEGylated silica nanospheres, mixed at different number fractions and size ratios, had large enough in-plane mobilities prior to jamming to form uniform monolayers reproducibly. From the collected nanometer-resolution images, local order and degree of mixing were assessed by standard metrics. For equimolar mixtures, a large-to-small size ratio of about 1.5 minimized correlated metrics for local orientational and positional order, as previously predicted in simulations of bidisperse disk jamming. Despite monolayer uniformity, structural and depletion interactions caused spheres of a similar size to cluster, a feature evident at size ratios above 2. Uniform nanoparticle monolayers of high packing disorder are sought in many liquid interface technologies, and these experiments outlined key design principles, buttressing extensive theory/simulation literature on the topic.

Simultaneously improving device efficiency and stability is the most important issue in perovskite solar cell (PSC) research. Here, we strategically introduce a multi-functional interface layer (MFIL) with integrated roles of: (1) electron transport, (2) moisture barrier, (3) near-infrared photocurrent enhancement, (4) trap passivation, and (5) ion migration suppression to enhance the device performance. The narrow-band-gap non-fullerene acceptor, Y6, was screened out to replace the most commonly used PCBM in the inverted PSCs. A significantly improved power conversion efficiency of 21.0% was achieved, along with a remarkable stability (up to 1,700 h) without encapsulation under various external stimuli (light, heat, and moisture). Furthermore, systematic studies of the molecular orientation or passivation and the charge carrier dynamics at the interface between perovskite and MFIL were presented. These results offer deep insights for designing advanced interlayers and establish the correlations between molecular orientation, interface molecular bonding, trap state density, non-radiation recombination, and the device performance.

The interfacial assembly of graphene oxide (GO) at the water/oil interface was investigated using pendant drop tensiometry as a function of the pH, GO size and concentration, and molecular weight of the polymer ligands. It was found that the smaller the lateral dimension of the GO sheets, the more rapidly the interfacial tension decreased, and the lower was the interfacial tension between the oil and water. The differences in the rates at which the interfacial tension decreased are related to the diffusion of the GO to the interface, the presentation of the GO at the interface, the degree of functionalization relative to the surface area, and the in-plane motion of the GO to accommodate the arrival of more GO at the interface to effectively cover the interface. The solidlike film formed at the interface had a modulus that increased with decreasing lateral GO dimensions.

Three fused-ring electron acceptors (FXIC-1, FXIC-2, and FXIC-3) were designed and synthesized. This FXIC series has similar electron-rich central units and the same electron-poor termini. Due to the different steric structures of fluorene, bifluorenylidene, and spirobifluorene, FXIC-1 is a one-dimensional (1D) crystal, while FXIC-2 and FXIC-3 are multidimensional (MD) amorphous materials. The conformations of the FXIC series have a slight impact on their absorption and energy levels. FXIC-1 has higher electron mobility than FXIC-2 and FXIC-3. When blending with different polymer donors (PTB7-Th, J71, and PM7), the FXIC-1-based organic solar cells have efficiencies higher than those of the FXIC-2/FXIC-3-based cells. Meanwhile, the ternary-blend cells based on PTB7-Th:F8IC with FXIC-1, FXIC-2, and FXIC-3 show similar efficiencies, which are all better than those of the binary-blend devices.

Using host–guest molecular recognition at the oil–water interface, a new type of photoresponsive nanoparticle surfactant (NPS) was designed and prepared to structure liquids. With the help of a polymeric surfactant, the interfacial host–guest interactions can be significantly enhanced, leading to the rapid formation and assembly of a NP monolayer and offering sufficient binding energy to hold the NPs in a jammed state. The assembly of the NPSs can be reversibly manipulated via a photoswitchable jamming-to-unjamming transition, endowing the interface as well as the macroscopic assemblies with responsiveness to the external trigger (photons). This study for the first time opens a pathway for the construction of multiresponsive, structured all-liquid systems by introducing host–guest chemistry, showing promising potential applications in encapsulation, delivery systems, and unique microfluidic devices.