Supercapacitors, as one of the energy storage devices, exhibit ultrahigh capacitance, high power density, and long cycle. High specific surface area, mechanical and chemical stability, and low cost ...are often required for supercapacitor materials. Graphene, as a new emerging carbon material, has attracted a lot of attention in energy storage field due to its intrinsic properties. Polymers are often incorporated into graphene for a number of enhanced or new properties as supercapacitors. In this paper, different polymers which are used to form composite materials for supercapacitor applications are reviewed. The functions, strategies, and the enhanced properties of graphene and polymer composites are discussed. Finally, the recent development of graphene and polymers for flexible supercapacitors are also discussed.
The number of DNA polymerases identified in each organism has mushroomed in the past two decades. Most newly found DNA polymerases specialize in translesion synthesis and DNA repair instead of ...replication. Although intrinsic error rates are higher for translesion and repair polymerases than for replicative polymerases, the specialized polymerases increase genome stability and reduce tumorigenesis. Reflecting the numerous types of DNA lesions and variations of broken DNA ends, translesion and repair polymerases differ in structure, mechanism, and function. Here, we review the unique and general features of polymerases specialized in lesion bypass, as well as in gap-filling and end-joining synthesis.
We identify the quantum metric dipole as the geometric origin of the nonreciprocal directional dichroism which describes the change in the refractive index upon reversing the light propagation ...direction. Specifically, we find that the static limit of the nonreciprocal directional dichroism corresponds to a quadrupolar transport current from the quantum metric dipole, in response to a quadrupolar electric field. Moreover, at a finite frequency, we demonstrate that the steepest slope of the averaged quantum metric dipole gives rise to a peak in the differential refractive index between counterpropagating lights. Finally, we illustrate both features in a low-energy model.
It is generally assumed that an enzyme-substrate (ES) complex contains all components necessary for catalysis and that conversion to products occurs by rearrangement of atoms, protons, and electrons. ...However, we find that DNA synthesis does not occur in a fully assembled DNA polymerase–DNA–deoxynucleoside triphosphate complex with two canonical metal ions bound. Using time-resolved x-ray crystallography, we show that the phosphoryltransfer reaction takes place only after the ES complex captures a third divalent cation that is not coordinated by the enzyme. Binding of the third cation is incompatible with the basal ES complex and requires thermal activation of the ES for entry. It is likely that the third cation provides the ultimate boost over the energy barrier to catalysis of DNA synthesis.
Monolayer graphene exhibits extraordinary properties owing to the unique, regular arrangement of atoms in it. However, graphene is usually modified for specific applications, which introduces ...disorder. This article presents details of graphene structure, including sp
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hybridization, critical parameters of the unit cell, formation of σ and π bonds, electronic band structure, edge orientations, and the number and stacking order of graphene layers. We also discuss topics related to the creation and configuration of disorders in graphene, such as corrugations, topological defects, vacancies, adatoms and sp
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-defects. The effects of these disorders on the electrical, thermal, chemical and mechanical properties of graphene are analyzed subsequently. Finally, we review previous work on the modulation of structural defects in graphene for specific applications.
Described for the first time is that carbon dioxide (CO2) can be successfully inserted into aryl C−H bonds of the backbone of a metal–organic framework (MOF) to generate free carboxylate groups, ...which serve as Brønsted acid sites for efficiently catalyzing the methanolysis of epoxides. The work delineates the very first example of utilizing CO2 for heterogeneous C−H activation and carboxylation reactions on MOFs, and opens a new avenue for CO2 chemical transformations under mild reaction conditions.
Framed: CO2 is utilized for heterogeneous C−H activation and carboxylation reactions on metal–organic frameworks (MOFs). The formed carboxylate groups serve as Brønsted acid sites and were shown to efficiently catalyze the methanolysis of epoxides. This work introduces a new avenue for CO2 chemical transformations under mild reaction conditions.
Ovarian clear cell carcinoma (OCCC) is a unique subtype of ovarian epithelial ovarian cancer. The number of chemotherapy cycles for early-stage patients is still debated. This study aimed to evaluate ...whether at least 4 cycles of adjuvant platinum-based chemotherapy have better prognostic value than 1-3 cycles in early-stage OCCC.
We retrospectively retrieved data from 102 patients with stage I-IIA OCCC between 2008 and 2017. All patients underwent complete surgical staging followed by adjuvant platinum-based chemotherapy. Kaplan-Meier curves and Multivariate Cox analysis were performed to estimate 5-year overall survival (OS) and progression-free (PFS) according to the number of chemotherapy cycles.
Among stage I-IIA disease, twenty (19.6%) patients received 1-3 cycles, and eighty-two (80.4%) patients received at least 4 cycles of adjuvant chemotherapy. Univariate analysis revealed that the patients in 1-3cycles group had not significantly improved 5-year OS and PFS than those in the ≥ 4 cycles group (5-year OS: hazard ratio HR 1.21; 95% confidence interval CI 0.25- 5.78, p = 0.1), and 5-year PFS: HR 0.79; 95% CI 0.26- 2.34, p = 0.1). In the multivariate analysis, there was no impact of 1-3 versus ≥ 4 cycles of chemotherapy on 5-year OS (HR 1.21, 95% CI 0.25-3.89, p = 0.8) or 5-year PFS (HR 0.94, 95% CI 0.32-2.71, p = 0.9). The potential independent risk factors associated with 5-year OS and PFS included the surgery approach and FIGO stage.
The number of cycles of platinum-based chemotherapy could not be associated with a survival benefit for patients with early-stage OCCC.
•A thermodynamic constitutive model is developed for geomaterials based on the tenet of particle reconstruction.•The concepts of particle entropy, particle temperature, migration coefficient and ...potential energy density function are introduced.•The proposed model is verified by saturated/unsaturated soils undergoing thermal loading.
A thermo-hydro-mechanical constitutive model is developed for geomaterials based on the tenet of particle rearrangement in porous granular materials undergoing thermodynamic processes. In this model, the concepts of particle entropy, particle temperature, migration coefficient and potential energy density function are introduced. The effects of temperature and saturation variation on energy dissipation and the soil–water characteristic curve of the geomaterials are also considered. This model can accurately describe the irreversible consolidation of normally consolidated saturated soils induced by thermal loading and the aging effect induced by cyclic thermal loading, which is attributed to the irreversible rearrangement of solid particles in the soils. However, as the overconsolidation ratio increases, volumetric expansion will likely become reversible. In this case, temperature-induced elastic deformation of the solid particles is more dominant than particle rearrangement. The constitutive model can accurately describe the effects of static stress, suction and temperature on the consolidation of unsaturated soils. An increase in temperature can cause thermal contraction at low suction but thermal expansion at high suction and the physical mechanism is the same as that of the thermal consolidation of saturated soils.
Peeling from strong adhesion is hard, and sometimes painful. Herein, an approach is described to achieve both strong adhesion and easy detachment. The latter is triggered, on‐demand, through an ...exposure to light of a certain frequency range. The principle of photodetachable adhesion is first demonstrated using two hydrogels as adherends. Each hydrogel has a covalent polymer network, but does not have functional groups for bonding, so that the two hydrogels by themselves adhere poorly. The two hydrogels, however, adhere strongly when an aqueous solution of polymer chains is spread on the surfaces of the hydrogels and is triggered to form a stitching polymer network in situ, in topological entanglement with the pre‐existing polymer networks of the two hydrogels. The two hydrogels detach easily when the stitching polymer network is so functionalized that it undergoes a gel–sol transition in response to a UV light. For example, two pieces of alginate–polyacrylamide hydrogels achieve adhesion energies about 1400 and 10 J m−2, respectively, before and after the UV radiation. Experiments are conducted to study the physics and chemistry of this strong and photodetachable adhesion, and to adhere and detach various materials, including hydrogels, elastomers, and inorganic solids.
Strong and photodetachable adhesion is achieved by forming a polymer network at the interface between two adherends. The network binds the two adherends and dissociates in response to an exposure to UV light. Three basic modes of interaction are described for different adherends. Through their combinations, strong and photodetachable adhesions are achieved for adherends of all kinds.
Herein, we report that a new flexible coordination network, NiL2 (L=4‐(4‐pyridyl)‐biphenyl‐4‐carboxylic acid), with diamondoid topology switches between non‐porous (closed) and several porous (open) ...phases at specific CO2 and CH4 pressures. These phases are manifested by multi‐step low‐pressure isotherms for CO2 or a single‐step high‐pressure isotherm for CH4. The potential methane working capacity of NiL2 approaches that of compressed natural gas but at much lower pressures. The guest‐induced phase transitions of NiL2 were studied by single‐crystal XRD, in situ variable pressure powder XRD, synchrotron powder XRD, pressure‐gradient differential scanning calorimetry (P‐DSC), and molecular modeling. The detailed structural information provides insight into the extreme flexibility of NiL2. Specifically, the extended linker ligand, L, undergoes ligand contortion and interactions between interpenetrated networks or sorbate–sorbent interactions enable the observed switching.
A new flexible coordination network, NiL2 (L=4‐(4‐pyridyl)‐biphenyl‐4‐carboxylic acid), undergoes extreme structural transformations, enabled by ligand contortion, between non‐porous (closed) and porous (open) phases as exemplified by a stepped isotherm.