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Epigallocatechin gallate (EGCG)-based nanosystems have garnered significant attention for their ability to alleviate inflammation due to their excellent anti-inflammatory properties and enhanced drug delivery capabilities. However, the degradation of EGCG in strongly acidic environments poses a challenge for potential administration, particularly in oral formulations, where gastric resistance is essential. In this study, we develop a "disintegration and reorganization" strategy to create acid-resistant antioxidant nanoparticles (EGA NPs) based on EGCG and 5-aminosalicylic acid (5-ASA) for mitigating inflammation in colitis and acute kidney injury. At acidic pH, the ester bond in EGCG breaks down, producing two building blocks. These, together with 5-ASA and formaldehyde, form oligomers through a combination of phenol-aldehyde condensation and the Mannich reaction. The resulting oligomers self-assemble into EGA NPs, which exhibit significant stability under both acidic and neutral pH conditions. This stability makes them suitable for oral administration, allowing them to withstand harsh gastric conditions, as well as for intravenous injection. Importantly, these oligomers retain the antioxidant and anti-inflammatory properties of EGCG, effectively scavenging reactive oxygen species and reducing intracellular oxidative stress. Additionally, EGA shows potential as a drug carrier, efficiently loading the anti-inflammatory agent curcumin (Cur) to form Cur@EGA NPs. In vivo studies demonstrate the efficacy of Cur@EGA and EGA in alleviating acute colitis and kidney injury following oral and intravenous administration, respectively. These nanoparticulate formulations exhibit superior inflammation reduction compared to free Cur in vivo. Overall, our findings introduce a novel acid-resistant nanoplatform based on EGCG for the treatment of acute inflammation.

Solid oxide electrolysis cells (SOECs) show significant promise in converting CO 2 to valuable fuels and chemicals, yet exploiting efficient electrode materials poses a great challenge. Perovskite oxides, known for their stability as SOEC electrodes, require improvements in electrocatalytic activity and conductivity. Herein, vanadium(V) cation is newly introduced into the B-site of Sr 2 Fe 1.5 Mo 0.5 O 6-δ perovskite to promote its electrochemical performance. The substitution of variable valence V 5+ for Mo 6+ along with the creation of oxygen vacancies contribute to improved electronic conductivity and enhanced electrocatalytic activity for CO 2 reduction. Notably, the Sr 2 Fe 1.5 Mo 0.4 V 0.1 O 6-δ based symmetrical SOEC achieves a current density of 1.56 A cm -2 at 1.5 V and 800 °C, maintaining outstanding durability over 300 h. Theoretical analysis unveils that V-doping facilitates the formation of oxygen vacancies, resulting in high intrinsic electrocatalytic activity for CO 2 reduction. These findings present a viable and facile strategy for advancing electrocatalysts in CO 2 conversion technologies.

Hydrogels are ideal for antifouling materials due to their high hydrophilicity and low adhesion properties. Herein, poly(ionic liquid) hydrogels integrated with zwitterionic copolymer-functionalized gallium-based liquid metal (PMPC-GLM) microgels were successfully prepared by a one-pot reaction. Poly(ionic liquid) hydrogels (IL-Gel) were obtained by chemical cross-linking the copolymer of ionic liquid, acrylic acid, and acrylamide, and the introduction of ionic liquid (IL) significantly increased the cross-linking density; this approach consequently enhanced the mechanical and antiswelling properties of the hydrogels. The swelling ratio of IL-Gel decreased eight times compared to the original hydrogels. PMPC-GLM microgels were prepared through grafting the zwitterionic polymer PMPC onto the GLM nanodroplet surface, which exhibited efficient antifouling performance attributed to the bactericidal effect of Ga 3+ and the antibacterial effect of the zwitterionic polymer layer PMPC. Based on the synergistic effect of PMPC-GLM microgels and IL, the composite hydrogels PMPC-GLM@IL-Gel not only exhibited excellent mechanical and antiswelling properties but also showed outstanding antibacterial and antifouling properties. Consequently, PMPC-GLM@IL-Gel hydrogels achieved inhibition rates of over 90% against bacteria and more than 85% against microalgae.

Balancing the accuracy and simplicity of aptasensors is a challenge in their construction. This study addresses this issue by leveraging the remarkable loading capacity and peroxidase-like catalytic activity of PtPdCu trimetallic nanoparticles, which reduces the reliance on precious metals. A dual-signal readout aptasensor for enrofloxacin (ENR) detection is designed, incorporating DNA dynamic network cascade reactions to further amplify the output signal. Exploiting the strong loading capacity of PtPdCu nanoparticles, they are self-assembled with thionine (Thi) to form a signal label capable of generating signals in two independent modes. The label exhibits excellent enzyme-like catalytic activity and enhances electron transfer capabilities. Differential pulse voltammetry (DPV) and square-wave voltammetry (SWV) are employed to independently read signals from the oxidation-reduction reaction of Thi and the catalytic oxidation of hydroquinone (HQ) to benzoquinone (BQ) by H 2 O 2 . The introduced DNA dynamic network cascade reaction modularizes sample processing and electrode surface signal generation, avoiding electrode contamination and efficiently increasing the output of the catalyzed hairpin assembly (CHA) cycle. Under optimized conditions, the developed aptasensor demonstrates detection limits of 0.112 (DPV mode) and 0.0203 pg/mL (SWV mode). Additionally, the sensor successfully detected enrofloxacin in real samples, expanding avenues for designing dual-mode signal amplification strategies.

Ferroelectric tunnel junctions (FTJs) have been regarded as one of the most promising candidates for next-generation devices for data storage and neuromorphic computing owing to their advantages such as fast operation speed, low energy consumption, convenient 3D stack ability, etc. Here, dramatically different from the conventional engineering approaches, we have developed a tunnel barrier decoration strategy to improve the ON/OFF ratio, where the ultrathin SrTiO 3 (STO) dielectric layers are periodically mounted onto the BaTiO 3 (BTO) ferroelectric tunnel layer using the high-throughput technique. The inserted STO enhances the local tetragonality of the BTO, resulting in a strengthened ferroelectricity in the tunnel layer, which greatly improves the OFF state and reduces the ON state. Combined with the optimized oxygen migration, which can further manipulate the tunneling barrier, a record-high ON/OFF ratio of ∼10 8 has been achieved. Furthermore, utilizing these FTJ-based artificial synapses, an artificial neural network has been simulated via back-propagation algorithms, and a classification accuracy as high as 92% has been achieved. This study screens out the prominent FTJ by the high-throughput technique, advancing the tunnel layer decoration at the atomic level in the FTJ design and offering a fundamental understanding of the multimechanisms in the tunnel barrier.

In this study, size-regulated MOFs (MZ) with high MBT loading were successfully synthesized by combining mercaptobenzothiazole (MBT), zinc salt, and 2-methylimidazole (2-MI). Subsequently, the MZ structure was utilized to encapsulate tannic acid-modified gallium-based liquid metal (GLM-TA), thereby acquiring a novel heterogeneous nanocomposite (GLM-TA@MZ). The results revealed that the as-prepared GLM-TA@MZ shows good antiwear and friction-reducing performance as an oil-based lubricant additive, the average friction coefficient was decreased to 0.091, and a wear volume was reduced to 0.95 × 10 4 μm 3 , which corresponds to a decrease of 52.3 and 97.2% as compared to base oil PAO. The excellent tribological properties of GLM-TA@MZ can be attributed to physical adsorption on the friction pair, followed by tribochemical reactions. As a result, a thick friction protection film (thickness of about 100 nm) containing Ga, Zn, and S elements was formed, which effectively reduced the contact area between the friction pairs, resulting in improved tribological performance. This study provides insights into the design of MOF-based nanocomposites for lubricating applications.

Solid oxide electrolysis cells (SOECs) show great promise in converting CO 2 to valuable products. However, their practicality for the CO 2 reduction reaction (CO 2 RR) is restricted by sluggish kinetics and limited durability. Herein, we propose a novel medium-entropy perovskite, Sr 2 (Fe 1.0 Ti 0.25 Cr 0.25 Mn 0.25 Mo 0.25 )O 6-δ (SFTCMM), as a potential electrode material for symmetrical SOEC toward CO 2 RR. Experimental and theoretical results unveil that the configuration entropy of SFTCMM perovskites contributes to the strengthened metal 3d-O 2p hybridization and the reduced O 2p bond center. This variation of electronic structure benefits oxygen vacancy creation and diffusion as well as CO 2 adsorption and activation and ultimately accelerates CO 2 RR and oxygen electrocatalysis kinetics. Notably, the SFTCMM-based symmetrical SOEC delivers an excellent current density of 1.50 A cm -2 at 800 °C and 1.5 V, surpassing the prototype Sr 2 Fe 1.5 Mo 0.5 O 6-δ (SFM, 1.04 A cm -2 ) and most of the state-of-the-art electrodes for symmetrical SOECs. Moreover, the SFTCMM-based symmetrical SOEC demonstrates stable CO 2 RR operation for 160 h.

Seeking highly efficient, stable, and cost-effective bifunctional electrocatalysts of rechargeable Zn-air batteries (ZABs) is the top-priority for developing new generation portable electronic devices. For this, the rational and effective structural design, interface engineering, and electron recombination on electrocatalysts should be taken into account to reduce the reaction overpotential and expedite the kinetics of oxygen reduction reaction (ORR) and oxygen evolution reaction (OER). Herein, we construct a MnCo-based metal organic framework-derived heterogeneous MnS-CoS nanocrystals, which are anchored on free-standing porous N-doped carbon fibers (PNCFs) by the in situ growth method and vulcanization process. Benefiting from the abundant vacancies and active sites, strong interfacial coupling as well as favorable conductivity, the MnS-CoS/PNCFs composite electrode delivers a mentionable oxygen electrocatalytic activity and stability with a half-wave potential of 0.81 V for ORR and an overpotential of 350 mV for OER in the alkaline medium. Of note, the flexible rechargeable ZAB using MnS-CoS/PNCFs as binder-free air cathode offers high power density of 86.7 mW cm -2 , large specific capacity of 563 mA h g -1 , and adapts to different bending degree of operation. In addition, the density functional theory calculation clarifies that the heterogeneous MnS-CoS nanocrystals reduces the reaction barrier and enhances the conductivity of the catalyst and the adsorption capacity of the intermediates during the ORR and OER process. This study opens up a new insight to the design of the self-supported air cathode for flexible electronic devices.

Sulfonated polyether ether ketone (SPEEK) has been widely investigated in proton exchange membrane fuel cells (PEMFCs) due to its excellent thermal stability, chemical stability, and low cost compared with Nafion. However, excessive degree of sulfonation will easily lead to the decrease in thermal stabilities and mechanical properties of SPEEK membranes, which limits the enhancement of proton conductivity. In this work, a series of Schiff-base networks (SNWs) with different contents are in situ synthesized in the SPEEK membrane by a Schiff-base co-condensation reaction, and then, the composite membranes are soaked in sulfonic acid for further improvement of proton conductivity. The highest doping amount of the SNW filler in SPEEK can reach 20 wt %. High loading and low leaching rate of H 2 SO 4 are easily achieved owing to the similar size between sulfuric acid molecules and micropores in SNW. Moreover, abundant amino and imine groups in SNW networks contribute to the anchoring of H 2 SO 4 into the pores by acid-base interactions. The proton conductivity of the SPEEK/S-SNW-15 composite membrane can reach 115.53 mS cm -1 at 80 °C and 100% RH. Meanwhile, the composite membrane also exhibits satisfied stability and mechanical property.

Atomically dispersed single-metal-site catalysts are hailed as the most promising category for the oxygen reduction reaction (ORR) with full metal utilization and complete exploitation of intrinsic activity. However, due to the inherent electronic structure of single-metal atoms in MN x , it is difficult to break the linear relationship between catalytic activity and adsorption energy of reaction intermediates, and the performance of such catalysts still falls short of expectations. Herein, we change the adsorption structure by constructing Fe-Ce atomic pairs to modulate the iron d-orbital electron configuration, breaking the linear relationship based on single-metal sites. The 4f cruise electrons of cerium element reduce the d-orbital center of iron in the synthesized FeCe-single atom dispersed hierarchical porous nitrogen-doped carbon (FeCe-SAD/HPNC) catalyst, and more orbital-occupied states appear near the fermi level, which weakens the adsorption strength in the active center and oxygen species, so that the rate-determining step was shifted from *OH desorption to *O > *OH, rendering the excellent ORR performances of the FeCe-SAD/HPNC catalyst. The synthesized FeCe-SAD/HPNC catalyst shows excellent activity, with a half-wave potential as high as 0.81 V for ORR in 0.1 M HClO 4 solution. Additionally, by constructing a three-phase reaction interface with a hierarchical porous structure, the H 2 -O 2 proton-exchange membrane fuel cell (PEMFC) assembled with FeCe-SAD/HPNC as cathode catalyst achieves a maximum power density of 0.771 W cm -2 and good stability.

Au nanozymes are extensively researched for their photothermal effect and catalytic performance, but overcoming the inherent defects of poor dispersibility and thermal stability through complementary materials will expand their prospects for biological applications. Herein, several novel CAu nanozymes were fabricated by in situ reduction of chloroauric acid on hollow carbon nanospheres (HCNs). Through regulating the number of reductions, sesame ball-shaped CAu (sCAu) with highly dispersed Au nanoparticles and diversity-shaped CAu (dCAu) were obtained. The number and morphology of loaded Au nanoparticles, absorption spectra, and hydrophilicity of CAu nanozymes were systematically characterized to demonstrate the flexibility of this novel method. The high-efficiency peroxidase-like sCAu0.3 nanozyme with hyperthermia-activated property was then screened for later bio-application. It is worth mentioning that its photothermal-promoted peroxidase-like activity could be achieved under near-infrared laser irradiation. Moreover, sCAu0.3 could specifically achieve glutathione detection in human blood samples. This method will provide a protocol for the regulation of CAu nanozymes to adapt to bio-detection applications.

Multidrug resistance in cancer stem cells (CSCs) is a major barrier to chemotherapy; hence, developing CSC-specific targeted nanocarriers for efficient drug delivery is critical. In this study, monodisperse hollow-structured MnO 2 (H-MnO 2 ) with a mesoporous shell was created for efficient targeted drug delivery. An effective therapeutic compound isoliquiritigenin (ISL) was confirmed to inhibit the lung cancer stem-cell phenotype by natural compound screening based on integrated microfluidic devices. The resultant H-MnO 2 showed a high drug-loading content of the potent CSC-targeting compound ISL and near-infrared fluorescent dye indocyanine green (ICG). In addition, H-MnO 2 was successively modified with hyaluronic acid (HA) to enhance targeting CSCs with high CD44 expression levels. The H-MnO 2 @(ICG + ISL)@HA nanocomposites displayed promising chemotherapeutic and photothermal treatment capabilities, as well as NIR-triggered drug release, which showed excellent CSC-killing effects and tumor inhibition efficacy. Meanwhile, the development of the tumor was effectively restrained by NIR-triggered phototherapy and prominent chemotherapy without obvious side effects after tail vein injection of the nanocomposites in vivo. In summary, the prepared nanocomposites accomplished synergistic cancer therapy that targets CSCs, offering a versatile platform for lung cancer diagnosis and treatment.

Most recently, the freestanding of an epitaxial single-crystal oxide has been greatly developed to its fundamental concerns and the possibility of integration with metal, two-dimensional, and organic materials for more promising functionalities. In an artificial ferromagnetic oxide heterostructure and superlattice, the release of the substrate constraint can induce a reasonable transformation of the magnetic structure because the change of the lattice field occurs. In this study, we have comprehensively investigated the evolution of magnetic properties of (La 0.7 Ca 0.3 MnO 3 /SrRuO 3 ) n [(LCMO/SRO) n ] ferromagnetic superlattices while they are epitaxially on SrTiO 3 and freestanding. It is found that the Curie temperature and the perpendicular exchange bias of the freestanding superlattices exhibit extreme sensitivity to the interface number and the thickness of LCMO and SRO, which can maximumly reach ∼293 K and ∼1150 Oe. These enhanced and bulk-beyond magnetic behaviors originate from the interfacial magnetic transition from ferromagnetic to antiferromagnetic via the charge reconstruction with the assistance of strain. Our study provides not only a reference for designing a high-performance flexible ferromagnetic architectural superlattice but also a deep understanding of the interfacial effect in freestanding ferromagnetic heterostructures benefiting flexible spintronics.

Ultrasensitive quantification of protein biomarkers has significant implications in disease diagnosis. Herein, we report a fluorescent bacteria counting immunoassay (FBCIA) strategy for protein biomarker detection based on a cascade signal conversion and amplification strategy including the copper metal-organic framework (Cu-MOF)-mediated Cu(I)-catalyzed azide-alkyne cycloaddition (CuAAC) for fluorescent bacteria immobilization that converted the concentration of target protein to countable bacterial number and the further self-proliferation of bacteria to amplify the detectable bacterial number. The developed low-background and enzyme-free cascade methodology achieved highly sensitive detection of carcinoembryonic antigen (CEA) and prostate-specific antigen (PSA) with detection limits down to 0.8 pg/mL and 64.5 fg/mL, respectively. On top of that, we also developed a smartphone device for visualizing individual bacteria and point-of-care counting of the resulting bacteria for the detection of clinical samples. The good consistency between FBCIA and clinical enzyme-linked immunosorbent assay (ELISA) validated the high reliability and promising potential of our developed platform in clinical applications.

Pyroptosis, as a novel mode of cell death, has been proven to have impressive antitumor effects. Dying cells undergoing pyroptosis can elicit antitumor immunity by the release of tumor-associated antigens (TAAs) and damage-associated molecular patterns (DAMPs). Accordingly, developing an effective, stable, and controllable nanoplatform that can promote these two side effects is a promising option for cancer therapy. In this study, we designed a carrier-free chemo-photodynamic nanoplatform (A-C/NPs) using a co-assembly strategy with cytarabine (Ara-C) and chlorin e6 (Ce6) to induce pyroptosis and a subsequent immune response against breast cancer. Mechanistically, A-C/NPs can trigger GSDME-mediated pyroptosis in a controllable manner through reactive oxygen species (ROS) accumulation, causing immunogenic cell death (ICD), in which dying cells release high-mobility group box 1 (HMGB1), adenosine triphosphate (ATP), and calcitonin (CRT). Additionally, Ara-C can stimulate the maturation of cytotoxic T lymphocytes to act synergistically with Ce6-mediated immunogenic cell death (ICD), collectively augmenting the anticancer effect of A-C/NPs. The A-C/NPs showed excellent suppressive effects on the growth of orthotopic, abscopal, and recurrent tumors in a breast cancer mouse model. The chemo-photodynamic therapy (PDT) using the proposed nanomedicine strategy could be a novel strategy for triggering pyroptosis and improving the global anticancer immune response.

Biomedical dressings have been comprehensively explored for wound healing; however, the complicated manufacturing process and mono-function of the dressing remain critical challenges for further applications. Here, a versatile extrusion three-dimensional (3D) printing strategy to prepare MXene and spidroin-incorporated microneedle scaffolds with photothermal responsive and self-healing properties for promoting wound healing is proposed. Inspired by the cactus, the microneedle scaffold is composed of a top porous scaffold, and microneedles whose inverse opal (IO) photonic crystal (PC) structure and the ample space between the scaffold gaps endow the microneedle scaffold with high drug-carrying capacity. Furthermore, the excellent electrical and photothermal properties of MXene allow the microneedle scaffold to perform sensitive wound movement monitoring and controlled drug release under near-infrared irradiation. Moreover, the extensive hydrogen bonding and Schiff base between the spidroin, polyurethane (PU), and aloe vera gel (avGel) molecules conferred high self-healing and mechanical performance to the microneedle scaffold. In vivo experiments with rat models of wounds have shown that drug-laden microneedle scaffolds under near-infrared (NIR) light can promote the recovery of full-skin wounds. These unique characteristics suggest that 3D-printed multifunctional microneedle scaffolds show great potential for applications in facilitating wound healing and will find widespread applications in wound management.

A simple rectangular-structured freestanding liquid-solid triboelectric nanogenerator (LS-TENG) was fabricated, which used fluorinated ethylene propylene (FEP) films and deionized water (DI) as friction materials. The LS-TENG can effectively convert mechanical energy into electrical energy under the extremely low-frequency shaking of 2 Hz and shows greatly reliable stability. The influence of liquid volume and units on the output performance of the LS-TENG was studied, and the mechanism of the triboelectric electrification process of the LS-TENG was analyzed by COMSOL Multiphysics software. The results show that friction materials, liquid types, and number of units have a great effect on the output performance of the LS-TENG. Under the optimized conditions, the designed array LS-TENG shows high output performance with the open-circuit voltage, short-circuit current, and transferred charge of 120 V, 3.9 μA, and 133 nC, respectively. The LS-TENG can be applied in capacitive storage, AC power, signal acquisition, and self-powered sensor. The multifunctional LS-TENG provides a potentially practical route for harvesting low-frequency mechanical energy in natural environments and enabling multifunctional applications.

Two-dimensional (2D) Dion-Jacobson (DJ) perovskites are drawing significant attention in optoelectronic fields because of their enhanced out-of-plane electron coupling and improved structure stability. However, the structural effects of organic cations on the in-plane charge transport properties of 2D DJ lead bromide perovskites have remained less explored. Herein, we adopt asymmetric 3-(dimethylamino)-1-propylammonium (DMPD) and symmetric butane-1,4-diammonium (BDA) to systematically investigate the influence of organic cations on the structural, optical, and in-plane charge transport properties of 2D lead bromide perovskites. The large penetration depth of DMPD 2+ induces a decreased perovskite layer distortion and a lower bandgap in DMPDPbBr 4 , compared with that of BDAPbBr 4 . Moreover, DMPDPbBr 4 is shown to possess a low exciton binding energy, a low defect density, and a low ion migration activation energy, thereby yielding a more efficient in-plane charge collection efficiency than BDAPbBr 4 . Density functional theory calculations suggest that the improved in-plane charge transport can be traced to the enlarged antibonding coupling between Pb-6s and Br-4p orbitals that enables a high band dispersion and a low carrier effective mass in the in-plane direction of DMPDPbBr 4 . Finally, the planar Ag/DMPDPbBr 4 /Ag photodetector delivers a satisfying detectivity of 1.73 × 10 12 Jones under an incident power intensity of 0.16 mW cm -2 and a high on/off ratio of 5.3 × 10 3 . The above findings offer novel insight for the design of 2D DJ lead bromide perovskites for optoelectronic devices.

Low-energy switching of ferroelectrics has been intensively studied for energy-efficient nanoelectronics. Mechanical force is considered as a low-energy consumption technique for switching the polarization of ferroelectric films due to the flexoelectric effect. Reduced threshold force is always desirable for the considerations of energy saving, easy domain manipulation, and sample surface protection. In this work, the mechanical switching behaviors of BaTiO 3 /SrRuO 3 epitaxial heterostructure grown on Nb:SrTiO 3 (001) substrate are reported. Domain switching is found to be induced by an extremely low tip force of 320 nN (estimated pressure ∼0.09 GPa), which is the lowest value ever reported. This low mechanical threshold is attributed to the small compressive strain, the low oxygen vacancy concentration in BaTiO 3 film, and the high conductivity of the SrRuO 3 electrode. The flexoelectricity under both perpendicular mechanical load (point measurement) and sliding load (scanning measurement) are investigated. The sliding mode shows a much stronger flexoelectric field for its strong trailing field. The mechanical written domains show several advantages in comparison with the electrically written ones: low charge injection, low energy consumption, high density, and improved stability. The ultralow-pressure switching in this work presents opportunities for next-generation low-energy and high-density memory electronics.

Environmental stress greatly decreases crop yield. The application of noninvasive techniques is one of the most practical and feasible ways of monitoring the health condition of plants under stress. However, it remains largely unsolved. A chemical fluorescent probe can be applied as a typical nondestructive method, but it has not been applied in living plants for stress detection to date. The abscisic acid (ABA) receptor plays a central role in conferring tolerance to environmental stresses and is an excellent target for developing fluorescent probes. Herein, we developed a fluorescence molecular imaging technology to monitor live plant stress by visualizing the protein expression level of the ABA receptor PYR1. A computer-aided designed indicator dye, flubactin, exhibited an 8-fold enhancement in fluorescence intensity upon interaction with PYR1. In vitro and in vivo experiments showed that flubactin is suitable to be used to detect salt stress in plants in real time. Moreover, the low toxicity of flubactin promotes its application in the future. Our work opens a new era for the nondestructive visualization of plant stress in vivo .

The abuse of chloramphenicol (CAP) in animal-derived products leads to serious food safety problems, so the sensitive and accurate determination of CAP residues has great noteworthiness for public health. Herein, we present a novel electrochemical aptasensor that incorporates a poly(diallyldimethylammonium chloride) functionalized graphene/Ag@Au nanosheets (PDDA-Gr/Ag@Au NSs) composite modified electrode and a DNAzyme signal amplification effect triggered by a triple-helix molecular switch (THMS) for detecting CAP. The PDDA-Gr/Ag@Au NSs composite has the advantages of high surface area, great conductivity, and dispersibility and has successfully improved the electrochemical performance of the electrode. Specific interaction with CAP will cause the signal transduction probe (STP) to be released from the THMS. After that, the DNAzyme will be activated with the help of Pb 2+ and remove the immobilized signal probe on the electrode surface. The signal change was recorded by square wave voltammetry (SWV) and led to an accurate quantification of CAP. With all these features, the proposed sensing strategy yielded a satisfactory analytical performance with linearity between 1 pM and 1 μM and a limit of detection of 18.6 fM. Furthermore, the aptasensor shows excellent specificity for CAP in the presence of other antibiotics and resists interference with other common metal ions. Importantly, the performance is not diminished when the constructed aptasensor is applied to measuring CAP in milk powder. This THMS-based method is easy to design, and alteration to different targets can be achieved by simply replacing the aptamer sequence in the THMS. Therefore, this method shows significant prospects as a flexible platform for accurate monitoring of antibiotic residues in foodstuffs.

Sodium borohydride is a promising candidate as hydrogen storage material. The direct borohydride fuel cell (DBFC) as an energy conversation device has attracted intensive attention owing to the low theoretical potential of borohydride oxidation reaction (BOR, -1.24 V vs SHE) on the anode. In this paper, the hierarchical sea urchin-like NiMoN@NC coated by thin carbon layer with optimal BH 4 - adsorption characteristic was synthesized as a superior electrocatalyst toward BOR. In 1 M NaOH-0.05 M NaBH 4 , the BOR working potentials are only -55 and 44 mV at the current densities of 10 and 200 mA cm -2 on NiMoN@NC, respectively. Furthermore, the membrane-free DBFC using NiMoN@NC as anodic electrocatalyst shows a maximum power density of 67 mW cm -2 at room temperature with appreciative stability. This well-designed carbon coated and nitrogen doped transition-metal material with hierarchical nano/microstructure as a highly efficient electrocatalyst shows promising potential and bright prospects in electrocatalysis research and practical application for energy conversion systems of DBFC.

Mangiferin (MGF) is found in many natural plants, such as Rhizoma Anemarrhenae, and has anti-diabetes effects. However, its clinical applications and development are limited by poor solubility and low-concentration enrichment in pancreatic islets. In this paper, targeted polymeric nanoparticles were constructed for MGF delivery with the desired drug loading content (6.86 ± 0.60%), excellent blood circulation, and missile-like delivery to the pancreas. Briefly, Glucagon-like peptide 1 (GLP-1) as an active targeting agent to the pancreas was immobilized on the block copolymer polyethyleneglycol-polycaprolactone (PEG-PCL) to obtain final GLP-1-PEG-PCL amphiphiles. Spherical MGF-loaded polymeric nanoparticles were acquired from the self-assembly of the targeted GDPP nanoparticles and MGF with a homogeneous size of 158.9 ± 1.7 nm and a negative potential for a good steady state in circulation. In this drug vehicle, GLP-1 acts as the missile vanguard via the GLP-1 receptor on the surface of the pancreas for improving the accumulation and efficiency of MGF in the pancreas, the hypoglycemic effect of MGF, and the restorative effect on pancreatic islets, which were investigated. As compared to free MGF, MGF/GDPP nanoparticles appeared to be more concentrated in the pancreas, with better blood glucose and glucose tolerance, enhanced insulin levels, increased β-cell proliferation, reduced β-cell apoptosis, and islet repair in vivo. This targeted drug delivery system provided a novel strategy and hope for enhancing MGF delivery and anti-diabetes efficacy.

The fabrication of ultrafiltration (UF) membranes with a small pore size (<20 nm) and high surface porosity is still a great challenge. In this work, a nanobubble-assisted nonsolvent-induced phase separation (BNIPS) technique was developed to prepare high-performance UF membranes by adding a tiny amount of CaCO 3 nanoparticles into the casting solution. The phase inversion occurred in a dilute-acid coagulation bath to simultaneously generate CO 2 nanobubbles, which regulated the membrane structure. The effects of the nano-CaCO 3 content in the casting solution on the structure and performance of poly(ethersulfone)/sulfonated polysulfone (PES/SPSf) UF membranes were studied. The UF membrane prepared from a casting solution with 0.3% nano-CaCO 3 achieved a surface porosity of 12%, a pore diameter of 10.2 nm, and a skin-layer thickness of 80.3 nm. The superior structure of the UF membrane was mainly attributed to the in situ generation of CO 2 nanobubbles because the CO 2 nanobubbles were amphiphobic to water and solvents to delay the phase inversion time and acted as nanosize porogens. The produced membrane showed an unprecedented separation performance, achieving a pure water permeance of up to 1128 L·m -2 ·h -1 ·bar -1 , 2.5 fold that of the control membrane. Similarly, a high bovine serum albumin rejection of above 99.0% was obtained. The overall permeability and selectivity were better than those of commercial and other previously reported UF membranes. This work provides insight toward a simple and cost-effective technique to address the trade-off between pure water permeance and solute rejection of UF membranes.

Lithium metal batteries (LMBs) are a promising candidate for next-generation energy storage devices. However, the high irreversibility and dead Li accumulation of the lithium metal anode caused by its fragile original solid electrolyte interface (SEI) seriously hinder the practical application of LMBs. Herein, a facile slurry-coating and one-step thermal fluorination reaction method is proposed to construct the 3D structural LiF-protected Li/G composite anode. The existence of a 3D LiF protection layer is convincingly confirmed and the function of the Li/G skeleton is discussed in detail. The 3D structural LiF protection layer results in superior electrochemical performance by improving the utilization of Li and suppressing the accumulation of dead Li in symmetric and full coin cells. Moreover, a 0.85 Ah pouch cell strictly following the parameters of the practical battery industry can work stably for 140 cycles with a gradual internal resistance increase. This novel Li/G composite anode indicates a promising strategy in lithium/carbon composite anodes for LMBs, and the facile thermal fluorination reaction method presented in this paper offers a new method for the construction of a 3D structural protection layer for lithium metal anodes.

Access to the potential applications of metal-organic frameworks (MOFs) depends on rapid fabrication. While there have been advances in the large-scale production of single-component MOFs, rapid synthesis of multicomponent MOFs presents greater challenges. Multicomponent systems subjected to rapid synthesis conditions have the opportunity to form separate kinetic phases that are each built up using just one linker. We sought to investigate whether continuous flow chemistry could be adapted to the rapid formation of multicomponent MOFs, exploring the UMCM-1 and MUF-77 series. Surprisingly, phase pure, highly crystalline multicomponent materials emerge under these conditions. To explore this, in situ WAXS was undertaken to gain an understanding of the formation mechanisms at play during flow synthesis. Key differences were found between the ternary UMCM-1 and the quaternary MUF-7, and key details about how the MOFs form were then uncovered. Counterintuitively, despite consisting of just two ligands UMCM-1 proceeds via MOF-5, whereas MUF-7 consists of three ligands but is generated directly from the reaction mixture. By taking advantage of the scalable high-quality materials produced, C6 separations were achieved in breakthrough settings.

Spinel oxide materials have been widely used as oxygen evolution catalysts to enhance the photoelectrochemical (PEC) performance of photoelectrodes. Herein, we demonstrate that the water splitting efficiency of a photoanode can be further enhanced by introducing its photothermal effect. Under near-infrared radiation, the temperature of the NiCo 2 O 4 /BiVO 4 photoanode increases moderately, leading to improved water oxidation kinetics and charge transport simultaneously. With the assistance of the photothermal effect, the obtained photoanode reaches a photocurrent density of 6.20 mA cm -2 at 1.23 V vs reversible hydrogen electrode. A series of spinel-type MCo 2 O 4 oxides (M = Mn, Zn, Cu, and Fe) are deposited on the surface of the BiVO 4 photoanode to show similar photothermally enhanced PEC performance. The research discovery provides a way for improving the catalytic activity of photoanode materials with a photothermal effect, which may be applied to various fields of energy conversion, including CO 2 reduction, N 2 fixation, and pollutant degradation.

Lithium loss during the initial charge process inevitably reduces the capacity and energy density of lithium-ion batteries. Cathode additives are favored with respect to their controllable prelithiation degree and scalable application; however, the insulating nature of their delithiation products retards electrode reaction kinetics in subsequent cycles. Herein, we propose a prelithiation separator by modifying a commercial separator with a Li 2 S/Co nanocomposite to compensate for the initial capacity loss. The Li 2 S/Co coating layer extracts active lithium ion during the charge process and shows a delithiation capacity of 993 mA h g -1 . When paired with a LiFePO 4 |graphite full cell, the reversible capacity is increased from 112.6 to 150.3 mA h g -1 , leading to a 29.5% boost in the energy density. The as-prepared pouch cell also demonstrates a stable cycling performance. The excellent electrochemical performance and the scalable production of the prelithiation separator reveal its great potential in lithium-ion battery industry application.

Protection of cardiomyocytes against oxidative stress is vital to alleviate myocardial ischemia/reperfusion injury (MI/RI). However, antioxidative treatment is hampered by the lack of safe and effective therapeutics. Polydopamine (PDA), as a biodegradable class of nanomaterial with excellent antioxidant properties, has shown great potential in treating MI/RI. To achieve site-specific antioxidative efficacy, we established a PDA-based biomimetic nanoplatform (PDA@M), which consisted of a polydopamine core and a macrophage membrane shell to form a shell-core structure. By inheriting the inherent migration capability of macrophages, PDA@M was able to target the infarcted myocardium and exert an antioxidative effect to protect the myocardium. The results demonstrated that the accumulation of the membrane-wrapped nanoparticles (NPs) in the infarcted myocardium was greatly increased as compared with PDA alone, which effectively relieved the MI/RI-induced oxidative stress. PDA@M largely decreased the infarct size and improved the cardiac function post-MI/RI. Our study revealed that PDA@M could inhibit cell pyroptosis by suppressing the NLRP3/caspase-1 pathway, which is known to play a significant role in the antioxidant signaling pathway. In summary, PDA@M can target the infarcted myocardium and exert antioxidative and antipyroptosis functions to protect the myocardium against MI/RI-induced oxidative stress, suggesting that it may prove to be a potential therapeutic agent for MI/RI.

The fragile electrolyte/Li interface is responsible for the long-lasting consumption of Li resources and fast failure of Li metal batteries. The polymer artificial interface with high mechanical flexibility is a promising candidate to maintain the stability of the electrolyte/Li interface; however, sluggish Li-ion transportation of the conventional polymer interface hinders the application. In this work, Li-functionalized graphene oxide (GO-ADP-Li 3 ), which is synthesized by covalent grafting of adenosine 5'-diphosphate lithium on GO nanosheets, is used as a functional additive to improve the Li-ion conductivity of the polymer artificial interface based on PVDF-HFP/LiTFSI. The enhanced Li-ion conductivity is contributed by accelerated Li-ion hopping at the surface between polymer chains and functionalized GO as well as the reduced crystallization degree of PVDF-HFP by this novel additive. The use of this modified polymer as an artificial interface on Li foil enables highly reversible Li stripping/plating and a high capacity retention of 78.4% after 150 cycles for a 0.2 A h Li metal pouch cell (Li/NCM811, strictly following practical conditions). This Li-grafted strategy on GO sheets provides an alternative for designing a compatible electrolyte/Li interface for practical Li metal batteries.

Mitochondrial drug delivery has attracted increasing attention in various mitochondrial dysfunction-associated disorders such as cancer owing to the important role of energy production. Herein, we report a lysosomal pH-activated mitochondrial-targeting polymer nanoparticle to overcome drug resistance by a synergy between mitochondrial delivery of doxorubicin (DOX, an anticancer drug) and erlotinib-mediated inhibition of drug efflux. The obtained nanoparticles, DE-NPs could maintain negative charge and have long blood circulation while undergoing charge reversal at lysosomal pH after internalization by cancer cells. Thereafter, the acidity-activated polycationic and hydrophobic polypeptide domains boost lysosomal escape and mitochondrial-targeting drug delivery, leading to mitochondrial dysfunction, ATP suppression, and cell apoptosis. Moreover, the suppressed ATP supply and erlotinib enabled dual inhibition of drug efflux by DOX-resistant MCF-7/ADR cells, leading to significantly augmented intracellular DOX accumulation and a synergistic anticancer effect with a 17-fold decrease of IC 50 relative to DOX. In vivo antitumor study demonstrates that DE-NPs efficiently suppressed the tumor burden in MCF-7/ADR tumor-bearing mice and led to negligible toxicity. This work establishes that a combination of mitochondrial drug delivery and drug efflux inhibition could be a promising strategy for combating multidrug resistance.

Dielectric polymer capacitors are extensively applied in advanced electronics by virtue of their extremely high power density. However, it remains a challenge to concurrently realize high energy density and high discharge efficiency. In order to solve this conundrum, we herein design a novel all-polymer trilayer structure, where the paraelectric poly(methyl methacrylate) (PMMA) is used as the top layer to obtain a high discharge efficiency, and ferroelectric P(VDF-HFP) is employed as the bottom layer to obtain a high energy density. Particularly, the PMMA/poly(vinylidene fluoride-hexafluoropropylene) (P(VDF-HFP)) blend composite is used as the middle layer to homogenize the electric field inside the trilayer composites, turning out an obviously boosted breakdown strength and elevated energy density. Consequently, an efficiency as high as 85% and an energy density up to 7.5 J/cm 3 along with excellent cycling stability are simultaneously realized at an ultrahigh electric field of 490 kV/mm. These attractive characteristics of the all-polymer trilayer structure suggest that the feasible pathway presented herein is significant to realize concurrently a high energy density and discharge efficiency.

Herein, a hierarchically porous Zr-MOF-labeled electrochemical aptasensor based on the composite of PtPd@Ni-Co hollow nanoboxes (PtPd@Ni-Co HNBs) and poly (diallyldimethylammonium chloride)-functionalized graphene (PDDA-Gr) was developed for ultrasensitive detection of chloramphenicol (CAP). PtPd@Ni-Co HNBs have excellent conductivity and provide binding sites for aptamers; the functionalized PDDA-Gr improves its dispersibility and conductivity as a substrate material, which can be successfully used to increase the electrode surface area and support more PtPd@Ni-CoHNBs. Besides, hierarchically porous Zr-MOFs (HP-UiO-66) were utilized as signal probes and showed a stronger load capacity for signal molecules than conventional UiO-66. In the presence of CAP, two ingeniously designed Exo III-assisted cyclic amplification strategies further improved the sensitivity of the aptasensor: CAP causes cycle I to release a large amount of trigger DNA (Tr DNA), and then, Tr DNA initiated cycle II, which causes the exposed capture DNA to further bind the signal probes. With these advantages, the constructed aptasensors performed with satisfactory sensitivity in a wide linear range (10 fM-10 nM) and a detection limit of 0.985 fM. Several signal amplification strategies adopted in this study have effectively improved the performance of the sensor, providing a new avenue for the development of ultrasensitive sensors in the food analysis field.

Using a coating layer to modify the separator in a practical Li metal battery has attracted wide attention; however, its function on Li-ion diffusion and Li plating/stripping has not been systematically investigated. Herein, in situ electrochemical Raman characterization using modified coin cell configuration is employed to directly reveal the anion adsorption mechanism of the coating layer. The adsorption ability of the MOF-based coating layer on the commercial separator is able to preserve high concentration of anions near the electrolyte/Li interface, which generates high local Li-ion concentration that delays the drain of Li + to uniform Li plating. The feasible and large-area fabrication of GO/ZIF-8-modified separator enables the assembly of pouch cell strictly following practical parameters. 0.4 Ah pouch cell (Li/NCM811) delivers stable capacity for over 100 cycles. The deep understanding of the mechanism of how a coating layer affects Li plating behavior is helpful for the designing and preparation of high-performance separators for Li metal batteries.

The all-inorganic cesium lead bromide (CsPbBr 3 ) perovskite solar cells (PSCs) have attracted considerable interest because of their outstanding environmental stability and low manufacturing cost. However, the state-of-the-art mesoscopic titanium dioxide (TiO 2 ) electron-transporting layers (ETLs) always present low electron mobility, are destructive to perovskites under ultraviolet light illumination, as well as possess high sintering temperature. Nanostructured tin dioxide (SnO 2 ) is a promising electron-transporting material for high-efficiency PSCs due to matching energy-level alignment with the perovskite layer, improved optical transparency, high electron mobility, excellent photostability, and low-temperature processing. Furthermore, rapid but poorly controlled perovskite crystallization makes it difficult to scale up planar PSCs for industrial applications. To address this issue, we adopt a dimensional SnO 2 ETL to change the surface wettability for uniform perovskite coverage over large areas and the growth of large-sized CsPbBr 3 grains, resulting in a maximum grain size of 1.65 μm. Moreover, the dimensional SnO 2 ETL could increase the interfacial contact area between the CsPbBr 3 layer and the ETL and enhance the electronic contact for efficient electron extraction to suppress or to eliminate the notorious hysteresis behavior. As expected, a power conversion efficiency (PCE) of 9.51% with an almost hysteresis-free phenomenon is achieved through dimensionality control of SnO 2 films attributed to the remarkably enhanced light harvesting, accelerated electron extraction, diminished defect density, and reduced charge recombination. Upon further interfacial modification with graphene quantum dots (GQDs), the PSC based on the two-dimensional SnO 2 ETL achieves a champion PCE of 10.34% due to the improved energy-level alignment at the device interface. Moreover, the best all-inorganic CsPbBr 3 PSC free of encapsulation retains 93% of initial efficiency over 10 days at 80% relative humidity. This work provides an effective dimensionality control strategy for optimized charge transportation and enlarged perovskite grain size to make stable and efficient all-inorganic CsPbBr 3 PSCs.

Membrane fouling is the obstacle that limits the practical application of membranes in efficient oil/water separation. The main reason for membrane fouling is the deposition of the dispersed phase (e.g., oil) on the membrane surface based on the sieving effect. The key challenge for solving the fouling problem is to achieve fouling removal via rationally considering hydrodynamics and interfacial science. Herein, a poly(vinylidene fluoride) membrane with a dual-scale hyperporous structure and rational wettability is designed to achieve a continuous "nonfouling" separation for oil/water emulsions via membrane demulsification. The membrane is fabricated via dual-phase separation (vapor and nonsolvent) and modified by in situ polymerization of poly(hydroxyethyl methylacrylate) (contact angle 59 ± 1°). The membrane shows stable permeability (1078 ± 50 Lm -2 h -1 bar -1 ) and high separation efficiency (>99.0%) in 2 h of continuous cross-flow without physicochemical washing compared to superwetting membranes. The permeation is composed of two distinct immiscible liquid phases via coalescence demulsification. The surface shearing and pore throat collision coalescence demulsification mechanism is proposed, and rational interface wettability facilitates the foulant/membrane interaction for "nonfouling" separation. Beyond superwetting surfaces, a new strategy for achieving "nonfouling" emulsion separation by designing membranes with a dual-scale hyperporous structure and rational wettability is provided.

The perovskite solar cells (PSCs) based on cesium lead bromide (CsPbBr 3 ) with outstanding environmental stability and low preparation cost are regarded as one of the most promising photovoltaic devices for commercial applications. However, the performance of CsPbBr 3 PSCs can be badly deteriorated by the intense charge recombination arising from the ionic defects at the grain boundaries of perovskite film. To cope with this issue, we adopt an amino acid of l-lysine with two amino and one carboxyl groups as a chemical additive to incorporate into perovskite film to simultaneously anchor the uncoordinated Pb 2+ (Cs + ) and halogen ion defects. Further, the grain size of CsPbBr 3 perovskite is boosted from 688 to over 1000 nm after l-lysine incorporation as a result of the decreased nucleation rate and the sufficient growth of perovskite, which effectively reduce the grain boundaries for load defects. As expected, the optimized device achieves a best power conversion efficiency of 9.69% attributed to the remarkably reduced charge recombination and enhanced charge extraction arising from the efficient defects dual-passivation and enlarged grain size of perovskite film as well as the improved energy level alignment at the device interface after the introduction of l-lysine, which is elevated by 61.23% in comparison to 6.01% efficiency of the pristine one. Moreover, the unencapsulated device with l-lysine incorporation exhibits remarkable long-term stability in air with 80% RH at 25 °C and 0% RH at 80 °C as well as under continuous illumination conditions. This work provides an effective multifunctional additive for imperfection passivation and grain size enlargement of perovskite to build PSCs with high efficiency and stability.

Garnet-type Li 7 La 3 Zr 2 O 12 (LLZO) is among the most attractive candidates for achieving solid-state lithium batteries. LLZO pellets with high density are preferred because of their potential to prevent dendritic Li growth and penetration. However, the presence of pores inside the LLZO electrolyte is inevitable if it is prepared by a traditional solid-state reaction. Large numbers of pores have an adverse influence on both the ionic conductivity and density of the LLZO pellets. In this work, we studied the origin of pore formation in Li 6.4 La 3 Zr 1.4 Ta 0.6 O 12 (LLZTO) and introduced a fast oxygen-assisted sintering method to eliminate the pores. All of the basic physical properties of the LLZTO sintered in oxygen for only 1 h are better than those of the LLZTO sintered in air. The conductivity and Vickers hardness of the LLZTO increased to 6.13 × 10 -4 S cm -1 and 9.82 GPa, corresponding to 12.3% and 62.8% enhancement, respectively, even at a low precalcined temperature of 600 °C. A Li||Li symmetric cell with the LLZTO sintered in oxygen also showed more stable and longer cycling at a higher current density (0.4 mA cm -2 ).

The merits of Li-O 2 batteries due to the huge energy density are shadowed by the sluggish kinetics of oxygen redox and massive side reactions caused by conductive carbon and a binder. Herein, Fe-Co inverse spinel oxide nanowires grown on Ni foam are fabricated as carbon-free and binder-free cathodes for Li-O 2 batteries. Superior high rate cycle durability and deep charge capability are obtained. For example, 300 cycles with a low overpotential under a fixed capacity of 500 mAh g -1 are achieved at a high current density of 500 mA g -1 . In the deep discharge/charge mode at 500 mA g -1 , the optimized Fe-Co oxide cathode can stably work for more than 30 cycles with the capacity maintained at about 2100 mAh g -1 . Owing to the appreciable incorporation of Fe 3+ into the surface of stable inverse spinel oxides, the regulated Fe-Co oxide cathodes possess a more stable and higher ratio of Co 3+ /Co 2+ , which offers improved adsorption ability of reactive oxygen intermediates and thus achieves the enhanced electrocatalytic performance in the higher current density. In addition, the morphology evolution from array to pyramid-like structure of nanowires further provides assurance in the superior cycle capability. By coupling pyramid-shaped nanowires with binary inverse spinel, the obtained Fe-Co oxide becomes a promising material for practical applications in Li-O 2 batteries. This work offers a general strategy to design efficient mixed metal oxide-based electrodes for the critical energy storage fields.

Aqueous rechargeable lithium-ion batteries (ARLIBs) as alternative energy storage devices have attracted tremendous attention because of their low cost and high safety. However, it is still a significant challenge to develop flexible high-performance ARLIBs for powering wearable devices because of the lack of all binder-free electrode materials. In this study, we develop one-step hydro-/solvothermal methods to design binder-free electrodes of LiCoO 2 polygonal-sheeted arrays and rugby ball-shaped NaTi 2 (PO 4 ) 3 on carbon nanotube fibers as the cathode (LCO@CNTF) and the anode (NTP@CNTF). Both the electrodes are prepared at low temperatures without an extra calcination process, which is a great improvement for the growth process. The electrodes deliver remarkable capacity and extraordinary rate performance in a saturated Li 2 SO 4 solution. Meanwhile, because of the synergy of LCO@CNTF and NTP@CNTF, an impressive capacity of 45.24 mA h cm -3 and an admirable energy density of 67.86 mW h cm -3 are achieved for the assembled quasi-solid-state fiber-shaped flexible ARLIB (FARLIB), which outperform most reported fiber-shaped aqueous rechargeable batteries. More encouragingly, our FARLIB possesses good flexibility, with a 94.74% capacity retention after bending 3000 times. Thus, this work represents a significant step toward developing FARLIBs and provides a new prospect in the design of wearable energy storage devices.

The defect passivation of perovskite films is an efficacious way to further boost the power conversion efficiency (PCE) and long-term stability of perovskite solar cells (PSCs). In this work, ionic liquids (ILs) of 1-butyl-2,3-dimethylimidazolium chloride ([BMMIm]Cl) are used as a modification layer in perovskite films in carbon-based CsPbBr 3 PSCs without a hole-transporting material (HTM) for passivating the surface defects. The preliminary results demonstrate that the [BMMIm]Cl modifier passivates the surface defects of the perovskite film and reduces the valence band of perovskite close to the work function of the carbon electrode, which causes a remarkably inhibited nonradiative and radiative charge recombination, improved energy-level matching, and decreased energy loss. After optimization, a champion efficiency of 9.92% with a V oc as high as 1.61 V is achieved for the [BMMIm]Cl tailored carbon-based CsPbBr 3 PSC without HTM, which is improved by 61.3% in comparison with 6.15% for the control device. Furthermore, the encapsulation-free PSC presents good long-term stability after storage in an air atmosphere with 70% RH at 20 °C or 0% RH at 80 °C as well as under continuous illumination conditions for 30 days. The significantly improved PCE and stability in high humidity or temperature suggest that the perovskite passivation by ILs is an effective strategy for fabricating high-PCE and stable PSCs.

In the present work, high-thickness zwitterionic polymer brushes based on imidazolium salts were successfully grafted via a novel subsurface-initiated ring-opening metathesis polymerization (subsurface-initiated ROMP) from polydimethylsiloxane (PDMS), and their antifouling performance was evaluated in detail. First, an initiator-embedded PDMS was prepared via copolymerization of PDMS prepolymer and ROMP initiator, and then zwitterionic polymer brushes were grafted via subsurface-initiated ROMP from surface to subsurface of the PDMS due to the implanted ROMP initiator. Results from a series of characterization methods such as infrared spectroscopy, X-ray photoelectron spectroscopy, contact angle, and atomic force microscopy proved the zwitterionic polymer brushes' successful grafting. The grafting thickness of zwitterionic polymer brushes via subsurface-initiated ROMP can reach the micron scale, and the as-prepared zwitterionic polymer based surfaces showed good lubricating properties compared to traditional surface-initiated ROMP, which hints that polymer brushes can be grafted not only on the surface but also on the subsurface of PDMS. The protein adhesion test and biofouling assay of zwitterionic polymer brushes were tested in the laboratory, and the results indicated that the zwitterionic polymer-functionalized PDMS can effectively resist the adhesion of bovine serum albumin and algae ( Porphyridium and Dunaliella ) and has good anti-bacterial activity against both Escherichia coli and Staphylococcus aureus .

Lithium-ion capacitors (LICs) are considered to be promising power sources due to their combination of high-rate capacitors and high-capacity batteries. However, development of a high-performance LIC is still restricted by the sluggish intercalation reaction and unsatisfied specific capacities in battery-type bulk anodes. To overcome these issues, herein, we utilize two-step atomic layer deposition (ALD) to realize a uniform coating of FeO x and TiO 2 on CuO nanorods, which results in the formation of ternary CuO@FeO x @TiO 2 composite. After further treatment in H 2 /Ar atmosphere, the as-derived Fe 3 O 4 is encapsulated between conductive Cu nanorod and hollow TiO 2 shell (denoted as Cu@Fe 3 O 4 @TiO 2 ). Owing to the rational design, the binder-free Cu@Fe 3 O 4 @TiO 2 electrode exhibits an ultrahigh Li-ion storage capacity (1585 mA h g -1 at 0.2 A g -1 ), superior rate capability, and excellent cycle performance (no decay after 1000 cycles), which could efficiently boost the energy-storage capability of LICs. By employing an anode of Cu@Fe 3 O 4 @TiO 2 and a cathode of activated carbon, the as-constructed full LIC device provides high energy//powder densities (154.8 Wh kg -1 at 200 W kg -1 ; 66.2 Wh kg -1 at 30 kW kg -1 ). These superior results demonstrate that ALD-enabled architectures hold great promise for synthesizing high-capacity anodes for LICs.

The development of an efficient, robust, and low-cost catalyst for water electrolysis is critically important for renewable energy conversion. Herein, we achieve a significant improvement in electrocatalytic activity for both the oxygen-evolution reaction (OER) and the hydrogen-evolution reaction (HER) by constructing a novel hierarchical PrBa 0.5 Sr 0.5 Co 2 O 5+δ (PBSC)@FeOOH catalyst. The optimized PBSC@FeOOH-20 catalyst consisted of layered perovskite PBSC nanorods and 20 nm thick amorphous FeOOH nanoflakes exhibiting an excellent electrocatalytic activity for the OER and the HER in 0.1 M KOH media, delivering a current density of 10 mA cm -2 at overpotentials of 390 mV for the OER and 280 mV for the HER, respectively. The substantially enhanced performance is probably attributed to the hierarchical nanostructure, the good charge-transfer capability, and the strong electronic interactions of FeOOH and PBSC. Importantly, an alkaline electrolyzer-integrated PBSC@FeOOH-20 catalyst as both the anode and cathode shows a highly active overall water splitting with a low voltage of 1.638 V at 10 mA cm -2 and high stability during continuous operation. This study provides new insights into exploring efficient bifunctional catalysts for overall water splitting, and it suggests that the rational design of the oxyhydroxide/perovskite heterostructure shows great potential as a promising type of electrocatalysts.

Extensive progress has been made in fiber-shaped asymmetric supercapacitors (FASCs) for portable and wearable electronics. However, positive and negative electrodes must be distinguished and low energy densities are a crucial challenge and thus limit their practical applications. This paper reports an efficient method to directly grow TiN nanowire arrays@V 2 O 5 nanosheets core-shell heterostructures on carbon nanotube fibers as nonpolarity electrodes. Benefiting from their unique heterostructure, single electrodes possess high specific capacitances of 195.1 and 230.7 F cm -3 as positive and negative electrodes, respectively. Furthermore, all-solid-state nonpolarity FASC devices with a maximum voltage of 1.6 V were successfully fabricated. Our devices achieve an outstanding specific capacitance of 74.25 F cm -3 and a remarkable energy density of 26.42 mW h cm -3 . More importantly, their electrochemical performance changed negligibly regardless of whether the charge-discharge process is in positive or negative direction, indicating excellent nonpolarity. Therefore, these high-performance nonpolarity FASCs pave the way for next-generation wearable energy storage devices.

Biomass with abundant resources and low price is regarded as potential sources of functionalized carbon-based energy storage and conversion electrode materials. Rational construction and development of biomass-derived carbon equipped with proper morphology, structure, and composition prove the key to highly efficient utilization of advanced energy storage systems. Herein, we use palm tree bark hair as a biomass source and prepare edge/defect-rich quasi-mesoporous carbon (QMC) by a direct pyrolysis followed by NaOH etching strategy. Then, the edge-rich quasi-mesoporous nitrogen-doped carbon (QMNC) is successfully fabricated through the hydrothermal method by making use of edge/defect-rich QMC and urea as carbon precursor and nitrogen source, respectively. The microstructure and composition of the resultant carbon materials are all detected by a series of techniques. In the meantime, the influence of the etching process on the preparation and electrochemical performance of edge-rich QMNC is systematically explored. The relevant results manifest that the as-prepared edge/defect-rich QMC not only possesses edge-rich plane, much increased specific surface area (SSA), and special quasi-mesopores but also reverses good conductivity and gains sufficient defects for subsequent N doping. After introducing N atoms, the obtained edge-rich QMNC exhibits outstanding capacitive property and oxygen reduction reaction performance, which are mainly attributed to the co-effect of edge-rich plane, large SSA, suitable pore structures, and effective N doping (including high doping amount and optimized N configurations). Clearly, our work not only offers an excellent biomass-derived carbon-based electrode material but also opens a fresh avenue for the development of advanced biomass-derived carbon-based electrode materials.

Water oxidation is the key process for many sustainable energy technologies containing artificial photosynthesis and metal-air batteries. Engineering inexpensive yet active electrocatalysts for water oxidation is mandatory for the cost-effective generation of solar fuels. Herein, we propose a novel hierarchical porous Ni-Co-mixed metal sulfide (denoted as NiCoS) on Ti 3 C 2 T x MXene via a metal-organic framework (MOF)-based approach. Benefiting from the unique structure and strong interfacial interaction between NiCoS and Ti 3 C 2 T x sheets, the hybrid guarantees an enhanced active surface area with prominent charge-transfer conductivity and thus a superior activity toward oxygen evolution reactions (OERs). Impressively, the hierarchical NiCoS in the hybrid is converted to nickel/cobalt oxyhydroxide-NiCoS assembly (denoted as NiCoOOH-NiCoS) by OER measurement, where NiCoOOH on the surface is confirmed as the intrinsic active species for the consequent water oxidation. The hybrid material is further applied to an air cathode for a rechargeable zinc-air battery, which exhibits low charging/discharging overpotential and long-term stability. Our work underscores the tuned structure and electrocatalytic OER performance of MOF derivatives by the versatility of MXenes and provides insight into the structure-activity relationship for noble metal-free catalysts.