摘要：As one of the most promising next-generation energy storage devices,the lithium-metal battery has been extensively ***,safety issues and undesired lithium dendrite growth hinder its *** application of solid-state electrolytes has attracted increasing attention as they can solve safety issues and show great potential to inhibit the growth of lithium *** oxide(PEO)-based electrolytes are very promising due to their enhanced safety and excellent ***,they suffer from low ionic conductivity at room temperature and cannot effectively inhibit lithium dendrites at high temperatures due to the intrinsic semicrystalline properties and poor mechanical *** this work,a novel coral-like Li_(6.25)Al_(0.25)La_(3)Zr_(2)O_(12)(C-LALZO)is synthesized to serve as an active ceramic filler in *** PEO with LALZO coral(PLC)exhibits increased ionic conductivity and mechanical strength,which leads to uniform deposition/stripping of lithium *** Li symmetric cells with PLC do not cause a short circuit after cycling for 1500 h at 60℃.The assembled LiFePO_(4)/PLC/Li batteries display excellent cycling stability at both 60 and 50℃.This work reveals that the electrochemical properties of the composite electrolyte can be effectively improved by tuning the microstructure of the filler,such as the C-LALZO architecture.

摘要：Sodium layered oxides generally suffer from deep-desodiation instability in P2 structure and sluggish kinetics in O3 *** will be great to design P2/O3 biphasic materials that bring the complementary merits of both ***,such exploration is hindered by the ambiguous mechanism of material ***,supported by theoretical simulations and various spectroscopies,we prove that P2/O3 biphasic structures essentially originate from the internal heterogeneity of cationic potential,which can be realized by constraining the temperature-driven ion diffusion during solid-state ***,P2/O3 biphasic Na_(0.7)Ni_(0.2)Cu_(0.1)Fe_(0.2)Mn_(0.5)O_(2)-δ with well-designed quaternary composition is successfully obtained,exhibiting much-improved rate capabilities(62 mAh g^(-1)at 2.4 A g^(-1)) and cycling stabilities(84%capacity retention after 500 cycles)than its single-phase ***,synchrotron-based diffraction and X-ray absorption spectroscopy are employed to unravel the underlying sodium-storage mechanism of the P2/O3 biphasic *** work presents new insights toward the rational design of advanced layered cathodes for sodium-ion batteries.

摘要：Tissue implant-related infections are among the most serious complications after surgical implantation,including orthopedics and *** with antibacterial ion release systems are efficient and economical antibiotic substitutes to fight against bacterial ***,the excessive amount of released antibacterial ions may cause biological toxicity while killing *** raises a fundamental issue on how to properly control the amounts of ions and their ***,we develop low-dose antibacterial ions-incorporated ferroelectric implants(copper-doped potassium sodium niobate,K0.5Na0.5NbO3-Cu,KNNCu)whose surface potential can be tuned via external *** released Cu2+ions can be targeted to bacteria via endogenous electric field(EEF)between KNNCu implants and negatively charged ***,the antibacterial efficacy of the implants is determined by the amount of Cu^2+ions that reaches bacteria,instead of the total amount of released Cu2+*** amount of Cu2+ions reaching bacteria from the high-surface-potential implant is 2.4 times that from the lowsurface-potential implant within 12 h,resulting in the increased antibacterial ratio from about 65%to 100%,while remaining low cell *** work provides insights into the specific role of the EEF in guiding mass transport between charged materials and living organisms,and a new perspective for the design of high-performance antibacterial biomaterials.

摘要：High-temperature proton exchange membrane fuel cells(HT-PEMFCs)bring new opportunities for portable power generation due to their outstanding advantages such as high tolerance to fuel/air impurities and simplified heat/water ***,carbon-supported nanostructured Pt-based catalysts running at temperatures over 150℃are challenged by the severe aggregation and carbon corrosion,thus leading to poor ***,we demonstrate that dendritic Pt-Ni nanoparticles supported on fluorinated carbon black(white carbon black)could significantly enhance the performance and durability of HT-PEMFCs as the cathode catalysts running at 160℃due to the strong interaction of the F and Ni atoms to form a Ni_(x)F_(y) interface on Pt-Ni *** the formation of a stable Ni_(x)F_(y) interface,this integrated HT-PEMFC reached peak power densities of 906 mW cm^(−2) and demonstrated excellent durability at 160℃ under anhydrous H_(2)/O_(2) *** mitigation strategy was applied to Pt-alloy/C electrocatalysts and resulted in the elimination of Pt dissolution in practical fuel cells.

摘要：Submicron scale temperature sensors are crucial for a range of applications,particularly in micro and na-noscale *** promising solution involves the use of active whispering gallery mode(WGM)*** resonators can be remotely excited and read out using free-space structures,simplifying the process of *** this study,we present a submicron-scale temperature sensor with a remarkable sensitivity up to 185 pm/℃based on a trian-gular MAPbI3 nanoplatelet(NPL)***,as temperature changes,the peak wavelength of the laser line shifts *** unique characteristic allows for precise temperature sensing by tracking the peak wavelength of the NPL *** optical modes are confined within the perovskite NPL,which measures just 85 nm in height,due to total internal *** NPL laser boasts several key features,including a high Q of~2610 and a low laser threshold of about 19.8μJ·cm^(−2).The combination of exceptional sensitivity and ultra-small size makes our WGM device an ideal candidate for integration into systems that demand compact temperature *** advancement paves the way for significant prog-ress in the development of ultrasmall temperature sensors,opening new possibilities across various fields.

摘要：Due to the unique interface and electronic structure,metal/metal oxide composite electrocatalysts have been designed and exploited for electrocatalytic oxygen evolution reaction(OER)in alkaline ***,how to fabricate metal/metal oxides with abundant interfaces and well-dispersed metal phases is a challenge,and the synergistic effect between metal and metal oxides on boosting the electrocatalytic activities is still ***,by controlling the lithium-induced conversion reaction of metal oxides,metal/metal oxide composites with plentiful interfaces and excellent electrical interconnection are fabricated,which can enhance the active sites,and accelerate the mass transfer during the electrocatalytic *** a result,the electrocatalytic oxygen evolution activities of the as-fabricated metal/metal oxide composite catalysts including NiCo/NiCo2O4,NiMn/NiMn2O4 and CoMn/CoMn2O4 are greatly *** catalytic mechanism is also explored using the in-situ X-ray and Raman spectroscopic tracking to uncover the real active centers and the synergistic effect between the metal and metal oxides during water *** functional theory plus U(DFT+U)calculation confirms the metal in the composite can optimize the catalytic reaction path and reduce the reaction barrier,thus boosting the electrocatalytic kinetics.

摘要：MnO_(2)作为超级电容器电极材料具有理论比电容高、成本低、环境友好等优点,但其低导电性和低利用率阻碍了其潜在应用.本研究首先在柔性碳布上电化学生长ZnO纳米棒阵列作为电极衬底,然后通过阳极电沉积法在ZnO纳米棒阵列表面外延生长了Mo和碳纳米管(CNTs)共掺杂的MnO_(2)薄膜,可控构筑了有效、高导电性的MnO_(2)纳米阵列电极(定义为ZnO@Mo-CNT-MnO_(2)NA).柔性ZnO@Mo-CNTMnO_(2)NA电极在100 A g^(-1)的大电流充放电密度下比电容可达237.5 F g^(-1),10,000次循环后电容保留率高达86%.采用ZnO@Mo-CNTMnO_(2)NA电极组装成水系非对称超级电容器,弯曲状态下在132.35 mW cm^(-3)(5mA cm^(-2))高功率密度下获得了1.13 mW h cm^(-3)的高能量密度,5mA cm^(-2)充放电倍率下循环7600次后电容保留率高达88%.本研究构筑的MnO_(2)基纳米阵列电极结构可提高其电导率和利用率,为柔性金属氧化物超级电容器电极的设计与制备提供新途径.

摘要：Due to their unique surface chemistry,highly adjustable metal components,hydrophilicity,and high carrier concentrations,MXenes are applied in a variety of *** to other two-dimensional(2D)materials,building heterostructures with additional materials to form a 3D porous architecture for MXenes can significantly enhance their functionality and ***,the open structures and well-defined pathways of these 3D structured MXenes can improve ionic and electronic transport,thereby promoting their applications in electrochemical energy storage,sensing,catalysis,and *** this review,the recent efforts made on preparing 3D porous MXenes with heterostructures,focusing on MXenes/C,MXenes/inorganics,and MXenes/polymers were *** discussion covers aspects ranging from the design to synthesis of 3D porous MXenes,and their applications in photocatalysis,environmental monitoring and electrochemical energy *** review is concluded by presenting the prospects and insights on exploring the relationships between the porosity formation mechanisms,properties and applications of the 3D porous MXenes *** review can provide meaningful guidance for the design,fabrication and application of 3D porous MXenes in high-performance materials and devices.

摘要：单价选择性阳离子交换膜(M-CEMs)已被广泛应用于环境修复和能量收集等领域,例如,从卤水和海水中提取Na^(+)或Li^(+)。然而,由于膜结构和材料的限制,M-CEMs存在渗透选择性低的问题。在此,我们提出了一种简单的方法以构建具有电荷Janus结构的新型M-CEMs,该结构由荷正电的均苯三甲酸/聚乙烯亚胺选择层和荷负电的商业阳离子交换膜(CEM)组成。选择性电渗析(SED)分析结果表明,具有电荷Janus结构的M-CEMs可以有效抑制多孔阳离子交换膜中存在的阴离子迁移问题,因而使这种具有电荷Janus结构的M-CEMs具有较高的渗透选择性和总阳离子通量。与最先进的单价选择性阳离子交换膜的分离性能相比,具有电荷Janus结构的M-CEMs对于Na^(+)/Mg^(2+)的最高渗透选择性可以达到145.77,这超过了目前单价选择性阳离子交换膜性能的“上限”,且对于Li^(+)/Mg^(2+)也具有优异的渗透选择性(14.11),在离子分离领域具有巨大的应用潜力。这项研究可以为具有电荷Janus结构的M-CEMs的设计提供新的见解,并应用于不同的环境和能源领域。

摘要：Recently,in-situ polymerization inside living cells has attracted much attention due to the efficient cellular internalization and elevated drug ***,the lack of tracking of the in-situ polymerization process and the unclear effects of polymerization on cellular functions restrict its biomedical ***,we designed a Y-shaped diacetylene-containing lipidated peptide amphiphile(YDLPA1)with positive charges,which underwent in-situ polymerization initiated by reactive oxygen species in the intracellular *** comparison,zwitterionic YDLPA2 and negatively charged Y-DLPA3 were polymerized in aqueous solution,but cannot polymerize in the intracellular *** polymerized Y-DLPA1 with red fluorescence provides a platform to label cells for long-term tracking *** polymerization reaction induced tumor cell apoptosis,increased cell viscosity and decreased cell motility,which potentially inhibited tumor metastasis and served as a novel antitumor *** work provides a novel strategy to track in-situ polymerization process and modulate cell biofunctions.