摘要：Nanoporous metals show promising performances in electrochemical *** this paper,we report a self-supporting bimetallic porous heterogeneous indium/copper structure synthesized with a eutectic gallium-indium(EGaIn)material on a copper *** nanoporous copper-indium heterostructure catalyst exhibits excellent performance in the reduction of carbon dioxide to *** ratio of H_(2)/CO is tunable from 0.47 to 2.0 by changing working *** catalyst is highly stable,showing 96%maintenance of the current density after a 70-h continuous *** functional theory calculations reveal that the indium/copper interface induces charge redistribution within the copper surface,leading to the formation of two distinct active sites,namely,Cu^(δ)and Cu0,and enabling a high-performance generation of CO and H_(2).This work provides a new strategy for obtaining self-supporting nanoporous metal electrode catalysts.

摘要：Owing to its photonic band gap(PBG)and slow light effects,aniline black(AB)-poly(vinylidene fluoride)(PVDF)inverse opal(IO)photonic crystal(PC)was constructed to promote the utility of light and realize photothermal synergetic *** a highly efficient reaction platform with the capability of restricting heat,a microreactor was introduced to further amplify the photothermal effects of near infrared(NIR)*** photocatalytic efficiency of ZnO/0.5AB-PVDF IO(Z0.5A)increases 1.63-fold compared to that of pure ZnO film under a full solar spectrum,indicating the effectiveness of synergetic promotion by slow light and photothermal ***,a 5.85-fold increase is achieved by combining Z0.5A with a microreactor compared to the film in a *** photon localization effect of PVDF IO was further exemplified by finite-difference time-domain(FDTD)*** conclusion,photonic crystal-microreactor enhanced photothermal catalysis has immense potential for alleviating the deteriorating water environment.

摘要：液晶弹性体(LCEs)是一种刺激响应性材料,具有较大且可逆变形的能力,在软致动器、人造肌肉、光子器件和生物医学工程等领域引起了广泛的关注.与具有永久交联网络的传统液晶弹性体不同,具有共价自适应网络的液晶弹性体(CAN-LCEs)可以通过键交换反应引起的网络重排将多畴液晶弹性体编程为单畴液晶弹性体.此外,CAN-LCEs还具有焊接、自修复、回收、再加工或重新编程的能力.本文综述了CAN-LCEs的最新研究成果,详细讨论了基于各种类型的键交换反应的CAN-LCEs及其设计策略.同时,本文还介绍了共价自适应网络给LCEs带来的新功能,包括焊接、自愈、重塑、回收、重新编程等,并探讨了CAN-LCEs在各种领域的应用前景.最后,本文总结了这一新兴研究领域面临的挑战和潜在的未来发展方向.

摘要：Based on aphid wax-honeydew marble and the hydrophobic wax structure of lotus and its derived applications with superareophilic and superhydrophobic properties,edible carnauba wax and beeswax particles were mixed and utilized to mimic lotus wax and wrap liquid,thus forming liquid marbles(LMs).Through the utilization of continuous production system(CPS),wax as an interfacial surfactant,water and solid,air-phase or mixed-phase marble content was *** edible liquid marble(ELM)could encapsulate water and food *** solid marble(ESM)and edible solid hollow marbles(ESHMs)could be fabricated by applying pectin or ***,through the heating of wax powders with different melting temperatures,stable tablets and hollow capsules could be *** wax powder as interfacial surfactant could firmly bind with pectin through hydrogen bonds on *** edible LMs can therefore be applied for residue reduction,corrosion reduction,biohazard prevention and cleaning in the food *** other phase LMs could act as novel tools in the pharmaceutical and food industries with the above-mentioned water transport,preservation,sustained releasing and selective releasing abilities.

摘要：剪切增稠型聚硼硅氧烷(PBS)通常以“silly putty”,“bouncing putty”或“solid-liquid”被熟知.因其独特的抗冲击性能,PBS广泛应用于防护装甲、运动器材、玩具等领域.然而,自第二次世界大战PBS被发明后,PBS材料的更新升级较少.本论文中,我们通过设计联硼/氧配位键制备了一类新型剪切增稠材料——聚联硼硅氧烷(PDBS).结果表明,与单硼/氧配位键相比,联硼/氧配位键具有更多的配位结构和更高的键能,导致PDBS具有更类固体性的剪切增稠行为.因此,PDBS具有比PBS更优异的抗冲击性能与防护功能,为新一代智能装备、阻尼器和传感器的开发提供了一类高性能防护材料.

摘要：Theranostic nanoprobes can potentially integrate imaging and therapeutic capabilities into a single platform,offering a new personalized cancer diagnostic ***,there is a growing concern that their clinical application is not safe,particularly due to metal-containing elements,such as the gadolinium used in magnetic resonance imaging(MRI).We demonstrate for the first time that the photothermal melting of the DNA duplex helix was a reliable and versatile strategy that enables the on-demand degradation of the gadolinium-containing MRI reporter gene from polydopamine(PDA)-based theranostic *** combination of chemotherapy(doxorubicin)and photothermal therapy,which leads to the enhanced anti-tumor *** vivo MRI tracking reveals that renal filtration was able to rapidly clear the free gadolinium-containing MRI reporter from the mice *** results in a decrease in the long-term toxic effect of theranostic MRI *** findings may pave the way to address toxicity issues of the theranostic nanoprobes.

摘要：It is a great challenge to develop highly active oxygen evolution reaction(OER)electrocatalysts with superior *** this study,a NiFe layered double hydroxidedecorated phosphide(NiFe LDH@CoP/NiP_(3))was constructed to display satisfactory OER activity and good stability for water splitting in alkaline *** an overpotential of 300 mV,NiFe LDH@CoP/NiP_(3) achieved a current density of 82 mA cm^(-2) for the OER,which was 9.1 and 2.3 times that of CoP/NiP_(3) and NiFe LDH,***,the reconstruction behavior,during which oxyhydroxides formed,was studied by a combination of X-ray photoelectron spectroscopy,Raman spectroscopy,and scanning electron microscopy.A synergistic effect between NiFe LDH and CoP/NiP_(3) was also observed for the hydrogen evolution ***,when NiFe LDH@CoP/NiP_(3) acted as both the cathode and anode for overall water splitting,a high current density of 100 mA cm^(-2) was maintained for more than 275 *** addition,under Xe light irradiation,a solar-to-hydrogen efficiency of 9.89% was achieved for solar-driven water *** work presents the coupling of different active compositions,and can provide a reference for designing bifunctional electrocatalysts.

摘要：The synthesis of nanocrystals(NCs)with defined morphology and surface structure provides an effective way to investigate the structure-activity relationship of nanocatalytsts,and it will facilitate the design of nanocatalysts with excellent catalytic *** this paper,we developed a facile method to synthesize PdH0.43 NCs with the shape of cube,octahedron and rhombic dodecahedron(RD),whose surface facets are{100},{111}and{110},*** asprepared PdH0.43 NCs are highly stable and exhibit enhanced catalytic activity and extremely low overpotential towards electro-oxidation of formic acid compared with the commercial Pd black and three types of Pd *** specific activity of the cubic PdH0.43 NCs is more than five times that of the commercial Pd black and two times that of the cubic Pd *** the three types of PdH0.43 NCs with different surface structure,the activity order is followed by PdH0.43{100}>PdH0.43{111}>PdH0.43{110}.

摘要：Solar‐energy‐driven catalytic CO_(2) reduction for the production of value‐added carbon‐based materials and chemical raw materials has attracted great interest to alleviate the global climate change and energy *** production of multicarbon(C2)products through CO_(2) reduction is extremely attractive,however,the yield and selectivity of C2 products remain low because of the low reaction temperature required and the low photoelectron density of the ***,we introduce WO3–x,which contains oxygen vacancies and exhibits an excellent photothermal conversion efficiency,to improve the generation of C2 products(C2H4 and C2H6)under simulated sunlight(UV‐Vis‐IR)***3–x produced 5.30 and 0.93μmol·g^(–1)C2H4 and C2H6,respectively,after 4 h,with a selectivity exceeding 34%.In situ Fourier transform infrared spectra and theoretical calculations showed that the oxygen vacancies enhanced the water activation and hydrogenation of adsorbed CO for the formation of C2 products via C–C coupling from CH2/CH3 *** findings of this study could assist in the design of highly active solar‐energy‐driven catalysts to produce C–C coupling products through CO2 reduction.

摘要：The catalytic hydrogenation of halonitroarenes to haloanilines is a green and sustainable process for the production of key nitrogen-containing intermediates in fine chemical *** hydrogenation poses a significant challenge,which requires the rational design of the catalysts with proper hydrogenation ability for nitro group and simultaneously preventing dehalogenation of halogen ***,a highly effective Rh@Al_(2)O_(3)@C single-atom catalyst(SAC)was developed for the hydrogenation of m-chloronitrobenzene(m-CNB)to m-chloroaniline(m-CAN),through an in-situ grafting of metal during the assembly of MIL-53(Al),followed by confined *** characterizations reveal an exquisite structure of the Rh@Al_(2)O_(3)@C,containing atomically dispersed Rh sites onto Al_(2)O_(3) confined by the amorphous *** five-coordinated aluminum(Al^(Ⅴ))species are essential for achieving the atomic dispersion of Rh atoms,providing the unsaturated coordinative sites for *** to the benchmark Rh/γ-Al_(2)O_(3) and Rh/C nanocatalysts,the Rh@Al_(2)O_(3)@C SAC affords an excellent turnover frequency of 2317 molm-CNB·molRh^(–1)·h^(–1),the highest value to date in heterogeneous catalyst systems for the hydrogenation of m-CNB at 313 K and 20 bar H2,together with a sustained selectivity to m-CAN(~98%)during five consecutive *** superior catalytic performance of the Rh@Al_(2)O_(3)@C is attributed to a proper modulation of electronic structure of hydrogenation metal by forming SAC,together with an enhanced accessibility of acid function sites.