摘要：Two non-ionic hydro-fluorocarbon hybrid surfactants with and without hydroxyl groups were synthesized and *** exhibited good thermal stability and superior surface *** was observed that the hydroxyl group had a profound effect on modifying the surface tension of their solutions and the morphology of the formed *** effect may be attributed to the rearranging of the alkane group from above the air/aqueous surface to below it and the disrupting of the interfacial water structure induced by the hydroxyl *** work provides a strategy to weaken the immiscibility between hydrocarbon and fluorocarbon chains by modifying their orientational structure at the interface,thus it is helpful for the design of surfactants with varied interfacial properties.

摘要：Lithium-ion capacitors(LICs),consisting of a battery-like negative electrode and a capacitive porous-carbon positive electrode,deliver more than twice the energy density of electric double-layer ***,their wide application suffers from low energy density and reduced cycle life at high ***,hierarchical meso±microporous carbon nanospheres with a highly disordered structure and nitrogen/phosphorous co-doped properties were synthesized through a facile template *** hierarchical porous structure facilitates rapid ion transport,and the highly disordered structure and high heteroatom content provide abundant active sites for Li+charge *** experiments demonstrated that the carbon nanosphere anode delivers large reversible capability,greatly improves rate capability and exhibits excellent cycle *** LIC fabricated with the carbon nanosphere anode and an activated carbon cathode yields a high energy density of 103 W h kg^(-1),an extremely high power density of 44,630 W kg^(-1),and longterm cyclability of over 10,000 *** work presents how structural control of carbon materials at the nano/atomic scale can significantly enhance electrochemical performance,enabling new opportunities for the design of high-performance energy-storage devices.

摘要：We investigated the hydrolysis of TiⅣ along with naturally abundant AlⅢ ions and reported the formation of a stable and semiconducting nanocluster. Interestingly, this compound exhibits an unusual odd-membered ring structure and also represents the largest Al-containing polyoxotitanium cluster(PTC) observed thus far. The presence of a shell of organic ligands as well as the incorporation of hetero-AlⅢ ions endowed the nanocluster with high air, thermal, and pH stabilities. The present compound exhibited a record photocatalytic hydrogen evolution of 402.88 μmol g–1 h–1 among PTC materials. This work not only paves the way towards stable PTC materials but also provides new insights into the design of novel photocatalysts.

摘要：The figure of merit is of crucial importance in materials design to search for candidates with optimal *** the field of photovoltaics,the bandgap(E_g)is a well-recognized figure of merit for screening solar cell absorbers subject to the Shockley-Queisser *** this paper,the bandgap as the figure of merit is challenged since an ideal solar cell absorber requires multiple criteria such as stability,optical absorption,and carrier *** criteria make the quantitative description of material candidates difficult and computationally *** halide perovskites as an example,we combine thermodynamic stability(ΔHd)and Eginto a unified figure of merit and use Bayesian optimization(BO)to accelerate materials *** have found that,in comparison to an exhaustive search via multiple parameters,BO based on the unified figure of merit can screen optimal candidates(E_g,PBEbetween 0.6–1.2 eV,ΔHd>-29 meV per atom)more ***,the proposed method opens a viable route for the search of optimal solar cell absorbers from a large amount of material candidates with less computational cost.

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 metal batteries are emerging as promising energy storage technologies owing to their high-energy density and rich ***,the challenge of achieving continuous operation at high areal capacity hinders the application of this ***,a robust two-dimensional tin/sodium‒tin alloy interface was introduced onto an Al substrate as an anode via an industrial electroplating *** the widely accepted in situ formation of Na15Sn4 alloys,the formation of Na_(9)Sn_(4)alloys results in a semi-coherent interface with sodium due to low lattice mismatch(20.84%),which alleviates the lattice stress of sodium deposition and induces subsequent dense sodium deposition under high areal *** addition,the strong interaction of Sn with anions allows more PF6−to preferentially participate in the interfacial solvation structure,thereby facilitating the formation of a thin(10 nm)NaF-rich solid electrolyte ***,the substrate can withstand a high areal capacity of 5 mA h cm^(-2),exhibiting a high average Coulombic efficiency of 99.7%.The full battery exhibits long-term cycling performance(600 cycles)with a low decay rate of 0.0018%per cycle at 60 mA g^(-1).

摘要：Photocatalytic hydrogen production coupled with selective oxidation of organic substrates to produce highvalue-added fine chemicals has drawn increasing ***,we report a noble metal-free photocatalyst for the highly efficient and simultaneous generation of hydrogen and the selective oxidation of benzyl alcohol into benzaldehyde over Cd S@Mo S2 heterostructures under visible *** the need for a sacrificial agent,Cd S@Mo S2 displayed an excellent hydrogen production rate of 4233μmol g^-1h^-1with0.3 mmol benzyl alcohol,which is approximately 53 times higher than that of bare Cd S nanorods(80μmol g^-1h^-1).The reaction system was highly selective for the oxidation of benzyl alcohol into *** the amount of benzyl alcohol increased to 1.0 mmol,the hydrogen production reached9033μmol g^-1h^-*** electron microscopy and transmission electron microscopy images revealed that p-type Mo S2 sheets with a flower-like structure closely adhered to n-type semiconductor Cd S nanorods through the formation of a p-n *** a potential Z-scheme photocatalyst,the Cd S@Mo S2 heterostructure effectively produces and separates electron-hole pairs under visible ***,the electrons are used for reduction to generate hydrogen,and the holes oxidize benzyl alcohol into ***,a mechanism of photogenerated charge transfer and separation was proposed and verified by photoluminescence,electrochemical impedance spectroscopy,photocurrent and Mott-Schottky *** results reveal that the Cd S@Mo S2 heterojunctions have rapid and efficient charge separation and transfer,thereby greatly improving benzyl alcohol *** work provides insight into the rational design of high-performance Z-scheme photocatalysts and the use of holes and electrons to obtain two valuable chemicals simultaneously.

摘要：Birefringence arises when the propagation speed and refractive index of light in an optically anisotropic crystal changes in response to the direction of ***,birefringence belongs to linear optical anisotropy and is a key parameter for linear optoelectronic functional crystals,such as birefringent crystals,which are widely used to modulate the polarization of light in optoelectronic areas[1].In terms of practical applications,there is still an urgent need for wide-bandgap birefringent crystals as they allow for the modulation of light polarization in short-wavelength UV waves and even in the deep-UV spectral region.

摘要：利用太阳能将CO_(2)光转化为化学燃料是前沿研究的热点.当前,科研的重点在于开发和优化各类光催化材料的性能.异质结构不仅用于增强无机半导体催化剂的活性,而且用于金属-有机框架(MOFs)光催化剂的构建.随着异质结技术的不断进步,新的相结概念应运而生.尽管关于无机半导体中的相结研究已取得一定进展,但是MOFs相结结构的探索尚处于起步阶段.本文中,我们成功设计并构建了一种具有卓越光催化CO_(2)还原性能的MOFs相结杂化材料.这种材料由具有高度连接性的卟啉配体(TCPP-Ni)与Zr6团簇紧密结合而成,在溶剂热反应条件下,PCN-222-Ni能够快速且均匀地成核.通过精准调控调节剂的用量,我们实现了同分异构体PCN-224-Ni在类似条件下较慢的晶体形成过程.最终制得的P@P杂化材料展现出高表面积、多孔性和卓越的结晶度.由于PCN-222-Ni和PCN-224-Ni之间的带隙匹配,光生载流子的分离和迁移得以促进,从而使P@P杂化材料展现出卓越的光还原CO_(2)性能.这一重大突破不仅标志着MOFs相结结构研究的重大进展,还拓宽了MOFs相结在CO_(2)光转化领域的应用前景.

摘要：单价Ag+或Li+引入到类金刚石结构的MQ22-(M=Ga,In;Q=S,Se)阴离子基团中能合成出良好的二阶非线性光学(NLO)晶体材料.然而,这些晶体分别面临着较低的抗激光损伤阈值(LIDT)或二氧化硅易被腐蚀等缺点,严重限制了其在高功率激光应用中的实用性.在本研究中,基于类金刚石结构的ZnSe,我们采用[Se_(4)Zn_(13)]Se_(2)4→[ClRb_(3)Ba]Se_(24)非常规的聚阳离子取代策略,设计并合成了一种新型的盐包硫属化合物[Rb_(3)BaCl][In_(8)Se_(14)](1).化合物1属于压缩黄铜矿型硒化物并保持了与AgInSe_(2)相同的晶体对称性(I-42d空间群).值得注意的是,由于InSe_(4)四面体结构单元的平行排列,化合物1具有相位匹配的强二次谐波(SHG)响应(2.0倍于AgGaS_(2)@2.90μm).此外,聚阳离子[Rb_(3)BaCl]^(4+)的引入促进了光学带隙(2.02 eV)的增强,有效地避免了对2.09μm激光的双光子吸收;同时结合较低的热膨胀系数,使得化合物1表现出高的LIDT(3.2倍于AgGaS2@2.09μm).本研究验证了在类金刚石结构中进行聚阳离子取代的可行性,并成功获得了性能优异的中远红外NLO材料.