摘要：The past 5 years have witnessed the rapid development of organic solar cells based on nonfullerene acceptors(NFAs)[1-26].The state-of-the-art NFA-based single-junction and tandem solar cells afforded 18.22%(certified 17.6%)and 17.36%(certified 17.29%)power conversion efficiencies(PCEs),respectively[27,28].Wide-bandgap(WBG)polymer donors are ideal partners for *** present complementary absorption with that of low-bandgap NFAs and deep the highest occupied molecular orbital(HOMO)***,solar cells based on a WBG polymer and a NFA can generate high short-circuit current density(Jsc)and open-circuit voltage(Voc)[29].Meanwhile,some WBG polymers show high crystallinity and mobility,gifting the solar cells high fill factors(FF)[30].Recently,our group first reported efficient WBG D-A copolymer donors based on fused-ring aromatic lactone(FRAL)acceptor units.

摘要：Herein,we report the excellent De-NO_(x)performance of La0.7Sr0.3MnO3(LSM)perovskite-supported Pd catalysts(Pd-LSM)in alternating lean-burn/fuel-rich atmospheres using C3H6 as reductant and describe the in situ activation of the Pd catalysts via metal-support interaction(MSI)*** NO_(x)reduction conversion of the Pd-LSM catalyst increased significantly from 56.1%to 90.1%and the production of N2O was *** results demonstrated that this behavior was mainly attributed to the in situ transformation of Pd2+into Pd0 during the *** generated Pd0 species could readily activate the C3H6 reductant and achieve an eight-fold higher turnover frequency than Pd2+for the reduction of NO_(x).Moreover,excessive MSIs inhibited the in situ generation of Pd0,and thereby,lowered the De-NO_(x)activity of the catalyst even at high Pd *** addition,the Pd-LSM catalysts exhibited much higher S tolerance than conventional Al_(2)O_(3)-supported *** study provides a new approach for analyzing and designing highly active metal catalysts operated under dynamic alternating oxidizing/reducing atmospheric conditions.

摘要：Flexible and Personalizable battery is a promising candidate for energy storage, but suffers from the weldablity and large-scale producibility of the electrode. To address the issues, we design a nickel foam catalyzed electroless deposition (NFED) derived 3D-metal-pattern embroidered electrodes. This is the first attempt to utilize this type of electrode in battery field. It is found that the current collector can be embroidered on any selected areas of any complex-shape electrodes, with high controllability and economical feasibility. As a result, the electronic conductivity of the flexible electrodes can be improved by nearly one order of magnitude, which can be easily and firmly weldded to the metal tab using the industry generic ultrasonic heating process. The embroidered electrodes could substantially promote the electrochemical performance under bending deformation, with both Li-S and Li-Li FePO4batteries as the models. This innovation is also suitable to embroider all the VIII group elements on any electrodes with personalized shapes, which is widely attractive for the development of next generation flexible and personalizable energy storage devices.

摘要：The thermal conduction of suspended few-layer hexagonal boron nitride （h-BN） sheets was experimentally investigated using a noncontact micro-Raman spectroscopy method. The first-order temperature coefficients for monolayer （1L）, bilayer （2L） and nine-layer （9L） h-BN sheets were measured to be -（3.41 ± 0.12）× 10-2, -（3.15 ± 0.14） × 10-2 and -（3.78 ±0.16）× 10-2 cm-1.K-1, respectively. The room-temperature thermal conductivity of few-layer h-BN sheets was found to be in the range from 227 to 280 W.m-1-K-1, which is comparable to that of bulk h-BN, indicating their potential use as important components to solve heat dissipation problems in thermal management configurations.

摘要：开发钙钛矿叠层太阳电池是一种可以突破单结太阳电池Shockley-Queisser极限的光伏技术.令人鼓舞的是,所有钙钛矿叠层器件,包括钙钛矿/硅、钙钛矿/钙钛矿、钙钛矿/铜铟镓硒和钙钛矿/有机叠层电池,都表现出比相应单结太阳电池更高的效率,显示出巨大的进一步突破的潜力.在叠层器件中,电荷传输材料是钙钛矿子电池的重要组成部分,它直接决定了器件的电荷传输和能量损失.一般来说,高导电性和透光性、良好的能级和化学稳定性是电荷传输材料叠层应用的关键.迄今为止,导电金属氧化物、有机分子、聚合物、富勒烯、自组装材料等各种电荷传输材料已被广泛应用于高效叠层电池.在本文中,我们首先总结了不同类型钙钛矿叠层电池的电荷传输材料的最新进展,详细讨论了材料的电学和光学性质及其对器件性能的影响.在此基础上,我们提出了叠层电池中电荷传输材料进一步发展所面临的挑战和展望.本综述将为不同钙钛矿叠层太阳电池的器件设计提供有效指导.

摘要：螺旋二色性利用无限的轨道角动量自由度,可以突破依赖于固有自旋自由度的圆二色性所受到的两态限制,为探索经典波体系中的手性效应提供了重要的手段.然而,在波与物质相互作用过程中,手性信号通常非常微弱,使得螺旋手性效应的有效增强极具挑战性.本文通过在非厄米梯度超构表面的内禀拓扑荷中构建手性奇异点,提出了一种实现最大螺旋二色性的新范式.由于奇异点所诱发的非对称手性耦合特性,非厄米梯度超构表面可以通过灵活地设计,实现多样化的极端手性调控:一种手性的涡旋场被非厄米超构表面完全反射,而相反手性的涡旋场则可以被完美吸收或传输到定制的涡旋模式.作为最大螺旋二色性的一种体现,本文提出完美手性选择的涡旋传输现象,并通过声学实验进行了验证.本研究为实现最大手性效应以及探索波与物质相互作用中的手性物理提供了新途径,有望推动诸如非对称手性调控、单向传播和信息多路复用等轨道角动量相关的基础研究和应用领域的发展.

摘要：Sintering inhibition of a catalyst at high temperatures is a challenge during heterogeneous catalysis. In this paper, we report that hexagonal boron nitride(h-BN) is an optimal material for anti-sintering γ-Al_(2)O_(3)-supported Pt nanoparticles(NPs) originating from the high thermal conductivity of h-BN. The high thermal conductivity of h-BN ensures maximal heat dissipation from Pt NPs to γ-Al_(2)O_(3),thereby causing both Ostwald ripening and particle coalescence of Pt NPs to be decelerated at elevated *** of Pt NP sintering is also shown in the reducible TiO^(2-)supported Pt NPs with the help of h-BN. The proposed anti-sintering strategy using thermal management is universal, providing new insight into the design of anti-sintering materials and structures for a wide range of applications in heterogeneous catalysis.

摘要：Herein,a novel photonic coordination polymer material was constructed by aggregation-induced emission luminogen(AIEgen)containing a tripyridyl moiety used as the linking *** displayed a spontaneous direct centrosymmetric to noncentrosymmetric phase transition in a single *** two crystals,before and after the phase transition,were both controllably synthesized and characterized by single-crystal X-ray *** being exposed to air,the centrosymmetric metastable phase(1-α)transitioned to a new stable phase with a noncentrosymmetric structure(1-β).Interestingly,the 1-βstructure exhibited a strong phasematching second-harmonic generation(SHG)response,about4.5 times higher than that of KH2PO4(KDP).In order to better understand the relationship between the structure and the nonlinear optical properties,the dipole moments were calculated and ***,the noncentrosymmetric phase with high thermal stability for 1-βretained and improved the initial photoluminescent properties of the AIEgen ligand after the structural phase transition from 1-α,and simultaneously produced the excellent SHG property,which are beneficial for the design and construction of excellent optical materials.

摘要：The anionic redox chemistry(O^2-→O^-)in P2-type sodium-ion battery cathodes has attracted much ***,determining how to tune the anionic redox reaction is still a major ***,we tune the activity and reversibility of both the anionic and cationic redox reactions of Na0.67Mn0.5Fe0.5O2 though an integrated strategy that combines the advantages of Li2SiO3 coating,Li doping and Si doping,and the initial capacity,rate performance and cycling stability are significantly *** in-depth modulation mechanism is revealed by means of neutron diffraction,X-ray absorption spectroscopy,in situ X-ray diffraction,electron paramagnetic resonance spectroscopy,first-principles calculations and so *** Li2SiO3 coating alleviates the side reactions and enhances the cycling ***^4+doping lowers the Na^+diffusion barrier due to the expanded interlayer ***,Si^4+doping improves the structural stability,oxygen redox activity and ***^+doping in Na sites further increases the structure *** electron density maps confirm the greater activity of Na and O in the modified *** density maps and bond-valence energy landscapes identify the Na^+migration pathway from Nae site to Naf site(the positions of the Na ions in the crystal structure).The proposed insights into the modulation mechanism of the anionic and cationic redox chemistry are also instructive for designing other oxide-based cathode materials.

摘要：Photoelectrochemical(PEC)water splitting for solar energy conversion into chemical fuels has attracted intense research *** semiconductor hematite(α-Fe_(2)O_(3)),with its earth abundance,chemical stability,and efficient light harvesting,stands out as a promising photoanode ***,its electron affinity is too deep for overall water splitting,requiring additional *** engineering has been used to reduce the onset potential of hematite *** we focus instead on energy band engineering hematite by shrinking the crystal lattice,and the water-splitting onset potential can be decreased from 1.14 to 0.61 V *** reversible hydrogen *** is the lowest record reported for a pristine hematite photoanode without surface modification.X-ray absorption spectroscopy and magnetic properties suggest the redistribution of 3d electrons in the as-synthesized grey hematite *** function theory studies herein show that the smaller-lattice-constant hematite benefits from raised energy bands,which accounts for the reduced onset potential.