摘要：Global demand for food and bioenergy production has increased rapidly,while the area of arable land has been declining for decades due to damage caused by erosion,pollution,sea level rise,urban development,soil salinization,and water scarcity driven by global climate *** order to overcome this conflict,there is an urgent need to adapt conventional agriculture to water-limited and hotter conditions with plant crop systems that display higher water-use efficiency(WUE).Crassulacean acid metabolism(CAM)species have substantially higher WUE than species performing C3 or C4 *** plants are derived from C3 photosynthesis ***,it is extremely unlikely that the C3 or C4 crop plants would evolve rapidly into CAM photosynthesis without human ***,there is growing interest in improving WUE through transferring CAM into C3 ***,engineering a major metabolic plant pathway,like CAM,is challenging and requires a comprehensive deep understanding of the enzymatic reactions and regulatory networks in both C3 and CAM photosynthesis,as well as overcoming physiometabolic limitations such as diurnal stomatal *** advances in CAM evolutionary genomics research,genome editing,and synthetic biology have increased the likelihood of successful acceleration of C3-to-CAM ***,we first summarize the systems biology-level understanding of the molecular processes in the CAM ***,we review the principles of CAM engineering in an evolutionary ***,we discuss the technical approaches to accelerate the C3-to-CAM transition in plants using synthetic biology toolboxes.

摘要：Capsule catalysts composed of pre-shaped core catalysts and layer zeolites have been widely used in the tandem reactions where multiple continuous reactions are combined into one process. They show excellent catalytic performance in heterogeneous catalysis, including the direct synthesis of middle isoparaflins or dimethyl ether from syngas, as compared to the conventional hybrid catalysts. The present review highlights the recent development in the design of capsule catalysts and their catalytic applications in heterogeneous catalysis. The capsule catalyst preparation methods are introduced in detail, such as hydrothermal synthe- sis method, dual-layer method, physically adhesive method and single crystal crystallization method. Purthermore, several new applications of capsule catalysts in heterogeneous cat- alytic processes are presented such as in the direct synthesis of liquefied petroleum gas from syngas, the direct synthesis of para-xylene from syngas and methane dehydroaromatization. In addition, the development in the design of multifunctional capsule catalysts is discussed, which makes the capsule catalyst not just a simple combination of two dill）rent catalysts, but has some special functions such as changing the surface hydrophobic or acid properties of the core catalysts. Finally, the future perspectives of the design and applications of capsule catalysts in heterogeneous catalysis are provided.

摘要：Rational design and controllable synthesis of efficient electrocatalysts for water oxidation is of significant importance for the development of promising energy conversion systems, in particular integrated photoelectrochemical water splitting devices. Cobalt oxide(Co3O4) nanostructures with mixed valences(Ⅱ,Ⅲ)have been regarded as promising electrocatalysts for the oxygen evolution reaction(OER). They are able to promote catalytic support of OER but with only modest activity. Here, we demonstrate that the OER performance of cubic Co3O4 electrocatalyst is obviously improved when they are anchored on delaminated two-dimensional(2D) Ti3C2 MXene nanosheets. Upon activation the overpotential of the hybrid catalyst delivers 300 m V at a current density of 10 m A cm(2) in basic solutions, which is remarkably lower than those of Ti3C2 MXene and Co3O4 nanocubes. The strong interfacial electrostatic interactions between two components contribute to the exceptional catalytic performance and stability. The enhanced OER activity and facile synthesis make these Co3O4 nanocubes-decorated ultrathin 2D Ti3C2 MXene nanosheets useful for constructing efficient and stable electrodes for high-performance electrochemical water splitting.

摘要：Rational composition design of trimetallic phosphide catalysts is of significant importance for enhanced surface reaction and efficient catalytic ***,hierarchical Co_(x)Ni_(y)Fe_(z)P with precise control of stoichiometric metallic elements(x:y:z=(1-10):(1-10):1)has been synthesized,and Co_(1.3)Ni_(0.5)Fe_(0.2)P,as the most optimal composition,exhibits remarkable catalytic activity(η=320 mV at 10 mA cm^(−2))and long-term stability(ignorable decrease after 10 h continuous test at the current density of 10 mA cm^(−2))toward oxygen evolution reaction(OER).It is found that the surface P in Co_(1.3)Ni_(0.5)Fe_(0.2)P was replaced by O under the OER *** density function theory calculations before and after long-term stability tests suggest the clear increasing of the density of states near the Fermi level of Co_(1.3)Ni_(0.5)Fe_(0.2)P/Co_(1.3)Ni_(0.5)Fe_(0.2)O,which could enhance the OH−adsorption of our electrocatalysts and the corresponding OER performance.

摘要：Nickel(Ni)-based materials act as one of the most promising candidates as platinum-group-metal-free(PGM-free)electrocatalysts for hydrogen oxidation reaction(HOR)in alkaline ***,the electrocatalytic activity of pure Ni is significantly limited due to the sluggish kinetics under alkaline *** accelerate the kinetics,constructing heterostructures and nitride structures have been developed as two representative ***,we combined the two methods and presented a facile synthesis of the sheet-like Ni_(3)N/MoO_(2)in-plane heterostructures for enhanced HOR in alkaline *** to Ni or Ni_(3)N,the Ni_(3)N/MoO_(2)in-plane heterostructures exhibited a significantly increased mass activity by 8.6-fold or 4.4-fold,*** studies revealed that the enhanced activity of Ni_(3)N/MoO_(2)could be attributed to the weakened hydrogen adsorption and strengthened hydroxyl *** work provides a facile approach to design high-efficiency catalysts for hydrogen-oxidation catalysis and beyond.

摘要：通过设计特定的时空调制,合成磁性的概念最近被提出以实现对光子和声子等电荷中性粒子的非互易操控,但现有方案存在着隔离度低、信号频率变化等问题.本文设计了一种新型耦合共振腔系统,其中动态耦合的相位作为实现声学合成磁场的新机制并打破了系统的时间反演对称性,最终取得了优异的声波非互易传输.基于旋转波近似方法,作者严格推导出了实现系统强非互易声传输的参数条件.通过优化动态耦合之间的相位差以及耦合强度,实验展示了隔离度达45-dB和正向传输率达0.85的优异单向声传输.此外,这种单向声传输具有始末态频率不变和隔离方向可电控等重要特性.该研究突破了现有声波单向操控机制在效率和隔离度方面的局限,并为实现弗洛奎和非线性声学拓扑绝缘体提供了新途径.

摘要：Corrugated reactors are known for their use in applications requiring UV-exposure, whereby media flowing within the corrugated channel react with a photo-active catalyst impregnated on the surface （i.e. TiO2）. The performance in these systems is dependent on catalyst properties and reactivity for a given light source, in conjunc-tion with the coupled transport of reactants within the media and photons falling incident to the catalyst surface. Experimental and computational analyses of local mass transfer and radiation pattems for a broad range of corrugation angles, depths, and non-idealities introduced during manufacture （i.e. fold curvature） are thus integrated to the design and optimization of these systems. This work explores techniques for determining incident energy distribu-tions on the surface of corrugated reactor geometries with non-ideal cross-sectional profiles, and the local and overall mass transfer rates obtained using computational fluid dynamics and experimental analysis. By examining the reaction kinetics for the photo-degradation of 4-chlorophenol over a TiO2 catalyst, the effects of surface area, energy incidence with photon recapture, and local mass transfer on overall reactor performance are presented to highlight ootimization concerns for these tvoes of reactors.

摘要：Rationally manipulating the in‐situ formed catalytically active surface of catalysts remains a great challenge for a highly efficient water ***,we report a cationic oxidation method which can adjust the leaching of the in‐situ catalyst and promote the reconstruction of dynamic surface for the oxygen evolution reaction(OER).The chlorine doping can reduce the possibility of triggering in‐situ cobalt oxidation and chlorine leaching,leading to a transformation of the surface chlorine doped LaCoO_(3)(Cl‐LaCoO_(3))into an intricate amorphous(oxygen)hydroxide *** thus,Cl‐LaCoO_(3)nanocrystals shows an ultralow overpotential of 342 mV at the current density of 10 mA cm^(–2)and Tafel slope of 76.2 mV dec–*** reconstructed Cl‐LaCoO_(3)is better than many of the most advanced OER catalysts and has proven significant *** work provides a new prospect for designing a high‐efficiency electrocatalyst with optimized perovskite‐structure in renewable energy system.

摘要：Inspired by the limitations of nanoparticles in cancer treatment caused by their low therapeutic effects and biotoxicity,biocompatible and photothermal enhanced copper oxide-decorated carbon nanospheres(CuO@CNSs)with doxorubicin hydrochloride(DOX)loading were *** as photothermal agents were synthesized by a hydrothermal *** was adsorbed on the surface of CNSs,which improved the photothermal conversion efficiency due to the electron transitions between C-2 p and Cu-3 *** addition,CuO would release Cu2+ions in the tumor microenvironment,which could produce hydroxyl radical(·OH)to induce cancer cells apoptosis via Haber-Weiss and Fenton-like *** as a chemotherapeutic agent was located on the surface of CuO@CNSs by electrostatic adsorption and released quickly in the tumor microenvironment to kill cancer *** CuO@CNSs-DOX nanoplatforms realized the combination therapy of photothermal therapy(PTT),chemodynamic therapy(CDT),and chemotherapy(CT),which have strong potential for cancer treatment.

摘要：Topological phase is an important development and unexplored degree of freedom of traditional band theory[1].Generally,it manifests in physics through the boundary states revealed by the bulkedge *** bulk topology implies various low-dimensional states at the boundary,giving extraordinary approaches to manipulate *** structure that encodes the band topology is the system associated with space–time evolution,such as Floquet topological insulator[2,3].Its quasistatic limit involves time-dependent dynamic adiabatic evolution[4,5].However,dynamic evolution is challenging as it requires fast modulation to overcome the dissipation of state before it is pumped from one edge to another[6].An alternative approach is to use an additional degree of freedom to replace the role of time,and an illuminating system is the weakly coupled waveguides,whose governing equation can be directly mapped to Schrodinger equation with time modulation replaced by wave propagation along the ***,such strategy has been largely explored to realize the pumping of topological boundary states in optics[7,8]and elastic wave[9,10].However,the strategy for acoustics is subtly different as the coupling of the acoustic waveguides is not weak for the fundamental waveguide *** exploring the possibility to realize two-dimensional(2D)topological acoustic pumping in a continuous regime remains an open question.