摘要：Aqueous zinc ion hybrid capacitors(ZIHCs)are considered one of the most promising electrochemical energy storage systems due to their high safety,environmental friendliness,low cost,and high power ***,the low energy density and the lack of sustainable design strategies for the cathodes hinder the practical application of ***,we design the N and O co-doped porous carbon cathode by annealing metal-organic framework(ZIF-8).ZIF-8 retains the original dodecahedral structure with a high specific surface(2814.67 m^(2)/g)and I_(G)/I_(D) ratio of 1.0 during carbonization and achieves self-doping of N and O *** defect sites are introduced into the porous carbon to provide additional active sites for ion adsorption after the activation of carbonized ZIF-8 by KOH *** ZIHCs assembled with modified ZIF-8 as the cathode and commercial zinc foil as the anode show an energy density of 125 W∙h/kg and a power density of 79 W/*** addition,this ZIHCs device achieves capacity retention of 77.8%after 9000 electrochemical cycles,which is attributed to the diverse pore structure and plentiful defect sites of ZIF-8-800(KOH).The proposed strategy may be useful in developing high-performance metal-ion hybrid capacitors for large-scale energy storage.

摘要：The central composite design in the modeling and optimization of catalytic dehydration of ethanol to ethylene was performed to improve the ethylene yield.A total of 20 experiments at random were conducted to investigate the effect of reaction temperature,Si/Al ratios of H-ZSM-5 catalyst and liquid hourly space velocity(LHSV) on the ethylene *** results show that the relationship between ethylene yield and the three significant independent variables can be approximated by a nonlinear polynomial model,with R-squared of 99.9%and adjusted R-squared of 99.8%.The maximal response for ethylene yield is 93.4%under the optimal condition of 328 ℃,Si/Al ratio 85,and LHSV 3.8 h-1.

摘要：光催化CO_(2)还原合成太阳能燃料对缓解CO_(2)排放引起的全球变暖和降低化石燃料消耗具有重要意义.然而,目前的光催化剂仍然存在反应动力学缓慢和选择性不理想的问题,特别是对于C_(2+)产物的生成,极大地限制了光催化的工业化进程.过去几十年中,关于太阳能驱动的CO_(2)还原的研究展示出鼓舞人心的结果,包括活性位点的构建.本综述重点介绍了通过构建活性位点制备原子级分散催化剂在光催化CO_(2)还原中的最新进展,包括两个独立的活性位点、成对双活性位点和基于活性位点构型的纳米团簇.此外,详细讨论了CO_(2)在活性位点上的活化机制和表征方法.特别是考虑到实验研究与实际应用之间的差距,整合实验和理论的结果,以实现潜在的结构-活性关系和高目标产物选择性发展.最后,概述了该领域存在的挑战,并展望了活性位点的合理设计和机理研究.

摘要：Aqueous zinc-ion batteries(AZIBs)are attracting worldwide attention due to their multiple merits such as extreme safety,low cost,feasible assembly,and environmentally friendly enabled by water-based *** present,AZIBs have experienced systematic advances in battery components including cathode,anode,and electrolyte,whereas research involving separators is *** separator is the crucial component of AZIBs through providing ion transport,forming contact with electrodes,serving as a container for electrolyte,and ensuring the efficient battery *** this great yet ignored significance,it is timely to present the latest advances in design strategies,the systematic classification and summary of *** summarize the separator optimization strategies mainly along two approaches including the modification of the frequently used glass fiber and the exploitation of new *** advantages and disadvantages of the two strategies are analyzed from the material types and the characteristics of different *** effects and mechanisms of various materials on regulating the uniform migration and deposition of Zn2+,balancing the excessively concentrated nucleation points,inhibiting the growth of dendrites,and the occurrence of side reactions were discussed using confinement,electric field regulation,ion interaction force,desolvation,***,potential directions for further improvement and development of AZIBs separators are proposed,aiming at providing helpful guidance for this booming field.

摘要：将多个响应分子整合到单晶体中是光机械晶体材料领域的一次全新尝试.本工作通过共晶制备了首个包含两种光响应分子的光机械晶体(9AC-NPE),每种分子都对应其独特的需要满足拓扑堆积条件的光二聚反应.紫外光照射下成功激发了晶体中的两种光二聚反应,同时表现出光显著效应、负光致变色和多发射峰的荧光增强.本文还将该共晶作为一个研究平台,比较和发现了两种光二聚反应在光反应速率和响应波长上的差异,这为制备具有复杂光机械行为的晶体材料提供了潜在的解决方案.此外,还发展了该共晶在光学打印中的概念设计.本工作加深了对光机械晶体材料设计和应用的理解,可作为该领域未来研究的重要参考.

摘要：石墨炔由于其高载流子迁移率和有序的孔隙结构被认为是一种很有应用前景的光催化材料.本研究通过交叉偶联合成了一种新型球状石墨炔,并与棒状Mn_(0.2)Cd_(0.8)S耦合构建了S型异质结用于光催化析氢.结果表明,Mn_(0.2)Cd_(0.8)S/石墨炔异质结光催化剂表现出优异的光催化活性,产氢性能分别较Mn_(0.2)Cd_(0.8)S和球形石墨炔单体催化剂提升了16.78和613.2倍.同时,该催化剂应用于平米级规模产氢取得较好效果.其优异的光催化活性可归因于石墨炔的独特性能及S-scheme异质结的有效构建.通过紫外光电子能谱、原位辐射X射线光电子能谱、电子顺磁共振能谱、密度泛函理论计算和其他表征技术探究了S-scheme异质结的形成和光催化活性的增强.该工作可为石墨炔的形貌可调性制备以及高效异质结光催化剂的设计和合成提供新参考.

摘要：近红外(NIR)光驱动水分解产生氢气(H_(2))一直以来都是光催化领域备受关注的问题,但由于其动力学和热力学方面的缺陷,迄今为止仍是一项艰巨的挑战.为了突破这一限制,我们通过简便的水热法设计出了富含硫空位的无贵金属二维(2D)ZnIn_(2)S_(4)-基光催化剂,并首次使用单组分ZnIn_(2)S_(4)-基材料实现了波长大于800 nm的近红外驱动制氢性能.根据价带光谱、紫外-可见-近红外DRS光谱、稳态PL光谱、瞬态光电流响应和EPR表征,我们揭示了存在一个高效的Urbach带尾吸收用于捕获近红外光.硫空位在ZnIn_(2)S_(4)纳米片中的成功构建不仅扩展了光谱吸收范围,而且具有出色的载流子扩散特性和丰富的活性位点.因此,我们的研究结果可能会为未来开发近红外响应的ZnIn_(2)S_(4)-基光催化剂用于实现高效近红外驱动制氢提供一定的指导.

摘要：The development of effective antifreeze peptides to control ice growth has attracted a significant amount of attention yet still remains a great ***,we propose a novel design method based on in-depth investigation of repetitive motifs in various ice-binding proteins(IBPs)with evolution *** this way,several peptides with notable antifreeze activity were *** particular,a designed antifreeze peptide named AVD exhibits ideal ice recrystallization inhibition(IRI),solubility,and biocompatibility,making it suitable for use as a cryoprotective agent(CPA).A mutation analysis and molecular dynamics(MD)simulations indicated that the Thr6 and Asn8 residues of the AVD peptide are fundamental to its ice-binding capacity,while the Ser18 residue can synergistically enhance their interaction with ice,revealing the antifreeze mechanism of ***,to evaluate the cryoprotection potential of AVD,the peptide was successfully employed for the cryopreservation of various cells,which demonstrated significant post-freezing cell *** work opens up a new avenue for designing antifreeze materials and provides peptide-based functional modules for synthetic biology.

摘要：Due to their tunable acidity,shape selectivity,and excellent stability,zeolites are of great importance as solid acid materials in industrial *** the properties of the acid sites in zeolites allows for the rational design and fabrication of catalysts for target *** ether(DME)carbonylation,a critical chain-growth reaction for C1 resource utilization,is selectively catalyzed by the Brønsted acid sites within the eight-membered rings(8-MRs)of mordenite(MOR).It is anticipated that strengthening the Brønsted acidity—particularly in 8-MRs—will improve the catalytic performance of *** this work,density functional theory(DFT)calculations are first employed and the results used to design a modified MOR with stannum(Sn)and to predict the corresponding changes in *** by the theoretical studies,a series of Sn-modified MOR are synthesized via a defect-engineering and subsequent heteroatom-substitution *** partial desilication,isolated tetrahedral Sn species in an open configuration are successfully synthesized for the first time,within which tetrahedrally coordinated Al sites are *** acidic characterization is used to confirm that the acidity of the Brønsted acid sites is enhanced by the introduction of the Sn species;as a result,the sample exhibits excellent activity in DME carbonylation *** and DFT studies reveal that this strengthened acidity facilitates the adsorption of DME and reduces the activation barriers of DME dissociation and acetyl formation,accounting for the improved *** work demonstrates mechanistic insights into the promoting effects of strong acidity on DME carbonylation and offers a promising strategy to precisely control the acidic strength of zeolites.

摘要：具有生物力学和生化活性的敷料在伤口护理和皮肤组织再生中起着至关重要的作用.然而,机械失配和药物释放管理所涉及的问题限制了当前敷料的有效使用.在本工作中,我们报道了一种简单的策略,即采用聚偏二氟乙烯(PVDF)作为底物,通过嵌入不同尺寸的沸石咪唑酸盐框架(ZIF-8)种子,以推动具有均匀蜂窝结构的高柔性金属有机框架(MOF)复合膜的受控生长,用于药物负载和释放.以嵌入的种子为控制中心,形成的多孔膜具有约0.7-3μm的宽孔隙.这种可调节的微尺度孔与ZIF-8中的固有纳米孔不仅可以有效地提高抗炎类药物的负载(姜黄素,CCM),而且还能够快速并可控地释放药物,大大提高了抗菌活性,同时促进细胞生长.其中,在40 nm种子上生长的0.7μm多孔膜的表现优于其他蜂窝膜,与2μm多孔膜(相当于裸PVDF基质)相比,细胞增殖能力提高了约2倍,针对金黄色葡萄球菌(***)和大肠杆菌(***)的抗菌活性分别提高了5倍和2.4倍,是基底抗菌活性的5倍,这是因为这种最佳孔几何结构具有CCM和Zn2+释放特性的平衡效应.这种可控分层孔阵列膜的独特性质有望真正用于伤口愈合,同时也为生物医学设计提供了新的指导.