摘要：The development of anode materials with high rate capability and long charge-discharge plateau is the key to improve per-formance of lithium-ion capacitors(LICs).Herein,the porous graphitic carbon(PGC-1300)derived from a new triply interpenetrated co-balt metal-organic framework(Co-MOF)was prepared through the facile and robust carbonization at 1300°C and washing by HCl *** as-prepared PGC-1300 featured an optimized graphitization degree and porous framework,which not only contributes to high plateau capacity(105.0 mAh·g^(−1)below 0.2 V at 0.05 A·g^(−1)),but also supplies more convenient pathways for ions and increases the rate capability(128.5 mAh·g^(−1)at 3.2 A·g^(−1)).According to the kinetics analyses,it can be found that diffusion regulated surface induced capa-citive process and Li-ions intercalation process are coexisted for lithium-ion ***,LIC PGC-1300//AC constructed with pre-lithiated PGC-1300 anode and activated carbon(AC)cathode exhibited an increased energy density of 102.8 Wh·kg^(−1),a power dens-ity of 6017.1 W·kg^(−1),together with the excellent cyclic stability(91.6%retention after 10000 cycles at 1.0 A·g^(−1)).

摘要：This paper is concerned with the scaled formation control problem for multi-agent systems(MASs)over fixed and switching ***,a modified resilient dynamic event-triggered(DET)mechanism involving an auxiliary dynamic variable(ADV)based on sampled data is *** the proposed DET mechanism,a random variable obeying the Bernoulli distribution is introduced to express the idle and busy situations of communication ***,the operation of absolute value is introduced into the triggering condition to effectively reduce the formation ***,a scaled formation control protocol with the proposed resilient DET mechanism is designed over fixed and switching *** scaled formation error system is modeled as a time-varying delay ***,several sufficient stability criteria are derived by constructing appropriate Lyapunov-Krasovskii functionals(LKFs).A co-design algorithm based on the sparrow search algorithm(SSA)is presented to design the control gains and triggering parameters ***,numerical simulations of multiple unmanned aerial vehicles(UAVs)are presented to validate the designed control method.

摘要：Solid oxide fuel cells(SOFCs)have attracted a great deal of interest because they have the highest efficiency without using any noble metal as catalysts among all the fuel cell ***,traditional SOFCs suffer from having a higher volume,current leakage,complex connections,and difficulty in gas *** solve these problems,Rolls-Royce has fabricated a simple design by stacking cells in series on an insulating porous support,resulting in the tubular segmented-in-series solid oxide fuel cells(SIS-SOFCs),which achieved higher output *** work systematically reviews recent advances in the structures,preparation methods,perform-ances,and stability of tubular SIS-SOFCs in experimental and numerical ***,the challenges and future development of tubular SIS-SOFCs are also *** findings of this work can help guide the direction and inspire innovation of future development in this field.

摘要：Because of its high purity and excellent orientation, mesophase pitch is a superior precursor for high-performance car-bon materials. However, the preparation of top-notch mesophase pitch faces challenges. Catalytic polycondensation at low temperat-ures is more favorable for synthesizing mesophase pitch, because it circumvents the high-temperature free radical reaction of other thermal polycondensation approaches. The reaction is gentle and can be easily controlled. It has the potential to significantly im-prove the yield of mesophase pitch and easily introduce naphthenic characteristics into the molecules, catalytic polycondensation is therefore a preferred method of synthesizing highly spinnable mesophase pitch. This review provides a synopsis of the selective pre-treatment of the raw materials to prepare different mesophase pitches, and explains the reaction mechanism and associated research advances for different catalytic systems in recent years. Finally, how to manufacture high-quality mesophase pitch by using a cata-lyst-promoter system is summarized and proposed, which may provide a theoretical basis for the future design of high-quality pitch molecules.

摘要：非质子锂氧电池基于锂金属与氧的可逆反应生成Li_(2)O_(2),可提供极高的理论能量密度.然而,Li_(2)O_(2)的成核/消除机制仍然不清楚.因此,构建能在原子水平上深入了解催化机理的催化剂体系,是开发高性能锂氧电池的关键.在此,我们报道了一种在富氧空位的Co_(3)O_(4)(Pd1-Co_(3)O_(4x))中实现Pd单原子选择性锚定的策略.原子水平表征技术揭示了Pd原子优先地结合到缺陷Co_(3)O_(4)的四面体位点.理论计算表明,选择性锚定的Pd单原子与氧空位的耦合引起了明显的电荷重分布,这可以有效地提高Pd 4d轨道在费米能级附近的能带占用率,促进电子转移,有利于中间体的吸附.这种双重相互作用不仅可以调节放电过程中Li_(2)O_(2)的成核生长过程,而且有利于Li_(2)O_(2)上的电子云的离域,减弱Li-O键的强度,从而促进Li_(2)O_(2)在充电过程中的分解.本研究对锂氧电池在原子水平上的催化机理和高效催化剂的合理设计提出了一些见解.

摘要：光生电荷的分离和转移被认为是影响BiVO_(4)基光阳极光电性能的核心因素之一.本文设计了在BiVO_(4)光阳极与析氧助催化剂之间插入空穴提取层的方法.Cu_(2)O作为空穴提取层引入到助催化剂层(FeOOH/NiOOH)和BiVO_(4)之间,可以有效优化空穴的迁移路径,延长光生空穴的寿命,从而提高电极的光电化学性能.与BiVO_(4)相比,调整后的BiVO_(4)/Cu_(2)O/FeOOH/NiOOH光阳极的电荷分离效率从70.6%提高到了92.0%.此外,该光阳极在1.23 VRHE(AM 1.5G照明下)下,还显示出了3.85 mA cm^(-2)的高光电流密度,是BiVO_(4)的2.77倍.我们的研究结果表明,电沉积Cu_(2)O空穴提取层是一种简单且可扩展的方法,能够有效提高BiVO_(4)的光电活性,可用于太阳能驱动水分解领域.

摘要：铂(Pt)是质子交换膜燃料电池(PEMFCs)阳极氢氧化反应(HOR)中最先进的电催化剂.然而,Pt催化剂对CO(工业低成本氢燃料中的杂质)极度敏感从而中毒,这会引起器件性能的急剧衰退,导致器件运行成本高.因此,提高Pt催化剂的CO耐受性对PEMFCs的商业化推广至关重要.在此,我们设计合成了一种独特的PtNiW@WO_(x)核壳纳米线来提高Pt基催化剂对CO的耐受能力.机理研究表明,表面无定形的WO_(x)壳层可以作为分子围栏,在动力学上阻碍CO扩散到达Pt位点.在热力学上,Ni和W元素合金化产生的电子效应可以使Pt的d带中心降低,减弱CO在Pt位点上的化学吸附.此外,亲氧W元素可以加速水的解离,提供更多OH活性物种,促进CO的氧化脱附.因此,在1000ppm CO/H_(2)条件下,所设计的PtNiW@WO_(x)核壳纳米线催化剂表现出优异的HOR抗CO中毒性能,在4000 s后仍能保持超过90%的HOR电流密度,超过了原始的PtNi纳米线和目前报道的绝大多数Pt基催化剂.

摘要：超高性能混凝土(UHPC)是一种具有巨大潜力的复合材料。为了降低UHPC的成本并获得更好的性能,有必要研究钢纤维在UHPC中的增强机理,实践中也需要一个有效的数值模型来促进UHPC的应用。钢纤维从UHPC中拔出时会产生新的裂纹面,进而需要消耗更多的能量。基于此,推导了新裂纹及其裂纹表面能的公式,提出了一种考虑钢纤维与UHPC基体之间界面断裂能的断裂相场模型。利用该模型,对含钢纤维的三维UHPC试样进行了单轴拉伸数值模拟;开展对比实验验证了所提模型的正确性。结果表明,模拟结果与实验结果吻合较好。通过分析不同试样的新裂纹面与拉伸强度间的关系,发现UHPC的抗拉强度和残余强度随钢纤维体积含量的增加而增加,随钢纤维直径的增加而降低。进一步分析发现,UHPC的抗拉强度与钢纤维的侧表面积成正比。理论分析、数值模拟和实验表明,钢纤维在UHPC中的增强机理为:钢纤维的加入使UHPC基体与钢纤维在断裂过程中产生了一些新的裂纹,这些新裂纹消耗了更多的能量。本文研究工作可为UHPC的性能设计和开发有效的UHPC数值模型提供理论依据。

摘要：p-d轨道之间的相互作用是一种提升电催化性能的有效方法.然而,其对主族金属的电催化CO_(2)还原(eCO_(2)RR)的增强机制尚不清晰.因此,我们向金属Bi纳米片中引入了一系列过渡金属氧化物(TMO:Fe_(2)O_(3)、Co_(3)O_(4)、NiO),并以此研究引入TMO对Bi物种eCO_(2)RR性能的影响.根据原位傅里叶变换红外光谱(FTIR)和CO_(2)-程序升温脱附(TPD)的结果,Bi/TMO中的TMO可以增强CO_(2)的吸附和活化能力.密度泛函理论(DFT)计算结果表明,Bi活性位点^(*)OCHO吸附能及p轨道的优化可以降低CO_(2)到^(*)OCHO过程和^(*)OCHO到HCOOH过程的理论过电位.同时,由于Bi与TMO之间因复合而发生的电子重排也促进了催化剂与反应物之间的电子传输.因此,在热力学和动力学的双重作用下,Bi/TMO中的Bi活性位点表现出最佳的催化能力,在更宽的电位区间内实现了更高的催化活性和甲酸选择性.其中,Bi/Fe_(2)O_(3)的增强效果最为显著.在500 mV的宽电位区间内达到较高的甲酸的法拉第效率(>90%),在-0.8 VRHE时,甲酸的法拉第效率达到最大值99.7%(Bi的1.11倍),甲酸局部电流密度达到12.65 mA cm^(-2)(Bi的1.86倍).这一研究不仅建立了eCO_(2)RR性能增强与引入TMO之间的关系,也为理性设计高性能电催化剂提供了一条实用的、可扩展的途径.

摘要：环保型CuInSe_(2)量子点具有高消光系数和宽光谱吸收范围,在光电化学催化应用中展现了良好的发展前景.然而,CuInSe_(2)量子点较低的载流子分离能力和严重的界面电荷复合降低了其光电化学性能,制约了其应用.因此,我们设计并合成了具有Ⅱ型能带排列的CuInSe_(2)/CuInS_(2)核/壳结构量子点,以促进载流子分离、减少界面缺陷;进一步通过调节In/Cu前驱体的摩尔比,产生铜空位.光物理性质研究表明,导带电子-铜空位捕获的空穴之间的辐射复合成为主要的复合方式,有效延长了载流子寿命,促进了载流子分离.因此,基于富铜空位的CuInSe_(2)/CuInS_(2)核壳量子点的光阳极获得了~8.0 mA cm^(-2)的最大饱和光电流密度,该性能是当前报道的CISe基量子点光电化学电池中的最高值之一.本工作提供了一种通过表面或内在缺陷的调控来促进光电化学应用中的电荷载流子分离和传输的有效方法.