摘要：Strongly regular (α,β)-reguli are a class of incidence structures with given conditions which were introduced by Hamilton and Mathon. We introduce two classes of codes constructed from strongly regular (α,β)-reguli within PG(k-1,q). The codes are related with two-weight codes intimately.

摘要：用在分离时间轴和反复的学习轴之间的类比，一条新分离时间的适应反复的学习控制(AILC ) 途径被开发与变化时间的参量的无常探讨非线性的系统的一个班。类似于适应控制，新 AILC 能合并一个设计算法，因此，学习获得能沿着学习的轴反复地被调节。当起始的状态是随机的，参考轨道是变化重复的时，新 AILC 能沿着反复的学习轴 asymptotically 在有限时间间隔上完成 pointwise 集中。

摘要：A new strategy of thermally activated delayed fluorescence(TADF)material-sensitized circularly polarized luminescence(CPL)has been proposed for improving the efficiencies of fluorescent circularly polarized organic lightemitting diodes(OLEDs)(CP-OLEDs).Consequently,a pair of helicene enantiomers,(P)-HAI and(M)-HAI,were *** helicene enantiomers with the rigid helicalπ-skeleton had highly thermal and enantiomeric stabilities,and they also showed excellent photophysical properties,especially,intense mirror-image CPL activities with large luminescence dissymmetry factor(|g_(lum)|)values of about 6×10^(-3).Notably,the CP-OLEDs with the helicene enantiomers as emitters and a TADF molecule as sensitizer not only displayed better performance of lower turn-on voltage(V_(T))of 2.6 V,four-fold maxmium-external quantum efficiency(EQE_(max))of 5.3%,and lower efficiencies roll-off of 1.9%at 1000 cd m^(-2),than those of the devices without TADF sensitizer,but also exhibited intense circularly polarized electroluminescence(CPEL)with the electroluminescence dissymmetry factor(g_(EL))values of-2.3×10^(-3)and+3.0×10^(-3).Meanwhile,this study also represents the first thermally activated sensitized fluorescent CP-OLEDs with markedly enhanced efficiencies and intense CPEL.

摘要：Hierarchical FeP nanoarray films composed of FeP nanopetals were successfully synthesized via a bio-inspired hydrothermal route followed by phosphorization. Glycerol as a crystal growth modifier, plays a significant role in controlling the morphology and structure of the FeO（OH） precursor during the biomineralization process, while the following transfer and pseudomorphic transformation of the FeO（OH） film successfully give rise to the FeP array film. The as-prepared FeP film electrodes exhibit excellent hydrogen evolution reaction （HER） performance over a wide pH range. Theoretical calculations reveal that the mixed P/Fe termination in the FeP film is responsible for the high catalytic activity of the nanostructured electrodes. This new insight will promote further explorations of efficient metal phosphoride-based catalysts for the HER. More importantly, this study bridges the gap between biological and inorganic self-assembling nanosystems and may open up a new avenue for the preparation of functional nanostructures with application in energy devices.

摘要：A heterojunction photocatalyst based on porous tubular g-C3N4 decorated with CdS nanoparticles was fabricated by a facile hydrothermal co-deposition *** one-dimensional porous structure of g-C3N4 provides a higher specific surface area,enhanced light absorption,and better separation and transport performance of charge carriers along the longitudinal direction,all of which synergistically contribute to the superior photocatalytic activity *** significantly enhanced catalytic efficiency is also a benefit originating from the fast transfer of photogenerated electrons and holes between g-C3N4 and CdS through a built-in electric field,which was confirmed by investigating the morphology,structure,optical properties,electrochemical properties,and photocatalytic *** degradation of rhodamine B(RhB)and photocatalytic hydrogen evolution reaction were also carried out to investigate its photocatalytic *** can be degraded completely within 60 min,and the optimum H2 evolution rate of tubular g-C3N4/CdS composite is as high as 71.6μmol h^–1,which is about 16.3 times higher than that of pure bulk *** as-prepared nanostructure would be suitable for treating environmental pollutants as well as for water splitting.

摘要：离子插层是提高Ti_(3)C_(2)TxMXene电化学性能的有效方法之一.然而,不同的插层离子对MXene的结构和电化学性能的影响是否相同这一问题尚不清楚.本文系统研究了Li+、Na+、K+、Cs+、Zn2+、Mg2+、SO_(4)2-和OH-等一系列离子插层后的MXene的结构特征和电化学性能.研究结果表明,插层离子的半径、电荷数和化学特性对插层效果都会产生影响.在所研究的插层剂中,由离子半径最大的一价阳离子Cs+和具有强碱性的阴离子OH-组成的插层剂CsOH对MXene具有较好的插层效果.插层后的MXene层间距增大,层间容纳了大量游离水,Ti的价态升高,片层表面有利于氧化还原反应的含O官能团增多,这都大大促进了电解液离子H+的扩散与存储.由此制备的电极的质量比电容大幅度提高,为原始MXene电极的7倍多,而且经过20,000次充放电循环后电容保持率未发生下降.本文为具有高电容性能的MXene和MXene基复合电极的合理设计和制备提供了指导.