Retracted: Dual Effects of Nanostructuring and Oxygen Vacancy on Photoelectrochemical Water Oxidation Activity of Superstructured and Defective Hematite Nanorods

An Ar atmospheric treatment is rationally used to etch and activate hematite nanoflakes (NFs) as photoanodes toward enhanced photoelectrochemical water oxidation. The formation of a highly ordered hematite nanorods (NRs) array containing a high density of oxygen vacancy is successfully prepared through in situ reduction of NFs in Ar atmosphere. Furthermore, a hematite (104) plane and an iron suboxide layer at the absorber/back‐contact interface are formed. The material defects produced by a thermal oxidation method can be critical for the morphology transformation from 2D NFs to 1D NRs. The resulting hematite NR photoanodes show high efficiency toward solar water splitting with improved light harvesting capabilities, leading to an enhanced photoresponse due to the artificially formed oxygen vacancies.     

In-situ synthesis of TiO2 nanostructures on Ti foil for enhanced and stable photocatalytic performance

TiO_2 nanostructures with strong interfacial adhesion and diverse morphologies have been in-situ grown on Ti foil substrate through a multiple-step method based on conventional plasma electrolytic oxidation(PEO) technology, hydrothermal reaction and ion exchange process. The PEO process is critical to the formation of TiO_2 seeding layer for the nucleation of Na_2Ti_3O_7 and H_2Ti_3O_7 mediates that are strongly attached to the Ti foil. An ion exchange reaction can finally lead to the formation of H_2Ti_3O_7 nanostructures with diverse morphologies and the calcination process can turn the H_2Ti_3O_7 nanostructures into TiO_2 nanostructures with enhanced crystallinity. The morphology of the TiO_2 nanostructures including nanoparticles(NP), nanowhiskers(NWK), nanowires(NW) and nanosheets(NS) can be easily tailored by controlling the NaOH concentration and reaction time during hydrothermal process. The morphology, composition and optical properties of TiO_2 photocatalysts were analyzed using scanning electron microscope(SEM), X-ray diffraction(XRD), photoluminescence(PL) spectroscopy and UV–vis absorption spectrum. Photocatalytic tests indicate that the TiO_2 nanosheets calcined at 500?C show good crystallization and the best capability of decomposing organic pollutants. The decoration of Ag cocatalyst can further improve the photocatalytic performance of the TiO_2 nanosheets as a result of the enhanced charger separation efficiency. Cyclic photocatalytic test using TiO_2 nanostructures grown on Ti foil substrate demonstrates the superior stability in the photodegradation of organic pollutant, suggesting the promising potential of in-situ growth technology for industrial application.     

Effects of redox-active interlayer anions on the oxygen evolution reactivity of NiFe-layered double hydroxide nanosheets

Nickel-iron layered double hydroxide (NiFe-LDH) nanosheets have shown optimal oxygen evolution reaction (OER) performance; however, the role of the intercalated ions in the OER activity remains unclear. In this work, we show that the activity of the NiFe-LDHs can be tailored by the intercalated anions with different redox potentials. The intercalation of anions with low redox potential (high reducing ability), such as hypophosphites, leads to NiFe-LDHs with low OER overpotential of 240 mV and a small Tafel slope of 36.9 mV/dec, whereas NiFe-LDHs intercalated with anions of high redox potential (low reducing ability), such as fluorion, show a high overpotential of 370 mV and a Tafel slope of 80.8 mV/dec. The OER activity shows a surprising linear correlation with the standard redox potential. Density functional theory calculations and X-ray photoelectron spectroscopy analysis indicate that the intercalated anions alter the electronic structure of metal atoms which exposed at the surface. Anions with low standard redox potential and strong reducing ability transfer more electrons to the hydroxide layers. This increases the electron density of the surface metal sites and stabilizes their high-valence states, whose formation is known as the critical step prior to the OER process.

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Layered double hydroxides with atomic-scale defects for superior electrocatalysis

Atomic composition tuning and defect engineering are effective strategies toenhance the catalytic performance of multicomponent catalysts by improvingthe synergetic effect; however, it remains challenging to dramatically tune the active sites on multicomponent materials through simultaneous defect engineeringat the atomic scale because of the similarities of the local environment. Herein,using the oxygen evolution reaction (OER) as a probe reaction, we deliberatelyintroduced base-soluble Zn(II) or Al(III) sites into NiFe layered double hydroxides(LDHs), which are one of the best OER catalysts. Then, the Zn(II) or Al(III) siteswere selectively etched to create atomic M(II)/M(III) defects, which dramaticallyenhanced the OER activity. At a current density of 20 mA·cm^?2, only 200 mV overpotential was required to generate M(II) defect-rich NiFe LDHs, which is the best NiFe-based OER catalyst reported to date. Density functional theory(DFT) calculations revealed that the creation of dangling Ni–Fe sites (i.e., unsaturated coordinated Ni–Fe sites) by defect engineering of a Ni–O–Fe site at the atomic scale efficiently lowers the Gibbs free energy of the oxygen evolutionprocess. This defect engineering strategy provides new insights into catalysts atthe atomic scale and should be beneficial for the design of a variety of catalysts.

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基于Sarsa算法和蚁群优化的监测网络路由控制设计

为了克服已有监测网络路由控制方法所具有的传输路径长和能量消耗高的缺点,设计了一种基于Sarsa算法和蚁群优化算法混合模型的路由控制策略;首先,建立了以MA(Mobile Agent)为基础的路由控制模型,并以访问时间和能耗消耗为基础设计了目标函数,然后,基于改进的蚁群算法设计了一种从数据发送节点到Sink节点的路由设计方法,采用节点之间的距离作为冗余度标准获取合理的下一跳邻居节点集,并采用Sarsa算法来对各路径的信息素进行更新,最后,对基于Sarsa算法和蚁群优化算法混合模型的路由控制算法进行了描述;在NS2环境下进行仿真实验,结果证明文中方法能有效实现网络路由控制,最优路由的获取过程的总仿真时间为300ms,是一种适用于监测网络路由控制的有效方法。     

基于GM(1,1)预测和虚拟机迁移的云计算负载均衡策略设计

针对云计算中心虚拟机集群负载的不均衡问题,设计了一种基于GM(1,1)预测和虚拟机迁移的负载均衡策略;首先,描述了云计算中心的负载均衡原理,介绍了经典ELB算法并总结了其缺点,然后,设计了基于GM(1,1)的虚拟机负载预测算法,能根据虚拟机的历史负载信息来预测下一时刻的负载信息,能有效克服ELB算法中仅依赖当前时刻负载而进行虚拟机的删除和增加,同时通过设定不同的阈值来实现虚拟机的增加、删除和迁移,最后,定义了基于预测机制和虚拟机迁移的负载均衡算法,能在创建虚拟机时根据用户的请求定制AMIs模板,从而提交用户请求的响应速度;在CloudSim环境下进行实验,实验结果表明文中方法能有效地实现云计算中心虚拟机集群的负载均衡,与其它方法相比,具有负载均衡高和负载均衡效率高的优点,是一种有效的云计算环境的负载均衡策略。     

The Character of Melting for Simple Molecules Deposited on Graphite

The microscopic character of melting for quasi–two dimensional N ₂ adlayers on graphite is examined for surface densities 0.2 1, where the upper limit corresponds to a complete monolayer. A Monte Carlo method, with the multiple histogram procedure, is employed to determine various thermodynamic quantities. Using the calculated specific heats and selected order parameters, determined at various surface densities, the mechanism for melting is shown to be vacancy mediated. The somewhat unusual behavior of the melting temperature versus density is shown to be entirely due to the vacancy concentration and their topology. Because this is determined by the free energy, our analysis should be general. Preliminary results for Xe on graphite supports this claim.     

Protein crystal growth in microgravity using a liquid/liquid diffusion method

Crystallization of proteins by liquid liquid diffusion method was performed in microgravity using the MDA Minilab aboard the US Space Shuttle. Three proteins, namely lysozyme, trichosanthin, and a new lechin, were crystallized in the space experiment. In contrast to the results of space experiments with a tube-like vapor diffusion method, the crystallization conditions for growing better crystals in space are remarkably different from the conditions optimized on earth. This may be due to difficulties in ground optimization, which are caused by gravity-dependent phenomena, in particular the specific convective flow occurring with liquid liquid diffusion.     

Property-microstructure correlation in in situ formed Al2O3, TiB2 and Al3Ti mixture-reinforced aluminium composites

The in situ formed Al₂O₃, TiB₂ and Al₃Ti mixture-reinforced aluminium composites were successfully fabricated by the reaction sintering of the TiO₂-B-Al system in a vacuum. With increasing boron content in the TiO₂-B-Al system, the amount of generated TiB₂ in the composites increased and Al₃Ti content decreased. At the same time the distribution uniformity of the in situ formed Al₂O₃ and TiB₂ particulates was obviously improved, and the size of the Al₃Ti particles was reduced. The in situ Al₂O₃ and TiB₂ particulates had sizes from 0.096–1.88 m. The interface between the in situ formed particulates and the aluminium matrix was clean, and no consistent crystallographic orientation relationship was found. The strength and elastic modulus of the composites was significantly improved by lowering the Al₃Ti content. When the boron content in the TiO₂-B-Al system rose, the morphology of the tensile fracture surface of the composites was changed from large fractured Al₃Ti blocks and fine dimples, to fine dimples and pulled-out particulates. The strengthening and fracture of the composites have been modelled.