Design and Implementation of Dance Online Teaching System Based on Optimized Load Balancing Algorithm.

With the continuous improvement of the network hardware environment, people turn the demand target to the network application environment and the construction of information resources. How to build a network teaching platform for general undergraduate teaching to ensure the stability of the system and high-quality services during operation especially large-scale concurrent access will inevitably lead to the increase in the business volume of each core part of the network, the number of visits, and data traffic. With the growth of the network, the corresponding processing power and computing intensity also increase rapidly, which causes problems such as overloading of core network equipment, network bottlenecks, and network congestion. Simply pursuing high-performance hardware to solve problems will undoubtedly result in high cost investment; moreover, equipment with excellent performance cannot meet the needs of the current rapidly growing business volume. According to the design goal of the dance online teaching platform, to meet the online teaching load requirements of many people at the same time, the pressure of the web server cluster must be great. Because many people in online at the same time put too much pressure on the web server, this part of the network cannot be processed in time, which leads to the phenomenon that the performance of this part and even the whole network is degraded. In severe cases, it will even cause network communication services to come to a standstill, that is, the so-called deadlock phenomenon. If the protocol software cannot detect congestion and reduce the packet sending rate, the network will be paralyzed due to congestion. This situation will cause the problem of movement delay for online dance teaching, which will seriously affect the quality of teaching. Therefore, the dance online course system should be continuously improved, the quality of online courses should be continuously improved, and the study of the practical application of load balancing technology in the network teaching environment has become an important means to solve the relationship between supply and demand of network teaching. According to the experimental analysis, when the number of Worker' actuators is fixed, the execution time span of MakeSpan increases with the increase of tasks, while the time required by the optimized load balancing algorithm proposed in this paper increases by 1.32 s on average with the increase of tasks, and the time required by heuristic algorithm and bee colony algorithm increases by 3.68 s and 3.45 s on average with the increase of tasks. On the whole, the optimized load balancing algorithm proposed in this paper has obvious advantages.

Two-atomic-layered optoelectronic device enabled by charge separation on graphene/semiconductor interface.

The Fermi level of graphene on different substrates usually changes significantly due to the interface difference between graphene and two-dimensional semiconductors. This feature opens many possibilities of manipulating optoelectronic devices by constructing graphene heterostructures through interface modification. Herein, we report the fabrication and optoelectronic response of an unconventional heterojunction device based on a graphene-MoSe2 hybrid interface. Different from the traditional three or more layered structure where the semiconductor is sandwiched between two electrodes, this device contains only two atomic layers: the MoSe2 layer serving as the photon absorber and the graphene layer functioning as the charge acceptor and both electrodes. This structure looks like short-circuited but shows an obvious photoelectric response, which is aided by electron transfers from MoSe2 to graphene. The photocurrent generation is explored quantitatively with electronic dynamics of graphene aided with ultrafast measurements. The two-layered architecture simplifies the fabrication of atomic-thick optoelectronic devices, allowing the as-grown semiconductors to be directly used and eliminating the damage-prone transfer process.

Photoluminescence of monolayer MoS2 modulated by water/O2/laser irradiation.

The low photoluminescence (PL) quantum yields of transition metal dichalcogenide monolayers have been a limiting factor for their optoelectronic applications. Various and even inconsistent mechanisms have been proposed to modulate their PL efficiencies. Herein, we use PL/Raman microspectroscopy and the corresponding in situ mapping, atomic force microscopy, and field-effect transistor (FET) characterization to investigate the changes in the structural and optical properties of monolayer MoS2. Relatively low power density (<4.08 × 105 W cm-2) of laser irradiation in ambient air can cause a slight PL suppression effect on monolayer MoS2, whereas relatively high power density (∼1.02 × 106 W cm-2) of laser irradiation brings significant PL enhancement. Experiments under different atmospheres reveal that the laser-irradiation-induced enhancement only occurs in the atmosphere containing O2 and is more remarkable in pure O2. In addition, physically adsorbed water can also induce PL enhancement of monolayer MoS2. FET devices suggest that the adsorbed water produces a p-doping effect on MoS2, and the laser irradiation in ambient air generates an n-doping effect, and both types of doping can enhance the PL intensity. The island-shaped defects caused by laser irradiation can be stabilized by oxygen atoms and act as trapping centers for excited trions or electrons, thus reducing the non-radiative recombination ratio and enhancing the PL intensity. The physically adsorbed water works in a similar way. A low power density of laser irradiation can sweep away the originally adsorbed H2O on the surface, thus reducing the PL.

Gas products generation mechanism during co-pyrolysis of styrene-butadiene rubber and natural rubber.

In this study, reaction molecular dynamics were combined with experiments to gain in-depth understanding of the gaseous pyrolysis products generation mechanism and optimal paths during natural rubber (NR), styrene-butadiene rubber (SBR) and mixed rubbers (NR-SBR) for effective recovery of waste rubber. The results show that the pyrolysis temperature of NR increases gradually with SBR addition. The monomers produced during the initial stage of SBR pyrolysis are mainly 1,3-butadiene and styrene, in which the energy barriers of the formed H and CH2=CH in styrene are higher than those in 1,3-butadiene, and during further pyrolysis the main gas products are H2 and CH4. During co-pyrolysis of NR-SBR, the reaction paths show that increasing H2 yield and decreasing CH4 yield take place easily as SBR content rises. By contrast to pyrolysis of NR, the path of generating CH2=CH in SBR is more difficult while that of CH2=CH abstracting H occurred easily, leading to first enhancement in produced CH2=CH2 followed by a decline. Fixed bed experiments and gas chromatography (GC) analysis identify the main gas products of the three rubbers (NR, SBR, NR-SBR)as H2, CH4 and CH2=CH2 and the change of yield caused by the increase of SBR content are consistent with the simulation results.

In Situ Laser Scattering Electrospray Ionization Mass Spectrometry and Its Application in the Mechanism Study of Photoinduced Direct C-H Arylation of Heteroarenes.

An in situ laser scattering electrospray ionization mass spectrometry (LS-ESI-MS) was developed, where the laser scattering was simply achieved through the laser radiation of the "media" modified on the capillary. The laser scattering extended the reaction window and powerfully promoted the reaction yield of the photoinduced organic reaction, which enables the trace intermediates to be efficiently tracked in real time. For instance, the key radical cation in the photoinduced direct C-H arylation of heteroarenes was captured inventively, which provided direct experimental evidence for the verification of the reaction mechanism. Together with the characterization of oxidative photocatalytic Ru(III) intermediate, the integral insight into the process of visible-light-mediated direct C-H arylation of heteroarenes was confirmed. This approach is facile, powerful, and promising in the mechanism study of organic reaction.

Author Correction: Ultrafast probes of electron-hole transitions between two atomic layers.

The original version of this Article omitted an affiliation of Xiewen Wen: 'College of Chemistry and Molecular Engineering, Beijing National Laboratory for Molecular Sciences, Peking University, Beijing 100871, China'. This has been corrected in both the PDF and HTML versions of the Article.

Ultrafast probes of electron-hole transitions between two atomic layers.

Phase transitions of electron-hole pairs on semiconductor/conductor interfaces determine fundamental properties of optoelectronics. To investigate interfacial dynamical transitions of charged quasiparticles, however, remains a grand challenge. By employing ultrafast mid-infrared microspectroscopic probes to detect excitonic internal quantum transitions and two-dimensional atomic device fabrications, we are able to directly monitor the interplay between free carriers and insulating interlayer excitons between two atomic layers. Our observations reveal unexpected ultrafast formation of tightly bound interlayer excitons between conducting graphene and semiconducting MoSe2. The result suggests carriers in the doped graphene are no longer massless, and an effective mass as small as one percent of free electron mass is sufficient to confine carriers within a 2D hetero space with energy 10 times larger than the room-temperature thermal energy. The interlayer excitons arise within 1 ps. Their formation effectively blocks charge recombination and improves charge separation efficiency for more than one order of magnitude.