Beijing University of Technology

About: Beijing University of Technology is a education organization based out in Beijing, Beijing, China. It is known for research contribution in the topics: Microstructure & Laser. The organization has 31929 authors who have published 31987 publications receiving 352112 citations. The organization is also known as: Běijīng Gōngyè Dàxué & Beijing Polytechnic University.

Temporal Task Scheduling With Constrained Service Delay for Profit Maximization in Hybrid Clouds

Abstract: As cloud computing is becoming growingly popular, consumers’ tasks around the world arrive in cloud data centers. A private cloud provider aims to achieve profit maximization by intelligently scheduling tasks while guaranteeing the service delay bound of delay-tolerant tasks. However, the aperiodicity of arrival tasks brings a challenging problem of how to dynamically schedule all arrival tasks given the fact that the capacity of a private cloud provider is limited. Previous works usually provide an admission control to intelligently refuse some of arrival tasks. Nevertheless, this will decrease the throughput of a private cloud, and cause revenue loss. This paper studies the problem of how to maximize the profit of a private cloud in hybrid clouds while guaranteeing the service delay bound of delay-tolerant tasks. We propose a profit maximization algorithm (PMA) to discover the temporal variation of prices in hybrid clouds. The temporal task scheduling provided by PMA can dynamically schedule all arrival tasks to execute in private and public clouds. The sub problem in each iteration of PMA is solved by the proposed hybrid heuristic optimization algorithm, simulated annealing particle swarm optimization (SAPSO). Besides, SAPSO is compared with existing baseline algorithms. Extensive simulation experiments demonstrate that the proposed method can greatly increase the throughput and the profit of a private cloud while guaranteeing the service delay bound.

Enhanced photocatalytic N2 fixation by promoting N2 adsorption with a co-catalyst

Abstract: Photocatalytic N2 fixation involves a nitrogen reduction reaction on the surface of the photocatalyst to convert N2 into ammonia. Currently, the adsorption of N2 is the limiting step for the N2 reduction reaction on the surface of the catalyst. Based on the concept of photocatalytic water splitting, the photocatalytic efficiency can be greatly enhanced by introducing a co-catalyst. In this report, we proposed a new strategy, namely, the loading of a NiS co-catalyst on CdS nanorods for photocatalytic N2 fixation. Theoretical calculation results indicated that N2 was effectively adsorbed onto the NiS/CdS surface. Temperature programmed desorption studies confirmed that the N2 molecules preferred to adsorb onto the NiS/CdS surface. Linear sweep voltammetry results revealed that the overpotential of the N2 reduction reaction was reduced by loading NiS. Furthermore, transient photocurrent and electrochemical impedance spectroscopy indicated that the charge separation was enhanced by introducing NiS. Photocatalytic N2 fixation was carried out in the presence of the catalyst dispersed in water without any sacrificial agent. As a result, 1.0 wt% NiS/CdS achieved an ammonia production rate of 2.8 and 1.7 mg L−1 for the first hour under full spectrum and visible light (λ > 420 nm), respectively. The catalyst demonstrated apparent quantum efficiencies of 0.76%, 0.39% and 0.09% at 420, 475 and 520 nm, respectively. This study provides a new method to promote the photocatalytic efficiency of N2 fixation.