arXiv subjects

Haifeng Li

Publications and source records attributed to Haifeng Li.

133 records · Page 8Linked to original sources

arXiv2014

An adaptive Simulated Annealing-based satellite observation scheduling method combined with a dynamic task clustering strategy

Efficient scheduling is of great significance to rationally make use of scarce satellite resources. Task clustering has been demonstrated to realize an effective strategy to improve the efficiency of satellite scheduling. However, the previous task clustering strategy is static. That is, it is integrated into the scheduling in a two-phase manner rather than in a dynamic fashion, without expressing its full potential in improving the satellite scheduling performance. In this study, we present an adaptive Simulated Annealing based scheduling algorithm aggregated with a dynamic task clustering strategy (or ASA-DTC for short) for satellite observation scheduling problems (SOSPs). First, we develop a formal model for the scheduling of Earth observing satellites. Second, we analyze the related constraints involved in the observation task clustering process. Thirdly, we detail an implementation of the dynamic task clustering strategy and the adaptive Simulated Annealing algorithm. The adaptive Simulated Annealing algorithm is efficient, with the endowment of some sophisticated mechanisms, i.e. adaptive temperature control, tabu-list based revisiting avoidance mechanism, and intelligent combination of neighborhood structures. Finally, we report on experimental simulation studies to demonstrate the competitive performance of ASA-DTC. Moreover, we show that ASA-DTC is especially effective when SOSPs contain a large number of targets or these targets are densely distributed in a certain area.

cs.AI↗

arXiv2013

Magnetic structures and the Ce-Fe coupling induced Fe spin reorientation in CeFeAsO single crystal

Neutron and synchrotron resonant X-ray magnetic scattering (RXMS) complemented by heat capacity and resistivity measurements reveal the evolution of the magnetic structures of Fe and Ce sublattices in single crystal CeFeAsO. The RXMS of magnetic reflections at the Ce $L_{\rm II}$-edge shows a magnetic transition that is specific to the Ce antiferromagnetic long-range ordering at $T_\texttt{Ce}\approx$ 4 K with short-range Ce ordering above $T_\texttt{Ce}$, whereas neutron diffraction measurements of a few magnetic reflections indicate a transition at $T^{*}\approx$ 12 K with unusual order parameter. Detailed order parameter measurements on several magnetic reflections by neutrons show a weak anomaly at 4 K which we associate with the Ce ordering. The successive transitions at $T_\texttt{Ce}$ and $T^{*}$ can also be clearly identified by two anomalies in heat capacity and resistivity measurements. The higher transition temperature at $T^{*}\approx$ 12 K is mainly ascribed to Fe spin reorientation transition, below which Fe spins rotate uniformly and gradually in the \textit{ab} plane. The Fe spin reorientation transition and short-range Ce ordering above $T_\texttt{Ce}$ reflect the strong Fe-Ce couplings prior to long-range ordering of the Ce. The evolution of the intricate magnetic structures in CeFeAsO going through $T^{*}$ and $T_\texttt{Ce}$ is proposed.

cond-mat.str-el↗

arXiv2012

Derivation of exact master equation with stochastic description: Models in quantum optics

The methodology of stochastic description for dissipation, a generic scheme to decouple the interaction between two subsystems, is applied to the study of dissipative dynamics in quantum optics. It is shown that the influence of the coupled thermal or vacuum field on the quantum mode can be exactly represented by the induced stochastic fields. The quantum mode thereby satisfies a stochastic differential equation and dissipation effect due to the coupling with the environment is obtained through statistical averaging. Within the framework of stochastic description, it is demonstrated how to derive the master equation for a single optical mode interacting with the bosonic bath. A numerical algorithm for solving the master equation in which the coefficients are determined by a set of integral equations is discussed and a comparison with the known results is displayed. The derivation of the master equation for the spontaneous decay of two-state atoms in the vacuum is also presented.

quant-ph↗

arXiv2011

Derivation of exact master equation with stochastic description: Dissipative harmonic oscillator

A systematic procedure for deriving the master equation of a dissipative system is reported in the framework of stochastic description. For the Caldeira-Leggett model of the harmonic-oscillator bath, a detailed and elementary derivation of the bath-induced stochastic field is presented. The dynamics of the system is thereby fully described by a stochastic differential equation and the desired master equation would be acquired with statistical averaging. It is shown that the existence of a closed-form master equation depends on the specificity of the system as well as the feature of the dissipation characterized by the spectral density function. For a dissipative harmonic oscillator it is observed that the correlation between the stochastic field due to the bath and the system can be decoupled and the master equation naturally comes out. Such an equation possesses the Lindblad form in which time dependent coefficients are determined by a set of integral equations. It is proved that the obtained master equation is equivalent to the well-known Hu-Paz-Zhang equation based on the path integral technique. The procedure is also used to obtain the master equation of a dissipative harmonic oscillator in time-dependent fields.

quant-ph↗

arXiv2010

The magnetic form factor of iron in SrFe2As2

The iron magnetic form factor in SrFe2As2 has been determined by neutron diffraction and by density functional theory (DFT). As noted previously, the magnitude of the calculated moment using DFT is sensitive to the Fe-As distance. However, the shape of the calculated form factor is practically insensitive to the Fe-As distance, and further we show that the form factor closely resembles that of bcc iron, and agrees well with experiment. The spin density exhibits some anisotropy due to geometry and As hybridization.

cond-mat.supr-con↗

arXiv2009

Magnetic and lattice coupling in single-crystal SrFe$_2$As$_2$: A neutron scattering study

A detailed elastic neutron scattering study of the structural and magnetic phase transitions in single-crystal SrFe$_2$As$_2$ reveals that the orthorhombic (O)-tetragonal (T) and the antiferromagnetic transitions coincide at $T_\texttt{O}$ = $T_\texttt{N}$ = (201.5 $\pm$ 0.25) K. The observation of coexisting O-T phases over a finite temperature range at the transition and the sudden onset of the O distortion provide strong evidences that the structural transition is first order. The simultaneous appearance and disappearance within 0.5 K upon cooling and within 0.25 K upon warming, respectively, indicate that the magnetic and structural transitions are intimately coupled. We find that the hysteresis in the transition temperature extends over a 1-2 K range. Based on the observation of a remnant orthorhombic phase at temperatures higher than \emph{T}$_\texttt{O}$, we suggest that the T-O transition may be an order-disorder transition.

cond-mat.str-el↗

arXiv2008

Three-Dimensional Grain Boundary Spectroscopy in Transparent High Power Ceramic Laser Materials

Using confocal Raman and fluorescence spectroscopic imaging in 3-dimensions, we show direct evidence for Nd3+-Nd3+ interactions across grain boundaries (GBs) in Nd3+:YAG laser ceramics. It is clearly shown that Nd3+ segregation takes place at GBs leading to self-fluorescence quenching which affects a volume fraction as high as 20%. In addition, we show a clear trend of increasing spatial inhomogeneities in Nd3+ concentration when the doping levels exceeds 3 at%, which is not detected by standard spectrometry techniques. These results could point the way to further improvements in what is already an impressive class of ceramic laser materials.

cond-mat.mtrl-sci↗