With the popularization of the Internet, the rapid development of intelligent education is promoted. They are a new platform for students to learn, and they can quickly help students improve and consolidate knowledge, as well as unlimited time, place, and space. However, due to a large number of learning resources, how to find the resources you need, and suitable from the massive resources is a problem that needs to be solved in this field. The individual characteristics of each learner are different, so when meeting their own needs, they have different requirements for individualization. The personalized learning resource recommendation system was born, according to the different characteristics of students to recommend corresponding learning resources. Since most of the recommendation systems currently recommend a large number of test questions or a large number of books, but each person’s needs are different, this article focuses on the above problems and selects a small piece of content course knowledge points in the learning resources, using course knowledge Come as a recommendation point and solve the above problems by designing a personal personalized learning mechanism. The main research contents of this article are as follows: (1) It is proposed to take curriculum knowledge points as the recommended objects. (2) Use collaborative filtering methods and cognitive diagnosis methods to design individual learning mechanisms. (3) Experiment. Through related experiments, the use of collaborative filtering method and cognitive diagnosis method based on curriculum knowledge points recommendation to confirm whether it is feasible.
The spin-forbidden O(3P2) + CO(X1Σ+, v) channel formed from photodissociation of CO2 in the low energy band centered 148 nm are investigated by using the time-sliced velocity-mapped ion imaging technique. The vibrational-resolved images of the O(3P2) photoproducts measured in the photolysis wavelength range of 144.62-150.45 nm are analyzed to give the total kinetic energy releases (TKER) spectra, CO(X1Σ+) vibrational state distributions and anisotropy parameters (β). The TKER spectra reveal the formation of correlated CO(X1Σ+) with well resolved v = 0-10 (or 11) vibrational bands. Several high vibrational bands observed in the low TKER region for each studied photolysis wavelength exhibit a bimodal structure. The CO(X1Σ+, v) vibrational distributions all present an inverted characteristics, and the most populated vibrational state changes from the low vibrational state to relatively high vibrational state with changing the photolysis wavelength from 150.45 to 144.62 nm. But, the vibrational-state specific β-values for different photolysis wavelength present a similar variation trend. The measured β-values show a significant bulge at the high vibrational levels in addition to the overall slow decreasing trend. The observed bimodal structures with mutational β-values for the highly vibrational excited CO(1Σ+) photoproducts suggest that the existence of more than one nonadiabatic pathway with different anisotropy in the formation of O(3P2) + CO(X1Σ+, v) photoproducts across the low energy band.
Understanding vacuum ultraviolet photodissociation dynamics of Carbonyl sulfide (OCS) is of considerable importance in the study of atmospheric chemistry. Yet, photodissociation dynamics of the CS(X1Σ+) + O(3Pj=2,1,0) channels following excitation to the 21Σ+(ν1′,1,0) state has not been clearly understood so far. Here, we investigate the O(3Pj=2,1,0) elimination dissociation processes in the resonance-state selective photodissociation of OCS between 147.24 and 156.48 nm by using the time-sliced velocity-mapped ion imaging technique. The total kinetic energy release spectra are found to exhibit highly structured profiles, indicative of the formation of a broad range of vibrational states of CS(1Σ+). The fitted CS(1Σ+) vibrational state distributions differ for the three 3Pj spin–orbit states, but a general trend of the inverted characteristics is observed. Additionally, the wavelength-dependent behaviors are also observed in the vibrational populations for CS(1Σ+, v). The CS(X1Σ+, v = 0) has a significantly strong population at several shorter wavelengths, and the most populated CS(X1Σ+, v) is gradually transferred to a higher vibrational state with the decrease in the photolysis wavelength. The measured overall β-values for the three 3Pj spin–orbit channels slightly increase and then abruptly decrease as the photolysis wavelength increases, while the vibrational dependences of β-values show an irregularly decreasing trend with increasing CS(1Σ+) vibrational excitation at all studied photolysis wavelengths. The comparison of the experimental observations for this titled channel and the S(3Pj) channel reveals that two different intersystem crossing mechanisms may be involved in the formation of the CS(X1Σ+) + O(3Pj=2,1,0) photoproducts via the 21Σ+ state.
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