Regularized Boolean operations have been widely used in 3D modeling systems. However, evaluating Boolean operations may be quite numerically unstable and time consuming, especially for iterated set operations. A novel...Regularized Boolean operations have been widely used in 3D modeling systems. However, evaluating Boolean operations may be quite numerically unstable and time consuming, especially for iterated set operations. A novel and unified technique is proposed in this paper for computing single and iterated set operations efficiently, robustly and exactly. An adaptive octree is combined with a nested constructive solid geometry （CSG） tree by this technique. The intersection handling is restricted to the cells in the octree where intersection actually occurs. Within those cells, a CSG tree template is instanced by the surfaces and the tree is converted to planebased binary space partitioning （BSP） for set evaluation; Moreover, the surface classification is restricted to the ceils in the octree where the surfaces only come from a model and are within the bounding-boxes of other polyhedrons. These two ways bring about the efficiency and scalability of the operations, in terms of runtime and memory. As all surfaces in such a cell have the same classification relation, they are classified as a whole. Robustness and exactness are achieved by integrating plane-based geometry representation with adaptive geometry predicate technique in intersection handling, and by applying divide-and-conquer arithmetic on surface classification. Experimental results demonstrate that the proposed approach can guarantee the robustness of Boolean computations and runs faster than other existing approaches.展开更多
表面增强拉曼散射(SERS)技术在农药残留的检测方面具有很大的潜力,但在痕量和定量分析方面仍存在局限性。提出了一种基于Au@4-ATP@Au凸多面纳米颗粒(NCPs-Au@4-ATP@Au)为增强基底的农药检测方法。XRD结果表明,由于探针分子对金前驱的选...表面增强拉曼散射(SERS)技术在农药残留的检测方面具有很大的潜力,但在痕量和定量分析方面仍存在局限性。提出了一种基于Au@4-ATP@Au凸多面纳米颗粒(NCPs-Au@4-ATP@Au)为增强基底的农药检测方法。XRD结果表明,由于探针分子对金前驱的选择性和诱导性,NCPs-Au@4-ATP@Au纳米颗粒与球形金纳米颗粒晶面结构信息有明显差异,具体体现在(200)处的强反射峰。结合扫描电镜与吸收光谱可以确定,NCPs-Au@4-ATP@Au同时具备球形与多面体结构特征。吸收峰较球形金纳米颗粒有明显红移,更加接近激发光波长,这在理论上更有利于SERS信号的增强。实验证明,以表面包覆高指数晶面,同时内嵌4-ATP作为探针分子的NCPs-Au@4-ATP@Au为增强基底,农药多菌灵(CBZ)的检测限(LODs)达到0.66 nmol·L^(-1)。通过对CBZ分子的拉曼与SERS光谱位移分析可以初步确定,CBZ分子是通过NH键和CO键吸附于金纳米颗粒上。Au@4-ATP@Au利用多凸面结构体提高灵敏度的同时,以4-ATP作为定标信号,归一后光谱稳定性和时效性也得到改善。内标峰强度矫正后光谱稳定性的相对标准偏差(relative standard deviation,RSD)低至7.03%,半个月内信号强度仅降低5.87%,RSD为2.94%。结果表明,NCPs-Au@4-ATP@Au提高了SERS在农药检测方面的痕量和定量检测能力,该基底有望推动SERS在实际中的应用。展开更多
Oxygen vacancies enable modulating surface reconstruction of transition metal oxides containing metal-oxygen polyhedrons into metallic oxyhydroxide for oxygen evolution reaction(OER),while revealing reconstructing mec...Oxygen vacancies enable modulating surface reconstruction of transition metal oxides containing metal-oxygen polyhedrons into metallic oxyhydroxide for oxygen evolution reaction(OER),while revealing reconstructing mechanism is stuck by the requirement to precisely control exact sites of these vacancies.Herein,oxygen vacancies are localized only within MoO_(4)tetrahedrons rather than CoO_(6)octahedrons in CoMoO_(4)catalyst,guaranteeing coherent reconstruction of CoO_(6)octahedrons into pure CoOOH with tunable activities for OER.Meanwhile,distorted tetrahedron accelerates the dissolution of Mo atoms into alkaline electrolyte,triggering spontaneous transition of partial CoMoO_(4)into Co(OH)_(2).CoO_(6)octahedrons in both CoMoO_(4)and Co(OH)_(2)can transform pure CoOOH completely at lower potential,resulting in excess intrinsic activity whose summit is identified by overpotential at 10 mA cm^(-2)with 22.9%reduction and Tafel slope with 65.3%reduction.Well-defined manipulation over the distorted polyhedrons offers one versatile knob to precisely modulate electronic structure of oxide catalysts with outstanding OER performance.展开更多
With the advantage of fast charge transfer,heterojunction engineering is identified as a viable method to reinforce the anodes'sodium storage performance.Also,vacancies can effectively strengthen the Na+adsorption...With the advantage of fast charge transfer,heterojunction engineering is identified as a viable method to reinforce the anodes'sodium storage performance.Also,vacancies can effectively strengthen the Na+adsorption ability and provide extra active sites for Na+adsorption.However,their synchronous engineering is rarely reported.Herein,a hybrid of Co_(0.85)Se/WSe_(2) heterostructure with Se vacancies and N-doped carbon polyhedron(CoWSe/NCP)has been fabricated for the first time via a hydrothermal and subsequent selenization strategy.Spherical aberration-corrected transmission electron microscopy confirms the phase interface of the Co_(0.85)Se/WSe_(2) heterostructure and the existence of Se vacancies.Density functional theory simulations reveal the accelerated charge transfer and enhanced Na+adsorption ability,which are contributed by the Co_(0.85)Se/WSe_(2) heterostructure and Se vacancies,respectively.As expected,the CoWSe/NCP anode in sodium-ion battery achieves outstanding rate capability(339.6 mAh g^(−1) at 20 A g^(−1)),outperforming almost all Co/W-based selenides.展开更多
基金supported by the Natural Science Foundation of China under Grant No.61202154 and No.61133009the National Basic Research Project of China under Grant No.2011CB302203+2 种基金Shanghai Pujiang Program under Grant No.13PJ1404500the Science and Technology Commission of Shanghai Municipality Program under Grant No.13511505000the Open Project Program of the State Key Lab of CAD&CG of Zhejiang University under Grant No.A1401
文摘Regularized Boolean operations have been widely used in 3D modeling systems. However, evaluating Boolean operations may be quite numerically unstable and time consuming, especially for iterated set operations. A novel and unified technique is proposed in this paper for computing single and iterated set operations efficiently, robustly and exactly. An adaptive octree is combined with a nested constructive solid geometry （CSG） tree by this technique. The intersection handling is restricted to the cells in the octree where intersection actually occurs. Within those cells, a CSG tree template is instanced by the surfaces and the tree is converted to planebased binary space partitioning （BSP） for set evaluation; Moreover, the surface classification is restricted to the ceils in the octree where the surfaces only come from a model and are within the bounding-boxes of other polyhedrons. These two ways bring about the efficiency and scalability of the operations, in terms of runtime and memory. As all surfaces in such a cell have the same classification relation, they are classified as a whole. Robustness and exactness are achieved by integrating plane-based geometry representation with adaptive geometry predicate technique in intersection handling, and by applying divide-and-conquer arithmetic on surface classification. Experimental results demonstrate that the proposed approach can guarantee the robustness of Boolean computations and runs faster than other existing approaches.
文摘表面增强拉曼散射(SERS)技术在农药残留的检测方面具有很大的潜力,但在痕量和定量分析方面仍存在局限性。提出了一种基于Au@4-ATP@Au凸多面纳米颗粒(NCPs-Au@4-ATP@Au)为增强基底的农药检测方法。XRD结果表明,由于探针分子对金前驱的选择性和诱导性,NCPs-Au@4-ATP@Au纳米颗粒与球形金纳米颗粒晶面结构信息有明显差异,具体体现在(200)处的强反射峰。结合扫描电镜与吸收光谱可以确定,NCPs-Au@4-ATP@Au同时具备球形与多面体结构特征。吸收峰较球形金纳米颗粒有明显红移,更加接近激发光波长,这在理论上更有利于SERS信号的增强。实验证明,以表面包覆高指数晶面,同时内嵌4-ATP作为探针分子的NCPs-Au@4-ATP@Au为增强基底,农药多菌灵(CBZ)的检测限(LODs)达到0.66 nmol·L^(-1)。通过对CBZ分子的拉曼与SERS光谱位移分析可以初步确定,CBZ分子是通过NH键和CO键吸附于金纳米颗粒上。Au@4-ATP@Au利用多凸面结构体提高灵敏度的同时,以4-ATP作为定标信号,归一后光谱稳定性和时效性也得到改善。内标峰强度矫正后光谱稳定性的相对标准偏差(relative standard deviation,RSD)低至7.03%,半个月内信号强度仅降低5.87%,RSD为2.94%。结果表明,NCPs-Au@4-ATP@Au提高了SERS在农药检测方面的痕量和定量检测能力,该基底有望推动SERS在实际中的应用。
基金supported by the National Natural Science Foundation of China(52171156,51771078)
文摘Oxygen vacancies enable modulating surface reconstruction of transition metal oxides containing metal-oxygen polyhedrons into metallic oxyhydroxide for oxygen evolution reaction(OER),while revealing reconstructing mechanism is stuck by the requirement to precisely control exact sites of these vacancies.Herein,oxygen vacancies are localized only within MoO_(4)tetrahedrons rather than CoO_(6)octahedrons in CoMoO_(4)catalyst,guaranteeing coherent reconstruction of CoO_(6)octahedrons into pure CoOOH with tunable activities for OER.Meanwhile,distorted tetrahedron accelerates the dissolution of Mo atoms into alkaline electrolyte,triggering spontaneous transition of partial CoMoO_(4)into Co(OH)_(2).CoO_(6)octahedrons in both CoMoO_(4)and Co(OH)_(2)can transform pure CoOOH completely at lower potential,resulting in excess intrinsic activity whose summit is identified by overpotential at 10 mA cm^(-2)with 22.9%reduction and Tafel slope with 65.3%reduction.Well-defined manipulation over the distorted polyhedrons offers one versatile knob to precisely modulate electronic structure of oxide catalysts with outstanding OER performance.
基金support from the Natural Science Foundation of Jilin Province(Grant No.20200201073JC)the National Natural Science Foundation of China(Grant No.52130101)+1 种基金Interdisciplinary Integration and Innovation Project of JLU(Grant No.JLUXKJC2021ZY01)the Fundamental Research Funds for the Central Universities.
文摘With the advantage of fast charge transfer,heterojunction engineering is identified as a viable method to reinforce the anodes'sodium storage performance.Also,vacancies can effectively strengthen the Na+adsorption ability and provide extra active sites for Na+adsorption.However,their synchronous engineering is rarely reported.Herein,a hybrid of Co_(0.85)Se/WSe_(2) heterostructure with Se vacancies and N-doped carbon polyhedron(CoWSe/NCP)has been fabricated for the first time via a hydrothermal and subsequent selenization strategy.Spherical aberration-corrected transmission electron microscopy confirms the phase interface of the Co_(0.85)Se/WSe_(2) heterostructure and the existence of Se vacancies.Density functional theory simulations reveal the accelerated charge transfer and enhanced Na+adsorption ability,which are contributed by the Co_(0.85)Se/WSe_(2) heterostructure and Se vacancies,respectively.As expected,the CoWSe/NCP anode in sodium-ion battery achieves outstanding rate capability(339.6 mAh g^(−1) at 20 A g^(−1)),outperforming almost all Co/W-based selenides.
