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Polyoxometalate (POM) presents great potential in oxidative desulfurization (ODS) reaction. However, the high dissolubility of POM in common solvents makes it difficult to recycle. Besides, the small specific surface area of POM also limits the interaction between them and the substrate. Depositing polyoxometalates onto three-dimensional (3D) network structured materials could largely expand the application of POM. Here, the surfaces of cellulose nanofibrils (CNFs) were modified with very few (3-Aminopropyl) trimethoxysilane (APTS) to endow positive charges on the surfaces of CNFs, and then phosphotungstic acid (PTA) was loaded to obtain the aerogel A-CNF/PTA as the ODS catalyst. FT-IR indicated the successful deposition of PTA onto aminosilane modified CNF surfaces. UV-VIS further suggested the stability of PTA in the aerogels. BET and SEM results suggested the increased specific surface area and the relatively uniform 3D network structure of the prepared aerogels. TGA analysis indicated that the thermal stability of the aerogel A-CNF/PTA50% was a little higher than that of the pure CNF aerogel. Most importantly, the aerogel A-CNF/PTA50% showed good catalytic performance for ODS. Catalysis results showed that the substrate conversion rate of the aerogel A-CNF/PTA50% reached 100% within 120 min at room temperature. Even after five cycles, the substrate conversion rate of the aerogel A-CNF/PTA50% still reached 91.2% during the dynamic catalytic process. This work provides a scalable and facile way to stably deposit POM onto 3D structured materials. 相似文献
43.
Lead-halide perovskite photovoltaics(PVs)have achieved impressive progress in power conversion efficiencies(PCEs)over the past ten years,accelerating their step forward to next-generation commercial PV technologies[1].As a leading candidate for perovskite PVs,monolithic all-perovskite tandem solar cells(PTSCs)have achieved the best24.8%for small-area devices(0.049 cm^2)in 2019。 相似文献
44.
首次报道了一种新型的基于铰链式六面顶压机的二级6-8模大腔体静高压装置的内置加热元件的设计与温度标定。此加热组装结构简单,升温快,保温效果好,并有效地解决了国外基于两面顶压机构架下的二级6-8模内加热组装中热电偶在施加压力时易断的问题。以低成本的碳管为加热元件,采用直接和间接两种加热方式,用双铂铑(Pt6%Rh-Pt30%Rt)B型热电偶进行温度测量,并根据实验过程中加热功率与腔内实际温度的关系,对不同压力下腔体内的温度进行了标定。实验结果表明:此加热系统的油压达到40 MPa(腔体压力约10 GPa)时,温度可以达到1 700 ℃以上;在油压为30 MPa、样品室温度为1 000 ℃时,保温时间可达2 h,甚至更长;实验中获得样品的直径可达3 mm,高度可达7 mm,实现了在高温超高压条件下大样品的制备,满足了实验对产生高温超高压条件的需要。 相似文献
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航天器对接相对位置姿态自主测量方法研究 总被引:2,自引:0,他引:2
航天器间相对位置姿态的准确测量是实现自主自动对接的先决条件。将三圆标志靶安装在目标航天器上;追踪航天器用数码相机对靶拍照。设计了亚像素处理方法实时处理数字照片,可精确测定圆心像点位置和特征直径的像长;用其作为基本特征参数,基于透视投影原理,建立了求圆心物空间坐标的公式,求出靶面的平面方程,可用来求两航天器间的相对位置姿态参数和实时标定相机的可变参数。计算机仿真结果表明,测距为2m时,测圆心像点位置的误差小于0.03个像素,测距误差小于1mm,测姿态角的误差小于0.01°。该方法也适用于无人直升飞机定点着陆时自主测量其相对位姿参数。 相似文献
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Rui M. Novais Frank Simon Petra Pötschke Tobias Villmow José A. Covas Maria C. Paiva 《Journal of polymer science. Part A, Polymer chemistry》2013,51(17):3740-3750
This work reports the study of the effect of chemical functionalization of carbon nanotubes on their dispersion in poly(lactic acid). The nanotubes were functionalized by the 1,3‐dipolar cycloaddition reaction, generating pyrrolidine groups at the nanotube surface. Further reaction of the pyrrolidine groups with poly(lactic acid) was studied in solution and in the polymer melt. The former involved refluxing the nanotubes in a dimethylformamide/polymer solution; the latter was carried out by direct melt mixing in a microcompounder. The carbon nanotubes collected after each process were characterized by thermogravimetry and by X‐ray photoelectron spectroscopy, showing evidence of polymer bonded to the nanotube surface only when the reaction was carried out in the polymer melt. The composites with polymer modified nanotubes present smaller average agglomerate area and a narrower agglomerate area distribution. In addition, they show improved tensile properties at low CNT concentration and present lower electrical resistivity. © 2013 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2013, 51, 3740–3750 相似文献
50.
Isovaleroyl oxokadsurane, a novel dibenzocyclooctadiene lignan pos-sessing a spirobenzofuranoid skeleton was isolated from the stems of Kadsura coccinea.Its structure and relative configuration were determined by X-ray diffraction analysis. 相似文献