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991.
Using the fact that for simple fluids the most general constitutive equation in constant stretch history flows for the extra
stress tensor τ is known in an explicit form, the Giesekus fluid model is cast into this (ω–D) form for two-dimensional flows. The three material functions needed to characterize τ are listed. The explicit results for
simple shear and planar elongation reveal that the parameter α should be restricted to values less than 0.5. It is demonstrated
that in this explicit form the constitutive equation is free from thermodynamic objections and can thus be used as a starting
point for numerical calculations of general, but steady, two-dimensional flows.
Received: 9 November 1998 Accepted: 20 May 1999 相似文献
992.
The properties of interface polarons in a strained (111)-oriented zinc-blende GaN/A1xGa1-xN heterojunc-tion at finite temperature under hydrostatic pressure are investigated by adopting a modified LLP variational method and a simplified coherent potential approximation. Considering the effect of hydrostatic pressure on the bulk longitu-dinal optical phonon mode, two branches interface-optical phonon modes and strain, respectively, we calculated the polaronic self-trapping energy and effective mass as functions of temperature, pressure and areal electron density. The numerical result shows that both of them near linearly increase with pressure but the self-trapping energies are nonlinear monotone increasing with increasing of the areal electron density. They are near constants below a range of temperature whereas decrease dramatically with increasing temperature beyond the range. The contributions from the bulk longitudinal optical phonon mode and one branch of interface optical phonon mode with higher frequency are important whereas the contribution from another branch of interface optical phonon mode with lower frequency is extremely small so that it can be neglected in the further discussion. 相似文献
993.
We have explored the fabrication of an InP/InGaAs single heterojunction bipolar transistor (HBT) and a wave guide p‐i‐n photodiode (PD) on two kinds of double stacked layers for the implementation of an optoelectronic millimeter‐wave monolithic integrated circuit (OEMMIC). We applied a photosensitive polyimide for passivation and integration to overcome the large difference between the HBT and PD layers of around 3 µm. Our experiment showed that the RF characteristics of the HBT were dependent on the location of the PD layer, while the dc performances of the HBTs and PDs were independent of the type of stacked layer used. The Ft and Fmax of the HBTs on the HBT/PD stacked layer were 10% lower than those of the HBTs on the PD/HBT stacked layer. 相似文献
994.
高性能新结构InGaP/GaAs异质结双极型晶体管 总被引:5,自引:5,他引:0
报道了一种采用 U形发射极新结构的高性能 In Ga P/ Ga As HBT.采用自对准发射极、L EU等先进工艺技术实现了特征频率达到 1 0 8GHz,最大振荡频率达到 1 4 0 GHz的频率特性 .这种新结构的 HBT的击穿电压达到 2 5 V,有利于在大功率领域应用 .而残余电压只有 1 0 5 m V,拐点电压只有 0 .5 0 V,使其更适用于低功耗应用 .同时 ,还对比了由于不同结构产生的器件性能的差异 相似文献
995.
996.
997.
We report a top-contact light emitting field-effect transistor based on an asymmetric vertical heterojunction using pentacene as a field-effect layer and tris-(8-hydroxyquinolinato) aluminum (Alq3) as an electron transport and luminescent material, which is fabricated on an indium tin oxide (ITO)-coated glass substrate with poly (methyl methacrylate) (PMMA) as a gate dielectric. The Alq3 layer underneath the drain electrode roughly occupies one half of the pentacene surface forming an asymmetric heterojunction with pentacene. A hole transport layer N,N′-Di(1-naphthyl)-N,N′-diphenyl-(1,1′-biphenyl)-4,4′-diamine (NPB) is introduced to occupy the other half of the pentacene surface underneath the source electrode to allow vertical hole transport in the device. We have realized the electrical switching functionality of a field-effect transistor (FET) and the control of electroluminescence (EL) simultaneously under ambient atmosphere. The device exhibits typical p-channel characteristics and green emission from Alq3 is observed adjacent to the drain electrode. A working principle of the device is discussed in detail. Furthermore, this device configuration enables high-spatial-resolution fluorescence imaging of device operation, which is a simple and powerful tool for studying organic luminescent materials. 相似文献
998.
Two molecules denoted as VC96 and VC97 have been synthesized for efficient (η = 6.13% @ 100 mW/cm2 sun-simulated light) small molecule solution processed organic solar cells. These molecules have been designed with the D1-A-D2-A-D1 structure bearing different central donor unit, same benzothiadiazole (BT) as π-acceptor and end capping triphenylamine. Moreover, the optical and electrochemical properties (both experimental and theoretical) of these molecules have been systematically investigated. The solar cells prepared from VC96:PC71BM and VC97:PC71BM (1:2) processed from CF (chloroform) exhibit a PCE (power conversion efficiency) of η = 4.06% (Jsc = 8.36 mA/cm2, Voc = 0.90 V and FF = 0.54) and η = 3.12% (Jsc = 6.78 mA/cm2, Voc = 0.92 V and FF = 0.50), respectively. The higher PCE of the device with VC96 as compared to VC97 is demonstrated to be due to the higher hole mobility and broader IPCE spectra. The devices based on VC96:PC71BM and VC97:PC71BM processed with solvent additive (3 v% DIO, 1,8-diiodooctane) showed PCE of η = 5.44% and η = 4.72%, respectively. The PCE device of optimized VC96:PC71BM processed with DIO/CF (thermal annealed) has been improved up to 6.13% (Jsc = 10.72 mA/cm2, Voc = 0.88 V and FF = 0.61). The device optimization results from the improvement of the balanced charge transport and better nanoscale morphology induced by the solvent additive plus the thermal annealing. 相似文献
999.
Donor–acceptor–acceptor–donor small molecules for solution processed bulk heterojunction solar cells
We report on the optical and electrochemical characterization (experimental and theoretical) of two donor substituted benzothiadiazole with different cyano based acceptor π-linkers, tetracyanobutadiene (TCBD) SM1 and dicyanoquinomethane (DCNQ) SM2, and explore them as the donor component for solution processed bulk heterojunction organic solar cells, along with PC71BM as the electron acceptor. The solution bulk heterojunction (BHJ) solar cells based on dichloromethane (DCM) processed active layer with SM1 and SM2 as donor and PC71BM as acceptor achieve power conversion efficiency (PCE) of 2.76% and 3.61%, respectively. The solar cells based on these two small molecules exhibit good Voc, which is attributed to their deep HOMO energy level. The higher PCE of the device based on SM2 compared to SM1 is attributed to the its small bandgap, broader absorption profile and enhanced hole mobility. Additionally, the PCE of the SM2:PC71BM based solar cells processed with 1-chloronaphthalene CN (3 v%)/DCM is further improved reaching upto 4.86%. This increase in PCE has been attributed to the improved nanoscale morphology and more balanced charge transport in the device, due to the solvent additive. 相似文献
1000.
Electronic Structures and Photoconversion Mechanism in Perovskite/Fullerene Heterojunctions
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Ming‐Fai Lo Zhi‐Qiang Guan Tsz‐Wai Ng Chiu‐Yee Chan Chun‐Sing Lee 《Advanced functional materials》2015,25(8):1213-1218
It has been generally believed and assumed that organometal halide perovskites would form type II P–N junctions with fullerene derivatives (C60 or PCBM), and the P–N junctions would provide driving force for exciton dissociation in perovskite‐based solar cell. To the best of our knowledge, there is so far no experiment proof on this assumption. On the other hand, whether photogenerated excitons can intrinsically dissociate into free carrier in the perovskite without any assistance from a P–N junction is still controversial. To address these, the interfacial electronic structures of a vacuum‐deposited perovskite/C60 and a solution‐processed perovskite/PCBM junctions is directly measured by ultraviolet photoelectron spectroscopy. Contrary to the common believes, both junctions are found to be type I N–N junctions with band gap of the perovskites embedded by that of the fullerenes. Meanwhile, device with such a charge inert junction can still effectively functions as a solar cell. These results give direct experimental evidence that excitons are dissociated to free carriers in the perovskite film even without any assistance from a P–N junction. 相似文献