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991.
光电耦合器件g-r噪声模型   总被引:1,自引:0,他引:1  
在宽范围偏置条件下,测量了光电耦合器件的g-r(产生-复合)噪声.实验结果表明,随着偏置电流的增加,g-r噪声逐渐向高频移动,其噪声幅值呈现先增加后减小的变化规律.通过测量前级噪声和后级噪声,发现光电耦合器件g-r噪声来源于后级的光敏三极管.基于载流子数涨落机制,建立了一个光电耦合器件g-r噪声的定量分析模型.实验结果和本文模型符合良好.  相似文献   
992.
Regarding the complex properties of various cations, the design of aqueous batteries that can simultaneously store multi-ions with high capacity and satisfactory rate performance is a great challenge. Here an amorphization strategy to boost cation-ion storage capacities of anode materials is reported. In monovalent (H+, Li+, K+), divalent (Mg2+, Ca2+, Zn2+) and even trivalent (Al3+) aqueous electrolytes, the capacity of the resulting amorphous MoOx is more than quadruple than that of crystalline MoOx and exceeds those of other reported multiple-ion storage materials. Both experimental and theoretical calculations reveal the generation of ample active sites and isotropic ions in the amorphous phase, which accelerates cation migration within the electrode bulk. Amorphous MoOx can be coupled with multi-ion storage cathodes to realize electrochemical energy storage devices with different carriers, promising high energy and power densities. The power density exceeded 15000 W kg−1, demonstrating the great potential of amorphous MoOx in advanced aqueous batteries.  相似文献   
993.
Conducting polymer hydrogels are widely used as strain sensors in light of their distinct skin-like softness, strain sensitivity, and environmental adaptiveness in the fields of wearable devices, soft robots, and human-machine interface. However, the mechanical and electrical properties of existing conducting polymer hydrogels, especially fatigue-resistance and sensing robustness during long-term application, are unsatisfactory, which severely hamper their practical utilities. Herein, a strategy to fabricate conducting polymer hydrogels with anisotropic structures and mechanics is presented through a combined freeze-casting and salting-out process. The as-fabricated conducting polymer hydrogels exhibit high fatigue threshold (>300 J m−2), low Young's modulus (≈100 kPa), as well as long-term strain sensing robustness (over 10 000 cycles). Such superior performance enables their application as strain sensors to monitor the real-time movement of underwater robotics. The design and fabrication strategy for conducting polymer hydrogels reported in this study may open up an enticing avenue for functional soft materials in soft electronics and robotics.  相似文献   
994.
Flexible sensing technologies that play a pivotal role in endowing robots with detection capabilities and monitoring their motions are impulsively desired for intelligent robotics systems. However, integrating and constructing reliable and sustainable flexible sensors with multifunctionality for robots remains an everlasting challenge. Herein, an entirely intrinsic self-healing, stretchable, and attachable multimodal sensor is developed that can be conformally integrated with soft robots to identify diverse signals. The dynamic bonds cross-linked networks including the insulating polymer and conductive hydrogel with good comprehensive performances are designed to fabricate the sensor with prolonged lifespan and improved reliability. Benefiting from the self-adhesiveness of the hydrogel, strong interfacial bonding can be formed on various surfaces, which promotes the conformable integration of the sensor with robots. Due to the ionic transportation mechanism, the sensor can detect strain and temperature based on piezoresistive and thermoresistive effect, respectively. Moreover, the sensor can work in triboelectric mode to achieve self-powered sensing. Various information can be identified from the electrical signals generated by the sensor, including hand gestures, soft robot crawling motions, a message of code, the temperature of objects, and the type of materials, holding great promise in the fields of environmental detection, wearable devices, human-machine interfacing, and robotics.  相似文献   
995.
Developing highly efficient and durable electrocatalysts toward oxygen evolution reaction (OER) is an urgent demand to produce clean hydrogen energy. In this study, a series of medium-entropy metal sulfides (MEMS) of (NiFeCoX)3S4 (where X = Mn, Cr, Zn) are synthesized by a facile one-pot solvothermal strategy using molecular precursors. Benefiting from the multiple-metal synergistic effect and the low crystallinity, these MEMS show significantly enhanced electrocatalytic OER activity compared with the binary-metal (NiFe)3S4 and ternary-metal (NiFeCo)3S4 counterparts. Especially, (NiFeCoMn)3S4 delivers a low overpotential of 289 mV at 10 mA cm−2, a decent Tafel slope of 75.6 mV dec−1 and robust catalytic stability in alkaline medium, outperforming the costly IrO2 benchmark electrocatalyst and the majority of the reported metal sulfide-based electrocatalysts until now. These MEMS with facile synthesis and excellent electrocatalytic performance bring a great opportunity to design desirable electrocatalysts for practical application.  相似文献   
996.
Magnetic skyrmions are localized particle-like nontrivial swirls that are promising in building high-performance topological spintronic devices. The read-out functions in skyrmionic devices require the translation of magnetic skyrmions to electrical signals. Here, combined real-space magnetic imaging and anisotropic magnetoresistance studies on dipolar skyrmions are reported. A single skyrmion chain and single skyrmion are observed using Lorentz transmission electron microscopy imaging. Meanwhile, the field, helicity, and skyrmion count dependence of anisotropic magnetoresistance of the Fe3Sn2 nanostructures are obtained simultaneously. These results demonstrate that the anisotropic magnetoresistance of skyrmions is independent of the helicity and proportional to the skyrmion count. This study promotes read-out operations in skyrmion-based spintronic devices.  相似文献   
997.
Temperature variation-induced thermoelectric catalytic efficiency of thermoelectric material is simultaneously restricted by its electrical conductivity, Seebeck coefficient, and thermal conductivity. Herein, Bi2Te3 nanosheets are in situ grown on reduced graphene oxides (rGO) to generate an efficient photo-thermoelectric catalyst (rGO-Bi2Te3). This system exhibits phonon scattering effect and extra carrier transport channels induced by the formed heterointerface between rGO and Bi2Te3, which improves the power factor value and reduces thermal conductivity, thus enhancing the thermoelectric performance of 2.13 times than single Bi2Te3. The photo-thermoelectric catalysis of rGO-Bi2Te3 significantly improves the reactive oxygen species yields, resulting from the effective electron–hole separation caused by the unique thermoelectric field and heterointerfaces of rGO-Bi2Te3. Correspondingly, the electrospinning membranes containing rGO-Bi2Te3 nanosheets exhibit high antibacterial efficiency in vivo (99.35 ± 0.29%), accelerated tissue repair ability, and excellent biosafety. This study provides an insight into heterointerface design in photo-thermoelectric catalysis.  相似文献   
998.
The exceptional photophysical properties of 3D organic–inorganic lead halide hybrids (OILHs) endow their significant potential for usage in optoelectronics, which has sparked intense research on novel 3D OILHs and associated applications. However, constructing new 3D OILHs based on large organic cations suffers from tough challenges due to the limitation of the Goldschmidt tolerance factor rule, let alone further explorations of their practical applications. Herein, a brand-new 3D lead chloride hybrid, (1MPZ)Pb4Cl10·H2O ( 1 , 1MPZ = 1-methylpiperazine) is reported, featuring a dense 3D lead chloride framework made of the corner-, edge-, and face-shared lead chloride polyhedra. 1 presents a broadband white light emission with a large Stokes shift and a nanosecond photoluminescence lifetime, which originates from radiative recombination of self-trapped excitons (STEs) induced by the highly distorted structure. Such a reabsorption-free and fast-decayed STEs emission coupling with the dense 3D architecture further enables 1 with effective X-ray scintillation with good sensitivity. Impressively, 1 also shows superior environmental and radiation stability. This study provides a new 3D OILH with appealing luminescence, not only expanding the 3D OILH family but also inspiring the exploitation of their optoelectronic applications.  相似文献   
999.
Here, a near-infrared (NIR)-absorbing small-molecule acceptor (SMA) Y-SeNF with strong intermolecular interaction and crystallinity is developed by combining selenophene-fused core with naphthalene-containing end-group, and then as a custom-tailor guest acceptor is incorporated into the binary PM6:L8-BO host system. Y-SeNF shows a 65 nm red-shifted absorption compared to L8-BO. Thanks to the strong crystallinity and intermolecular interaction of Y-SeNF, the morphology of PM6:L8-BO:Y-SeNF can be precisely regulated by introducing Y-SeNF, achieving improved charge-transporting and suppressed non-radiative energy loss. Consequently, ternary polymer solar cells (PSCs) offer an impressive device efficiency of 19.28% with both high photovoltage (0.873 V) and photocurrent (27.88 mA cm−2), which is one of the highest efficiencies in reported single-junction PSCs. Notably, ternary PSC has excellent stability under maximum-power-point tracking for even over 200 h, which is better than its parental binary devices. The study provides a novel strategy to construct NIR-absorbing SMA for efficient and stable PSCs toward practical applications.  相似文献   
1000.
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