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1.
Leucokinins (LKs) constitute a family of neuropeptides identified in numerous insects and many other invertebrates. LKs act on G-protein-coupled receptors that display only distant relations to other known receptors. In adult Drosophila, 26 neurons/neurosecretory cells of three main types express LK. The four brain interneurons are of two types, and these are implicated in several important functions in the fly’s behavior and physiology, including feeding, sleep–metabolism interactions, state-dependent memory formation, as well as modulation of gustatory sensitivity and nociception. The 22 neurosecretory cells (abdominal LK neurons, ABLKs) of the abdominal neuromeres co-express LK and a diuretic hormone (DH44), and together, these regulate water and ion homeostasis and associated stress as well as food intake. In Drosophila larvae, LK neurons modulate locomotion, escape responses and aspects of ecdysis behavior. A set of lateral neurosecretory cells, ALKs (anterior LK neurons), in the brain express LK in larvae, but inconsistently so in adults. These ALKs co-express three other neuropeptides and regulate water and ion homeostasis, feeding, and drinking, but the specific role of LK is not yet known. This review summarizes Drosophila data on embryonic lineages of LK neurons, functional roles of individual LK neuron types, interactions with other peptidergic systems, and orchestrating functions of LK.  相似文献   
2.
为了解决醇胺法燃烧后捕集二氧化碳再生能耗过高的问题,研究了一种向胺溶液中添加金属离子以降低其CO2解吸能耗的方法,称之为金属离子络合物热缓冲自热利用技术。以广泛商业化应用的单乙醇胺(MEA)溶液为研究载体,并在MEA溶液中分别添加金属离子铜或镍, 通过建立含有金属离子的MEA捕集CO2体系的化学反应模型,解释金属离子热缓冲剂效应的内在机理。机理显示在MEA-金属离子-CO2-H2O体系中,金属-MEA络合物作为一种有效的反应热缓冲剂,将有机胺吸收CO2过程中释放的反应热(放热反应)存储于金属络合物的解离键能中(吸热反应),在CO2高温解吸中通过其络合放热反应将储存的能量释放出来用于CO2解吸,形成自热再生低能耗CO2捕集技术,从而降低了MEA再生的能耗。本文进行了综合的实验测定来评价金属离子对MEA溶液捕集CO2过程的性能提升影响,包括CO2反应热、解吸速率、吸收-解吸循环负载、汽液平衡溶解度等。实验结果表明铜离子或镍离子作为添加剂,能增加MEA的CO2平衡循环负载14%~20%或7%~10%,同时能够降低MEA的CO2反应热值6.6%~24%或6.0%~20%。  相似文献   
3.
The damage induced in 3C-SiC epilayers on a silicon wafer by 2.3-MeV Si ion irradiation for fluences of 1014, 1015, and 1016 cm−2, was studied by conventional and high-resolution transmission electron microscopy (TEM/HRTEM). The evolution of extended defects and lattice disorder is followed in both the 3C-SiC film and Si substrate as a function of ion fluence, with reference to previous FTIR spectroscopy data. The likelihood of athermal unfaulting of native stacking faults by point defect migration to the native stacking faults is discussed in relation to damage recovery. Threshold energy densities and irradiation doses for dislocation loop formation and amorphous phase transformation are deduced from the damage depth profile by nuclear collisions. The role of electronic excitations on the damage recovery at high fluence is also addressed for both SiC and Si.  相似文献   
4.
张璐璐  谭伯川  李文坡 《化工学报》2021,72(10):5402-5411
采用简单的一步电沉积方法制备了Cu2+掺杂的MnO2材料。通过XRD、SEM、TEM等方法对材料进行了表征,结果表明其具有蓬松多孔的纳米结构,作为电池正极材料时有利于Zn2+的存储,具有较高的电池容量。与未掺杂样品相比Cu2+掺杂的MnO2材料有更好的电化学性能,在电流密度为200 mA/g时,比容量达到235 mAh/g,增加了47.8%,阻抗也由997.3 Ω降到了564.3 Ω。  相似文献   
5.
Perfluorosulfonic acid ionomer membranes have been widely used as proton conducting membranes in various electrochemical processes such as polymer electrolyte fuel cells and water electrolysis. While their thermal stability has been studied by thermogravimetry and analysis of low molecular weight products, their decomposition mechanism is little understood. In this study a newly developed methodology of thermal desorption and pyrolysis in combination with direct analysis in real time mass spectrometry is applied for Nafion membrane. An ambient ionization source and a high-resolution time-of-flight mass spectrometer enabled unambiguous assignment of gaseous products. Thermal decomposition is initiated by side chain detachment above 350°C, which leaves carbonyls on the main chain at the locations of the side chains. Perfluoroalkanes are released above 400°C by main chain scission and their further decomposition products dominate above 500 °C. DFT calculation of reaction energies and barrier heights of model compounds support proposed decomposition reactions.  相似文献   
6.
Biofuel cells (BFCs) that produce electrical energy from organic resources through enzymatic reactions have been attracting significant attention. Owing to the high electrical conductivity of carbon nanotubes (CNTs), their modification on the electrode surface of a BFC is expected to increase the current, and their high specific surface area may be useful in increasing the power output. Previously, we constructed a biocathode by immobilizing multicopper oxidase from Pyrobaculum aerophilum (McoP) with a carbon nanotube binding peptide (CBP) sequence on the CNTs. This resulted in higher current densities than when using enzymes without CBP sequences. However, owing to the randomly stacked CNTs on the surface of the electrodes, their conductive properties were impaired and performance as biocathodes was poor. Herein, we constructed a biocathode in which single-walled CNTs (SWCNTs) were oriented one-dimensionally and McoP is immobilized on the surface of an SWNCT via CBP. The current density was successfully increased by two-fold by orienting the CNTs and orienting and immobilizing McoP on their surfaces. This technology provides insights into the development of biodevices with controlled orientation of both the SWCNTs and enzymes immobilized on their surfaces.  相似文献   
7.
In this study,nano-sized SnO_2 decorated on carbon cloth(SnO_2/CC) is prepared through a simple and facile solid method.The nano-sized SnO_2 is uniformly distributed on the surface of carbon fibers in carbon cloth,providing sufficient free space to relieve volume expansion and reduce electrode pulverization during cycling.The as-prepared SnO_2/CC as a flexible,self-supporting and additive-free anode electrode for sodium-ion/lithium-ion batteries(SIBs/LIBs) can demonstrate outstanding electrochemical performance.SnO_2/CC after annealing at 350℃(SC-350) as an anode for SIBs can deliver a reversible capacity of 0.587 mA h cm~(-2) at the current density of 0.3 mA cm~(-2) after 100 cycles.In addition,when cycling at 1.5 mA cm~(-2),SC-350 can maintain 1.69 mA h cm~(-2) after 500 cycles when used as LIB anode.These results illustrate that the as-prepared SnO_2/CC can be a promising flexible anode material for flexible SIBs/LIBs and provide a simple and practical method for designing new flexible electrode materials.  相似文献   
8.
《Ceramics International》2021,47(23):32710-32719
The formation of micro-cracks in Ni-rich LiNi0.8Co0.1Mn0.1O2 (NCM811) cathode particles is an extremely important factor affecting the electrochemical characteristics after long-term cycling. Generally, cracks can be divided into intergranular crack and intracrystalline crack according to their positions. Coating has been confirmed as a highly effective strategy to relieve intergranular cracks. However, the intracrystalline cracks of primary-like particles have rarely been studied. In this work, ethoxy functional polysiloxane (EPS) was directly coated on the surface of original NCM811 by tetraethyl orthosilicate (TEOS) hydrolytic polycondensation method without any additives. Then, the microstructure, micromorphology, surface state and electrochemical properties were investigated in detail by XRD, SEM, TEM, CV and EIS. The results displayed that the micro-cracks of primary-like particles were effectively suppressed under appropriate EPS coating. Accordingly, excellent capacity retention of 95.6% (100 cycles, 1C) and rate performance (144.6 mA h/g, 5C) were obtained. These improved mechanical and electrochemical properties are considered to be related to the EPS stress buffer layer, suppressed oxygen vacancies, inhibited phase transition and reduced volume change.  相似文献   
9.
Aqueous solutions of poly(vinylpyrrolidone) (PVP) of various concentrations (20, 25, and 28 wt%) were successfully spun into fibers by centrifugal spinning. The pristine PVP fibers were annealed and carbonized to produce flexible carbon fibers for use as binder-free anodes in lithium-ion batteries. These flexible carbon fibers were prepared by developing a novel three-step heat treatment to reduce the residual stresses in the pristine PVP precursor fibers, and to prevent fiber degradation during carbonization. The thermogravimetric analysis data showed that the annealed fibers yielded a residual mass percentage of 36.0% while the pristine PVP fibers suffered a higher mass loss and only retained 26.5% of original mass above 450 °C (under nitrogen). The electrochemical performance of the carbon-fiber anodes was evaluated by conducting galvanostatic charge/discharge, rate performance, and cycle voltammetry experiments. The 20, 25, and 28 wt% derived binder-free anodes delivered specific charge capacities of 205, 189, and 275 mAh g−1, respectively, after the first cycle at a current density of 100 mA g−1. The results obtained in this work indicate that a feasible pathway towards a large-scale production of carbon-fiber anodes from a 100% aqueous solution can be achieved via centrifugal spinning and subsequent heat treatment.  相似文献   
10.
目的 在保证膜层耐蚀性能的前提下,降低镁锂合金等离子电解氧化过程中的能量消耗.方法 分别使用常规NaOH-Na2SiO3电解体系与自研的NaOH-Na2SiO3-Na2B4O7-Na3C6H5O7·2H2O(柠檬酸钠)低能耗电解体系,对LA91型镁锂合金进行等离子电解氧化,并探究其放电过程.采用扫描电子显微镜(SEM)、能谱仪(EDS)、掠入射X射线衍射仪(GIXRD),表征等离子电解氧化膜层的表面形貌、元素组成、物相组成.通过电化学极化曲线、盐雾试验,测试膜层的耐蚀性.结果 使用低能耗体系对镁锂合金进行等离子电解氧化处理,可将膜层的单位体积能耗降低至12.87 kJ/(dm2·μm),节约能耗约50.34%.在两个体系中制备的膜层表面均产生等离子电解氧化的特征性孔洞.低能耗体系膜层孔洞数量较少,但孔洞直径差异较大,孔隙率为14.21%;常规体系膜层孔洞大小均匀,但数量较多,孔隙率为13.93%.两个膜层表面的主要元素均为O、Mg、Na和Si.在低能耗体系中制备的膜层,主要物相为方镁石型MgO,而在常规体系中制备的膜层,物相组成较为复杂.盐雾试验和电化学极化曲线结果显示,在两种体系中进行等离子电解氧化,均能提升镁锂合金的耐蚀性.低能耗等离子氧化处理后,镁锂合金的腐蚀电流密度降低约3个数量级,腐蚀速率降低约2个数量级,自腐蚀电位正移0.261 V,有效地提升了镁锂合金的耐蚀性,并且耐蚀性的提升程度要优于常规体系.结论 使用低能耗体系电解液进行等离子电解氧化,能够形成孔洞特征不同于常规体系的等离子电解氧化膜层.与常规体系下制备的膜层相比,其厚度、孔隙率并无较大差异,但能够在节约较多能耗的情况下制备出耐蚀性能更好的等离子电解氧化膜层.  相似文献   
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