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91.
为减少多硫化锂(LIPs) “穿梭效应” 及锂枝晶对锂硫电池的影响,采用刮涂法制备中空碳材料修饰隔膜。接触角测试表明修饰隔膜对 LIPs具有更强的吸引力, 其对 LIPs “穿梭” 的有效抑制也可以通过渗透性实验进一步得到印证。在隔膜的正极对称电池测试中, 电流响应显示中空碳材料的催化使 LIPs快速转化为Li2S。通过隔膜的负极对称电池测试发现修饰隔膜呈现出更稳定的电压-时间曲线。为证明隔膜修饰对锂硫电池性能改进的效果, 分别采用聚丙烯(PP)隔膜、单面改性和双面改性的 PP隔膜组装成纽扣电池并进行电化学测试, 其中电极材料的硫负载量为 1.8~2.0 mg·cm-2。GITT(恒电流间歇滴定法)测试和锂离子扩散系数计算表明, 改性隔膜的离子传输更快且阻抗较小。通过分析第 1、5、10、50及 100次的充放电循环阻抗谱图发现, 中空碳材料的多通道能够为锂离子的传输提供更多的通道, 因此能够使锂离子具有更加稳定的扩散行为。在电流密度为 0.2 C时, 由双面改性隔膜组装的锂硫电池在首次充放电时有 1 035 mAh·g-1的可逆比容量, 700圈后仍有 500 mAh·g-1的高比容量,并在高硫负载时表现出 500 mAh·g-1的可逆比容量。双面修饰隔膜赋予了锂硫电池优异的电化学性能, 这是由于中空碳材料的修饰加速了 LIPs的转化和吸附, 有效缓解了 LIPs的穿梭效应, 且对锂枝晶有很好的抑制作用, 提高了锂硫电池的安全性。 相似文献
92.
The kinetics of the nucleation and growth of PbO2 during the potentiostatic oxidation of PbSO4 in a lead anodic film was studied using linear sweep voltammetry, potential-step and ac impedance tracing methods. The film investigated is the partially reduced anodic PbO2 film formed by polarizing a lead electrode in 4.5 M H2SO4 solution first at 1.3 V vs. Hg|HgSO4 for 20 min and then at 0.9 V for 5 min. The nucleation and growth process begins some time after the potential step and is completed within 60 s. The pre- and post-nucleation and growth processes correspond to the growth of the anodic film formed by the oxidation of the lead substrate. The mathematical equations representing the current-time and capacitance-time transients are derived taking the background oxidation current into account. The experimental results are well fitted by these equations. The process obeys the laws of two-dimensional instantaneous nucleation and growth. 相似文献
93.
LiNi0.3Co0.7O2的结构及其锂电池行为的研究 总被引:4,自引:0,他引:4
章福平 《高等学校化学学报》1995,16(5):770-774
利用XRD、XPS、CV等方法研究了LiNi0.3Co0.7O2的结构及其锂电池行为。结果表明:LiNi0.3Co0.7O2具有六方晶系空间群结构,其晶胞参数a=0.2826nm,c=1.4130nm;其表面存在Li2O;Li+在其中的化学扩散系数为1~7×10-8cm2·s-1;其锂电池在4.30~3.00V间放电容量可达120~140mA·h·g-1,放电机理为Li+在其中进行两步嵌入反应。 相似文献
94.
Sri R. Narayan Archith Nirmalchandar Advaith Murali Bo Yang Lena Hoober-Burkhardt Sankarganesh Krishnamoorthy G.K. Surya Prakash 《Current Opinion in Electrochemistry》2019
The battery industry is seeking solutions for large-scale energy storage that are affordable, durable, and safe. Aqueous redox flow batteries (RFBs) have the inherent properties to meet these requirements. While much has been learned over the past decade on the properties of redox materials, the focus of next-generation systems must be primarily on lowering redox material cost and increasing durability. In this context, in addition to inexpensive materials such as iron salts, redox couples based on small organic molecules have shown significant promise. A considerable level of understanding has been gained on the factors affecting the durability of aqueous RFB systems, specifically relating to molecular stability and crossover. New molecular classes, substituent strategies, and cell configurations have been identified to enhance the durability of systems in the future. Next-generation systems will also need to focus on designing molecules for achieving high energy efficiency and power density as well. Furthermore, the application of computational methods for screening of chemical stability could accelerate discovery of new molecular architectures. 相似文献
95.
96.
97.
L. Sánchez J. L. Tirado C. Pérez Vicente J. C. Jumas 《Journal of Solid State Electrochemistry》1998,2(5):328-333
Lithium and sodium have been topotactically inserted in the lattice of TaFe1.25Te3 by electrochemical procedures. The existence of electronically unequivalent sites occupied by tellurium atoms conditions
a two-step insertion process. In each step, the alkali metal ions occupy empty sites in the structure which are coordinated
by tellurium atoms of a different set of sites. The␣thermodynamic and kinetic parameters of Li
x
TaFe1.25Te3 and Na
x
TaFe1.25Te3 have been determined and compared with other inserted binary and ternary chalcogenides. The values of the free energy of
intercalation are less negative than those previously reported for TaTe2 and close to those found for the misfit layer compound (PbS)1.13TaS2. The values of alkali metal ion diffusivity are closer to those reported for the binary telluride, due to the similarities
in the atoms exposed to the interlayer space.
Received: 14 October 1997 / Accepted: 14 November 1997 相似文献
98.
固态电池发展至今,许多比能量高、贮存性能好的新型电池产品不断涌向市场,而目前广泛用于正极材料的大多数物质是层状化合物[1],如聚乙炔,聚苯胺等化合物,它们贮存能量的方式主要是通过插入化学反应来实现,本工作将合成一种高分子材料——2.5-二巯基-1,3... 相似文献
99.
锂离子二次电池碳负极材料的改性 总被引:5,自引:1,他引:5
作为锂离子二次电池的碳负极材料,其改性方面的研究内容主要有:引入非金属元素,引入金属元素,处理表面及其它方面。纺入的非金属元素有硼,硅,氮,磷和硫。引入的金属元素有钾,铝,镓和钒,镍,钴,铜,铁等过渡金属元素。表面处理的方法包括氧化,形成表面层等。 相似文献
100.
Flexible Na-ion storage cathodes are still very few due to the challenge in achieving both reliable mechanical flexibility and excellent electrochemical performances.Herein,a new type of flexible Na_3(VOPO_4)_2F cathode with nanocubes tightly assembled on carbon cloth is fabricated by a facile solvothe rmal method for the first time.The cathode is able to exhibit superior rate capability and stable cycling performa nce up to 1000 cycles,due to the surface-assembling of crystalline nanocubes on carbon fibers.In addition,it shows good mechanical flexibility,nearly no capacity decay is observed after continuous bending of 500 times.With this novel cathode and a directly-grown Na_2Ti_2O_5 anode,a fully binde r-free Na-ion battery is assembled.It can deliver a high wo rking voltage and increased gravimetric energy/power densities(maximum values:220.2 Wh/kg;5674,7 W/kg),and can power a LED indicator at bending angles fro m 0° to 180°. 相似文献