首页 | 本学科首页   官方微博 | 高级检索  
文章检索
  按 检索   检索词:      
出版年份:   被引次数:   他引次数: 提示:输入*表示无穷大
  收费全文   9420篇
  免费   1410篇
  国内免费   1776篇
化学   4792篇
晶体学   283篇
力学   2299篇
综合类   50篇
数学   384篇
物理学   2355篇
无线电   2443篇
  2025年   71篇
  2024年   272篇
  2023年   235篇
  2022年   387篇
  2021年   469篇
  2020年   430篇
  2019年   382篇
  2018年   267篇
  2017年   361篇
  2016年   428篇
  2015年   386篇
  2014年   502篇
  2013年   564篇
  2012年   570篇
  2011年   580篇
  2010年   549篇
  2009年   644篇
  2008年   659篇
  2007年   746篇
  2006年   516篇
  2005年   501篇
  2004年   494篇
  2003年   458篇
  2002年   345篇
  2001年   279篇
  2000年   245篇
  1999年   196篇
  1998年   174篇
  1997年   154篇
  1996年   150篇
  1995年   107篇
  1994年   103篇
  1993年   66篇
  1992年   67篇
  1991年   53篇
  1990年   38篇
  1989年   27篇
  1988年   30篇
  1987年   21篇
  1986年   23篇
  1985年   9篇
  1984年   7篇
  1983年   4篇
  1982年   7篇
  1981年   7篇
  1979年   10篇
  1978年   3篇
  1974年   3篇
  1971年   2篇
  1957年   2篇
排序方式: 共有10000条查询结果,搜索用时 15 毫秒
971.
(NH4)2[Zn2(O3PCH2CH2COO)2]⋅5 H2O (BIRM-1) is a new metal phosphonate material, synthesized through a simple hydrothermal reaction between zinc nitrate and 3-phosphonopropionic acid, using urea and tetraethylammonium bromide as the reaction medium. In common with other metal–organic framework materials, BIRM-1 has a large three-dimensional porous structure providing potential access to a high internal surface area. Unlike most others, it has the advantage of containing ammonium cations within the pores and has the ability to undergo cation exchange. Additionally, BIRM-1 also exhibits a reversible dehydration behavior involving an amorphization-recrystallization cycle. The ability to undergo ion exchange and dynamic structural behavior are of interest in their own right, but also increase the range of potential applications for this material. Here the crystal structure of this new metal phosphonate and its ion exchange behavior with K+ as an exemplar are studied in detail, and its unusual structure-reviving property reported.  相似文献   
972.
    
This study presents a sensitive voltammetric determination of terbutaline (TER) on a platform based on carbon nanotubes (CNTs) and europium oxide nanoparticles (Eu2O3NPs) coated glassy carbon electrodes (GCEs). An ultrasonic bath was performed for the preparation of composite material. The material was characterized by energy dispersive X‐ray spectroscopy (EDX), X‐ray diffraction method (XRD) and scanning electron microscopy (SEM). The Eu2O3NPs/CNTs/GCE system was assessed for the oxidation of terbutaline (TER). A broad oxidation peak was appeared at 0.71 V using a bare GCE. However, the voltammetry of TER has been improved at a GCE coated with CNTs and a well‐defined anodic peak exhibited at 0.61 V. Furthermore, the nanoparticles of Eu2O3 and CNTs coated GCE has greatly improved the electrochemical behaviour of TER and a sharp peak was appeared at 0.59 V. Cyclic voltammetry at Eu2O3NPs/CNTs/GCE also reveals a high catalytic effect for the oxidation of TER with an oxidation peak that is distinctly enhanced compared to GCE and CNTs/GCE. Eu2O3 nanoparticles were utilized to enhance the surface area of GCE and then improve the sensitivity of the procedure. The response of TER was linear over a concentration range of 2.0×10?8 M ?9.5×10?6 M with an LOD of 3.7×10?9 M. Square wave voltammetric analysis of tablets by Eu2O3NPs/CNTs/GCE yielded a recovery of 99.2 % with an RSD% of 3.2. The modified electrode (EuO2NPs/CNTs/GCE) provides accuracy and precision to the analysis of samples.  相似文献   
973.
974.
    
N‐(2‐mercaptoethyl) acrylamide (MEAM) monomer was synthesized by acrylation of cysteamine and was cross‐linked with ethylene glycol dimethacrylate (EGDMA) via dispersion polymerization forming poly(N‐(2‐mercaptoethyl) acrylamide) (p(MEAM)) microgel. Then, the prepared microgels were tested for potential biomedical use, eg, antioxidant capacity and blood compatibility, cytotoxicity, apoptotic, and necrotic cell death; drug delivery properties were determined. Antioxidant studies of p(MEAM) microgels revealed a super antioxidant capability with total phenol content and trolox equivalent antioxidant capacity as 6.05 ± 1.15 mg/L gallic acid equivalency and 40.96 ± 2.40 mM trolox/g, respectively. Moreover, the blood compatibility of p(MEAM) microgels on fresh blood was resulted in lower than 1.0% hemolysis ratios for all the studied concentration range, and the blood clotting index was determined as 60.66% at 2.0 mg/mL at microgel concentration. The biocompatibility studies employing WST‐1 test on L929 fibroblast cells and DLD‐1 colon cancer cells have shown that p(MEAM) microgel was biocompatible up to 200 μg/mL concentration with the cell viability values of 84.54% and 86.15% on L929 fibroblast and DLD‐1 colon cancer cells, respectively. Using Captopril was used as model drug to test p(MEAM) microgel as drug delivery device for in vitro release studies at different pHs. Release profile of Captopril was found linear up to 5 hours with the released amounts of 9.81, 12.24, and 13.78 mg g‐1microgel at the pH 1.5, 7.4, and 9.0, respectively.  相似文献   
975.
    
This Review provides a comprehensive overview of LiNiO2 (LNO), almost 30 years after its introduction as a cathode active material. We aim to highlight the physicochemical peculiarities that make LNO a complex material in every aspect. We specifically stress the effect of the Li off‐stoichiometry (Li1?zNi1+zO2) on every property of LNO, especially the electrochemical ones. The key instability issues that plague the compound and the strategies that have been implemented so far to overcome them are discussed in detail. Finally, the open questions that remain to be addressed by the scientific community are summarized, and the research directions that seem the most promising to enable LNO to be fully exploited are elucidated.  相似文献   
976.
977.
978.
    
Metal oxides have a large storage capacity when employed as anode materials for lithium‐ion batteries (LIBs). However, they often suffer from poor capacity retention due to their low electrical conductivity and huge volume variation during the charge–discharge process. To overcome these limitations, fabrication of metal oxides/carbon hybrids with hollow structures can be expected to further improve their electrochemical properties. Herein, ZnO‐Co3O4 nanocomposites embedded in N‐doped carbon (ZnO‐Co3O4@N‐C) nanocages with hollow dodecahedral shapes have been prepared successfully by the simple carbonizing and oxidizing of metal–organic frameworks (MOFs). Benefiting from the advantages of the structural features, i.e. the conductive N‐doped carbon coating, the porous structure of the nanocages and the synergistic effects of different components, the as‐prepared ZnO‐Co3O4@N‐C not only avoids particle aggregation and nanostructure cracking but also facilitates the transport of ions and electrons. As a result, the resultant ZnO‐Co3O4@N‐C shows a discharge capacity of 2373 mAh g?1 at the first cycle and exhibits a retention capacity of 1305 mAh g?1 even after 300 cycles at 0.1 A g?1. In addition, a reversible capacity of 948 mAh g?1 is obtained at a current density of 2 A g?1, which delivers an excellent high‐rate cycle ability.  相似文献   
979.
    
Novel, potassium-deficient, layered P3-K0.45Mn0.9Mg0.1O2 is successfully prepared through a simple solid-state reaction method; its electrochemical performance as a cathode material for K-ion batteries is explored for the first time. The as-prepared K0.45Mn0.9Mg0.1O2 delivers a high reversible capacity of 108 mAh g−1 at a current density of 20 mA g−1 in the potential region from 1.5 to 4.0 V. Moreover, the cyclability is enhanced by Mg substitution. After 100 cycles, the capacity of K0.45Mn0.9Mg0.1O2 can remain at about 80.8 mAh g−1 at 20 mA g−1. It also presents an excellent rate performance of 69.8 mAh g−1 even at a high current density of 200 mA g−1. Furthermore, the potassium storage mechanism is studied by using the ex situ XRD technique. These results contribute to the development of rechargeable K-ion batteries based on earth-abundant elements.  相似文献   
980.
    
We consider here a mathematical model describing the bilateral frictional contact between a thermo‐piezoelectric body and a thermally conductive foundation. We model the behavior of the material with a linear thermo‐electro‐elastic constitutive law. The process is assumed to be quasistatic and the contact is modeled with a nonlocal version of Coulomb's dry friction law, in which the frictional heat generated in the process, is taken into account. We drive a variational formulation of the problem and establish the existence of its weak solution.  相似文献   
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号