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   22368篇
  免费   4582篇
  国内免费   5681篇
化学   16729篇
晶体学   730篇
力学   1336篇
综合类   494篇
数学   2984篇
物理学   10358篇
  2024年   56篇
  2023年   358篇
  2022年   840篇
  2021年   935篇
  2020年   1011篇
  2019年   1013篇
  2018年   893篇
  2017年   1077篇
  2016年   1053篇
  2015年   1268篇
  2014年   1575篇
  2013年   2014篇
  2012年   2120篇
  2011年   2218篇
  2010年   1823篇
  2009年   1760篇
  2008年   1980篇
  2007年   1678篇
  2006年   1552篇
  2005年   1300篇
  2004年   998篇
  2003年   759篇
  2002年   667篇
  2001年   656篇
  2000年   662篇
  1999年   428篇
  1998年   242篇
  1997年   191篇
  1996年   208篇
  1995年   154篇
  1994年   137篇
  1993年   148篇
  1992年   117篇
  1991年   114篇
  1990年   81篇
  1989年   102篇
  1988年   65篇
  1987年   54篇
  1986年   57篇
  1985年   49篇
  1984年   39篇
  1983年   42篇
  1982年   36篇
  1981年   18篇
  1980年   21篇
  1979年   14篇
  1978年   9篇
  1977年   7篇
  1957年   5篇
  1936年   5篇
排序方式: 共有10000条查询结果,搜索用时 125 毫秒
991.
JPC – Journal of Planar Chromatography – Modern TLC - Brazilin, a constituent of the Chinese medicine heartwood, exhibits pronounced anti-tumor effects. To date, brazilin quantification...  相似文献   
992.
胡灿  梅宏成  郭洪玲  孙振文  刘占芳  朱军 《色谱》2021,39(4):376-383
炸药的深度比对与溯源对于爆炸案事件的侦破具有重大意义,以不同地域来源的原料或不同生产工艺生产的炸药,其组成元素的稳定同位素比值具有差异,因而稳定同位素比值可作为炸药深度比对与溯源的重要指标。稳定同位素比值质谱法(IRMS)作为一种高精度的稳定同位素比值测量手段,已逐渐发展成熟,与元素分析仪、气相色谱仪、液相色谱仪等仪器联用,在食品安全、环境保护、法庭科学等领域应用广泛。IRMS在炸药比对与溯源上亦发挥了重要作用,自1975年IRMS被应用于区分不同国家生产的三硝基甲苯(TNT)以来,IRMS已成功用于多种炸药的分析。但目前尚未见有文献系统地总结常见炸药的稳定同位素比值分析研究进展。该文介绍了稳定同位素比值分析的相关原理、仪器组成及特点,分别总结了硝酸铵、黑火药、TNT、太恩、黑索金等常见炸药的稳定同位素比值分析方法,汇总了文献报道的不同国家生产的硝酸铵、黑火药、TNT等炸药的稳定同位素比值。文章就不同炸药的稳定同位素比值差异、炸药生产、存储过程中相关因素对同位素比值的影响,爆炸前后稳定同位素比值的变化情况等内容进行了分析。本文还指出了目前炸药的稳定同位素比值分析研究中存在的问题,对可能的解决办法进行了讨论,对未来的发展方向提出了建议。  相似文献   
993.
Photoelectrochemical(PEC) technology is considered to be a promising approach for solar-driven hydrogen production with zero emissions. Bismuth vanadate(BiVO_4) is a kind of photocatalytic material with strong photoactivity in the visible light region and appropriate band gap for PEC water splitting.However, the solar-to-hydrogen efficiency(STH) of BiVO_4 is far away from the 10% target needed for practical application due to its poor charge separation ability. Therefore, this review attempts to summarize the strategies for improving the photocurrent density and especially hydrogen production of BiVO_4 materials through PEC techniques in the last three years, such as doping nonmetal and metal elements, depositing noble metals, constructing heterojunctions, coupling with carbon and metalorganic framework(MOF) materials to further enhance the PEC performance of BiVO_4 photoanode. This review aims to serve as a general guideline to fabricate highly efficient BiVO_4-based materials for PEC water splitting.  相似文献   
994.
Metal organic frameworks (MOFs) derived carbonaceous materials have a wide range of applications in the fields of energy storage, catalysis, adsorption and separation, etc. Especially, zeolitic imidazolate framework-8 (ZIF-8) is an excellent candidate to synthesize porous carbon due to the large surface area and high nitrogen content. However, the dominated microporous structure of ZIF-8-derived carbon significantly hinders ionic mass transfer, limiting the improvement of performance. Herein, MOF-derived mesoporous carbon was prepared using ZIF-8 as carbon precursor and cheap sodium silicate (Na2SiO3) as activator. The introduction of Na2SiO3 created rich mesoporous structure and increased specific surface area, as well as the effects of pyrolysis temperature and Na2SiO3 dosage on performance was also investigated. The obtained ZIF-derived porous carbon exhibits good electrochemical performance with specific capacitance of 263 F/g at 1 A/g and excellent cycle life (96.07% after 10,000 GCD cycles) in supercapacitor. The use of cheap Na2SiO3 activator provides a new orientation for the preparation of MOF-derived carbons with rich pores, high surface area, and facilitates the large-scale application of MOF-derived carbons.  相似文献   
995.
A facile tandem route has been developed for constructing quinazolinones from various aminobenzamides and in-situ generated aldehydes. Visible light was found to play a dual role: first oxidizes the alcohol to the aldehyde and then facilitates its cyclization with o-substituted aniline. Furthermore, alcohols are perfect alternatives to aldehydes because they are greener, more available, more economical, more stable, and less toxic than aldehydes. The first reaction step continuously provides material for the second step, which effectively reduces loss through volatilization, oxidation, and polymerization of the aldehyde, while avoiding its toxicity. A variety of quinazolinones can be prepared in the presence of visible light without any additional photocatalyst. The developed synthesis protocol proceeds with the merits of mild conditions, broad substrate scope, operational simplicity, and high atom efficiency, with an eco-energy source under metal-free, photocatalyst-free, and ambient conditions.  相似文献   
996.
997.
Guoqiang Liu  Lei Wen  Yue Li  Yulong Kou 《Ionics》2015,21(4):1011-1016
The pure phase P2-Na2/3Ni1/3Mn2/3O2 was synthesized by a solid reaction process. The optimum calcination temperature was 850 °C. The as-prepared product delivered a capacity of 158 mAh g?1 in the voltage range of 2–4.5 V, and there was a phase transition from P2 to O2 at about 4.2 V in the charge process. The P2 phase exhibited excellent intercalation behavior of Na ions. The reversible capacity is about 88.5 mAh g?1 at 0.1 C in the voltage range of 2–4 V at room temperature. At an elevated temperature of 55 °C, it could remain as an excellent capacity retention at low current rates. The P2-Na2/3Ni1/3Mn2/3O2 is a potential cathode material for sodium-ion batteries.  相似文献   
998.
999.
1000.
Xiao  Jin  Yuan  Hongchun  Chen  Lei  Xiong  Chao  Liu  Wei 《Ionics》2015,21(4):1193-1199
Ionics - A novel cobalt-free perovskite La0.6Ba0.4Fe0.8Ni0.2O3 − δ (LBFN) powder was synthesized using a combustion method. The phase composition, electrical conductivity, thermal...  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