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1.
通过改装多旋翼无人机(UAV)和搭载各类载荷以及联合地基观测设备对大柴旦地区大气、环境以及气溶胶参数进行测量。利用获得的数据资料,对该地区近地层气溶胶粒子数浓度(即单位体积空气中气溶胶粒子的数目)、消光系数以及气象要素等特征进行了分析。结果表明,在大柴旦地区,近地层气溶胶粒子数浓度日变化显著,呈现双峰形态,气溶胶粒子数浓度的变化范围为75~220 cm-3,消光系数的变化范围为0.004~0.038 km-1;当风速小于6 m/s时,气溶胶粒子数浓度与风速呈负相关关系;当风速大于6 m/s时,二者呈正相关关系;相对湿度对气溶胶粒子的影响较小,这可能是由于该地区以沙尘型气溶胶为主,吸湿性较弱。本研究基于多旋翼无人机探测平台,可以有效地获得近地层精细化大气、环境结构,有助于研究人员了解该地区气溶胶的结构、变化特征以及建立气溶胶模式,同时也为气溶胶及大气环境参数探测方法提供了技术支撑及思路拓展。 相似文献
2.
In this paper, the authors consider the asymptotic synchronization of a linear dissipative system with multiple feedback dampings. They ?rst show that under the observability of a scalar equation, Kalman’s rank condition is su?cient for the uniqueness of solution to a complex system of elliptic equations with mixedobservations. The authors then establish a general theory on the asymptotic stability and the asymptotic synchronization for the corresponding evolutional system subjected to mixed dampings of various natures. Some classic models are presented to illustrate the ?eld of applications of the abstract theory. 相似文献
3.
以过渡金属为催化衬底的化学气相沉积法(Chemical Vapor Deposition,CVD)已经可以制备与机械剥离样品相媲美的石墨烯,是实现石墨烯工业应用的关键技术之一。原子尺度理论研究能够帮助我们深刻理解石墨烯生长机理,为实验现象提供合理的解释,并有可能成为将来实验设计的理论指导。本文从理论计算的角度,总结了各种金属衬底在石墨烯CVD生长过程中的各种作用与相应的机理,包括在催化碳源裂解、降低石墨烯成核密度等,催化加快石墨烯快速生长,修复石墨烯生长过程中产生的缺陷,控制外延生长石墨烯的晶格取向,以及在降温过程中石墨烯褶皱与金属表面台阶束的形成过程等。在本文最后,我们对当前石墨烯生长领域中亟需解决的理论问题进行了深入探讨与展望。 相似文献
4.
制备了混合导体膜反应器,通过电化学方法捕获CO2,并将其用于甲烷二氧化碳干重整反应中.采用XRD, SEM,TPR等技术系统研究了LaNi0.5Co0.5O3催化剂在膜反应器中对甲烷二氧化碳干重整反应的影响.结果表明:LaNi0.5Co0.5O3催化剂在甲烷干重整反应中能原位析出纳米金属Ni和Co,对反应起到了较好的催化作用,同时抑制了积碳.催化剂还具有良好的氧化还原性能,可以循环利用. 相似文献
5.
Jihua Liu Huizhu Gan Ting Li Jia Wang Guangguang Du Yang An Xiaojing Yan Cong Geng 《Biomedical chromatography : BMC》2020,34(8):e4856
Ocotillol, pseudo-ginsenoside RT5 (RT5), and pseudo-ginsenoside F11 (PF11) are ocotillol-type saponins that have the same aglycone structure but with different numbers of glucose at the C-6 position. In this study, the metabolites of ocotillol, RT5, and PF11 in rat plasma, stomach, intestine, urine, and feces after oral administration were investigated by ultra-performance liquid chromatography coupled with time-of-flight mass spectrometry. The results showed that RT5 was easily biotransformed into metabolites in vivo, whereas PF11 and RT5 were difficult to be biotransformed. Hydrogenation, dehydrogenation, dehydration, deglycosylation, deoxygenation, hydration, phosphorylation, deoxidation, glucuronidation, and reactions combining amino acid were speculated to be involved in the biotransformation of ocotillol, RT5, and PF11. Based on the structural analysis of metabolites, it was deduced that hydrogenation, dehydration, deoxidation, and reactions combining amino acid occurred on the aglycone structure, whereas deglycosylation, hydration, and phosphorylation occurred on the glycosyl chain. Further, metabolites in plasma, urine, feces, and tissues were different: First, glucuronidation products were found in urine, stomach, intestine, and feces, but not in plasma. Second, the ocotillol prototype was not identified in urine samples. Third, the RT5 prototype was found in stomach, intestine, feces, and urine, but not in plasma. 相似文献
6.
Ding Wenwen He Yongjia Lu Linnu Rao Meijuan Wang Fazhou 《Journal of Thermal Analysis and Calorimetry》2019,135(4):2009-2018
Journal of Thermal Analysis and Calorimetry - The present task is to investigate the influence of iron on the mineral composition and microstructure of the phase Q (C20A13M3S3, in the text below... 相似文献
7.
Acta Mathematicae Applicatae Sinica, English Series - This paper summarizes the parameter estimation of systems with set-valued signals, which can be classified to three catalogs: one-time... 相似文献
8.
受Peng-中心极限定理的启发,本文主要应用G-正态分布的概念,放宽Peng-中心极限定理的条件,在次线性期望下得到形式更为一般的中心极限定理.首先,将均值条件E[X_n]=ε[X_n]=0放宽为|E[X_n]|+|ε[X_n]|=O(1/n);其次,应用随机变量截断的方法,放宽随机变量的2阶矩与2+δ阶矩条件;最后,将该定理的Peng-独立性条件进行放宽,得到卷积独立随机变量的中心极限定理. 相似文献
9.
Jilloju Parameshwara Chary Persoons Leentje Kurapati Sathish Kumar Schols Dominique De Jonghe Steven Daelemans Dirk Vedula Rajeswar Rao 《Molecular diversity》2022,26(3):1357-1371
A new series of (?±)-(3-(3,5-dimethyl-1H-pyrazol-1-yl)-6-phenyl-6,7-dihydro-5H-[1,2,4]triazolo[3,4-b][1,3,4]thiadiazin-7-yl)(phenyl)methanones were efficiently synthesized starting from 4-amino-5-hydrazinyl-4H-1,2,4-triazole-3-thiol 1, acetyl acetone 2, various aromatic and heterocyclic aldehydes 3 and phenacyl bromides 4. All the newly synthesized compounds were tested for their antiviral and antitumoral activity. It was shown that subtle structural variations on the phenyl moiety allowed to tune biological properties toward antiviral or antitumoral activity. Mode-of-action studies revealed that the antitumoral activity was due to inhibition of tubulin polymerization.
Graphic abstract 相似文献10.
Ke Xu Evan T. Vickers Longshi Rao Dr. Sarah A. Lindley A'Lester C. Allen Prof. Binbin Luo Prof. Xueming Li Prof. Jin Zhong Zhang 《Chemistry (Weinheim an der Bergstrasse, Germany)》2019,25(19):5014-5021
CH3NH3PbBr3 perovskite quantum dots (PQDs) are synthesized by using four different linear alkyl phosphonic acids (PAs) in conjunction with (3-aminopropyl)triethoxysilane (APTES) as capping ligands. The resultant PQDs are characterized by means of XRD, TEM, Raman spectroscopy, FTIR spectroscopy, UV/Vis, photoluminescence (PL), time-resolved PL, and X-ray photoelectron spectroscopy (XPS). PA chain length is shown to control the PQD size (ca. 2.9–4.2 nm) and excitonic absorption band positions (λ=488–525 nm), with shorter chain lengths corresponding to smaller sizes and bluer absorptions. All samples show a high PL quantum yield (ca. 46–83 %) and high PL stability; this is indicative of a low density of band gap trap states and effective surface passivation. Stability is higher for smaller PQDs; this is attributed to better passivation due to better solubility and less steric hindrance of the shorter PA ligands. Based on the FTIR, Raman, and XPS results, it is proposed that Pb2+ and CH3NH3+ surface defects are passivated by R−PO32− or R−PO2(OH)−, whereas Br− surface defects are passivated by R−NH3+ moieties. This study establishes the combination of PA and APTES ligands as a highly effective dual passivation system for the synergistic passivation of multiple surface defects of PQDs through primarily ionic bonding. 相似文献