全文获取类型
收费全文 | 12851篇 |
免费 | 2420篇 |
国内免费 | 2001篇 |
专业分类
化学 | 9039篇 |
晶体学 | 216篇 |
力学 | 904篇 |
综合类 | 149篇 |
数学 | 1486篇 |
物理学 | 5478篇 |
出版年
2024年 | 24篇 |
2023年 | 282篇 |
2022年 | 463篇 |
2021年 | 545篇 |
2020年 | 534篇 |
2019年 | 542篇 |
2018年 | 452篇 |
2017年 | 435篇 |
2016年 | 646篇 |
2015年 | 625篇 |
2014年 | 790篇 |
2013年 | 949篇 |
2012年 | 1183篇 |
2011年 | 1167篇 |
2010年 | 958篇 |
2009年 | 867篇 |
2008年 | 878篇 |
2007年 | 776篇 |
2006年 | 781篇 |
2005年 | 668篇 |
2004年 | 438篇 |
2003年 | 356篇 |
2002年 | 360篇 |
2001年 | 294篇 |
2000年 | 280篇 |
1999年 | 253篇 |
1998年 | 203篇 |
1997年 | 212篇 |
1996年 | 189篇 |
1995年 | 175篇 |
1994年 | 152篇 |
1993年 | 120篇 |
1992年 | 97篇 |
1991年 | 90篇 |
1990年 | 86篇 |
1989年 | 79篇 |
1988年 | 63篇 |
1987年 | 36篇 |
1986年 | 53篇 |
1985年 | 37篇 |
1984年 | 20篇 |
1983年 | 15篇 |
1982年 | 17篇 |
1981年 | 8篇 |
1980年 | 10篇 |
1975年 | 7篇 |
1973年 | 4篇 |
1972年 | 7篇 |
1965年 | 6篇 |
1964年 | 6篇 |
排序方式: 共有10000条查询结果,搜索用时 15 毫秒
991.
Efficient top-emitting white organic light emitting device with an extremely stable chromaticity and viewing-angle
下载免费PDF全文
![点击此处可从《中国物理 B》网站下载免费的PDF全文](/ch/ext_images/free.gif)
In this paper,we report on the fabrication of a top-emitting electrophosphorescent p-i-n white organic lightemitting diode on the basis of a low-reflectivity Sm/Ag semi-transparent cathode together with a thickness-optimized ZnS out-coupling layer.With a 24-nm out-coupling layer,the reflectivity of the cathode is reduced to 8% at 492 nm and the mean reflectivity is 24% in the visible area.By introducing an efficient electron blocking layer tris(1phenylpyrazolato,N,C2 ’)iridium(III)(Ir(ppz) 3) to confine the exciton recombination area,the current efficiency and the colour stability of the device are effectively improved.A white emission with the Ir(ppz) 3 layer exhibits a maximum current efficiency of 9.8 cd/A at 8 V,and the Commission Internationale de L’Eclairage(CIE) chromaticity coordinates are almost constant during a large voltage change of 6 V-11 V.There is almost no viewing angular dependence in the spectrum when the viewing angle is no more than 45,with a CIE x,y coordinate variation of only(±0.0025,±0.0008).Even at a large viewing angle(75),the CIE x,y coordinate change is as small as(±0.0087,±0.0013). 相似文献
992.
近些年发展起来的近场动力学方法对于模拟复杂的断裂破坏问题具有显著优势.然而,计算精度不高一直是影响该方法进一步发展的瓶颈问题之一.区域积分不精确和键缺失导致的边界效应是降低该方法计算精度的两个主要原因.针对一维键型近场动力学模型,本文通过修正微模量提高区域积分的精度,通过理性构建固定边界和力边界虚拟键改善边界效应,建立... 相似文献
993.
Lu Xiao Bo Li Fan Xiao Cong Fu Liang Wei Yanfeng Dang Xiu-Qin Dong Chun-Jiang Wang 《Chemical science》2022,13(17):4801
The development of enantioselective annulation reactions using readily available substrates for the construction of structurally and stereochemically diverse heterocycles is a compelling topic in diversity-oriented synthesis. Herein, we report efficient catalytic asymmetric formal 1,3-dipolar (3 + 4) cycloadditions of azomethine ylides with 4-indolyl allylic carbonates for the construction of azepino[3,4,5-cd]-indoles fused with a challenging seven-membered N-heterocycle, a frequently occurring tricyclic indole scaffold in bioactive compounds and pharmaceuticals. Through cooperative Cu/Ir-catalyzed asymmetric allylic alkylation followed by intramolecular Friedel–Crafts reaction, an array of azepino[3,4,5-cd]-indoles were obtained in good yields with excellent diastereo-/enantioselective control. More importantly, the full stereodivergence of this transformation was established via synergistic catalysis followed by acid-promoted epimerization, and up to eight stereoisomers of the cycloadducts bearing three stereogenic centers could be predictably achieved from the same set of starting materials for the first time. Quantum mechanical computations established a plausible mechanism for the synergistic Cu/Ir catalysis to stereodivergently introduce two vicinal stereocenters whose stereochemical information is remotely delivered across the fused azepine ring to control the third chiral center. Epimerization of the last center involves protonation-enabled reversal of the thermodynamically controlled relative configuration.A stereodivergent synthesis of azepino[3,4,5-cd]-indoles bearing three stereogenic centers was established via synergistic dual-metal catalysis followed by acid-promoted epimerization, and up to all eight stereoisomers could be predictably achieved. 相似文献
994.
Temperature effect on dissipative holographicscreening-photovoltaic solitons in a biased dissipative system
下载免费PDF全文
![点击此处可从《中国物理 B》网站下载免费的PDF全文](/ch/ext_images/free.gif)
In a biased dissipative photovoltaic-photorefractive system, this paper investigates the temperature effect on the evolution and the self-deflection of the dissipative holographic screening-photovoltaic (DHSP) solitons. The results reveal that, the evolution and the self-deflection of the bright and dark DHSP solitons are influenced by the system temperature. At a given temperature, for a stable DHSP soliton originally formed in the dissipative system, it attempts to evolve into another DHSP soliton when the temperature change is appropriately small, whereas it will become unstable or break down if the temperature departure is large enough. Moreover, the self-deflection degree of the solitary beam centre increases as temperature rises in some range, while it is decided by the system parameters and is slight under small-signal condition. The system temperature can be adjusted to change the formation and the self-deflection of the solitary beam in order to gain certain optical ends. In a word, the system temperature plays a role for the DHSP solitons in the dissipative system. 相似文献
995.
本文利用红外光解离光谱研究了第三族金属氧化物离子对二氧化碳分子的转化机制. 研究表明,对于[ScO(CO2)n]+体系,在n≤4时,形成了溶剂化结构;在n=5时,形成了碳酸盐结构,实现了二氧化碳的转化. 对于[YO(CO2)n]+体系,需要4个二氧化碳分子就可以实现二氧化碳的转化. 而在[YO(CO2)n]+体系中,只发现了溶剂化结构,没有观察到碳酸盐结构. 理论计算表明,[YO(CO2)n]+体系拥有最小的溶剂化结构向碳酸盐结构转化能垒,[LaO(CO2)n]+体系拥有最大的溶剂化结构向碳酸盐结构转化能垒. 本文从分子水平揭示了不同金属氧化物离子对二氧化碳分子转化的影响规律. 相似文献
996.
997.
998.
As one of the most attractive non-radiative power transfer mechanisms without cables,efficient magnetic resonance wireless power transfer(WPT)in the near field has been extensively developed in recent years,and promoted a variety of practical applications,such as mobile phones,medical implant devices and electric vehicles.However,the physical mechanism behind some key limitations of the resonance WPT,such as frequency splitting and size-dependent efficiency,is not very clear under the widely used circuit model.Here,we review the recently developed efficient and stable resonance WPT based on non-Hermitian physics,which starts from a completely different avenue(utilizing loss and gain)to introduce novel functionalities to the resonance WPT.From the perspective of non-Hermitian photonics,the coherent and incoherent effects compete and coexist in the WPT system,and the weak stable of energy transfer mainly comes from the broken phase associated with the phase transition of parity-time symmetry.Based on this basic physical framework,some optimization schemes are proposed,including using nonlinear effect,using bound states in the continuum,or resorting to the system with high-order parity-time symmetry.Moreover,the combination of non-Hermitian physics and topological photonics in multi-coil system also provides a versatile platform for long-range robust WPT with topological protection.Therefore,the non-Hermitian physics can not only exactly predict the main results of current WPT systems,but also provide new ways to solve the difficulties of previous designs. 相似文献
999.
本文系统研究了臭氧修饰对(001)主导晶面锐钛矿型TiO2光催化剂降解甲苯性能的影响. 利用自行搭建的光催化VOCs降解装置对催化剂光降解甲苯的性能进行了测试. 通过多种表征手段,结合原位DRIFTS和DFT计算研究了臭氧表面修饰及甲苯吸附和降解机理. 结果表明,用臭氧进行表面修饰可以显著提高(001)主导晶面TiO2光催化降解甲苯的性能. (001)晶面上丰富的5c-Ti不饱和配位是臭氧分子的吸附位点,其解离后形成的Ti-O键与H2O分子结合,在表面生成大量孤立的Ti5c-OH. Ti5c-OH 是甲苯分子的吸附位,它的形成显著提高了对甲苯分子的吸附能力. 在光照下Ti5c-OH与光生空穴结合能形成·OH自由基. 通过臭氧解离产生的O2也可以与光生电子结合形成超氧自由基. 这些具有强氧化性活性自由基的形成促进了对气相甲苯的光催化降解速率. 相似文献
1000.
A silicon-on-insulator (SOI) high performance lateral double-diffusion metal oxide semiconductor (LDMOS) on a compound buried layer (CBL) with a step buried oxide (SBO CBL SOI) is proposed.The step buried oxide locates holes in the top interface of the upper buried oxide (UBO) layer.Furthermore,holes with high density are collected in the interface between the polysilicon layer and the lower buried oxide (LBO) layer.Consequently,the electric fields in both the thin LBO and the thick UBO are enhanced by these holes,leading to an improved breakdown voltage.The breakdown voltage of the SBO CBL SOI LDMOS increases to 847 V from the 477 V of a conventional SOI with the same thicknesses of SOI layer and the buried oxide layer.Moreover,SBO CBL SOI can also reduce the self-heating effect. 相似文献