全文获取类型
收费全文 | 2928篇 |
免费 | 222篇 |
国内免费 | 78篇 |
专业分类
化学 | 1179篇 |
晶体学 | 5篇 |
力学 | 67篇 |
综合类 | 28篇 |
数学 | 1314篇 |
物理学 | 635篇 |
出版年
2024年 | 2篇 |
2023年 | 32篇 |
2022年 | 44篇 |
2021年 | 73篇 |
2020年 | 112篇 |
2019年 | 85篇 |
2018年 | 55篇 |
2017年 | 62篇 |
2016年 | 95篇 |
2015年 | 98篇 |
2014年 | 86篇 |
2013年 | 135篇 |
2012年 | 116篇 |
2011年 | 305篇 |
2010年 | 256篇 |
2009年 | 366篇 |
2008年 | 298篇 |
2007年 | 255篇 |
2006年 | 214篇 |
2005年 | 109篇 |
2004年 | 77篇 |
2003年 | 81篇 |
2002年 | 43篇 |
2001年 | 38篇 |
2000年 | 20篇 |
1999年 | 23篇 |
1998年 | 17篇 |
1997年 | 18篇 |
1996年 | 13篇 |
1995年 | 14篇 |
1994年 | 4篇 |
1993年 | 12篇 |
1992年 | 4篇 |
1991年 | 3篇 |
1990年 | 9篇 |
1989年 | 2篇 |
1988年 | 2篇 |
1987年 | 4篇 |
1986年 | 12篇 |
1985年 | 4篇 |
1984年 | 4篇 |
1983年 | 2篇 |
1981年 | 2篇 |
1979年 | 2篇 |
1977年 | 2篇 |
1972年 | 3篇 |
1971年 | 3篇 |
1970年 | 5篇 |
1967年 | 1篇 |
1966年 | 1篇 |
排序方式: 共有3228条查询结果,搜索用时 93 毫秒
51.
Defect Chemistry of Singly and Doubly Doped Ceria: Correlation between Ion Transport and Energetics 下载免费PDF全文
Dr. Salih Buyukkilic Prof. Sangtae Kim Prof. Alexandra Navrotsky 《Angewandte Chemie (International ed. in English)》2014,53(36):9517-9521
Earlier studies have shown a strong correlation between the enthalpy of formation, ΔHf,ox, and the ionic conductivity, σi, near room temperature in doped ceria systems, which are promising solid electrolytes for intermediate‐temperature solid oxide fuel cells (IT‐SOFCs). The present work demonstrates that this correlation holds at the operating temperature of IT‐SOFCs, 600–700 °C. Solid solutions of Ce1?xNdxO2?0.5x, Ce1?xSmxO2?0.5x, and Ce1?xSm0.5xNd0.5xO2?0.5x are studied. The ΔHf,ox at 702 °C is determined by considering the excess heat content between 25 and 702 °C combined with the value of ΔHf,ox at 25 °C. Both σi and ΔHf,ox show maxima at x=0.15 and 0.20 for the singly and doubly doped ceria, respectively, suggesting that the number of mobile oxygen vacancies in these solid solutions reaches a maximum near those compositions. An increase in temperature results in a shift of the maximum in both ΔHf,ox and σi towards higher concentrations. This shift results from a gradual increase in dissociation of the defect associates. 相似文献
52.
《中国化学会会志》2017,64(6):574-588
This review is aimed at the current research progression of a unique class of Pt(II ) metal complexes bearing at least one azolate‐containing bidentate chelate. The azole fragment can link to a neutral heteroaromatic entity or another azole and form bidentate chelates, such as monoanionic 3‐pyridyl‐1H ‐pyrazole and derivatives, dianionic 3,3′‐bi‐1H ‐pyrazole, 3,3′‐(1‐methylethylidene)‐bis‐1H ‐pyrazole, and their analogs. These azole‐containing chelates readily react with a variety of Pt(II) reagents to afford the corresponding bis‐bidentate Pt(II) complexes. Most of them were highly emissive in solution, doped polymer matrix, thin film, and even as crystal or powder, due to the high ligand field strength exerted by these chelates and their high propensity in forming the singular square‐planar architecture and intermolecular aggregates with substantially strengthened Pt⋯Pt interaction, according to their structural design. Therefore, they hold bright prospects in academic research and future optoelectronic applications such as organic light‐emitting diodes. 相似文献
53.
Stephen E. Fosdick Kyle N. Knust Karen Scida Prof. Richard M. Crooks 《Angewandte Chemie (International ed. in English)》2013,52(40):10438-10456
A bipolar electrode (BPE) is an electrically conductive material that promotes electrochemical reactions at its extremities (poles) even in the absence of a direct ohmic contact. More specifically, when sufficient voltage is applied to an electrolyte solution in which a BPE is immersed, the potential difference between the BPE and the solution drives oxidation and reduction reactions. Because no direct electrical connection is required to activate redox reactions, large arrays of electrodes can be controlled with just a single DC power supply or even a battery. The wireless aspect of BPEs also makes it possible to electrosynthesize and screen novel materials for a wide variety of applications. Finally, bipolar electrochemistry enables mobile electrodes, dubbed microswimmers, that are able to move freely in solution. 相似文献
54.
Alexandre Zagdoun Dr. Aaron J. Rossini Dr. Matthew P. Conley Wolfram R. Grüning Martin Schwarzwälder Dr. Moreno Lelli Dr. W. Trent Franks Prof. Dr. Hartmut Oschkinat Prof. Dr. Christophe Copéret Prof. Dr. Lyndon Emsley Dr. Anne Lesage 《Angewandte Chemie (International ed. in English)》2013,52(4):1222-1225
55.
Dr. Jun‐ichi Matsuo Prof. Dr. Masahiro Murakami 《Angewandte Chemie (International ed. in English)》2013,52(35):9109-9118
A directed cross‐aldol reaction of silyl enol ethers with carbonyl compounds, such as aldehydes and ketones, promoted by a Lewis acid, a reaction which is now widely known as the Mukaiyama aldol reaction. It was first reported in 1973, and this year marks the 40th anniversary. The directed cross‐aldol reactions mediated by boron enolates and tin(II) enolates also emerged from the Mukaiyama laboratory. These directed cross‐aldol reactions have become invaluable tools for the construction of stereochemically complex molecules from two carbonyl compounds. This Minireview provides a succinct historical overview of their discoveries and the early stages of their development. 相似文献
56.
Dr. Claudia Kolbeck Dr. Alexey Deyko Dr. Takashi Matsuda Florian T. U. Kohler Prof. Dr. Peter Wasserscheid Dr. Florian Maier Prof. Dr. Hans-Peter Steinrück 《Chemphyschem》2013,14(16):3726-3730
We present the first systematic study of the influence of temperature on the degree of surface enrichment of 1-alkyl-3-methylimidazolium-based ionic liquids (ILs). Using angle-resolved X-ray photoelectron spectroscopy, we demonstrate that the degree of surface enrichment strongly decreases with increasing temperature for all the studied ILs. For ILs with the same cation, but different anions, [C8C1Im]Br, [C8C1Im][TfO] and [C8C1Im][Tf2N], no significant differences of the temperature-induced partial loss of surface enrichment are found. Measurements for [C4C1Im][TfO], [C8C1Im][TfO] and [C18C1Im][TfO] indicate a small effect of the chain length. For [C18C1Im][TfO], a continuous decrease of alkyl surface enrichment is found with increasing temperature, with no abrupt changes at the phase-transition temperature from the smectic A to the isotropic phase, indicating that the surface enrichment is not affected by this phase transition. 相似文献
57.
以乙二胺四乙酸为配位剂采用水热法制备了棒状LiFePO4/C材料。采用X射线衍射、扫描电镜、透射电镜、循环伏安、交流阻抗和恒电流充放电测试等对材料进行表征。结果表明:乙二胺四乙酸对材料的形貌和电性能均有很大影响。通过加入乙二胺四乙酸, 材料的形貌由不规则的颗粒变为棒状的颗粒且颗粒的厚度由140~200 nm减少至40~90 nm, 材料的表面包覆约3.5 nm的均匀碳层, 且该材料极化较小且界面阻抗较低。0.1C放电比容量为167 mAh·g-1(接近理论容量170 mAh·g-1)。 相似文献
58.
酒石酸铅锆的制备、表征及其燃烧催化作用 总被引:1,自引:0,他引:1
以酒石酸、硝酸氧锆和硝酸铅为原料,合成出了双金属盐酒石酸铅锆,采用有机元素分析、X射线荧光光谱和FTIR对其进行了表征。在程序升温条件下,利用TG/DTG、DSC、固相原位反应池/FTIR联用技术,研究了酒石酸铅锆的热行为和热分解机理,描述了酒石酸铅锆的热分解过程,分析得出其最终分解产物为ZrO2、PbO和C。利用螺压工艺制备了含酒石酸铅锆的推进剂样品,研究了酒石酸铅锆对双基系推进剂燃烧性能的影响,分析了其燃烧催化作用。结果表明,酒石酸铅锆对双基系推进剂的燃烧具有良好的催化作用,是一种高效的燃烧催化剂;酒石酸铅锆热分解的最终产物PbO是催化燃烧的主要活性物质,推进剂燃烧过程中形成了氧化铅-铅循环催化体系,而锆和碳则起辅助催化的作用。 相似文献
59.
60.