全文获取类型
收费全文 | 13910篇 |
免费 | 2672篇 |
国内免费 | 3019篇 |
专业分类
化学 | 11027篇 |
晶体学 | 343篇 |
力学 | 716篇 |
综合类 | 294篇 |
数学 | 1650篇 |
物理学 | 5571篇 |
出版年
2024年 | 31篇 |
2023年 | 250篇 |
2022年 | 435篇 |
2021年 | 594篇 |
2020年 | 612篇 |
2019年 | 617篇 |
2018年 | 533篇 |
2017年 | 593篇 |
2016年 | 711篇 |
2015年 | 773篇 |
2014年 | 964篇 |
2013年 | 1186篇 |
2012年 | 1299篇 |
2011年 | 1324篇 |
2010年 | 1085篇 |
2009年 | 1067篇 |
2008年 | 1177篇 |
2007年 | 1002篇 |
2006年 | 962篇 |
2005年 | 777篇 |
2004年 | 580篇 |
2003年 | 461篇 |
2002年 | 437篇 |
2001年 | 404篇 |
2000年 | 328篇 |
1999年 | 264篇 |
1998年 | 205篇 |
1997年 | 149篇 |
1996年 | 131篇 |
1995年 | 105篇 |
1994年 | 102篇 |
1993年 | 83篇 |
1992年 | 71篇 |
1991年 | 57篇 |
1990年 | 62篇 |
1989年 | 37篇 |
1988年 | 31篇 |
1987年 | 16篇 |
1986年 | 22篇 |
1985年 | 15篇 |
1984年 | 4篇 |
1983年 | 8篇 |
1982年 | 8篇 |
1981年 | 3篇 |
1980年 | 6篇 |
1979年 | 7篇 |
1976年 | 2篇 |
1975年 | 2篇 |
1974年 | 2篇 |
1959年 | 2篇 |
排序方式: 共有10000条查询结果,搜索用时 578 毫秒
11.
Dr. Feifan Wang Jie Tian Dr. Mengzhu Li Dr. Weizhen Li Dr. Lifang Chen Xiaozhi Liu Dr. Jian Li Aidaer Muhetaer Prof. Dr. Qi Li Prof. Dr. Yuan Wang Prof. Dr. Lin Gu Prof. Dr. Ding Ma Prof. Dr. Dongsheng Xu 《Angewandte Chemie (Weinheim an der Bergstrasse, Germany)》2020,132(21):8280-8286
Fully utilizing solar energy for catalysis requires the integration of conversion mechanisms and therefore delicate design of catalyst structures and active species. Herein, a MOF crystal engineering method was developed to controllably synthesize a copper–ceria catalyst with well-dispersed photoactive Cu-[O]-Ce species. Using the preferential oxidation of CO as a model reaction, the catalyst showed remarkably efficient and stable photoactivated catalysis, which found practical application in feed gas treatment for fuel cell gas supply. The coexistence of photochemistry and thermochemistry effects contributes to the high efficiency. Our results demonstrate a catalyst design approach with atomic or molecular precision and a combinatorial photoactivation strategy for solar energy conversion. 相似文献
12.
A new asymmetric Salamo‐based ligand H2L was synthesized using 3‐tert‐butyl‐salicylaldehyde and 6‐methoxy‐2‐[O‐(1‐ethyloxyamide)]‐oxime‐1‐phenol. By adjusting the ratio of the ligand H2L and Cu (II), Co (II), and Ni (II) ions, mononuclear, dinuclear, and trinuclear transition metal (II) complexes, [Cu(L)], [{Co(L)}2], and [{Ni(L)(CH3COO)(CH3CH2OH)}2Ni] with the ligand H2L possessing completely different coordination modes were obtained, respectively. The optical spectra of ligand H2L and its Cu (II), Co (II) and Ni (II) complexes were investigated. The Cu (II) complex is a mononuclear structure, and the Cu (II) atom is tetracoordinated to form a planar quadrilateral structure. The Co (II) complex is dinuclear, and the two Co (II) atoms are pentacoordinated and have coordination geometries of distorted triangular bipyramid. The Ni (II) complex is a trinuclear structure, and the terminal and central Ni (II) atoms are all hexacoordinated, forming distorted octahedral geometries. Furthermore, optical properties including UV–Vis, IR, and fluorescence of the Cu (II), Co (II), and Ni (II) complexes were investigated. Finally, the antibacterial activities of the Cu (II), Co (II), and Ni (II) complexes were explored. According to the experimental results, the inhibitory effect was found to be enhanced with increasing concentrations of the Cu (II), Co (II), and Ni (II) complexes. 相似文献
13.
Dongping Wang Jie Dong Wenjing Fan Prof. Dr. Xiang-Ai Yuan Prof. Dr. Jian Han Prof. Dr. Jin Xie 《Angewandte Chemie (Weinheim an der Bergstrasse, Germany)》2020,132(22):8508-8512
An unprecedented Mn(I)-catalyzed selective hydroarylation and hydroalkenylation of unsaturated amides with commercially available organic boronic acids is reported. Alkenyl boronic acids have been successfully employed for the first time in Mn(I)-catalyzed carbon–carbon bond formation. A wide array of β-alkenylated amide products can be obtained in moderate to good yields, which offers practical access to five- and six-membered lactams. This protocol has predictable regio- and chemoselectivity, excellent functional group compatibility and ease of operation in air, representing a significant step-forward towards manganese-catalyzed C−C coupling. 相似文献
14.
Guangrui Chen Yuxing Yan Dr. Jie Wang Prof. Yong Sik Ok Guiyuan Zhong Prof. Bu Yuan Guan Prof. Yusuke Yamauchi 《Angewandte Chemie (Weinheim an der Bergstrasse, Germany)》2020,132(44):19831-19836
Mesoporous core–shell nanostructures with controllable ultra-large open channels in their nanoshells are of great interest. However, soft template-directed cooperative assembly to mesoporous nanoshells with highly accessible pores larger than 30 nm, or even above 50 nm into macroporous range, remains a significant challenge. Herein we report a general approach for precisely tailored coating of hierarchically macro-/mesoporous polymer and carbon shells, possessing highly accessible radial channels with extremely wide pore size distribution from ca. 10 nm to ca. 200 nm, on diverse functional materials. This strategy creates opportunities to tailor the interfacial assembly of irregular mesostructured nanounits on core materials and generate various core–shell nanomaterials with controllable pore architectures. The obtained Fe,N-doped macro-/mesoporous carbon nanoshells show enhanced electrochemical performance for the oxygen reduction reaction in alkaline condition. 相似文献
15.
The sunset diagram of λφ4 theory is evaluated numerically in cutoff scheme and a nonzero finite term(in accordance with dimensional regularization (DR) result) is found in contrast to published calculations. This findingdramatically reduces the critical couplings for symmetry breaking in the two-loop effective potential discussed in ourprevious work. 相似文献
16.
用波导产生倍频波时,如果倍频波进入辐射模区,仍然有相匹配问题。契伦可夫辐射式倍频不是自动地实现相匹配的。相匹配要求导波基波模式场,倍频传输场(自由波),倍频触发场,以及经多次反射透射后的辐射场的迭加形成的总辐射场处于同步的相匹配状态。根据这个相匹配的分析,提出波导契伦可夫相匹配的特有的方法,那就是对波导的模色散进行设计,并指出非对称波导的特有优点,是改变一个边界上的反射相变,即选择不同色散的线性材料作包层,由此可得到相匹配的高效契伦可夫倍频辐射。 相似文献
17.
本文提出了一个含有两类相互作用的准自旋模型,讨论了模型Hamilton量在SU(2)×SU(2)基中的严格解、基态相变和波函数的K结构,并用此模型探讨了HF近似的有效性。 相似文献
18.
采用基于第一性原理的密度泛函理论研究了四角晶相二氧化铪(t-HfO2)体相及 其(001)表面的原子几何与电子结构.理论计算结果表明,t-HfO2(001)表面不会 产生重构现象.与体相电子结构相比, t-HfO2(001)表面态密度明显高于体相态 密度.其次,表面原子的态密度更靠近费米能级(EF),价带往低能量处移动,并 有表面态产生.计算结果表明了t-HfO2表面禁带宽度明显低于体相的禁带宽度. t-HfO2(001)的表面态产生以及表面禁带宽度减小是由于Hf原子与O原子的配位 数减少,表面原子周围的环境发生变化而引起的.
关键词:
密度泛函理论
2(001)')" href="#">t-HfO2(001)
表面电子结构 相似文献
19.
本文介绍一种用牛顿力学研究赛跑运动的物理模型,给出两种情形下跑步时间的最优化结果.这一结果与优秀运动员的实际比赛成绩很好地相符. 相似文献
20.
在保持非负定性不变的前提下,本文对矩阵每一元素容许多大的扰动作了进一步的研究, 将本文的结论和C.R.Johnson提出的部分正定阵的正定完备化进行比较,容易发现对已知的正定矩阵求扰动,本文的结论比用C.R.Johnson的正定完备化计算扰动形式上更简单,同时也给出了不同于C.R.Johnson的部分正定阵的正定完备化表示的另外一个公式,推出了这些正定完备化矩阵应具有的若干性质. 相似文献