全文获取类型
收费全文 | 969篇 |
免费 | 218篇 |
国内免费 | 282篇 |
专业分类
化学 | 1015篇 |
晶体学 | 57篇 |
力学 | 144篇 |
综合类 | 9篇 |
数学 | 41篇 |
物理学 | 203篇 |
出版年
2024年 | 2篇 |
2023年 | 13篇 |
2022年 | 42篇 |
2021年 | 51篇 |
2020年 | 79篇 |
2019年 | 48篇 |
2018年 | 50篇 |
2017年 | 42篇 |
2016年 | 64篇 |
2015年 | 82篇 |
2014年 | 71篇 |
2013年 | 112篇 |
2012年 | 54篇 |
2011年 | 62篇 |
2010年 | 45篇 |
2009年 | 57篇 |
2008年 | 69篇 |
2007年 | 67篇 |
2006年 | 55篇 |
2005年 | 59篇 |
2004年 | 49篇 |
2003年 | 76篇 |
2002年 | 46篇 |
2001年 | 28篇 |
2000年 | 23篇 |
1999年 | 18篇 |
1998年 | 20篇 |
1997年 | 26篇 |
1996年 | 14篇 |
1995年 | 9篇 |
1994年 | 7篇 |
1993年 | 4篇 |
1992年 | 6篇 |
1991年 | 2篇 |
1990年 | 2篇 |
1989年 | 4篇 |
1988年 | 2篇 |
1987年 | 2篇 |
1986年 | 3篇 |
1985年 | 2篇 |
1982年 | 1篇 |
1957年 | 1篇 |
排序方式: 共有1469条查询结果,搜索用时 15 毫秒
71.
Liangliang Liang Wei Yan Xian Qin Xiao Peng Han Feng Yu Wang Ziyu Zhu Lingmei Liu Yu Han Qinghua Xu Junle Qu Xiaogang Liu 《Angewandte Chemie (International ed. in English)》2020,59(2):746-751
Stimulated emission depletion (STED) microscopy enables ultrastructural imaging of biological samples with high spatiotemporal resolution. STED nanoprobes based on fluorescent organosilica nanohybrids featuring sub‐2 nm size and near‐unity quantum yield are presented. The spin–orbit coupling (SOC) of heavy‐atom‐rich organic fluorophores is mitigated through a silane‐molecule‐mediated condensation/dehalogenation process, resulting in bright fluorescent organosilica nanohybrids with multiple emitters in one hybrid nanodot. When harnessed as STED nanoprobes, these fluorescent nanohybrids show intense photoluminescence, high biocompatibility, and long‐term photostability. Taking advantage of the low‐power excitation (0.5 μW), prolonged singlet‐state lifetime, and negligible depletion‐induced re‐excitation, these STED nanohybrids present high depletion efficiency (>96 %), extremely low saturation intensity (0.54 mW, ca. 0.188 MW cm?2), and ultra‐high lateral resolution (ca. λem/28). 相似文献
72.
《Journal of Saudi Chemical Society》2020,24(10):715-732
The mechanistic aspects of improved aqueous removal of methyl orange (MO) dyes using high performance novel magnetic MgAlNi barium-ferrite (MgAlNi-BaFe) ternary double layer hydroxide (LDH) nanocomposites is reported in this study. Detailed surface characterization coupled with kinetic, equilibrium, thermodynamics and regeneration studies were undertaken under different operational conditions of temperature (298–318 K), initial concentration (20–100 mg/L), pH (2–6). The kinetic results show that MO sorption was mainly, associated with pseudo-second order and intra-particular diffusion process. The MO adsorption onto the MgAlNi-BaFe nanocomposites suggests a multi-layered sorption process that is endothermic and spontaneous in nature. The MO adsorption mechanism insight taken in cognizance of FTIR, XRD, pKa, zeta potential, the adsorbates surface functional groups and the adsorbate-adsorbent surface charges interactions suggest involvement of hydrogen bonding and n-π interactions, predominantly via physisorption process (ΔG° = −7.406 to −5.69 kJ/mol). The excellent adsorptive performance of the MgAlNi-BaFe adsorbents for removal of MO from water compared with other magnetic LDH nanocomposites was further elucidated via the MgAlNi-BaFe nanomaterials high rates of regeneration and superior performances for three successive desorption-adsorption cycles. This study demonstrates the high potentials of employing MgAlNi-BaFe nanomaterials for removal of dyes from water and wastewater. 相似文献
73.
Sebastian Grieger Beata M. Szydowska Vaishnavi J. Rao Eva Steinmann Marcus Dodds Zahra Gholamvand Georg S. Duesberg Jana Zaumseil Claudia Backes 《Angewandte Chemie (International ed. in English)》2020,59(33):13785-13792
In recent years, various functionalization strategies for transition‐metal dichalcogenides have been explored to tailor the properties of materials and to provide anchor points for the fabrication of hybrid structures. Herein, new insights into the role of the surfactant in functionalization reactions are described. Using the spontaneous reaction of WS2 with chloroauric acid as a model reaction, the regioselective formation of gold nanoparticles on WS2 is shown to be heavily dependent on the surfactant employed. A simple model is developed to explain the role of the chosen surfactant in this heterogeneous functionalization reaction. The surfactant coverage is identified as the crucial element that governs the dominant reaction pathway and therefore can severely alter the reaction outcome. This study shows the general importance of the surfactant choice and how detrimental or beneficial a certain surfactant can be to the desired functionalization. 相似文献
74.
75.
二维WS2是一种层状过渡金属硫化物,因其具有特殊的层状结构、可调带隙及稳定的物理化学性质而备受关注。结合玻尔兹曼输运方程(BTE)和密度泛函理论(DFT),利用第一性原理研究了单层WS2声子的输运特性,分析了声子的谐性效应和非谐性效应对WS2晶格热导率的影响机理,计算了其声子的临界平均自由程,提出通过调整阻断频率的方法来调控WS2的晶格热导率。研究结果表明:单层WS2在300 K时的本征晶格热导率为149.12 W/(m·K),且随温度的升高而降低;从各声子支对总热导率的贡献来看,声学声子支起主要作用,特别是纵向声学(longitudinal acoustic, LA)声子支对单层WS2热导率的贡献百分比最大(44.28%);单层WS2声学声子支和光学声子支之间的较大带隙(声光学声子支之间无散射)导致其具有较高的晶格热导率。本文研究可为基于单层WS2纳米电子器件的设计和改进提供借鉴和理论指导。 相似文献
76.
77.
Z. Mikulová P. Čuba J. Balabánová T. Rojka F. Kovanda K. Jirátová 《Chemical Papers》2007,61(2):103-109
The effect of hydrothermal treatment on properties (crystallinity, porous structure, reducibility, acidity, basicity, and
catalytic activity and selectivity in toluene and ethanol total oxidation) of Ni—Al layered double hydroxide precursors and
related mixed oxides was examined. The hydrothermal treatment increased considerably both the content of crystalline phase
and LDH crystallite size. On the other hand, only a slight effect of the precursor hydrothermal treatment on crystallinity
of the related Ni—Al mixed oxides obtained by calcination at 450°C was observed. The reducibility of NiO particles appeared
to be hindered considerably compared to the reducibility of pure NiO. Catalytic activity of the Ni—Al mixed oxides prepared
from the precursors hydrothermally treated for a short time (4 h) was the highest. The highest amount of acetaldehyde formed
during the total oxidation of ethanol, i.e. the worst selectivity was found for the calcined Ni—Al LDH without hydrothermal treatment.
Presented at the 33rd International Conference of the Slovak Society of Chemical Engineering, Tatranské Matliare, 22–26 May
2006. 相似文献
78.
采用水热合成法,在Ti网上原位生长多孔层状Co_3O_4纳米片,并优化了电荷转移电阻。通过X射线衍射(XRD)、扫描电子显微镜(SEM)和透射电子显微镜(TEM)对产物的结构、形貌进行表征,及对电极的电化学性能进行测试。结果表明,材料是由排列良好的微米矩形二维薄片组成,且具有均匀的孔隙分布。这种独特的微纳米结构的超级电容器电极材料降低了电极的电荷转移电阻,增强了活性物质的结构稳定性,从而提高了电极的电化学性能,在电流密度为100 mA·g-1时,电极循环1 000次后,电容保持率为91.8%,电荷转移电阻(Rct)为0.29Ω。这些显著的超电容性能归因于合理的二维层状结构在柔性基底钛网上的生长及柔性Co_3O_4/Ti电极活性材料的高利用率。 相似文献
79.
Xiaokai Ding Dong Luo Jiaxiang Cui Huixian Xie Qingqing Ren Zhan Lin 《Angewandte Chemie (International ed. in English)》2020,59(20):7778-7782
Voltage decay and capacity fading are the main challenges for the commercialization of Li‐rich Mn‐based layered oxides (LLOs). Now, a three‐in‐one surface treatment is designed via the pyrolysis of urea to improve the voltage and capacity stability of Li1.2Mn0.6Ni0.2O2 (LMNO), by which oxygen vacancies, spinel phase integration, and N‐doped carbon nanolayers are synchronously built on the surface of LMNO microspheres. Oxygen vacancies and spinel phase integration suppress irreversible O2 release and help lithium ion diffusion, while N‐doped carbon nanolayer mitigates the corrosion of electrolyte with excellent conductivity. The electrochemical performance of LMNO after the treatment improves significantly; the capacity retention rate after 500 cycles at 1 C is still as high as 89.9 % with a very small voltage fading rate of 1.09 mV cycle?1. This three‐in‐one surface treatment strategy can suppress the voltage decay and capacity fading of LLOs. 相似文献
80.
通过酚醛树酯包覆和碳热反应在富锂正极材料表面原位构建碳和尖晶石双壳保护结构, 对这种核壳结构的正极材料进行了结构和形貌表征, 并研究了其电化学性能. 研究发现, 尖晶石相为材料提供了三维锂离子迁移通道, 碳包覆层显著提高了正极材料的电子电导率, 两种效应的共同作用极大降低了材料的电化学阻抗, 提升了材料的放电比容量, 这种多壳层结构正极材料还具有优异的倍率性能, 在5C倍率下放电比容量可达到135.1 mA·h/g. 相似文献