全文获取类型
收费全文 | 16525篇 |
免费 | 3497篇 |
国内免费 | 5563篇 |
专业分类
化学 | 12523篇 |
晶体学 | 514篇 |
力学 | 1312篇 |
综合类 | 725篇 |
数学 | 2165篇 |
物理学 | 8346篇 |
出版年
2024年 | 32篇 |
2023年 | 184篇 |
2022年 | 555篇 |
2021年 | 520篇 |
2020年 | 574篇 |
2019年 | 585篇 |
2018年 | 571篇 |
2017年 | 726篇 |
2016年 | 698篇 |
2015年 | 922篇 |
2014年 | 1061篇 |
2013年 | 1404篇 |
2012年 | 1369篇 |
2011年 | 1448篇 |
2010年 | 1406篇 |
2009年 | 1375篇 |
2008年 | 1561篇 |
2007年 | 1372篇 |
2006年 | 1415篇 |
2005年 | 1244篇 |
2004年 | 976篇 |
2003年 | 727篇 |
2002年 | 712篇 |
2001年 | 734篇 |
2000年 | 732篇 |
1999年 | 457篇 |
1998年 | 262篇 |
1997年 | 229篇 |
1996年 | 224篇 |
1995年 | 177篇 |
1994年 | 185篇 |
1993年 | 159篇 |
1992年 | 150篇 |
1991年 | 106篇 |
1990年 | 118篇 |
1989年 | 109篇 |
1988年 | 98篇 |
1987年 | 80篇 |
1986年 | 70篇 |
1985年 | 45篇 |
1984年 | 33篇 |
1983年 | 38篇 |
1982年 | 21篇 |
1981年 | 17篇 |
1980年 | 14篇 |
1979年 | 21篇 |
1971年 | 5篇 |
1966年 | 5篇 |
1965年 | 19篇 |
1964年 | 8篇 |
排序方式: 共有10000条查询结果,搜索用时 31 毫秒
951.
952.
953.
A novel method based on plastic processing and equipment for preparing ultra-fine metal fibers and particles is reported. With this new method, metal fibers and particles can both be produced on the same equipment and the surfaces of the fibers and particles can be protected from oxidation by the polymers or solvents during the preparation process. Metal-alloy powders with lower melt point were filled into polymer by an extruder, followed by a die-drawing process at a temperature lower than the melt temperature of the metal alloy. Metal fibers or particles were obtained after the polymer matrix was washed away. Metal alloy fibers can be obtained when a polymer that strongly interacts with metal alloy, such as a special polyvinyl alcohol with a low alcoholysis degree, is used as the polymer matrix. Metal-alloy particles can be obtained when a polymer with weak interaction with metal alloy, such as polyethylene (PE), is used as the polymer matrix. Based on the principle of this new method, it is possible to produce finer or even nano-sized metal fibers and particles with higher melting points. 相似文献
954.
955.
Yu-Yu DAI Wei-Jun LI Shuan-Ma YAN Shi-Zhao WANG Yue YU Mi OUYANG Li-Tao CHEN Cheng ZHANG 《物理化学学报》2017,33(11):2268-2276
A series of multi-branched dithienylpyrrole (SNS) monomers with rigid phenyl (PhSNS) and biphenyl rings (BPhSNS) as bridges were designed and synthesized, and were fabricated to form cross-linked polymers (pPhSNS, pBPhSNS) by electrochemical polymerization. Cyclic voltammetry (CV) results showed that PhSNS and BPhSNS exhibited similar oxidative properties except for one new higher-potential oxidative peak appearing in the curves of PhSNS. Theoretical calculations indicated that it should be attributed to the different steric configuration between the two dithienylpyrrole (SNS) units in PhSNS. One SNS unit possessed a larger twist angle (40.2°) between thiophene and pyrrole rings than the other one (21.2°), which indicated that PhSNS possessed a relatively larger energy gap (~0.4 eV) between HOMO-1 and HOMO than BPhSNS, for which HOMO and HOMO-1 levels were of almost the same energy. However, both PhSNS and BPhSNS showed similar onset oxidation potentials. The CV curves of pPhSNS and pBPhSNS showed that they presented similar oxidative properties, which enabled their corresponding electrochemical polymers to exhibit similar electrochromic properties. The UV-vis spectra of the corresponding polymers showed that both pPhSNS and pBPhSNS possessed similar optical absorption and similar multicolor switching between yellow (-0.8 V), greyish-green (0.9 V) and gray (1.1 V) colors. Besides, pPhSNS and pBPhSNS showed fast switching times of 0.57 s and 0.93 s at 1100 nm, respectively and reasonable contrasts of 46% and 31% at 1100 nm, respectively. These investigations may help understand the relationship between structural configuration and the electrochemistry/electrochromic properties for polymer electrochromic (PEC) materials research. 相似文献
956.
Jessica K. Su Zexin Jin Rui Zhang Gang Lu Peng Liu Yan Xia 《Angewandte Chemie (Weinheim an der Bergstrasse, Germany)》2019,131(49):17935-17940
Ring‐opening metathesis polymerization (ROMP) has become one of the most important living polymerizations. Cyclopropenes (CPEs) remain underexplored for ROMP. Described here is that the simple swap of 1‐methyl to 1‐phenyl on 1‐(benzoyloxymethyl)CPEs elicited strikingly different modes of reactivity, switching from living polymerization to either selective single‐addition or living alternating ROMP. The distinct reactivity stems from differences in steric repulsions at the Ru alkylidene after CPE ring opening. Possible olefin or oxygen chelation from ring‐opened CPE substituents was also observed to significantly affect the rate of propagation. These results demonstrate the versatility of CPEs as a new class of monomers for ROMP, provide mechanistic insights for designing new monomers with rare single‐addition reactivity, and generate a new functionalizable alternating copolymer scaffold with controlled molecular weight and low dispersity. 相似文献
957.
959.
研究了3种不同阳极(铜丝,镀锌铁丝和镍丝)材料对在熔盐中电化学还原CO_(2)制备的碳材料结构和形貌的影响,并探究了制备的3种碳材料,中空四面体碳(HQC,Cu作为阳极时的还原产物)、碳纳米片(CNS,Fe作为阳极时的还原产物)和海绵状多孔碳(SPC,Ni作为阳极时的还原产物),对2电子氧还原反应(2e;ORR)的电催化性能。研究表明,使用镀锌铁丝作为阳极材料制备的CNS由大量的碳纳米片构成,且该纳米片上具有丰富的孔洞结构以及较大的I_(D)/I_(C)(Raman光谱中D峰与G峰的强度之比,其比值反映材料的缺陷程度)值(0.996)。与HQC和SPC相比,CNS表现出最高的2e;ORR电催化活性和H_(2)O_(2)选择性(接近90%)。CNS的高活性和高选择性归因于其高的I_(D)/I_(C)值和高C—O/C=O比值,说明结构缺陷和C—O/C=O官能团对CNS催化性能至关重要。此外,CNS还具有非常优异的电催化稳定性,在长达14 h的恒电压电化学催化测试后,环电流几乎无衰减。这种以CO_(2)为碳源合成可用于电催化合成过氧化氢(H_(2)O_(2))的碳材料的方法,不仅可以作为缓解温室效应的潜在选项,也为CO_(2)衍生碳的实际应用提供了新的思路。 相似文献
960.
QI Yuxue LI Tingting HU Yajie XIANG Jiahong SHAO Wenqian CHEN Wenhua MU Xueqin LIU Suli CHEN Changyun YU Min MU Shichun 《高等学校化学研究》2022,38(5):1282-1286
Constructing atomically dispersed active sites with densely exposed and dispersed double metal-Sx catalytic sites for favorable OER catalytic activity remains rare and challenging. Herein, we design and construct a Fe1Sx@Co3S4 electrocatalyst with Fe single atoms epitaxially confined in Co3S4 nanosheets for catalyzing the sluggish alkaline oxygen evolution reaction(OER). Consequently, in ultralow concentration alkaline solutions(0.1 mol/L KOH), such a catalyst is highly active and robust for OER with low overpotentials of 300 and 333 mV at current densities of 10 and 30 mA/cm2, respectively, accompanying long-term stability without significant degradation even for 350 h. In addition, Fe1Sx@Co3S4 shows a turnover frequency(TOF) value of 0.18 s−1, nearly three times that of Co3S4(0.07 s−1), suggesting the higher atomic utilization of Fe single atoms. Mössbauer and in-situ Raman spectra confirm that the OER activity of Fe1Sx@Co3S4 origins from a thin catalytic layer of Co(Fe)OOH that interacts with trace-level Fe species in the electrolyte, creating dynamically stable active sites. Combined with experimental characterizations, it suggests that the most active S-coordinated dual-metal site configurations are 2S-bridged (Fe-Co)S4, in which Co-S and Fe-S moieties are shared with two S atoms, which can strongly regulate the adsorption energy of reaction intermediates, accelerating the OER reaction kinetics. 相似文献