全文获取类型
收费全文 | 109篇 |
免费 | 6篇 |
国内免费 | 1篇 |
专业分类
化学 | 84篇 |
力学 | 2篇 |
数学 | 12篇 |
物理学 | 18篇 |
出版年
2023年 | 1篇 |
2022年 | 2篇 |
2021年 | 1篇 |
2020年 | 1篇 |
2019年 | 5篇 |
2018年 | 3篇 |
2017年 | 1篇 |
2016年 | 2篇 |
2015年 | 3篇 |
2014年 | 4篇 |
2013年 | 7篇 |
2012年 | 9篇 |
2011年 | 10篇 |
2010年 | 3篇 |
2009年 | 5篇 |
2008年 | 8篇 |
2007年 | 8篇 |
2006年 | 8篇 |
2005年 | 7篇 |
2004年 | 6篇 |
2003年 | 7篇 |
2002年 | 7篇 |
2001年 | 2篇 |
2000年 | 1篇 |
1999年 | 1篇 |
1998年 | 1篇 |
1990年 | 1篇 |
1987年 | 1篇 |
1985年 | 1篇 |
排序方式: 共有116条查询结果,搜索用时 15 毫秒
21.
Guowen Peng S.J. Sibener George C. Schatz Manos Mavrikakis 《Surface science》2012,606(13-14):1050-1055
Hydrogen (H) in the subsurface of transition-metal surfaces exhibits unique reactivity for heterogeneously catalyzed hydrogenation reactions. Here, we explore the potential of subsurface H for hydrogenating carbon dioxide (CO2) on Ni(110). The energetics of surface and subsurface H reacting with surface CO2 to form formate, carboxyl, and formic acid on Ni(110) is systematically studied using self-consistent, spin-polarized, periodic density functional theory (DFT-GGA-PW91) calculations. We show that on Ni(110), CO2 can be hydrogenated to formate by surface H. However, further hydrogenation of formate to formic acid by surface H is hindered by a larger activation energy barrier. The relative energetics of hydrogenation barriers is reversed for the carboxyl-mediated route to formic acid. We suggest that the energetics of subsurface H emerging to the surface is suitable for providing the extra energy needed to overcome the barrier to formate hydrogenation. CO2 hydrogenation to formic acid could take place on Ni(110) when subsurface H is available to react with CO2. Additional electronic-structure based dynamic calculations would be needed to elucidate the detailed reaction paths for these transformations. 相似文献
22.
Anyfantakis M Loppinet B Fytas G Mantzaridis C Pispas S Butt HJ 《Optics letters》2012,37(13):2487-2489
We report on the versatile effect of weak red laser light impinging on diblock copolymer [poly(isoprene-b-styrene)] dispersions in two selective solvents for each block. In the strongly scattering but transparent micellar solutions in hexane (a good solvent for polyisoprene), higher refractive index copolymer-rich fibers were formed. In the turbid dispersions of the same copolymer in ethyl acetate (a good solvent for polystyrene), the effect of self-induced transparency was observed. A two-step patterning mechanism caused the generation of a transparent microchannel, increasing light transmission. The analogy between the current effect and that observed in homopolymer polyisoprene solutions in different solvents is discussed toward an understanding of the unanticipated light-soft-matter interaction. 相似文献
23.
Dr. Manos Anyfantakis Dr. Venkata S. R. Jampani Dr. Rijeesh Kizhakidathazhath Prof. Bernard P. Binks Prof. Jan P. F. Lagerwall 《Angewandte Chemie (Weinheim an der Bergstrasse, Germany)》2020,132(43):19422-19429
Liquid marbles have potential to serve as mini-reactors for fabricating new materials, but this has been exploited little and mostly for conventional chemical reactions. Here, we uncover the unparalleled capability of liquid marbles to act as platforms for controlling the self-assembly of a bio-derived polymer, hydroxypropyl cellulose, into a cholesteric liquid crystalline phase showing structural coloration by Bragg reflection. By adjusting the cholesteric pitch via quantitative water extraction, we achieve liquid marbles that we can tailor for structural color anywhere in the visible range. Liquid marbles respond with color change that can be detected by eye, to changes in temperature, exposure to toxic chemicals and mechanical deformation. Our concept demonstrates the advantages of using liquid marbles as a miniature platform for controlling the liquid crystal self-assembly of bio-derived polymers, and their exploitation to fabricate sustainable, responsive soft photonic objects. 相似文献
24.
Yulin Huang Evangelia Perperi George Manos David J. Cole-Hamilton 《Journal of molecular catalysis. A, Chemical》2004,210(1-2):17-21
During fluorous biphasic hydroformylation 1-octene is transferred from the fluorous into the organic product phase and then from the product layer back to the fluorous layer again, due to the immiscibility of nonanal with PFMCH. The effect of the temperature and the total amount of octene on the above behaviour were also studied. 相似文献
25.
Dr. Tibor Szilvási Nanqi Bao Dr. Karthik Nayani Huaizhe Yu Dr. Prabin Rai Prof. Dr. Robert J. Twieg Prof. Dr. Manos Mavrikakis Prof. Dr. Nicholas L. Abbott 《Angewandte Chemie (International ed. in English)》2018,57(31):9665-9669
Surface‐supported liquid crystals (LCs) that exhibit orientational and thus optical responses upon exposure to ppb concentrations of Cl2 gas are reported. Computations identified Mn cations as candidate surface binding sites that undergo redox‐triggered changes in the strength of binding to nitrogen‐based LCs upon exposure to Cl2 gas. Guided by these predictions, μm‐thick films of nitrile‐ or pyridine‐containing LCs were prepared on surfaces decorated with Mn2+ binding sites as perchlorate salts. Following exposure to Cl2, formation of Mn4+ (in the form of MnO2 microparticles) was confirmed and an accompanying change in the orientation and optical appearance of the supported LC films was measured. In unoptimized systems, the LC orientational transitions provided the sensitivity and response times needed for monitoring human exposure to Cl2 gas. The response was also selective to Cl2 over other oxidizing agents such as air or NO2 and other chemical targets such as organophosphonates. 相似文献
26.
Strachan JD Bitter M Ramsey AT Zarnstorff MC Arunasalam V Bell MG Bretz NL Budny R Bush CE Davis SL Dylla HF Efthimion PC Fonck RJ Fredrickson E Furth HP Goldston RJ Grisham LR Grek B Hawryluk RJ Heidbrink WW Hendel HW Hill KW Hsuan H Jaehnig KP Jassby DL Jobes F Johnson DW Johnson LC Kaita R Kampershroer J Knize RJ Kozub T LeBlanc B Levinton F La Marche PH Manos DM Mansfield DK McGuire K McNeill DH Meade DM Medley SS Morris W Mueller D Nieschmidt EB Owens DK Park H Schivell J Schilling G 《Physical review letters》1987,58(10):1004-1007
27.
28.
Turn‐On Luminescence Sensing and Real‐Time Detection of Traces of Water in Organic Solvents by a Flexible Metal–Organic Framework 下载免费PDF全文
Antigoni Douvali Dr. Athanassios C. Tsipis Dr. Svetlana V. Eliseeva Prof. Stéphane Petoud Dr. Giannis S. Papaefstathiou Dr. Christos D. Malliakas Dr. Ioannis Papadas Dr. Gerasimos S. Armatas Dr. Irene Margiolaki Prof. Mercouri G. Kanatzidis Dr. Theodore Lazarides Dr. Manolis J. Manos 《Angewandte Chemie (International ed. in English)》2015,54(5):1651-1656
The development of efficient sensors for the determination of the water content in organic solvents is highly desirable for a number of chemical industries. Presented herein is a Mg2+ metal–organic framework (MOF), which exhibits the remarkable capability to rapidly detect traces of water (0.05–5 % v/v) in various organic solvents through an unusual turn‐on luminescence sensing mechanism. The extraordinary sensitivity and fast response of this MOF for water, and its reusability make it one of the most powerful water sensors known. 相似文献
29.
30.