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81.
George W. Bright 《School science and mathematics》1984,84(3):208-219
82.
Alavi-Harati A Alexopoulos T Arenton M Barbosa RF Barker AR Barrio M Bellantoni L Bellavance A Blucher E Bock GJ Bown C Bright S Cheu E Coleman R Corcoran MD Cox B Erwin AR Escobar CO Ford R Glazov A Golossanov A Gomes RA Gouffon P Graham J Hamm J Hanagaki K Hsiung YB Huang H Jejer V Jensen DA Kessler R Kobrak HG Kotera K LaDue J Lai N Ledovskoy A McBride PL Monnier E Nelson KS Nguyen H Ping H Prasad V Qi XR Quinn B Ramberg EJ Ray RE Ronquest M Santos E Senyo K Shanahan P Shields J Slater W 《Physical review letters》2004,93(2):021805
The KTeV/E799 experiment at Fermilab has searched for the rare kaon decay K(L)-->pi(0)e(+)e(-). This mode is expected to have a significant CP violating component. The measurement of its branching ratio could support the standard model or could indicate the existence of new physics. This Letter reports new results from the 1999-2000 data set. One event is observed with an expected background at 0.99+/-0.35 events. We set a limit on the branching ratio of 3.5x10(-10) at the 90% confidence level. Combining with the previous result based on the data set taken in 1997 yields the final KTeV result: BR(K(L)-->pi(0)e(+)e(-))<2.8x10(-10) at 90% C.L. 相似文献
83.
Alavi-Harati A Albuquerque IF Alexopoulos T Arenton M Arisaka K Averitte S Barker AR Bellantoni L Bellavance A Belz J Ben-David R Bergman DR Blucher E Bock GJ Bown C Bright S Cheu E Childress S Coleman R Corcoran MD Corti G Cox B Crisler MB Erwin AR Ford R Glazov A 《Physical review letters》2000,84(23):5279-5282
We report on a search for the decay K(L)-->pi(0)&mgr;(+)&mgr;(-) carried out as a part of the KTeV experiment at Fermilab. This decay is expected to have a significant CP violating contribution and a direct measurement will either support the Cabibbo-Kobayashi-Maskawa mechanism for CP violation or point to new physics. Two events were observed in the 1997 data with an expected background of 0.87+/-0.15 events, and we set an upper limit B(K(L)-->pi(0)&mgr;(+)&mgr;(-))<3. 8x10(-10) at the 90% confidence level. 相似文献
84.
Kausar Ali Khawaja Dr. Yeasin Khan Dr. Yu Jung Park Jin Hee Lee Dr. Ju Hwan Kang Kiwoong Kim Yeonjin Yi Prof. Jung Hwa Seo Prof. Bright Walker 《化学:亚洲杂志》2021,16(20):3151-3161
Despite the exceptional efficiency of perovskite solar cells (PSCs), further improvements can be made to bring their power conversion efficiencies (PCE) closer to the Shockley-Queisser limit, while the development of cost-effective strategies to produce high-performance devices are needed for them to reach their potential as a widespread energy source. In this context, there is a need to improve existing charge transport layers (CTLs) or introduce new CTLs. In this contribution, we introduced a new polyelectrolyte (lithium poly(styrene sulfonate (PSS))) (Li:PSS) polyelectrolyte as an HTL in inverted PSCs, where Li+ can act as a counter ion for the PSS backbone. The negative charge on the PSS backbone can stabilize the presence of p-type carriers and p-doping at the anode. Simple Li:PSS performed poorly due to poor surface coverage and voids existence in perovskite film as well as low conductivity. PEDOT:PSS was added to increase the conductivity to the simple Li:PSS solution before its use which also resulted in lower performance. Furthermore, a bilayer of PEDOT:PSS and Li:PSS was employed, which outperformed simple PEDOT:PSS due to high quality of perovskite film with large grain size also the large electron injection barrier (ϕe) impeded back diffusion of electrons towards anode. As a consequence, devices employing PEDOT:PSS / Li:PSS bilayers gave the highest PCE of 18.64%. 相似文献
85.
Biologically-based recognition elements (e.g., antibodies, aptamers, enzymes, etc.) are used as the recognition element within a wide variety of assays and sensor systems. There are, however, compelling reasons for researchers to develop inexpensive, robust, and reusable alternatives for these expensive and unstable biorecognition elements. This review summarizes recent research efforts on the development of molecularly templated (sometimes called molecularly imprinted) organic and inorganic polymers as possible replacements for expensive/labile biorecognition elements. The review begins with a briefing on biosensing and the pertinent issues and limitations. The focus then swings toward molecularly templating within organic and inorganic (xerogels) polymers to create materials with analyte binding characteristics akin to a biorecognition element. The review then describes several recent developments wherein analyte recognition and an analyte-dependent transduction methodology are simultaneously incorporated directly within the templated materials. The review ends by outlining the current state-of-the-art and the remaining issues and impediments. 相似文献
86.
Page PM McCarty TA Baker GA Baker SN Bright FV 《Langmuir : the ACS journal of surfaces and colloids》2007,23(2):843-849
We compare how (i) four ionic liquids (ILs) (1-butyl-3-methylimidazolium tetrafluoroborate ([C4mim][BF4]), 1-butyl-3-methylimidazolium bis(trifluoromethylsulfonyl)imide ([C4mim][Tf2N]), 1-butyl-1-methylpyrrolidinium bis(trifluoromethylsulfonyl)imide ([C4mpy][Tf2N]), and trihexyltetradecylphosphonium bis(trifluoromethylsulfonyl)imide ([P(C6)3C14][Tf2N])) and (ii) two conventional molecular liquids (methanol and 1-octanol) solvate/wet luminescent organic moieties that are covalently attached to the surface of silica controlled pore glass (CPG). A series of aminopropyl CPG particles that have been covalently tagged with the solvatochromic fluorescent probe group dansyl were used in this study. The results demonstrate that ILs solvate/wet the silica surface differently in comparison to molecular liquids (MLs). Specifically, when comparing ILs and MLs that appear to solvate the free probe, dansylpropylsulfonamide (DPSA), equally in solution, we find that ILs do not solvate/wet the silica surfaces as well as the corresponding MLs. The cation component in these ILs is the significant factor in how the ILs solvate/wet silica surfaces. Solvation/wetting of surface-bound species at a silica surface depends on the cation size. Chlorosilane end-capping of the surface silanol and amine residues attenuates the cation's affects. 相似文献
87.
Roggemann Michael C. Bright Victor M. Welsh Byron M. Cowan William D. Lee Max 《Optical and Quantum Electronics》1999,31(5-7):451-468
Controlling optical aberrations is one of the enduring problems in optics. Recent advances in adaptive optics for astronomical applications have shown the promise of adaptive optics technology for controlling aberrations. Micro-electro-mechanical deformable mirrors (MEM-DMs) offer an alternative to conventional adaptive optics which, due to the inexpensive nature of MEM-DM technology, will enable a wide range of commercial and scientific applications for optical wave front control. In this paper we describe MEM-DMs, present results of modelling the performance of an MEM-DM for optical aberration control, and present results of experiments to verify that MEM-DMs can control optical aberrations. 相似文献
88.
Ido Bright 《Journal of Differential Equations》2011,250(3):1267-1284
We introduce an averaging framework, where the solution of a time-varying equation with a small amplitude is approximated by the solution of a slowly-varying auxiliary system, generated by convolving the original equation with a kernel function. The effect of the convolution is smoothing of the equation, thus, making it more amenable to numerical computations. We present tight results on the approximation error for general classes of vector fields and kernels. 相似文献
89.
Duc T. Duong Bright Walker Jason Lin Chunki Kim John Love Balaji Purushothaman John E. Anthony Thuc‐Quyen Nguyen 《Journal of Polymer Science.Polymer Physics》2012,50(20):1405-1413
Although the fabrication procedures for bulk heterojunction (BHJ) solar cells are routinely optimized to accommodate new organic materials, the influence of solvent properties and cohesive forces on the film‐forming process and the self‐assembly of donor and acceptor molecules on the nanoscale are poorly understood. In this study, we measure the solubility of a variety of organic semiconductors in a range of solvents and calculate cohesive forces including dispersion forces, dipole interactions, and hydrogen bonding via Hansen Solubility Parameters (HSPs). HSPs were calculated by measuring the solubilities of various organic semiconductors in 27 solvents and the influence of solvent identity on film morphology of different BHJ mixtures was explored via atomic force microscopy (AFM). The possibility of correlations between HSPs and film morphology was considered; however, it is apparent that the HSP values alone do not play a critical role in determining the morphology of the films of conjugated polymers and molecules. This collection of solubility data constitutes the first of its type for organic semiconducting materials, and may act as a useful reference for the organic semiconductor community to aid in the understanding and selection of solvents for donor–acceptor BHJ mixtures. © 2012 Wiley Periodicals, Inc. J Polym Sci Part B: Polym Phys, 2012 相似文献
90.
Schulz MN Landström J Bright K Hubbard RE 《Journal of computer-aided molecular design》2011,25(7):611-620
Cheminformatics protocols have been developed and assessed that identify a small set of fragments which can represent the
compounds in a chemical library for use in fragment-based ligand discovery. Six different methods have been implemented and
tested on Input Libraries of compounds from three suppliers. The resulting Fragment Sets have been characterised on the basis
of computed physico-chemical properties and their similarity to the Input Libraries. A method that iteratively identifies
fragments with the maximum number of similar compounds in the Input Library (Nearest Neighbours) produces the most diverse
library. This approach could increase the success of experimental ligand discovery projects, by providing fragments that can
be progressed rapidly to larger compounds through access to available similar compounds (known as SAR by Catalog). 相似文献