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Hui-Ling Li De-Jiang Qi Qing-Quan Jiang Shu-Zheng Yang 《International Journal of Theoretical Physics》2006,45(12):2428-2436
An extension of the Parikh-Wilczek's semi-classical quantum tunneling method, the tunneling radiation of the charged particle from a torus-like black hole is investigated. Difference from the uncharged mass-less particle, the geodesics of the charged massive particle tunneling from the black hole is not light-like, but determined by the phase velocity. The derived result shows that the tunneling rate depends on the emitted particle's energy and electric charge, and takes the same functional form as uncharged particle. It proves also that the exact emission spectrum is not strictly pure thermal, but is consistent with the underlying unitary theory.
PACS Numbers: 04.70.Dy, 97.60.Lf, 05.30.Ch. 相似文献
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Applying Parikh-Wilzcek‘s semi-classical quantum tunneling model, we study the Hawking radiation of charged particles as tunneling from the event horizon of a cylindrically symmetric black hole in anti-de Sitter space-time.The derived result shows that the tunneling rate of charged particles is related to the change of Bekenstein-Hawking entropy and that the radiation spectrum is not strictly pure thermal after taking the black hole background dynamical and self-gravitation interaction into account, but is consistent with the underlying unitary theory. 相似文献
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Microchip capillary electrophoresis (μCE) with amperometric detection at Cu electrode benefited fast separation and direct detection of carbohydrates. The working electrode of 50-μm Cu wire attached nearly against the channel outlet—4 μm, where it benefited collecting detection current and suppressing overwhelming noise. The use of alkaline medium was essential to separating and detecting carbohydrates, which dissociated into the sensitive alcolate anions. The 10-cm serpentine chip, though lengthening the migration time, it provided better efficiency. Sucrose, cellobiose, glucose, and fructose migrated from the outlet in 400 s +2000 V. The linear calibration plots ranging from 10 to 1000 μM with regression coefficients better than 0.996 were obtained. The injection-to-injection reproducibility of 1.24% (n=7) for glucose in peak current and 0.6% for migration times were excellent. The detection limit was low, down to 2.3 μM for glucose (S/N=3) or 27.6 attomole in mass detection. 相似文献
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Fe3O4/TiO2 纳米材料靶上脱盐的基质辅助激光解析/电离质谱新方法研究 总被引:1,自引:0,他引:1
建立了一种简便、高效的靶上脱盐新方法。利用Fe3O4/TiO2磁性纳米材料对肽段的吸附作用,将其作为载体用于靶上肽段富集和脱盐。在对纳米材料使用量、浸洗条件进行优化的基础上,成功地鉴定了溶于10mol/L尿素溶液的100fmol的肌红蛋白样品,也对溶于3mol/L尿素溶液中的10fmol的肌红蛋白样品进行了成功地分析鉴定。通过对肌红蛋白样品进行预处理和质谱分析重复实验,表明该方法重现性好,且简便、高效,所需时间短,一次可同时处理多个样品,易于实现通量化,为有效地解决目前蛋白质组分析中所面临的基质辅助激光解析/离子化飞行时间质谱耐盐性差的问题提供了一种新的手段。 相似文献
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Yen YS Lin YC Huang SL Liu YH Sung HL Wang Y 《Journal of the American Chemical Society》2005,127(51):18037-18045
The cationic complex {[Ru]=C=CHCPh2CH2CH=CH2}BF4 (3a, [Ru] = (eta5-C5H5)(PPh3)2Ru) in solution transforms to {[Ru]=C=CHCH2CPh2CH=CH2}BF4 (4a) via a new metathesis process of the terminal vinyl group with the C=C of the vinylidene group which is confirmed by 13C labeling studies. This transformation is irreversible as revealed by deuteration and decomplexation studies. The cationic complex {[Ru]=C=CHCPh2CH2CMe=CH2}BF4 (3b) undergoes a cyclization process yielding 6b containing a eta2-cyclic allene ligand which is fully characterized by single-crystal X-ray diffraction analysis. Analogous complexes 4a' and 6b' ([Ru] = (eta5-C5H5)(dppe)Ru) containing dppe ligands were similarly obtained from protonation of the corresponding acetylide complexes via formation of vinylidene intermediate. Protonation of the acetylide complex containing a terminal alkynyl group [Ru]-CCCPh2CH2CCH (2c) generates the vinylidene complex {[Ru]=C=CHCPh2CH2CCH}BF4 (3c) which again undergoes an irreversible transformation to give {[Ru]=C=CHCH2CPh2CCH}BF4 (4c) possibly via a pi-coordinated alkynyl complex followed by hydrogen and metal migration. No similar transformation is observed for the analogous dppe complex 3c'. With an extra methylene group, complex {[Ru]=C=CHCPh2CH2CH2CH=CH2}BF4 (3d) and complex {[Ru]=C=CHCPh2CH2Ph}BF4 (3e) are stable. The presence of a gem-diphenylmethylene moiety at the vinylidene ligand with the appropriate terminal vinyl or alkynyl group along with the correct steric environment implements such a novel reactivity in the ruthenium vinylidene complexes. 相似文献
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反胶束法合成氧化锌微晶及其荧光特性 总被引:1,自引:0,他引:1
0引言材料的结构(微结构)、尺寸和形貌等因素对其特性及其实际应用具有重要的影响。对无机材料特别是氧化物半导体进行结构控制的研究近年来引起了人们极大的关注。氧化锌作为一种宽带隙(3.2eV)半导体材料,可广泛应用于压电材料、气体传感器、橡胶添加剂和光学器件等领域,而且还因其在室温下可产生激射现象使其成为纳米光学材料研究领域中的一大热点[1 ̄6]。目前,除了传统的固相-气相(V S)反应外,用于氧化锌微晶的制备方法主要有共沉淀法[7]、多羟基化合物水解法[8]、有机金属气相沉积法[9 ̄12]和水热法[13]等。通过选择不同的制备方法和… 相似文献