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61.
Pd-catalyzed annulation of aryne and aryl ketone O-acetyloxime via C–H bond activation was realized. Through the C–H bond activation/insertion/cyclization/elimination reaction sequence, phenanthridines are successfully constructed, providing an attractive strategy to approach substituted heterocycle without preactivation of starting materials. 相似文献
62.
Xiaojuan Liao Lei Guo Junxia Chang Sha Liu Meiran Xie Guosong Chen 《Macromolecular rapid communications》2015,36(16):1492-1497
Pillararene‐containing thermoresponsive polymers are synthesized via reversible addition–fragmentation chain transfer polymerization using pillararene derivatives as the effective chain transfer agents for the first time. These polymers can self‐assemble into micelles and form vesicles after guest molecules are added. Furthermore, such functional polymers can be further applied to prepare hybrid gold nanoparticles, which integrate the thermoresponsivity of polymers and molecular recognition of pillararenes.
63.
Ning Zuozhou Zhang Zhicheng Yan Qingsong Zhou Naifu Wen Linzi Peng Xichao Tang Yu Feng Pengju 《中国科学:化学(英文版)》2022,65(10):1962-1967
Science China Chemistry - A mild and practical protocol for selectively time-dependent dehydrogenative C-C coupling, as well as tandem coupling-cyclization reaction between indoles or/and other... 相似文献
64.
Jun Zhou Prof. Sha Yang Yesen Tan Huaisheng Cheng Dr. Jinsong Chai Prof. Manzhou Zhu 《化学:亚洲杂志》2021,16(19):2973-2977
The change in the valence state of nanocluster can induce remarkable changes in the properties and structure. However, achieving the valence state changes in nanoclusters is still a challenge. In this work, we use Cu2+ as dopant to “oxidize” [Ag62S12(SBut)32]2+ (4 free electrons) to obtain the new nanocluster: [Ag62−xCuxS12(SBut)32]4+ with 2 free electrons. As revealed by its structure, the [Ag62−xCuxS12(SBut)32]4+ (x=10∼21) has a similar structure to that of [Ag62S12(SBut)32]2+ precursor and all the Cu atoms occupy the surface site of nanocluster. It′s worth noting that with the Cu atoms doping, the [Ag62−xCuxS12(SBut)32]4+ nanocluster is more stable than [Ag62S12(SBut)32]2+ at higher temperature and in electrochemical cycle. This result has laid a foundation for the subsequent application and exploration. Overall, this work reveals crystals structure of a new Ag−Cu nanocluster and offers a new insight into the electron reduction/oxidation of nanocluster. 相似文献
65.
硅氧化物(SiOx, 0<x≤2)具有高的比容量和低的嵌锂电位, 且体积膨胀率显著低于纯硅负极, 因而被认为是替代传统石墨负极材料的理想选择之一. 然而SiOx负极在首次嵌锂过程中表面形成的固体电解质界面膜(SEI)以及大量的不可逆产物, 造成其首次库伦效率偏低, 严重阻碍了SiOx负极的实际应用. 本文从SiOx的结构模型出发, 系统阐述了SiOx负极的嵌锂机理以及首次库伦效率低的原因; 归纳了SiOx负极首次库伦效率的提升策略及其研究进展; 并对提升SiOx负极首次库伦效率的未来发展方向进行了展望. 相似文献
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68.
Xiaofeng Wang Zheng You Hailiang Sha Zhaolan Sun Wei Sun 《Journal of Solid State Electrochemistry》2014,18(1):207-213
In this paper, a Fe3O4@SiO2 core-shell structure microsphere was synthesized and used to investigate the direct electron transfer of myoglobin (Mb) with a 1-butylpyridinium hexafluorophosphate based carbon ionic liquid electrode (CILE) as the substrate electrode. The mixture of Mb and Fe3O4@SiO2 microsphere could form an organic–inorganic composite, which was immobilized on the surface of CILE with a chitosan (CS) film. Cyclic voltammetric experiments indicated that a pair of well-defined quasi-reversible redox peaks appeared on CS/Mb-Fe3O4@SiO2/CILE with the formal peak potential (E 0′) located at ?0.31 V (vs. saturated calomel electrode), which was corresponded to the electroactive center of Mb heme Fe(III)/Fe(II) redox couples. Direct electrochemical behaviors of Mb in CS-Fe3O4@SiO2 composite film were carefully investigated with the electrochemical parameters calculated. The CS/Mb-Fe3O4@SiO2/CILE showed good electrocatalytic behaviors to the reduction of trichloroacetic acid in the concentration range from 0.2 to 11.0 mmol L?1 with the detection limit of 0.18 mmol L?1 (3σ). Based on CS/Mb-Fe3O4@SiO2/CILE, a new third-generation reagentless electrochemical biosensor was constructed with higher sensitivity and reproducibility. 相似文献
69.
Youqian Bai Mengyu Gan Wei Qiu Feifei Cheng Dandan Fu Zhitao Li Sha Li 《Polymer Science Series B》2014,56(3):377-383
The polyaniline-gold (PANI-AuNPs) fibrillar nanocomposites were prepared via a simple one-pot synthesis route in ethylene glycol (EG) medium. The morphology of PANI-AuNPs was characterized by transmission electron microscopy (TEM), and their electrochemical properties were studied by CV, TAF and EIS measurement using an electrochemical workstation. The results show that the morphology of nanocomposites can be controlled by changing the temperature. The diameter of PANI-AuNPs composite nanofiber reduce from about 80 to 30 nm, and the size of AuNP also reduce from about 20 to 4 nm, with the rise of synthesized temperature. When the synthesized temperature is 10°C, the distribution of AuNPs is the best, and the amount of AuNPs dispersed in PANI is the most, as well as the electrochemical performance of PANI-AuNPs is the most excellent. 相似文献
70.
Guan Wu ;Ran Ran ;Bote Zhao ;Yujing Sha ;Chao Su ;Yingke Zhou ;Zongping Shao 《天然气化学杂志》2014,(3):363-375
Amorphous carbon and graphene co-modified LiFePO_4 nanocomposite has been synthesized via a facile polyol process in connection with a following thermal treatment.Various characterization techniques,including XRD.Mossbauer spectra,Raman spectra,SEM,TEM,BET,O_2-TPO,galvano charge-discharge,CV and EIS were applied to investigate the phase composition,carbon content,morphological structure and electrochemical performance of the synthesized samples.The effect of introducing way of carbon sources on the properties and performance of LiFePO_4/C/graphene composite was paid special attention.Under optimized synthetic conditions,highly crystalized olivine-type LiFePO_4was successfully obtained with electron conductive Fe_2P and FeP as the main impurity phases.SEM and TEM analyses demonstrated the graphene sheets were randomly distributed inside the sample to create an open structured LiFePO_4 with respect to graphene,while the glucosederived carbon mainly coated over LiFeP04 particles which effectively connected the graphene sheets and LiFePO_4 particles to result in a more efficient charge transfer process.As a result,favorable electrochemical performance was achieved.The performance of the amorphous carbon-graphene co-modified LiFePO_4 was further progressively improved upon cycling in the first 200 cycles to reach a reversible specificcapacity as high as 97 mAh·g~(-1) at 10 C rate. 相似文献