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71.
One Step Preparation of Reduced Graphene Oxide/Pd–Fe3O4@Polypyrrole Composites and Their Application in Catalysis 下载免费PDF全文
Dr. Tongjie Yao Hao Wang Quan Zuo Dr. Jie Wu Dr. Xiao Zhang Dr. Fang Cui Dr. Tieyu Cui 《化学:亚洲杂志》2015,10(9):1940-1947
The simple preparation of catalysts with superior catalytic activity and good reusability is highly desirable. Herein, we report a novel strategy to construct reduced graphene oxide (rGO)/Pd–Fe3O4@polypyrrole (PPy) catalysts with Pd and Fe3O4 nanoparticles anchored on a rGO nanosheet surface and wrapped in a PPy shell. The synthesis and assembly of both the Pd and Fe3O4 nanoparticles, the preparation of the PPy layer, and the reduction of graphene oxide nanosheets were finished in one step. In the system, the PPy layer not only prevented aggregation of Pd and Fe3O4 nanoparticles, but also generated a synergistic effect with precursor Pd2+ ions, which led to a high dispersity of as‐prepared Pd nanoparticles. Although the procedure was simplified to one step, the catalytic activity and reusability were not sacrificed. In the reduction of 4‐nitrophenol, their catalytic performance was better than that in recent reports. Moreover, the catalysts showed good reusability owing to their magnetic properties. 相似文献
72.
Electrochemical reduction of CO2 has the benefit of turning greenhouse gas emissions into useful resources. We performed a comparative study of the electrochemical reduction of CO2 on stepped Pb(211) and Sn(112) surfaces based on the results of density functional theory slab calculations. We mapped out the potential energy profiles for electrochemical reduction of CO2 to formate and other possible products on both surfaces. Our results show that the first step is the formation of the adsorbed formate(HCOO*) species through an Eley-Rideal mechanism. The formate species can be reduced to HCOO- through a oneelectron reduction in basic solution, which produces formic acid as the predominant product. The respective potentials of forming HCOO* are predicted to be -0.72 and -0.58 V on Pb and Sn. Higher overpotentials make other reaction pathways accessible, leading to different products. On Sn(112), CO and CH4 can be generated at -0.65 V following formate formation. In contrast, the limiting potential to access alternative reaction channels on Pb(211) is -1.33 V, significantly higher than that of Sn. 相似文献
73.
Nan Zhang Tao Bing Xiangjun Liu Cui Qi Luyao Shen Linlin Wang Dihua Shangguan 《Chemical science》2015,6(7):3831-3838
Guanine-rich oligonucleotides (GROs) have attracted considerable attention as anticancer agents, because they exhibit cancer-selective antiproliferative activity and can form G-quadruplex structures with higher nuclease resistance and cellular uptake. Recently, a GRO, AS1411 has reached phase II clinical trials for acute myeloid leukemia and renal cell carcinoma. The antiproliferative activity of GROs has been associated with various protein targets; however the real mechanisms of action remain unclear. In this study, we showed evidence that antiproliferative activity of GROs (including AS1411) is mainly contributed by the cytotoxicity of their guanine-based degradation products, such as monophosphate deoxyguanosine (dGMP), deoxyguanosine (dG) and guanine. The GROs with lower nuclease resistance exhibited higher antiproliferative activity. Among nucleotides, nucleosides and nucleobases, only guanine-based compounds showed highly concentration-dependent cytotoxicity. Our results suggest that it is necessary to reconsider the cancer-selective antiproliferative activity of GROs. Since guanine-based compounds are endogenous substances in living organisms, systematic studies of the cytotoxicity of these compounds will provide new information for the understanding of certain diseases and offer useful information for drug design. 相似文献
74.
This paper considers a Schelling model in an arbitrary fixed network where there are no vacant houses. Agents have preferences either for segregation or for mixed neighborhoods. Utility is non-transferable. Two agents exchange houses when the trade is mutually beneficial. We find that an allocation is stable when for two agents of opposite-color each black (white) agent has a higher proportion of neighbors who are black (white). This result holds irrespective of agents’ preferences. When all members of both groups prefer mixed neighborhoods, an allocation is also stable provided that if an agent belongs to the minority (majority), then any neighbor of opposite-color is in a smaller minority (larger majority). 相似文献
75.
Yaodong Cui Xiang Song Yan Chen Yi-Ping Cui 《The Journal of the Operational Research Society》2017,68(3):269-280
In the one-dimensional cutting stock problem with usable leftovers (1DCSPUL), items of the current order are cut from stock bars to minimize material cost. Here, stock bars include both standard ones bought commercially and old leftovers generated in processing previous orders, and cutting patterns often include new leftovers that are usable in processing subsequent orders. Leftovers of the same length are considered to be of the same type. The number of types of leftovers should be limited to simplify the cutting process and reduce the storage area. This paper presents an integer programming model for the 1DCSPUL with limited leftover types and describes a heuristic algorithm based on a column-generation procedure to solve it. Computational results show that the proposed approach is more effective than several published algorithms in reducing trim loss, especially when the number of types of leftovers is limited. 相似文献
76.
Yongqiao Wang Donghe Pei Xiupeng Cui 《Mathematical Methods in the Applied Sciences》2017,40(18):7151-7161
We introduce the notions of the pseudospherical normal Darboux images for the curve on a lightlike surface in Minkowski 3‐space and study these Darboux images by using technics of the singularity theory. Furthermore, we give a relation between these Darboux images and Darboux frame from the viewpoint of Legendrian dualities. 相似文献
77.
Metalloproteins have inspired chemists for many years to synthesize artificial catalysts that mimic native enzymes.As a complementary approach to studying native enzymes or making synthetic models,biosynthetic approach using small and stable proteins to model native enzymes has offered advantages of incorporating non-covalent secondary sphere interactions under physiological conditions.However,most biosynthetic models are restricted to natural amino acids.To overcome this limitation,incorporating unnatural amino acids into the biosynthetic models has shown promises.In this review,we summarize first synthetic,semisynthetic and biological methods of incorporates unnatural amino acids(UAAs)into proteins,followed by progress made in incorporating UAAs into both native metalloproteins and their biosynthetic models to fine-tune functional properties beyond native enzymes or their variants containing natural amino acids,such as reduction potentials of azurin,O_2 reduction rates and percentages of product formation of HCO models in Mb,the rate of radical transport in ribonucleotide reductase(RNR)and the proton and electron transfer pathways in photosystemⅡ(PSⅡ).We also discuss how this endeavour has allowed systematic investigations of precise roles of conserved residues in metalloproteins,such as Metl21 in azurin,Tyr244 that is cross-linked to one of the three His ligands to CuB in HCO,Tyr122,356,730 and 731 in RNR and TyrZ in PSⅡ.These examples have demonstrated that incorporating UAAs has provided a new dimension in our efforts to mimic native enzymes and in providing deeper insights into structural features responsible high enzymatic activity and reaction mechanisms,making it possible to design highly efficient artificial catalysts with similar or even higher activity than native enzymes. 相似文献
78.
Meiling Peng Wei Xu Weihao Cui Tao Wang Sheng Wang 《Journal of Solid State Electrochemistry》2017,21(2):391-401
This study reports the synthesis of octahedral Pd-Pt bimetallic alloy nanocrystals through a facile, one-pot, templateless, and seedless hydrothermal method in the presence of glucose and hexadecyl trimethyl ammonium bromide. The morphologies, compositions, and structures of the Pd-Pt nanocrystals were fully characterized by various physical techniques, thereby demonstrating their highly alloying octahedral nanostructures. The formation or growth mechanism of the Pd-Pt bimetallic alloy nanocrystals was explored and is discussed here based on the experimental observations. In addition, the synthesized Pd-Pt nanocrystals were applied to the methanol oxidation reaction (MOR) in alkaline media, which proved that the as-prepared catalysts exhibit enhanced electrocatalytic activity for MOR. Pd1Pt3 exhibited the best stability and durability, and its mass activity was 3.4 and 5.2 times greater than those of Pt black and Pd black catalysts, respectively. The facile synthetic process and excellent catalytic performance of the as-prepared catalysts demonstrate that they have the potential to be used in direct methanol fuel cell techniques. 相似文献
79.
Shu Xia Wang Yan Qin Yongqiang Yu Cuiping Zhang Jianfang Zhao Jiebo Cui Jiewu Cui Lihua Zheng Hongmei Zhang Yong Wang Wenfang Wu Yucheng 《Journal of Solid State Electrochemistry》2017,21(5):1489-1497
Journal of Solid State Electrochemistry - Binder-free, high-performance electrode materials play a critical role for supercapacitors. In this paper, through the electrochemical anodization process,... 相似文献
80.
Dr. Qiang Gao Chuan-Qi Huang Yi-Ming Ju Dr. Min-Rui Gao Dr. Jian-Wei Liu Duo An Dr. Chun-Hua Cui Dr. Ya-Rong Zheng Prof. Dr. Wei-Xue Li Prof. Dr. Shu-Hong Yu 《Angewandte Chemie (International ed. in English)》2017,56(27):7769-7773
Cobalt-based nanomaterials have been intensively explored as promising noble-metal-free oxygen evolution reaction (OER) electrocatalysts. Herein, we report phase-selective syntheses of novel hierarchical CoTe2 and CoTe nanofleeces for efficient OER catalysts. The CoTe2 nanofleeces exhibited excellent electrocatalytic activity and stablity for OER in alkaline media. The CoTe2 catalyst exhibited superior OER activity compared to the CoTe catalyst, which is comparable to the state-of-the-art RuO2 catalyst. Density functional theory calculations showed that the binding strength and lateral interaction of the reaction intermediates on CoTe2 and CoTe are essential for determining the overpotential required under different conditions. This study provides valuable insights for the rational design of noble-metal-free OER catalysts with high performance and low cost by use of Co-based chalcogenides. 相似文献