全文获取类型
收费全文 | 2003篇 |
免费 | 212篇 |
国内免费 | 50篇 |
专业分类
电工技术 | 17篇 |
综合类 | 49篇 |
化学工业 | 604篇 |
金属工艺 | 112篇 |
机械仪表 | 107篇 |
建筑科学 | 10篇 |
矿业工程 | 125篇 |
能源动力 | 197篇 |
轻工业 | 94篇 |
石油天然气 | 54篇 |
武器工业 | 5篇 |
无线电 | 92篇 |
一般工业技术 | 395篇 |
冶金工业 | 377篇 |
原子能技术 | 20篇 |
自动化技术 | 7篇 |
出版年
2024年 | 6篇 |
2023年 | 53篇 |
2022年 | 62篇 |
2021年 | 85篇 |
2020年 | 96篇 |
2019年 | 81篇 |
2018年 | 84篇 |
2017年 | 77篇 |
2016年 | 77篇 |
2015年 | 64篇 |
2014年 | 98篇 |
2013年 | 133篇 |
2012年 | 77篇 |
2011年 | 117篇 |
2010年 | 72篇 |
2009年 | 89篇 |
2008年 | 77篇 |
2007年 | 65篇 |
2006年 | 84篇 |
2005年 | 50篇 |
2004年 | 59篇 |
2003年 | 73篇 |
2002年 | 67篇 |
2001年 | 75篇 |
2000年 | 64篇 |
1999年 | 68篇 |
1998年 | 66篇 |
1997年 | 58篇 |
1996年 | 28篇 |
1995年 | 53篇 |
1994年 | 29篇 |
1993年 | 22篇 |
1992年 | 11篇 |
1991年 | 9篇 |
1990年 | 10篇 |
1989年 | 6篇 |
1988年 | 5篇 |
1987年 | 3篇 |
1986年 | 1篇 |
1985年 | 1篇 |
1984年 | 1篇 |
1982年 | 1篇 |
1981年 | 1篇 |
1980年 | 1篇 |
1979年 | 3篇 |
1978年 | 1篇 |
1951年 | 2篇 |
排序方式: 共有2265条查询结果,搜索用时 31 毫秒
1.
《Ceramics International》2022,48(14):19971-19977
Molybdenum diboride is unique among transition metal diborides because it exists in both hexagonal (AlB2-type) and rhombohedral structures. However, it is difficult to stabilize the superconducting AlB2-type phase, which requires either extreme synthesis condition or suitable chemical doping. Here we report the structural and physical properties of Sc-doped nonstoichiometric molybdenum diborides (Mo0.95Sc0.05)1-xB2 and (Mo1-yScy)0.71B2 prepared by the common arc melting method. The AlB2-type phase is found to form over wide ranges of 0 ≤ x ≤ 0.29 and 0.025 ≤ y ≤ 0.30 for the first time, and bulk superconductivity with Tc up to 7.9 K is observed. Tc increases with increasing x in the (Mo0.95Sc0.05)1-xB2 series, but evolves nonmonotonically with varying y in the (Mo1-yScy)0.71B2 series. Despite this contrast, Tc of both borides follows nearly the same linear dependence on the electron-phonon coupling constant, suggesting that it is mainly controlled by the electron-phonon interaction. In addition, the stabilization of AlB2-type structure is attributed to the decrease in the number of d electrons as a consequence of Sc doping, which suggests that a similar effect may be achieved by substituting Mo with other d electron-poorer metal elements. 相似文献
2.
《International Journal of Hydrogen Energy》2022,47(72):31014-31057
In the scope of the rapid technological advancements, nanoparticles (NPs) have gained prominence due to their excellent and tunable biological, and physicochemical properties. Nowadays, different methods are used for their synthesis. In particular, the green synthesis of metal precursors for the synthesis of NPs, represents a cost-effective, environmentally friendly, and hazardous chemical-free method for developing a large variety of NPs. By exploiting plant extracts, the production rate of NPs is relatively faster. Due to fossil reserves and high fuel consumption, renewable and clean energy materials are urgently needed to improve environmental sustainability. With outstanding electrochemical and physicochemical characteristics, molybdenum-based NPs (Mo-NPs) are gaining increasing attention in the fields of energy conversion and storage. Considering the significance of Mo-NPs synthesized from greener routes and their energy applications, it is necessary to review recent trends and developments in this field. This review summarizes important research studies and future research guidelines for the preparation of Mo-NPs through green routes and their applications to meet global energy and environmental demands. Moreover, future research directions are also highlighted to achieve sustainable greener precursors and Mo-NPs based energy storage devices. 相似文献
3.
Ryan J. Grohsmeyer Laura Silvestroni Gregory E. Hilmas Fredêric Monteverde William G. Fahrenholtz Andrea D’Angió Diletta Sciti 《Journal of the European Ceramic Society》2019,39(6):1948-1954
The mechanical behavior of ZrB2-MoSi2 ceramics made of ZrB2 powder with three different particle sizes and MoSi2 additions from 5 to 70 vol% was characterized up to 1500 °C. Microhardness (12–17 GPa), Young’s modulus (450–540 GPa) and shear modulus (190–240 GPa) decreased with both increasing MoSi2 content and with decreasing ZrB2 grain size. Room temperature fracture toughness was unaffected by grain size or silicide content, whilst at 1500 °C in air it increased with MoSi2 and ZrB2 grain size, from 4.1 to 8.7 MPa m½. Room temperature strength did not trend with MoSi2 content, but increased with decreasing ZrB2 grain size from 440 to 590 MPa for the largest starting particle size to 700–800 MPa for the finest due to the decreasing size of surface grain pullout. At 1500 °C, flexure strength for ZrB2 with MoSi2 contents above 25 vol% were roughly constant, 400–450 MPa, whilst for lower content strength was controlled by oxidation damages. Strength for compositions made using fine and medium ZrB2 powders increased with increasing MoSi2 content, 250–450 MPa. Ceramics made with coarse ZrB2 displayed the highest strengths, which decreased with increasing MoSi2 content from 600 to 450 MPa. 相似文献
4.
Xinran Zhao Fengxiang Yin Xiaobo He Biaohua Chen Guoru Li 《International Journal of Hydrogen Energy》2021,46(40):20905-20918
To meet the demand of producing hydrogen at low cost, a molybdenum (Mo)-doped cobalt oxide (Co3O4) supported on nitrogen (N)-doped carbon (x%Mo–Co3O4/NC, where x% represents Mo/Co molar ratio) is developed as an efficient bifunctional electrocatalyst for hydrogen evolution reaction (HER) and oxygen evolution reaction (OER). This defect engineering strategy is realized by a facile urea oxidation method in nitrogen atmosphere. Through X-ray diffraction (XRD) refinement and other detailed characterizations, molybdenum ion (Mo4+) is found to be doped into Co3O4 by substituting cobalt ion (Co2+) at tetrahedron site, while N is doped into carbon matrix simultaneously. 4%Mo–Co3O4/NC is the optimized sample to show the lowest overpotentials of 91 and 276 mV to deliver 10 mA cm?2 for HER and OER in 1 M potassium hydroxide solution (KOH), respectively. The overall water splitting cell 4%Mo–Co3O4/NC||4%Mo–Co3O4/NC displays a voltage of 1.62 V to deliver 10 mA cm?2 in 1 M KOH. The Mo4+ dopant modulates the electronic structure of active cobalt ion (Co3+) and boosts the water dissociation process during HER, while the increased amount of lattice oxygen and formation of pyridinic nitrogen due to Mo doping benefits the OER activity. Besides, the smaller grain size owing to Mo doping leads to higher electrochemically active surface area (ECSA) on 4%Mo–Co3O4/NC, resulting in its superior bifunctional catalytic activity. 相似文献
5.
The potential energy profile of the reaction between dimethyl disulfide and OH? radicals is explored by utilizing ab initio and hybrid meta density functional theory methods. Having the energies and structural data of the stationary points, statistical rate theories, such as transition state theory and variable reaction coordinate-transition state theory, are employed to compute the overall rate constants, and discuss the mechanism and product channels. On the basis of the calculations, the overall rate coefficient is predicted to be 2.49?×?10?10?cm3?molecule?1?s?1 at 298?K. It is found that in the most favorable pathway, the reaction proceeds via formation of the relatively unstable intermediate CH3S?(OH)SCH3 decomposing rapidly to yield CH3S?+CH3SOH. 相似文献
6.
《International Journal of Hydrogen Energy》2020,45(15):8497-8506
A facile, one-pot, solvothermal synthesis of MoS2 microflowers (S1) and the heterostructures MoS2/g-C3N4 with varying ratios of 1:1 (S2), 1:2 (S3) and 1:3 (S4) exhibiting enhanced visible-light-assisted H2 generation by water splitting has been reported. The compounds were thoroughly characterized by PXRD, FESEM, HRTEM, EDS, UV–vis and XPS techniques. FESEM and HRTEM analyses showed the presence of microflowers composed of nano-sized petals in case of pure MoS2 (S1), while the MoS2 microflowers covered with g-C3N4 nanosheets in case of MoS2/g-C3N4 heterostructure, S4. XPS analysis of S2 showed the presence of 2H phase of MoS2 with g-C3N4. The Eosin-Y/dye-sensitized visible-light-assisted photocatalytic investigation of the samples in the absence of any noble metal co-catalyst revealed very good water splitting activity of MoS2/g-C3N4 heterostructure, S2 with hydrogen generation rate of 1787 μmol h−1g−1 which is about 6 and 40 times higher than pure MoS2 and g-C3N4 respectively. The relatively higher catalytic activity of the heterostructure, S2 has been ascribed to the efficient spatial separation of photo-induced charge carriers owing to the synergistic interaction between MoS2 and g-C3N4. A possible mechanism for the Eosin-Y-sensitized photocatalytic H2 generation activity of MoS2/g-C3N4 heterostructures has also been presented. The enhanced activity of S2 was further supported by fluorescence measurements. Thus, the present study highlights the importance of non-noble metal based MoS2/g-C3N4 heterojunction photocatalysts for efficient visible-light-driven H2 production from water splitting. 相似文献
7.
《International Journal of Hydrogen Energy》2020,45(30):15063-15075
Electrochemical hydrogen evolution reaction (HER) via the splitting of water has required electrocatalysts with cost-effectiveness, environmentally friendliness, high catalytic activity, and superior stability to meet the hydrogen economy in future. In this context, we report the successful synthesis of self-standing mesoporous Ni2P–MoP2 nanorod arrays on nickel foam (Ni2P–MoP2 NRs/3D-NF) through an effective phosphidization of the corresponding NiMoO4 NRs/3D-NF. The as-synthesis Ni2P–MoP2 NRs/3D-NF, as an efficient HER electrocatalyst, exhibits small overpotential of 82.2 and 124.7 mV to reach current density of 10 and 50 mA cm−2, a low Tafel slope of 52.9 mV dec−1 and it retains its catalytic performance for at least 20 h in alkaline condition. Our work also offers a new strategy in designing and using transition metal phosphide-based 3D nanoarrays catalysts with enhanced catalytic efficiency for mass production of hydrogen fuels. 相似文献
8.
《International Journal of Hydrogen Energy》2020,45(31):15507-15520
Sulfonated poly(ether sulfone) (SPES) based proton exchange membranes (PEMs) are fabricated using sulfonated molybdenum disulfide (S-MoS2) nanosheets via facile solution casting method. SPES (DS = 30%) and S-MoS2 are synthesized and sulfonation is evidently observed in FTIR and XRD analysis. The anchoring of sulfonic acid group on exfoliated molybdenum disulfide (E-MoS2) and elemental composition of S-MoS2 are confirmed by XPS spectrum. Physico-chemical characteristics such as ion-exchange capacity (IEC), water uptake, swelling ratio and oxidation stability are found to be increases after the addition of S-MoS2 into SPES matrix. Increment in S-MoS2 content in SPES matrix decreases the surface contact angle due to the increase in hydrophilicity. Further, the dispersing ability of S-MoS2 in SPES matrix is evidently shown by an increase in surface roughness, tensile strength and thermal stability of the SPES/S-MoS2 nanocomposite membranes. On the whole, SPES/S-MoS2-1 membrane showed the highest proton conductivity of 5.98 × 10−3 Scm−1, selectivity of 19.6 × 104 Scm−3s, peak power density of 28.28 mWcm−2 and lesser methanol permeability of 3.05 × 10−8 cm2s−1. The strong interfacial interaction between SPES and S-MoS2 in nanocomposite membranes create strong hydrogen bond network to facilitate the proton conduction pathway via both vehicle and Grotthuss type mechanisms. Overall results suggested that the SPES/S-MoS2 nanocomposite membranes are superior and appropriate alternative for commercially high-cost Nafion® membranes for use in renewable direct methanol fuel cell (DMFC) devices. 相似文献
9.
《International Journal of Hydrogen Energy》2020,45(3):1435-1443
The size-controlled preparation of Mo powders is always a challenge and important task in the molybdenum metallurgy. In the current study, Mo powders with controllable sizes are synthesized by hydrogen reduction of MoO2 powders with the assistance of Mo nuclei in the range of 900–1100 °C. The influences of the particle sizes of Mo nuclei, the additive amount as well as reaction temperature on the morphology and particle sizes of the final products are studied. For the hydrogen reduction of MoO2 without any additive, the obtained Mo powders always have large particle sizes. However, the addition of small amounts of nuclei in MoO2 can help Mo nucleate dispersedly, and the growth of Mo could be also controlled by adjusting the sizes of added nuclei, amount of addition and the reaction temperature. With the addition of Mo nuclei, the different sizes of Mo powders with the good dispersity can be prepared. As adding commercial Mo powders with the particle size of about 2.03 μm, the micron-sized Mo powders ranged from 2.11 μm to 3.25 μm could be prepared. While for the case of adding ultrafine Mo nuclei of about 170 nm, Mo powders from 0.28 μm to 0.88 μm can be obtained. Moreover, the more the amounts of nuclei added and the lower the reaction temperature (in the range of 900–1100 °C) is, the smaller the particle size of the prepared Mo powder will be. The current method is a facile and feasible method, and is potential to be used for industrial production of Mo powder with controllable particle sizes. 相似文献
10.
利用简单的一步水热法制备了MoS2纳米片并用于修饰不锈钢纤维毡阳极(MoS2-SSFF),与未修饰不锈钢纤维毡阳极(SSFF)和多壁碳纳米管修饰阳极(CNT-SSFF)进行了对比研究。装配MFC运行的测试结果表明,MoS2-SSFF/MFC的功率密度为714 m W/m2,略高于CNT-SSFF/MFC的功率密度693 m W/m2,远高于未修饰SSFF/MFC的功率密度197 m W/m2。利用扫描电子显微镜(SEM)观察到MoS2纳米片呈簇状附着于MoS2-SSFF电极表面,显著增加了电极的比表面积。MoS2纳米片修饰改善了SSFF阳极的生物相容性,修饰电极在循环伏安测试(CV)中表现出良好的氧化还原性能。水热法制备的MoS2纳米片用于修饰阳极是一种高效、经济、简单的阳极修饰方法。 相似文献