全文获取类型
收费全文 | 17352篇 |
免费 | 1978篇 |
国内免费 | 665篇 |
专业分类
电工技术 | 109篇 |
综合类 | 1007篇 |
化学工业 | 4809篇 |
金属工艺 | 539篇 |
机械仪表 | 262篇 |
建筑科学 | 430篇 |
矿业工程 | 246篇 |
能源动力 | 824篇 |
轻工业 | 7084篇 |
水利工程 | 173篇 |
石油天然气 | 575篇 |
武器工业 | 45篇 |
无线电 | 736篇 |
一般工业技术 | 2703篇 |
冶金工业 | 269篇 |
原子能技术 | 62篇 |
自动化技术 | 122篇 |
出版年
2025年 | 8篇 |
2024年 | 528篇 |
2023年 | 662篇 |
2022年 | 636篇 |
2021年 | 791篇 |
2020年 | 784篇 |
2019年 | 867篇 |
2018年 | 655篇 |
2017年 | 816篇 |
2016年 | 707篇 |
2015年 | 709篇 |
2014年 | 806篇 |
2013年 | 967篇 |
2012年 | 1121篇 |
2011年 | 1158篇 |
2010年 | 741篇 |
2009年 | 868篇 |
2008年 | 718篇 |
2007年 | 983篇 |
2006年 | 948篇 |
2005年 | 750篇 |
2004年 | 636篇 |
2003年 | 570篇 |
2002年 | 455篇 |
2001年 | 436篇 |
2000年 | 394篇 |
1999年 | 242篇 |
1998年 | 189篇 |
1997年 | 157篇 |
1996年 | 123篇 |
1995年 | 112篇 |
1994年 | 92篇 |
1993年 | 78篇 |
1992年 | 75篇 |
1991年 | 39篇 |
1990年 | 31篇 |
1989年 | 38篇 |
1988年 | 22篇 |
1987年 | 12篇 |
1986年 | 10篇 |
1985年 | 13篇 |
1984年 | 11篇 |
1983年 | 4篇 |
1982年 | 3篇 |
1980年 | 8篇 |
1979年 | 2篇 |
1974年 | 2篇 |
1973年 | 3篇 |
1959年 | 1篇 |
1951年 | 9篇 |
排序方式: 共有10000条查询结果,搜索用时 0 毫秒
981.
A New Salt‐Baked Approach for Confining Selenium in Metal Complex‐Derived Porous Carbon with Superior Lithium Storage Properties
下载免费PDF全文
![点击此处可从《Advanced functional materials》网站下载免费的PDF全文](/ch/ext_images/free.gif)
Xiaona Li Jianwen Liang Zhiguo Hou Wanqun Zhang Yan Wang Yongchun Zhu Yitai Qian 《Advanced functional materials》2015,25(32):5229-5238
For lithium‐selenium batteries, commercial applications are hindered by the inferior electrical conductivity of selenium and the low utilization ratio of the active selenium. Here, we report a new baked‐in‐salt approach to enable Se to better infiltrate into metal‐complex‐derived porous carbon (Se/MnMC‐B). The approach uses the confined, narrow space that is sandwiched between two compact NaCl solid disks, thus avoiding the need for protection with argon or a vacuum environment during processing. The electrochemical properties for both lithium and sodium storage of our Se/MnMC‐B cathode were found to be outstanding. For lithium storage, the Se/MnMC‐B cathode (with 72% selenium loading) exhibited a capacity of 580 mA h g?1 after 1000 cycles at 1 C, and an excellent rate capability was achieved at 20 C and 510 mA h g?1. For sodium storage, a specific capacity of 535 mA h g?1 was achieved at 0.1 C after 150 cycles. These results demonstrate the potential of this approach as a new effective general synthesis method for confining other low melting point materials into a porous carbon matrix. 相似文献
982.
Porous Coordination Polymers: Unveiling the Mechanism of Water‐Triggered Diplex Transformation and Correlating the Changes in Structures and Separation Properties (Adv. Funct. Mater. 41/2015)
下载免费PDF全文
![点击此处可从《Advanced functional materials》网站下载免费的PDF全文](/ch/ext_images/free.gif)
Li‐Hui Cao Yong‐Sheng Wei Hong Xu Shuang‐Quan Zang Thomas C. W. Mak 《Advanced functional materials》2015,25(41):6556-6556
983.
Design of Hierarchical NiCo@NiCo Layered Double Hydroxide Core–Shell Structured Nanotube Array for High‐Performance Flexible All‐Solid‐State Battery‐Type Supercapacitors
下载免费PDF全文
![点击此处可从《Advanced functional materials》网站下载免费的PDF全文](/ch/ext_images/free.gif)
Yan Liu Nianqing Fu Guoge Zhang Ming Xu Wei Lu Limin Zhou Haitao Huang 《Advanced functional materials》2017,27(8)
A novel hierarchical nanotube array (NTA) with a massive layered top and discretely separated nanotubes in a core–shell structure, that is, nickel–cobalt metallic core and nickel–cobalt layered double hydroxide shell (Ni?Co@Ni?Co LDH), is grown on carbon fiber cloth (CFC) by template‐assisted electrodeposition for high‐performance supercapacitor application. The synthesized Ni?Co@Ni?Co LDH NTAs/CFC shows high capacitance of 2200 F g?1 at a current density of 5 A g?1, while 98.8% of its initial capacitance is retained after 5000 cycles. When the current density is increased from 1 to 20 A g?1, the capacitance loss is less than 20%, demonstrating excellent rate capability. A highly flexible all‐solid‐state battery‐type supercapacitor is successfully fabricated with Ni?Co LDH NTAs/CFC as the positive electrode and electrospun carbon fibers/CFC as the negative electrode, showing a maximum specific capacitance of 319 F g?1, a high energy density of 100 W h kg?1 at 1.5 kW kg?1, and good cycling stability (98.6% after 3000 cycles). These fascinating electrochemical properties are resulted from the novel structure of electrode materials and synergistic contributions from the two electrodes, showing great potential for energy storage applications. 相似文献
984.
985.
Shengyan Yin Yulia Goldovsky Moshe Herzberg Lei Liu Hang Sun Yanyan Zhang Fanben Meng Xuebo Cao Darren D. Sun Hongyu Chen Ariel Kushmaro Xiaodong Chen 《Advanced functional materials》2013,23(23):2972-2978
Fabricating free‐standing, three‐dimensional (3D) ordered porous graphene structure can service a wide range of functional materials such as environmentally friendly materials for antibacterial medical applications and efficient solar harvesting devices. A scalable solution processable strategy is developed to create such free‐standing hierarchical porous structures composed of functionalized graphene sheets via an “on water spreading” method. The free‐standing film shows a large area uniform honeycomb structure and can be transferred onto any substrate of interest. The graphene‐based free‐standing honeycomb films exhibit superior broad spectrum antibacterial activity as confirmed using green fluorescent protein labeled Pseudomonas aeruginosa PAO1 and Escherichia coli as model pathogens. Functional nanoparticles such as titanium dioxide (TiO2) nanoparticles can be easily introduced into conductive graphene‐based scaffolds by premixing. The formed composite honeycomb film electrode shows a fast, stable, and completely reversible photocurrent response accompanying each switch‐on and switch‐off event. The graphene‐based honeycomb scaffold enhances the light‐harvesting efficiency and improves the photoelectric conversion behavior; the photocurrent of the composite film is about two times as high as that of the pure TiO2 film electrode. Such composite porous films combining remarkably good electrochemical performance of graphene, a large electrode/electrolyte contact area, and excellent stability during the photo‐conversion process hold promise for further applications in water treatment and solar energy conversion. 相似文献
986.
987.
988.
Chang‐Woo Kwon Ji‐Won Son Jong‐Ho Lee Hyun‐Mi Kim Hae‐Weon Lee Ki‐Bum Kim 《Advanced functional materials》2011,21(6):1154-1159
Micro‐solid oxide fuel cells (μ‐SOFCs) are fabricated on nanoporous anodic aluminum oxide (AAO) templates with a cell structure composed of a 600‐nm‐thick AAO free‐standing membrane embedded on a Si substrate, sputter‐deposited Pt electrodes (cathode and anode) and an yttria‐stabilized zirconia (YSZ) electrolyte deposited by pulsed laser deposition (PLD). Initially, the open circuit voltages (OCVs) of the AAO‐supported μ‐SOFCs are in the range of 0.05 V to 0.78 V, which is much lower than the ideal value, depending on the average pore size of the AAO template and the thickness of the YSZ electrolyte. Transmission electron microscopy (TEM) analysis reveals the formation of pinholes in the electrolyte layer that originate from the porous nature of the underlying AAO membrane. In order to clog these pinholes, a 20‐nm thick Al2O3 layer is deposited by atomic layer deposition (ALD) on top of the 300‐nm thick YSZ layer and another 600‐nm thick YSZ layer is deposited after removing the top intermittent Al2O3 layer. Fuel cell devices fabricated in this way manifest OCVs of 1.02 V, and a maximum power density of 350 mW cm?2 at 500 °C. 相似文献
989.
990.
多层间隔式结构多孔硅冷阴极电子发射的研究 总被引:2,自引:0,他引:2
在多孔硅(PS)表面电子发射冷阴极中采用间隔式多层结构。由此,器件电子发射效率显著提高,在32.5V偏压下,发射效率达13.5%,发射电流密度29μA/cm^2;工作电流和发射电流的波动性明显减小;器件稳定性得到提高。 相似文献