全文获取类型
收费全文 | 75532篇 |
免费 | 18716篇 |
国内免费 | 4061篇 |
出版年
2024年 | 72篇 |
2023年 | 608篇 |
2022年 | 958篇 |
2021年 | 3144篇 |
2020年 | 3852篇 |
2019年 | 5893篇 |
2018年 | 5818篇 |
2017年 | 5563篇 |
2016年 | 6208篇 |
2015年 | 7016篇 |
2014年 | 7398篇 |
2013年 | 8206篇 |
2012年 | 6483篇 |
2011年 | 5686篇 |
2010年 | 5495篇 |
2009年 | 4084篇 |
2008年 | 3369篇 |
2007年 | 2626篇 |
2006年 | 2276篇 |
2005年 | 1905篇 |
2004年 | 1666篇 |
2003年 | 1503篇 |
2002年 | 1298篇 |
2001年 | 1169篇 |
2000年 | 1009篇 |
1999年 | 912篇 |
1998年 | 504篇 |
1997年 | 440篇 |
1996年 | 438篇 |
1995年 | 413篇 |
1994年 | 420篇 |
1993年 | 281篇 |
1992年 | 329篇 |
1991年 | 289篇 |
1990年 | 221篇 |
1989年 | 179篇 |
1988年 | 144篇 |
1987年 | 106篇 |
1986年 | 84篇 |
1985年 | 74篇 |
1984年 | 49篇 |
1983年 | 46篇 |
1982年 | 26篇 |
1981年 | 22篇 |
1980年 | 13篇 |
1979年 | 6篇 |
1889年 | 1篇 |
1882年 | 1篇 |
1881年 | 1篇 |
1873年 | 1篇 |
排序方式: 共有10000条查询结果,搜索用时 15 毫秒
991.
Jin Zhao Yi‐Zhou Zhang Jianyu Chen Wenli Zhang Du Yuan Rodney Chua Husam N. Alshareef Yanwen Ma 《Liver Transplantation》2020,10(18)
The pursuit of more efficient carbon‐based anodes for sodium‐ion batteries (SIBs) prepared from facile and economical methods is a very important endeavor. Based on the crystallinity difference within carbon materials, herein, a low‐temperature selective burning method is developed for preparing oxygen and nitrogen codoped holey graphene aerogel as additive‐free anode for SIBs. By selective burning of a mixture of graphene and low‐crystallinity carbon at 450 °C in air, an elastic porous graphene monolith with abundant holes on graphene sheets and optimized crystallinity is obtained. These structural characteristics lead to an additive‐free electrode with fast charge (ions and electrons) transfer and more abundant Na+ storage active sites. Moreover, the heteroatom oxygen/nitrogen doping favors large interlayer distance for rapid Na+ insertion/extraction and provides more active sites for high capacitive contribution. The optimized sample exhibits superior sodium‐ion storage capability, i.e., high specific capacity (446 mAh g?1 at 0.1 A g?1), ultrahigh rate capability (189 mAh g?1 at 10 A g?1), and long cycle life (81.0% capacity retention after 2000 cycles at 5 A g?1). This facile and economic strategy might be extended to fabricating other superior carbon‐based energy storage materials. 相似文献
992.
993.
Shijian Jin Eric M. Fell Lucia Vina‐Lopez Yan Jing P. Winston Michalak Roy G. Gordon Michael J. Aziz 《Liver Transplantation》2020,10(20)
A highly stable phosphonate‐functionalized viologen is introduced as the redox‐active material in a negative potential electrolyte for aqueous redox flow batteries (ARFBs) operating at nearly neutral pH. The solubility is 1.23 m and the reduction potential is the lowest of any substituted viologen utilized in a flow battery, reaching ?0.462 V versus SHE at pH = 9. The negative charges in both the oxidized and the reduced states of 1,1′‐bis(3‐phosphonopropyl)‐[4,4′‐bipyridine]‐1,1′‐diium dibromide ( BPP?Vi ) effect low permeability in cation exchange membranes and suppress a bimolecular mechanism of viologen decomposition. A flow battery pairing BPP?Vi with a ferrocyanide‐based positive potential electrolyte across an inexpensive, non‐fluorinated cation exchange membrane at pH = 9 exhibits an open‐circuit voltage of 0.9 V and a capacity fade rate of 0.016% per day or 0.00069% per cycle. Overcharging leads to viologen decomposition, causing irreversible capacity fade. This work introduces extremely stable, extremely low‐permeating and low reduction potential redox active materials into near neutral ARFBs. 相似文献
994.
Tika R. Kafle Bhupal Kattel Shanika Wanigasekara Ti Wang Wai‐Lun Chan 《Liver Transplantation》2020,10(10)
In organic semiconductors, optical excitation does not necessarily produce free carriers. Very often, electron and hole are bound together to form an exciton. Releasing free carriers from the exciton is essential for the functioning of photovoltaics and optoelectronic devices, but it is a bottleneck process because of the high exciton binding energy. Inefficient exciton dissociation can limit the efficiency of organic photovoltaics. Here, nanoscale features that can allow the free carrier generation to occur spontaneously despite being an energy uphill process are determined. Specifically, by comparing the dissociation dynamics of the charge transfer (CT) exciton at two donor–acceptor interfaces, it is found that the relative orientation of the electron and hole wavefunction within a CT exciton plays an important role in determining whether the CT exciton will decompose into the higher energy free electron–hole pair or relax to the lower energy tightly‐bound CT exciton. The concept of the entropic driving force is combined with the structural anisotropy of typical organic crystals to devise a framework that can describe how the orientation of the delocalized electronic wavefunction can be manipulated to favor the energy‐uphill spontaneous dissociation of CT excitons over the energy‐downhill CT exciton cooling. 相似文献
995.
996.
Marko Jot Benjamin Lipovek Botjan Glaar Amran Al‐Ashouri Kristijan Brecl Gaper Mati
Artiom Magomedov Vytautas Getautis Marko Topi
Steve Albrecht 《Liver Transplantation》2020,10(25)
Perovskite solar cells (PSC) have shown that under laboratory conditions they can compete with established photovoltaic technologies. However, controlled laboratory measurements usually performed do not fully resemble operational conditions and field testing outdoors, with day‐night cycles, changing irradiance and temperature. In this contribution, the performance of PSCs in the rooftop field test, exposed to real weather conditions is evaluated. The 1 cm2 single‐junction devices, with an initial average power conversion efficiency of 18.5% are tracked outdoors in maximum power point over several weeks. In parallel, irradiance and air temperature are recorded, allowing us to correlate outside factors with generated power. To get more insight into outdoor device performance, a comprehensive set of laboratory measurements under different light intensities (10% to 120% of AM1.5) and temperatures is performed. From these results, a low power temperature coefficient of ?0.17% K?1 is extracted in the temperature range between 25 and 85 °C. By incorporating these temperature‐ and light‐dependent PV parameters into the energy yield model, it is possible to correctly predict the generated energy of the devices, thus validating the energy yield model. In addition, degradation of the tested devices can be tracked precisely from the difference between measured and modelled power. 相似文献
997.
Energy generation and consumption have always been an important component of social development. Interests in this field are beginning to shift to indoor photovoltaics (IPV) which can serve as power sources under low light conditions to meet the energy needs of rapidly growing fields, such as intelligence gathering and information processing which usually operate via the Internet‐of‐things (IoT). Since the power requirements for this purpose continue to decrease, IPV systems under low light may facilitate the realization of self‐powered high‐tech electronic devices connected through the IoT. This review discusses and compares the characteristics of different types of IPV devices such as those based on silicon, dye, III‐V semiconductors, organic compounds, and halide perovskites. Among them, specific attention is paid to perovskite photovoltaics which may potentially become a high performing IPV system due to the fascinating photophysics of the halide perovskite active layer. The limitations of such indoor application as they relate to the toxicity, stability, and electronic structure of halide perovskites are also discussed. Finally, strategies which could produce highly functional, nontoxic, and stable perovskite photovoltaics devices for indoor applications are proposed. 相似文献
998.
Mingzi Sun Alan William Dougherty Bolong Huang Yuliang Li Chun‐Hua Yan 《Liver Transplantation》2020,10(12)
Atomic catalysts (AC) are emerging as a highly attractive research topic, especially in sustainable energy fields. Lack of a full picture of the hydrogen evolution reaction (HER) impedes the future development of potential electrocatalysts. In this work, the systematic investigation of the HER process in graphdyine (GDY) based AC is presented in terms of the adsorption energies, adsorption trend, electronic structures, reaction pathway, and active sites. This comprehensive work innovatively reveals GDY based AC for HER covering all the transition metals (TM) and lanthanide (Ln) metals, enabling the screening of potential catalysts. The density functional theory (DFT) calculations carefully explore the HER performance beyond the comparison of sole H adsorption. Therefore, the screened catalysts candidates not only match with experimental results but also provide significant references for novel catalysts. Moreover, the machine learning (ML) technique bag‐tree approach is innovatively utilized based on the fuzzy model for data separation and converse prediction of the HER performance, which indicates a similar result to the theoretical calculations. From two independent theoretical perspectives (DFT and ML), this work proposes pivotal guidelines for experimental catalyst design and synthesis. The proposed advanced research strategy shows great potential as a general approach in other energy‐related areas. 相似文献
999.
1000.
Yinglin Xiao Bing Han Yi Zeng Shang‐Sen Chi Xianzhe Zeng Zijian Zheng Kang Xu Yonghong Deng 《Liver Transplantation》2020,10(14)
Lithium–sulfur batteries (LSBs) are considered promising candidates for the next‐generation energy‐storage systems due to their high theoretical capacity and prevalent abundance of sulfur. Their reversible operation, however, encounters challenges from both the anode, where dendritic and dead Li‐metal form, and the cathode, where polysulfides dissolve and become parasitic shuttles. Both issues arise from the imperfection of interphases between electrolyte and electrode. Herein, a new lithium salt based on an imide anion with fluorination and unsaturation in its structure is reported, whose interphasial chemistries resolve these issues simultaneously. Lithium 1, 1, 2, 2, 3, 3‐hexafluoropropane‐1, 3‐disulfonimide (LiHFDF) forms highly fluorinated interphases at both anode and cathode surfaces, which effectively suppress formation of Li‐dendrites and dissolution/shuttling of polysulfides, and significantly improves the electrochemical reversibility of LSBs. In a broader context, this new Li salt offers a new perspective for diversified beyond Li‐ion chemistries that rely on a Li‐metal anode and active cathode materials. 相似文献