全文获取类型
收费全文 | 107043篇 |
免费 | 8989篇 |
国内免费 | 8604篇 |
出版年
2023年 | 1264篇 |
2022年 | 1608篇 |
2021年 | 5003篇 |
2020年 | 3825篇 |
2019年 | 4724篇 |
2018年 | 4467篇 |
2017年 | 3282篇 |
2016年 | 4669篇 |
2015年 | 6773篇 |
2014年 | 7949篇 |
2013年 | 8430篇 |
2012年 | 10127篇 |
2011年 | 9109篇 |
2010年 | 5627篇 |
2009年 | 5038篇 |
2008年 | 5798篇 |
2007年 | 5225篇 |
2006年 | 4529篇 |
2005年 | 3552篇 |
2004年 | 3027篇 |
2003年 | 2769篇 |
2002年 | 2329篇 |
2001年 | 1900篇 |
2000年 | 1725篇 |
1999年 | 1689篇 |
1998年 | 1019篇 |
1997年 | 991篇 |
1996年 | 930篇 |
1995年 | 838篇 |
1994年 | 796篇 |
1993年 | 629篇 |
1992年 | 839篇 |
1991年 | 633篇 |
1990年 | 479篇 |
1989年 | 452篇 |
1988年 | 367篇 |
1987年 | 354篇 |
1986年 | 278篇 |
1985年 | 291篇 |
1984年 | 160篇 |
1983年 | 166篇 |
1982年 | 103篇 |
1981年 | 85篇 |
1980年 | 65篇 |
1979年 | 79篇 |
1977年 | 59篇 |
1975年 | 60篇 |
1974年 | 53篇 |
1973年 | 60篇 |
1972年 | 50篇 |
排序方式: 共有10000条查询结果,搜索用时 0 毫秒
991.
Yingke Zhu Yujie Zhu Xingyi Huang Jin Chen Qi Li Jinliang He Pingkai Jiang 《Liver Transplantation》2019,9(36)
Polymer dielectrics such as poly(vinylidene fluoride) (PVDF) have drawn tremendous attention in high energy density capacitors because of their high dielectric constant and ease of processing. However, the discharged energy density attained with these materials is restrained by the inferior breakdown strength and electric resistivity. Herein, PVDF composite films with a nanosized interlayer of assembled boron nitride nanosheets (BNNSs) that is aligned along the in‐plane direction are prepared through a simple layer‐by‐layer solution‐casting process. Compared to the pristine PVDF, the composite films show remarkably suppressed leakage current, resulting in a high breakdown strength and a superior energy density which are 136% and 275%, respectively, that of the pristine PVDF. The experimental results and computational simulations reveal that the compact and successive interlayer of assembled BNNSs can largely mitigate the local field distortion and block the propagation of electrical treeing, which is advantageous over the conventional dielectric polymer nanocomposites. Notably, unlike the previous dielectric polymer nanocomposites that are usually incorporated with a high volume fraction of nanofillers, i.e., 5–10 vol%, the present composites contain only an extremely low content of nanfillers, e.g., 0.16 vol%. These findings offer a novel paradigm for fabricating high energy density and high efficiency polymer dielectrics. 相似文献
992.
Heng Zhang Xabier Judez Alexander Santiago Maria Martinez‐Ibaez Miguel ngel Muoz‐Mrquez Javier Carrasco Chunmei Li Gebrekidan Gebresilassie Eshetu Michel Armand 《Liver Transplantation》2019,9(25)
Amongst post‐Li‐ion battery technologies, lithium–sulfur (Li–S) batteries have captured an immense interest as one of the most appealing devices from both the industrial and academia sectors. The replacement of conventional liquid electrolytes with solid polymer electrolytes (SPEs) enables not only a safer use of Li metal (Li°) anodes but also a flexible design in the shape of Li–S batteries. However, the practical implementation of SPEs‐based all‐solid‐state Li–S batteries (ASSLSBs) is largely hindered by the shuttling effect of the polysulfide intermediates and the formation of dendritic Li° during the battery operation. Herein, a fluorine‐free noble salt anion, tricyanomethanide [C(CN)3?, TCM?], is proposed as a Li‐ion conducting salt for ASSLSBs. Compared to the widely used perfluorinated anions {e.g., bis(trifluoromethanesulfonyl)imide anion, [N(SO2CF3)2)]?, TFSI?}, the LiTCM‐based electrolytes show decent ionic conductivity, good thermal stability, and sufficient anodic stability suiting the cell chemistry of ASSLSBs. In particular, the fluorine‐free solid electrolyte interphase layer originating from the decomposition of LiTCM exhibits a good mechanical integrity and Li‐ion conductivity, which allows the LiTCM‐based Li–S cells to be cycled with good rate capability and Coulombic efficiency. The LiTCM‐based electrolytes are believed to be the most promising candidates for building cost‐effective and high energy density ASSLSBs in the near future. 相似文献
993.
Wenzhi Tian Baojuan Xi Zhenyu Feng Haibo Li Jinkui Feng Shenglin Xiong 《Liver Transplantation》2019,9(36)
Lithium‐sulfur batteries (LSBs) have been regarded as a competitive candidate for next‐generation electrochemical energy‐storage technologies due to their merits in energy density. The sluggish redox kinetics of the electrochemistry and the high solubility of polysulfides during cycling result in insufficient sulfur utilization, severe polarization, and poor cyclic stability. Herein, sulfiphilic few‐layered MoSe2 nanoflakes decorated rGO (MoSe2@rGO) hybrid has been synthesized through a facile hydrothermal method and for the first time, is used as a conceptually new‐style sulfur host for LSBs. Specifically, MoSe2@rGO not only strongly interacts with polysulfides but also dynamically strengthens polysulfide redox reactions. The polarization problem is effectively alleviated by relying on the sulfiphilic MoSe2. Moreover, MoSe2@rGO is demonstrated to be beneficial for the fast nucleation and uniform deposition of Li2S, contributing to the high discharge capacity and good cyclic stability. A high initial capacity of 1608 mAh g?1 at 0.1 C, a slow decay rate of 0.042% per loop at 0.25 C, and a high reversible capacity of 870 mAh g?1 with areal sulfur loading of 4.2 mg cm?2 at 0.3 C are obtained. The concept of introducing sulfiphilic transition‐metal selenides into the LSBs system can stimulate engineering of novel architectures with enhanced properties for various energy‐storage devices. 相似文献
994.
Xingfeng He Qiang Bai Yunsheng Liu Adelaide M. Nolan Chen Ling Yifei Mo 《Liver Transplantation》2019,9(43)
As technologically important materials for solid‐state batteries, Li super‐ionic conductors are a class of materials exhibiting exceptionally high ionic conductivity at room temperature. These materials have unique crystal structural frameworks hosting a highly conductive Li sublattice. However, it is not understood why certain crystal structures of the super‐ionic conductors lead to high conductivity in the Li sublattice. In this study, using topological analysis and ab initio molecular dynamics simulations, the crystal structures of all Li‐conducting oxides and sulfides are studied systematically and the key features pertaining to fast‐ion conduction are quantified. In particular, a unique feature of enlarged Li sites caused by large local spaces in the crystal structural framework is identified, promoting fast conduction in the Li‐ion sublattice. Based on these quantified features, the high‐throughput screening identifies many new structures as fast Li‐ion conductors, which are further confirmed by ab initio molecular dynamics simulations. This study provides new insights and a systematic quantitative understanding of the crystal structural frameworks of fast ion‐conductor materials and motivates future experimental and computational studies on new fast‐ion conductors. 相似文献
995.
Jingsi Yi Jiahua Chen Zheng Yang Yang Dai Weimin Li Jiang Cui Francesco Ciucci Ziheng Lu Chunlei Yang 《Liver Transplantation》2019,9(38)
A facile and scalable approach is reported to stabilize the lithium‐metal anode by regulating the Li nucleation and deposition kinetics with laser‐induced graphene (LIG). By processing polyimide (PI) films on copper foils with a laser, a 3D‐hierarchical composite material is constructed, consisting of a highly conductive copper substrate, a pillared array of flexible PI, and most importantly, porous LIG on the walls of the PI pillars. The high number of defects and heteroatoms present in LIG significantly lowers the Li nucleation barrier compared to the copper foil. An overpotential‐free Li nucleation process is identified at current densities lower than 0.2 mA cm?2. Theoretical computations reveal that the defects serve as nucleation centers during the heterogeneous nucleation of lithium. By adopting such composites, ultrastable lithium‐metal anodes are obtained with high Coulombic efficiencies of ≈99%. Full lithium‐metal cells based on LiFePO4 cathodes with a material loading of ≈15 mg cm?2 and a negative/positive ratio of 5/1 could be cycled over 250 times with a capacity loss of less than 10%. The current work highlights the importance of nucleation kinetics on the stability of metallic anodes and demonstrates a practical method toward long lasting Li‐metal batteries. 相似文献
996.
Qi Li Yao Zhao Wenke Zhou Zhengyuan Han Rui Fu Fang Lin Dapeng Yu Qing Zhao 《Liver Transplantation》2019,9(46)
The performance of perovskite solar cells (PSCs) relies on the synthesis method and chemical composition of the perovskite materials. So far, PSCs that have adopted two‐step sequential deposited perovskite with the state‐of‐art composition (FAPbI3)1?x(MAPbBr3)x (x < 0.05) have achieved record power conversion efficiency (PCE), while their one‐step antisolvent dripping counterparts with typical composition Cs0.05FA0.81MA0.14Pb(I0.85Br0.15)3 with more bromine have exhibited much better long‐term operational stability. Thus, halogen engineering that aims to elevate bromine content in sequential deposited perovskite film would push operational stability of PSCs toward that of antisolvent dripping deposited perovskite materials. Here, a Br‐rich seeding growth method is devised and perovskite seed solution with high bromine content is introduced into a PbI2 precursor, leading to bromine incorporation in the resulting perovskite film. Photovoltaic devices fabricated by Br‐rich seeding growth method exhibit a PCE of 21.5%, similar to 21.6% for PSCs having lower bromine content. Whereas, the operational stability of PSCs with higher bromine content is significantly enhanced, with over 80% of initial PCE retained after 500 h tracking at maximum power point under 1‐sun illumination. This work highlights the vital importance of halogen composition for the operational stability of PSCs, and introduces an effective way to incorporate bromine into mixed‐cation‐halide perovskite film via sequential deposition method. 相似文献
997.
Nonaqueous metal–gas batteries based on halogenated reactants exhibit strong potential for future high‐energy electrochemical systems. The lithium–sulfur hexafluoride (Li–SF6) primary battery, which utilizes a safe, noncombustible, energy‐dense gas as cathode, demonstrates attractive eight‐electron transfer reduction during discharge and high attainable capacities (>3000 mAh g?1carbon) at voltages above 2.2 VLi. However, improved rate capability is needed for practical applications. Here, two viable strategies are reported to achieve this by targeting the solubility of the passivating discharge product, lithium fluoride (LiF). Operating at moderately elevated temperatures, e.g., 50 °C, in DMSO dramatically improves LiF solubility and promotes sparser and larger LiF nuclei on gas diffusion layer electrodes, leading to capacity improvements of ≈10× at 120 µA cm?2. More aggressive chemical modification of the electrolyte by including a tris(pentafluorophenyl)borane anion receptor further promotes LiF solubilization; capacity increases even at room temperature by a factor of 25 at 120 µA cm?2, with attainable capacities up to 3 mAh cm?2. This work shows that bulk fluoride‐forming conversion reactions can be strongly manipulated by tuning the electrolyte environment to be solvating toward F?, and that significantly improved rates can be achieved, leading a step closer to practical applications. 相似文献
998.
Zhe Hu Zhixin Tai Qiannan Liu Shi‐Wen Wang Huile Jin Shun Wang Weihong Lai Mingzhe Chen Lin Li Lingna Chen Zhanliang Tao Shu‐Lei Chou 《Liver Transplantation》2019,9(8)
Sodium ion batteries are now attracting great attention, mainly because of the abundance of sodium resources and their cheap raw materials. 2D materials possess a unique structure for sodium storage. Among them, transition metal chalcogenides exhibit significant potential for rechargeable battery devices due to their tunable composition, remarkable structural stability, fast ion transport, and robust kinetics. Herein, ultrathin TiS2 nanosheets are synthesized by a shear‐mixing method and exhibit outstanding cycling performance (386 mAh g?1 after 200 cycles at 0.2 A g?1). To clarify the variations of galvanostatic curves and superior cycling performance, the mechanism and morphology changes are systematically investigated. This facile synthesis method is expected to shed light on the preparation of ultrathin 2D materials, whose unique morphologies could easily enable their application in rechargeable batteries. 相似文献
999.
Jianwen Liang Xiaona Li Yang Zhao Lyudmila V. Goncharova Weihan Li Keegan R. Adair Mohammad Norouzi Banis Yongfeng Hu Tsun‐Kong Sham Huan Huang Li Zhang Shangqian Zhao Shigang Lu Ruying Li Xueliang Sun 《Liver Transplantation》2019,9(38)
Li metal is a promising anode material for all‐solid‐state batteries, owing to its high specific capacity and low electrochemical potential. However, direct contact of Li metal with most solid‐state electrolytes induces severe side reactions that can lead to dendrite formation and short circuits. Moreover, Li metal is unstable when exposed to air, leading to stringent processing requirements. Herein, it is reported that the Li3PS4/Li interface in all‐solid‐state batteries can be stabilized by an air‐stable LixSiSy protection layer that is formed in situ on the surface of Li metal through a solution‐based method. Highly stable Li cycling for over 2000 h in symmetrical cells and a lifetime of over 100 cycles can be achieved for an all‐solid‐state LiCoO2/Li3PS4/Li cell. Synchrotron‐based high energy X‐ray photoelectron spectroscopy in‐depth analysis demonstrates the distribution of different components within the protection layer. The in situ formation of an electronically insulating LixSiSy protection layer with highly ionic conductivity provides an effective way to prevent Li dendrite formation in high‐energy all‐solid‐state Li metal batteries. 相似文献
1000.
Qing Zhang Christophe Didier Wei Kong Pang Yajie Liu Zhijie Wang Sean Li Vanessa K. Peterson Jianfeng Mao Zaiping Guo 《Liver Transplantation》2019,9(30)
Potassium‐ion batteries (PIBs) are an emerging, affordable, and environmentally friendly alternative to lithium‐ion batteries, with their further development driven by the need for suitably performing electrode materials capable of reversibly accommodating the relatively large K+. Layer‐structured manganese oxides are attractive as electrodes for PIBs, but suffer from structural instability and sluggish kinetics of K+ insertion/extraction, leading to poor rate capability. Herein, cobalt is successfully introduced at the manganese site in the KxMnO2 layered oxide electrode material and it is shown that with only 5% Co, the reversible capacity increases by 30% at 22 mA g‐1 and by 92% at 440 mA g‐1. In operando synchrotron X‐ray diffraction reveals that Co suppresses Jahn–Teller distortion, leading to more isotropic migration pathways for K+ in the interlayer, thus enhancing the ionic diffusion and consequently, rate capability. The detailed analysis reveals that additional phase transitions and larger volume change occur in the Co‐doped material as a result of layer gliding, with these associated with faster capacity decay, despite the overall capacity remaining higher than the pristine material, even after 500 cycles. These results assert the importance of understanding the detailed structural evolution that underpins performance that will inform the strategic design of electrode materials for high‐performance PIBs. 相似文献