全文获取类型
收费全文 | 22023篇 |
免费 | 3419篇 |
国内免费 | 2418篇 |
专业分类
化学 | 15593篇 |
晶体学 | 253篇 |
力学 | 1317篇 |
综合类 | 188篇 |
数学 | 2301篇 |
物理学 | 8208篇 |
出版年
2024年 | 13篇 |
2023年 | 409篇 |
2022年 | 443篇 |
2021年 | 669篇 |
2020年 | 837篇 |
2019年 | 818篇 |
2018年 | 698篇 |
2017年 | 717篇 |
2016年 | 1001篇 |
2015年 | 1001篇 |
2014年 | 1137篇 |
2013年 | 1578篇 |
2012年 | 1855篇 |
2011年 | 1997篇 |
2010年 | 1297篇 |
2009年 | 1271篇 |
2008年 | 1467篇 |
2007年 | 1351篇 |
2006年 | 1220篇 |
2005年 | 970篇 |
2004年 | 774篇 |
2003年 | 653篇 |
2002年 | 592篇 |
2001年 | 449篇 |
2000年 | 436篇 |
1999年 | 473篇 |
1998年 | 403篇 |
1997年 | 414篇 |
1996年 | 453篇 |
1995年 | 363篇 |
1994年 | 375篇 |
1993年 | 270篇 |
1992年 | 252篇 |
1991年 | 232篇 |
1990年 | 166篇 |
1989年 | 130篇 |
1988年 | 116篇 |
1987年 | 98篇 |
1986年 | 96篇 |
1985年 | 85篇 |
1984年 | 58篇 |
1983年 | 49篇 |
1982年 | 38篇 |
1981年 | 28篇 |
1980年 | 31篇 |
1979年 | 17篇 |
1978年 | 10篇 |
1977年 | 8篇 |
1975年 | 7篇 |
1973年 | 6篇 |
排序方式: 共有10000条查询结果,搜索用时 62 毫秒
991.
992.
Kaikai Wen Lifen Wu Xiaoxi Wu Ying Lu Tao Duan Han Ma Aidong Peng Qinqin Shi Hui Huang 《Angewandte Chemie (International ed. in English)》2020,59(31):12756-12761
Cancer possesses normoxic and hypoxia microenvironments with different levels of oxygen, needing different efficacies of photothermal and photodynamic therapies. It is important to precisely tune the photothermal and photodynamic effects of phototherapy nano‐agents for efficient cancer treatment. Now, a series of copolymeric nanoparticles (PPy‐Te NPs) were synthesized in situ by controlled oxidative copolymerization with different ratios of pyrrole to tellurophene by FeCl3. The photothermal and photodynamic effects of semiconducting nano‐agents under the first near‐infrared (NIR) irradiation were precisely and systematically tuned upon simply varying the molar ratio of the pyrrole to tellurophene. The PPy‐Te NPs were used for cancer treatment in mice, exhibiting excellent biocompatibility and therapeutic effect. This work presents a simple method to tune photothermal and photodynamic therapies effect in semiconducting nano‐agents for cancer treatment. 相似文献
993.
Siyuan Li Weidong Zhang Qiang Wu Lei Fan Xinyang Wang Xiao Wang Zeyu Shen Yi He Yingying Lu 《Angewandte Chemie (International ed. in English)》2020,59(35):14935-14941
A rechargeable Li metal anode coupled with a high‐voltage cathode is a promising approach to high‐energy‐density batteries exceeding 300 Wh kg?1. Reported here is an advanced dual‐additive electrolyte containing a unique solvation structure and it comprises a tris(pentafluorophenyl)borane additive and LiNO3 in a carbonate‐based electrolyte. This system generates a robust outer Li2O solid electrolyte interface and F‐ and B‐containing conformal cathode electrolyte interphase. The resulting stable ion transport kinetics enables excellent cycling of Li/LiNi0.8Mn0.1Co0.1O2 for 140 cycles with 80 % capacity retention under highly challenging conditions (≈295.1 Wh kg?1 at cell‐level). The electrolyte also exhibits high cycling stability for a 4.6 V LiCoO2 (160 cycles with 89.8 % capacity retention) cathode and 4.95 V LiNi0.5Mn1.5O4 cathode. 相似文献
994.
Qun‐Liang Zhang Qin Xiong Miao‐Miao Li Wei Xiong Bin Shi Yu Lan Liang‐Qiu Lu Wen‐Jing Xiao 《Angewandte Chemie (International ed. in English)》2020,59(33):14096-14100
Higher‐order cycloadditions, particularly [8+2] cycloadditions, are a straightforward and efficient strategy for constructing significant medium‐sized architectures. Typically, configuration‐restrained conjugated systems are utilized as 8π‐components for higher‐order concerted cycloadditions. However, for this reason, 10‐membered monocyclic skeletons have never been constructed via catalytic asymmetric [8+2] cycloaddition with high peri‐ and stereoselectivity. Here, we accomplished an enantioselective [8+2] dipolar cycloaddition via the merger of visible‐light activation and asymmetric palladium catalysis. This protocol provides a new route to 10‐membered monocyclic architectures bearing chiral quaternary stereocenters with high chemo‐, peri‐, and enantioselectivity. The success of this strategy relied on the facile in situ generation of Pd‐containing 1,8‐dipoles and their enantioselective trapping by ketene dipolarophiles, which were formed in situ via a photo‐Wolff rearrangement. 相似文献
995.
Yanan Jiang Wenjie Ma Yujuan Qiao Yifei Xue Jiahao Lu Jun Gao Nannan Liu Fei Wu Ping Yu Lei Jiang Lanqun Mao 《Angewandte Chemie (International ed. in English)》2020,59(31):12795-12799
Biological ion channels and ion pumps with sub‐nanometer sizes modulate ion transport in response to external stimuli. Realizing such functions with sub‐nanometer solid‐state nanopores has been an important topic with wide practical applications. Herein, we demonstrate a biomimetic photoresponsive ion channel and photodriven ion pump using a porphyrin‐based metal–organic framework membrane with pore sizes comparable to hydrated ions. We show that the molecular‐size pores enable precise and robust optoelectronic ion transport modulation in a broad range of concentrations, unparalleled with conventional solid‐state nanopores. Upon decoration with platinum nanoparticles to form a Schottky barrier photodiode, photovoltage across the membrane is generated with “uphill” ion transport from low concentration to high concentration. These results may spark applications in energy conversion, ion sieving, and artificial photosynthesis. 相似文献
996.
Ze‐Fan Yao Zi‐Yuan Wang Hao‐Tian Wu Yang Lu Qi‐Yi Li Lin Zou Jie‐Yu Wang Jian Pei 《Angewandte Chemie (International ed. in English)》2020,59(40):17467-17471
Controlling the solution‐state aggregation of conjugated polymers for producing specific microstructures remains challenging. Herein, a practical approach is developed to finely tune the solid‐state microstructures through temperature‐controlled solution‐state aggregation and polymer crystallization. High temperature generates significant conformation fluctuation of conjugated backbones in solution, which facilitates the polymer crystallization from solvated aggregates to orderly packed structures. The polymer films deposited at high temperatures exhibit less structural disorders and higher electron mobilities (up to two orders of magnitude) in field‐effect transistors, compared to those deposited at low temperatures. This work provides an effective strategy to tune the solution‐state aggregation to reveal the relationship between solution‐state aggregation and solid‐state microstructures of conjugated polymers. 相似文献
997.
Zhaohong Lu Stephen L. Buchwald 《Angewandte Chemie (International ed. in English)》2020,59(37):16128-16132
Arenes with β‐stereogenic centers are important substructures in pharmaceuticals and natural products. We have developed an asymmetric anti‐Markovnikov hydroarylation of 1,1‐disubstituted olefins by dual palladium and copper hydride catalysis as a convenient and general approach to access these substructures. This efficient one‐step process addresses several limitations of the traditional stepwise approaches. The use of cesium benzoate as a base and a common phosphine ligand for both the Cu‐ and Pd‐catalyzed processes were important discoveries that allow these challenging olefin substrates to be efficiently transformed. A variety of aryl bromide coupling partners, including numerous heterocycles, were coupled with 1,1‐disubstituted alkenes to generate arenes with β‐stereogenic centers. 相似文献
998.
999.
Ding Yi Fei Lu Fengchu Zhang Shoujie Liu Bo Zhou Denglei Gao Xi Wang Jiannian Yao 《Angewandte Chemie (International ed. in English)》2020,59(37):15855-15859
Single‐atom catalysts have attracted much attention. Reported herein is that regulating charge transfer of lattice oxygen atoms in serial single‐atom‐doped titania enables tunable hydrogen evolution reaction (HER) activity. First‐principles calculations disclose that the activity of lattice oxygen for the HER can be regularly promoted by substituting its nearest metal atom, and doping‐induced charge transfer plays an essential role. Besides, the realm of the charge transfer of the active site can be enlarged to the second nearest atom by creating oxygen vacancies, resulting in further optimization for the HER. Various single‐atom‐doped titania nanosheets were fabricated to validate the proposed model. Taking advantage of the localized charge transfer to the lattice atom is demonstrated to be feasible for realizing precise regulation of the electronic structures and thus catalytic activity of the nanosheets. 相似文献
1000.
Yanying Lu Tianyu Zhu Wessel van den Bergh Morgan Stefik Kevin Huang 《Angewandte Chemie (International ed. in English)》2020,59(39):17004-17011
Developing high capacity and stable cathodes is a key to successful commercialization of aqueous Zn‐ion batteries (ZIBs). Pure layered V2O5 has a high theoretical capacity (585 mAh g?1), but it suffers severe capacity decay. Pre‐inserting cations into V2O5 can substantially stabilize the performance, but at an expense of lowered capacity. Here we show that an atomic layer deposition derived V2O5 can be an excellent ZIB cathode with high capacity and exceptional cycle stability at once. We report a rapid in situ on‐site transformation of V2O5 atomic layers into Zn3V2O7(OH)2?2 H2O (ZVO) nanoflake clusters, also a known Zn‐ion and proton intercalatable material. High concentration of reactive sites, strong bonding to the conductive substrate, nanosized thickness and binder‐free composition facilitate ionic transport and promote the best utilization of the active material. We also provide new insights into the V2O5‐dissolution mechanisms for different Zn‐salt aqueous electrolytes and their implications to the cycle stability. 相似文献