首页 | 本学科首页   官方微博 | 高级检索  
文章检索
  按 检索   检索词:      
出版年份:   被引次数:   他引次数: 提示:输入*表示无穷大
  收费全文   91篇
  免费   60篇
  国内免费   8篇
  2023年   5篇
  2022年   1篇
  2021年   3篇
  2020年   20篇
  2019年   32篇
  2018年   22篇
  2017年   14篇
  2016年   9篇
  2015年   4篇
  2014年   14篇
  2013年   3篇
  2012年   2篇
  2011年   3篇
  2010年   3篇
  2009年   2篇
  2008年   3篇
  2007年   4篇
  2006年   2篇
  2005年   1篇
  2004年   1篇
  2003年   1篇
  2002年   3篇
  2001年   2篇
  1999年   1篇
  1997年   1篇
  1993年   1篇
  1989年   1篇
  1988年   1篇
排序方式: 共有159条查询结果,搜索用时 78 毫秒
91.
This paper complements our recent survey [1] of experimental and theoretical work on the optical spectra of high-temperature superconductors. The emphasis is laid on experiments involving single crystals and good textured ceramic samples. Data have been collected on chemically doped samples, as well as on samples in which carriers are created by photodoping. One of the most remarkable consequences is the observation of a photoinduced superconductivity and a phase separation of photoexcited carriers. The theory has offered a few main suggestions but they have all failed to produce the magic formula for understanding the optical response. Nevertheless, bipolaron models seem somewhat closer to reality. Future experimental, theoretical, and practical developments are considered.  相似文献   
92.
The future large‐scale deployment of rechargeable zinc–air batteries requires the development of cheap, stable, and efficient bifunctional electrocatalysts for the oxygen reduction reaction (ORR) and oxygen evolution reaction (OER). In this work, a highly efficient bifunctional electrocatalyst is prepared by depositing 3–5 nm NiFe layered double hydroxide (NiFe‐LDH) nanoparticles on Co,N‐codoped carbon nanoframes (Co,N‐CNF). The NiFe‐LDH/Co,N‐CNF electrocatalyst displayed an OER overpotential of 0.312 V at 10 mA cm?2 and an ORR half‐wave potential of 0.790 V. The outstanding performance of the electrocatalyst is attributable to the high electrical conductivity and excellent ORR activity of Co,N‐CNF, together with the strong anchoring of 3–5 nm NiFe‐LDH nanoparticles, which preserves active sites. Inspired by the excellent OER and ORR performance of NiFe‐LDH/Co,N‐CNF, a prototype rechargeable zinc–air battery is developed. The battery exhibited a low discharge–charge voltage gap (1.0 V at 25 mA cm?2) and long‐term cycling durability (over 80 h), and superior overall performance to a counterpart battery constructed using a mixture of IrO2 and Pt/C as the cathode. The strategy developed here can easily be adapted to synthesize other bifunctional CNF‐based hybrid electrodes for ORR and OER, providing a practical route to more efficient rechargeable zinc–air batteries.  相似文献   
93.
Na‐ion batteries are promising for large‐scale energy storage applications, but few cathode materials can be practically used because of the significant difficulty in synthesizing an electrode material with superior comprehensive performance. Herein, an effective strategy based on synergetic contributions of rationally selected metal ions is applied to design layered oxides with excellent electrochemical performances. The power of this strategy is demonstrated by the superior properties of as‐obtained NaFe0.45Co0.5Mg0.05O2 with 139.9 mA h g?1 of reversible capacity, 3.1 V of average voltage, 96.6% of initial Coulombic efficiency, and 73.9 mA h g?1 of capacity at 10 C rate, which benefit from the synergetic effect of Fe3+ (high redox potential), Co3+ (good kinetics), and inactive Mg2+ with compatible radii (stabilizing structure). Moreover, it is clarified that the superior property is not the simple superposition of performance for layered oxides with single metal ions. With the assistance of density functional theory calculations, it is evidenced that the wide capacity range (>70%) of prismatic Na+‐occupied sites during sodiation/desodiation is responsible for its high rate performance. This rational strategy of designing high‐performance cathodes based on the synergetic effect of various metal ions might be a powerful step forward in the development of new Na‐ion‐insertion cathodes.  相似文献   
94.
透光分层疏透度测定及其在次生林结构研究中的应用   总被引:12,自引:0,他引:12  
朱教君 《应用生态学报》2003,14(8):1229-1233
次生林是中国森林的主体,对其进行合理的经营无疑对中国天然林资源保护及国家生态安全建设具有重大意义.次生林的结构(尤其是垂直结构)是该林种合理经营的重要因素.本文在以往研究的基础上,引入了分层疏透度的概念,并以透光分层疏透度表征林分的垂直结构;详细介绍了应用全天照片测定透光分层疏透度的方法与步骤.分析了透光分层疏透度在次生林结构研究和次生林的经营理论与技术研究中的应用前景.  相似文献   
95.
96.
A new and promising P2‐type layered oxide, Na5/6[Li1/4Mn3/4]O2 is prepared using a solid‐state method. Detailed crystal structures of the sample are analyzed by synchrotron X‐ray diffraction combined with high‐resolution neutron diffraction. P2‐type Na5/6[Li1/4Mn3/4]O2 consists of two MeO2 layers with partial in‐plane √3a × √3a‐type Li/Mn ordering. Na/Li ion‐exchange in a molten salt results in a phase transition accompanied with glide of [Li1/4Mn3/4]O2 layers without the destruction of in‐plane cation ordering. P2‐type Na5/6[Li1/4Mn3/4]O2 translates into an O2‐type layered structure with staking faults as the result of ion‐exchange. Electrode performance of P2‐type Na5/6[Li1/4Mn3/4]O2 and O2‐type Lix[Li1/4Mn3/4]O2 is examined and compared in Na and Li cells, respectively. Both samples show large reversible capacity, ca. 200 mA h g?1, after charge to high voltage regardless of the difference in charge carriers. Structural analysis suggests that in‐plane structural rearrangements, presumably associated with partial oxygen loss, occur in both samples after charge to a high‐voltage region. Such structural activation process significantly influences electrode performance of the P2/O2‐type phases, similar to O3‐type Li2MnO3‐based materials. Crystal structures, phase‐transition mechanisms, and the possibility of the P2/O2‐type phases as high‐capacity and long‐cycle‐life electrode materials with the multi‐functionality for both rechargeable Li/Na batteries are discussed in detail.  相似文献   
97.
98.
99.
The synthesis of a new layered cathode material, Na0.5[Ni0.23Fe0.13Mn0.63]O2, and its characterization in terms of crystalline structure and electrochemical performance in a sodium cell is reported. X‐ray diffraction studies and high resolution scanning electron microscopy images reveal a well‐defined P2‐type layered structure, while the electrochemical tests demonstrate excellent characteristics in terms of high capacity and cycle life. This performance, the low cost, and the environmental compatibility of its component poses Na0.5[Ni0.23Fe0.13Mn0.63]O2 to be among the most promising materials for the next generation of sodium‐ion batteries.  相似文献   
100.
Li‐rich layered materials are considered to be the promising low‐cost cathodes for lithium‐ion batteries but they suffer from poor rate capability despite of efforts toward surface coating or foreign dopings. Here, spinel‐layered Li‐rich Li‐Mn‐Co‐O microspheres are reported as a new high‐rate cathode material for Li‐ion batteries. The synthetic procedure is relatively simple, involving the formation of uniform carbonate precursor under solvothermal conditions and its subsequent transformation to an assembled microsphere that integrates a spinel‐like component with a layered component by a heat treatment. When calcined at 700 °C, the amount of transition metal Mn and Co in the Li‐Mn‐Co‐O microspheres maintained is similar to at 800 °C, while the structures of constituent particles partially transform from 2D to 3D channels. As a consequence, when tested as a cathode for lithium‐ion batteries, the spinel‐layered Li‐rich Li‐Mn‐Co‐O microspheres obtained at 700 °C show a maximum discharge capacity of 185.1 mA h g?1 at a very high current density of 1200 mA g?1 between 2.0 and 4.6 V. Such a capacity is among the highest reported to date at high charge‐discharge rates. Therefore, the present spinel‐layered Li‐rich Li‐Mn‐Co‐O microspheres represent an attractive alternative to high‐rate electrode materials for lithium‐ion batteries.  相似文献   
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号