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排序方式: 共有497条查询结果,搜索用时 15 毫秒
491.
Dr. Angel T. Garcia-Esparza Dr. Tatsuya Shinagawa Dr. Samy Ould-Chikh Muhammad Qureshi Dr. Xuyuan Peng Dr. Nini Wei Dr. Dalaver H. Anjum Dr. Alain Clo Dr. Tsu-Chien Weng Dr. Dennis Nordlund Dr. Dimosthenis Sokaras Prof. Jun Kubota Prof. Kazunari Domen Prof. Kazuhiro Takanabe 《Angewandte Chemie (Weinheim an der Bergstrasse, Germany)》2017,129(21):5874-5878
For overall water-splitting systems, it is essential to establish O2-insensitive cathodes that allow cogeneration of H2 and O2. An acid-tolerant electrocatalyst is described, which employs a Mo-coating on a metal surface to achieve selective H2 evolution in the presence of O2. In operando X-ray absorption spectroscopy identified reduced Pt covered with an amorphous molybdenum oxyhydroxide hydrate with a local structural order composed of polyanionic trimeric units of molybdenum(IV). The Mo layer likely hinders O2 gas permeation, impeding contact with active Pt. Photocatalytic overall water splitting proceeded using MoOx/Pt/SrTiO3 with inhibited water formation from H2 and O2, which is the prevailing back reaction on the bare Pt/SrTiO3 photocatalyst. The Mo coating was stable in acidic media for multiple hours of overall water splitting by membraneless electrolysis and photocatalysis. 相似文献
492.
Toshio Kawanami Kentaro Ishizuka Hiroshi Furuno Yoshihito Shiota Kazunari Yoshizawa Junji Inanaga 《Tetrahedron: Asymmetry》2017,28(11):1587-1590
A chiral BINOL dimer, (R,R)-3′,3″-BiBINOL, which possesses both rigid (atropos) and dynamic (tropos) axial chiralities, was found to work as an effective NMR chiral solvating reagent for the determination of the enantiomeric purities of various chiral sulfoxides. The unique chiral discrimination mechanism was also revealed by using DFT calculations and X-ray crystallographic analysis. 相似文献
493.
Lihua Lin Pongpen Kaewdee Vikas Nandal Ryota Shoji Hiroyuki Matsuzaki Kazuhiko Seki Mamiko Nakabayashi Naoya Shibata Xiaoping Tao Xizhuang Liang Yiwen Ma Takashi Hisatomi Tsuyoshi Takata Prof. Kazunari Domen 《Angewandte Chemie (International ed. in English)》2023,62(42):e202310607
Photocatalytic water splitting is an ideal means of producing hydrogen in a sustainable manner, and developing highly efficient photocatalysts is a vital aspect of realizing this process. The photocatalyst Y2Ti2O5S2 (YTOS) is capable of absorbing at wavelengths up to 650 nm and exhibits outstanding thermal and chemical durability compared with other oxysulfides. However, the photocatalytic performance of YTOS synthesized using the conventional solid-state reaction (SSR) process is limited owing to the large particle sizes and structural defects associated with this synthetic method. Herein, we report the synthesis of YTOS particles by a flux-assisted technique. The enhanced mass transfer efficiency in the flux significantly reduced the preparation time compared with the SSR method. In addition, the resulting YTOS showed improved photocatalytic H2 and O2 evolution activity when loaded with Rh and Co3O4 co-catalysts, respectively. These improvements are attributed to the reduced particle size and enhanced crystallinity of the material as well as the slower decay of photogenerated carriers on a nanosecond to sub-microsecond time range. Further optimization of this flux-assisted method together with suitable surface modification is expected to produce high-quality YTOS crystals with superior photocatalytic activity. 相似文献
494.
495.
Takuya Hashimoto Kazunari Takagi Kenji Tsuda Michiyoshi Tanaka Kaori Yoshida Hiroaki Tagawa Masayuki Dokiya 《ChemInform》2001,32(10):no-no
ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable via the “References” option. 相似文献
496.
497.
Kazunari Akiyoshi Masaharu Kohara Kensuke Ito Shinichi Kitamura Junzo Sunamoto 《Macromolecular rapid communications》1999,20(3):112-115
Amphiphilic A‐B block copolymers, ω‐methoxypoly(ethylene oxide)‐amylose copolymers (MPEO‐amylose), were synthesized by an enzymatic reaction using potato phosphorylase from an MPEO (Mw = 5.0×103)‐maltopentaosylamine derivative as a primer and α‐D ‐glucose‐1‐phosphate as a substrate. MPEO‐amyloses with various molecular weights of amylose (DP = 26, 36, 73 and 112) were obtained. None of the MPEO‐amyloses (5 mg/ml) precipitate in water containing 10 vol.‐% DMSO even after 24 h. The MPEO‐amyloses effectively form complexes with iodine in water. 相似文献