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In this paper, we propose a mechanism on how to construct long MDS self-dual codes from short ones. These codes are special types of generalized Reed-Solomon (GRS) codes or extended generalized Reed-Solomon codes. The main tool is utilizing additive structure or multiplicative structure on finite fields. By applying this method, more MDS self-dual codes can be constructed. 相似文献
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The complex-scaled Green's function(CGF)method is employed to explore the single-proton resonance in 15F.Special attention is paid to the first excited resonant state 5/2+,which has been widely studied in both theory and experiments.However,past studies generally overestimated the width of the 5/2+state.The predicted energy and width of the first excited resonant state 5/2+by the CGF method are both in good agreement with the experimental value and close to Fortune's new estimation.Furthermore,the influence of the potential parameters and quadruple deformation effects on the resonant states are investigated in detail,which is helpful to the study of the shell structure evolution. 相似文献
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Kwon Yongsoo Yang Heejung Chun Wanjoo Kim Myong Jo Yang Jinfeng 《Chemistry of Natural Compounds》2022,58(3):424-425
Chemistry of Natural Compounds - Phytochemical investigation of the MeOH extract of Angelica polymorpha stem led to the isolation of a new chromone (compound 9, named polymorphachromic acid). Based... 相似文献
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Shuyan Gong Mingze Sun Yiyang Lee Nigel Becknell Jiangwei Zhang Zhongqi Wang Liang Zhang Zhiqiang Niu 《Angewandte Chemie (International ed. in English)》2023,62(4):e202214516
Single crystal surfaces with highly coordinated sites very often hold high specific activities toward oxygen reduction reaction (ORR) and others. Transposing their high specific activity to practical high-surface-area electrocatalysts remains challenging. Here, ultrathin Pt(100) alloy surface is constructed via epitaxial growth. The surface shows 3.1–6.9 % compressive strain and bulk-like characteristics as demonstrated by site-probe reactions and different spectroscopies. Its ORR activity exceeds that of bulk Pt3Ni(100) and Pt(111) and presents a 19-fold increase in specific activity and a 13-fold increase in mass activity relative to commercial Pt/C. Moreover, the electrochemically active surface area (ECSA) is increased by 4-fold compared to traditional thin films (e.g. NSTF), which makes the catalyst more tolerant to voltage loss at high current densities under fuel cell operation. This work broadens the family of extended surface catalysts and highlights the knowledge-driven approach in the development of advanced electrocatalysts. 相似文献
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采用密度泛函理论平面波赝势的方法,计算了LiFeSO_4F和LiTi_(0.25)Fe_(0.75)SO_4F正极材料的电子结构。计算结果表明:当锂嵌入材料后,S、O和F的原子布居变化较小,电子主要填充在过渡金属的3d轨道,导致过渡金属被还原,成为电化学反应的活性中心。在嵌锂态中,锂和氧(氟)之间形成了离子键,而过渡金属(Ti和Fe)与氧(氟)之间则形成了共价键,S-O键的共价性最强。态密度的计算结果则表明:Ti和Fe均保持高自旋排列结构;LiFeSO_4F的两个自旋通道的带隙分别为2.88和2.29 e V,其导电性很差;Ti掺杂使体系的带隙消失,显著地提高了正极材料的导电性;LiTi_(0.25)Fe_(0.75)SO_4F系统中Ti-O和Ti-F键均比纯相中的Fe-O和Fe-F键的共价性更强,因此Ti掺杂材料具有更好的结构稳定性。 相似文献
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A novel quinoline-functionalized Schiff-base derivative PY was designed and synthesized. Sensor PY displayed highly selective and sensitive fluorescence enhancement and naked-eye color change to Fe3+ in the presence of other competing cations. The mechanisms have been supported by Job’s plot evaluation, FT-MS and theoretical calculations. The in situ generated PY-Fe3+ complex solution exhibited a high selectivity toward PPi via Fe3+ displacement approach. The detection limits of sensor PY to Fe3+ and PY-Fe3+ complex to PPi were estimated to be 4.24 × 10?8 M and 8.18 × 10?8 M, respectively. This successive recognition feature of sensor PY makes it has a potential utility for Fe3+ and PPi detection in aqueous solution. A B3LYP/6-31G(d,p) basis set was employed for optimization of PY and PY-Fe3+ complex. 相似文献