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61.
One-dimensional (1D) organic nanoribbons built on N-p-nitrophenylsalicylaldimine cadmium complex were synthesized via a facile solvothermal route. Scanning electron microscope images revealed that the as-synthesized products were ribbon like with widths of 500 nm,thicknesses of about 50nm, and lengthes up to several hundred micrometers. Fourier transform infrared spectrum was employed to characterize the structure. The conductivity of a bundle of nanoribbons was also measured,which showed that Schiff base cadmium nanoribbons had good photoconductive property. This work might enrich organic photoconductive materials and be applicable in nano photoswitch devices in the future. 相似文献
62.
Study on phenol adsorption from aqueous solutions on exfoliated graphitic nanoplatelets 总被引:1,自引:0,他引:1
Alina C. Ion Alla AlpatovaI. Ion Alina Culetu 《Materials Science and Engineering: B》2011,176(7):588-595
In this study we report first data on exfoliated graphitic nanoplatelets (xGnPs) as a sorbent for phenol removal and preliminary evaluated the ability of different type of natural organic matter (NOM) to effectively disperse exfoliated graphitic nanoplatelets. 相似文献
63.
Highly dispersed,high performance Pt and PtRu catalysts,supported on multiwalled carbon nanotubes(CNTs),were prepared by a high pressure organic colloid method.The particle sizes of the active components were as small as 1.2 nm for Pt and 1.1 nm for PtRu,and the active Pt surface areas were 295 and 395 m2/g,respectively.The catalysts showed very high activities toward the anodic oxidation of methanol,evaluated by cyclic voltammetry,being up to 4 times higher than that of commercial Johnson Matthey Hispec 20... 相似文献
64.
Der-Fong Juang Chao-Hsien Lee Chung-Shin Yuan 《The Science of the total environment》2010,408(20):4524-4531
To understand the potential threat of volatile organic compounds (VOCs) to the health of residents living close to a heavily polluted river, this study investigated the species and the concentration of VOCs evaporating from a river and surveyed the health condition of the nearby residents. Air samples were taken seasonally at the upstream, midstream, and downstream water surfaces of the river, and at different locations at certain distances from the river. These samples were analyzed qualitatively and quantitatively through gas chromatography and electron capture detector (GC/ECD) for chlorinated organic compounds, and through gas chromatography and flame ionization detector (GC/FID) for ordinary hydrocarbons. The health data obtained from valid health questionnaires of 908 residents were analyzed through Statistical Package for Social Science (SPSS) software. Twenty-six species of VOCs were identified in the environment adjacent the river, many of which are carcinogenic or believed to be carcinogenic to humans. However, results of this study shows that the VOCs evaporating from the polluted river have not been definitively identified as a major factor of cancer in the residents. However, the risk of suffering from certain chronic diseases may increase in residents living less than 225 m away from the river due to the high levels of evaporated VOCs. Residents living less than 225 m away from the river and with nearby specific industries are 3.130 times more at risk of suffering from chronic diseases than those with no nearby specific industries. 相似文献
65.
This study addresses two key issues, stability and efficiency, of polymer solar cells based on blended poly(3‐hexylthiophene) (P3HT) and [6,6]‐phenyl‐C61‐butyric acid methyl ester (PCBM) by demonstrating a film‐forming process that involves low‐temperature drying (?5 °C) and subsequent annealing of the active layer. The low‐temperature process achieves 4.70% power conversion efficiency (PCE) and ~1250 h storage half‐life at 65 °C, which are significant improvements over the 3.39% PCE and ~143 h half‐life of the regular room‐temperature process. The improvements are attributed to the enhanced nucleation of P3HT crystallites as well as the minimized separation of the P3HT and PCBM phases at the low drying temperature, which upon post‐drying annealing results in a morphology consisting of small PCBM‐rich domains interspersed within a densely interconnected P3HT crystal network. This morphology provides ample bulk‐heterojunction area for charge generation while allowing for facile charge transport; moreover, the P3HT crystal network serves as an immobile frame at heating temperatures less than the melting point (Tm) of P3HT, thus preventing PCBM/P3HT phase separation and the corresponding device degradation. 相似文献
66.
Unprecedented Homoleptic Bis‐Tridentate Iridium(III) Phosphors: Facile,Scaled‐Up Production,and Superior Chemical Stability 下载免费PDF全文
Jun Lin Yang Wang Premkumar Gnanasekaran Yu‐Cheng Chiang Chun‐Chieh Yang Chih‐Hao Chang Shih‐Hung Liu Gene‐Hsiang Lee Pi‐Tai Chou Yun Chi Shun‐Wei Liu 《Advanced functional materials》2017,27(35)
Bis‐tridentate Ir(III) metal complexes are expected to show great potential in organic light‐emitting diode (OLED) applications due to the anticipated, superb chemical and photochemical stability. Unfortunately, their exploitation has long been hampered by lack of adequate methodology and with inferior synthetic yields. This hurdle can be overcome by design of the first homoleptic, bis‐tridentate Ir(III) complex [Ir(pzpyph)(pzHpyph)] ( 1 ), for which the abbreviation (pzpyph)H (or pzHpyph) stands for the parent 2‐pyrazolyl‐6‐phenyl pyridine chelate. After that, methylation and double methylation of 1 afford the charge‐neutral Ir(III) complex [Ir(pzpyph)(pzMepyph)] ( 2 ) and cationic complex [Ir(pzMepyph)2][PF6] ( 3 ), while deprotonation of 1 gives formation of anionic [Ir(pzpyph)2][NBu4] ( 4 ), all in high yields. These bis‐tridentate Ir(III) complexes 2 – 4 are highly emitted in solution and solid states, while the charge‐neutral 2 and corresponding t ‐butyl substituted derivative [Ir(pzpyBuph)(pzMepyBuph)] ( 5 ) exhibit superior photostability versus the tris‐bidentate references [Ir(ppy)2(acac)] and [Ir(ppy)3] in toluene under argon, making them ideal OLED emitters. For the track record, phosphor 5 gives very small efficiency roll‐off and excellent overall efficiencies of 20.7%, 66.8 cd A?1, and 52.8 lm W?1 at high brightness of 1000 cd m?2. These results are expected to inspire further studies on the bis‐tridentate Ir(III) complexes, which are judged to be more stable than their tris‐bidentate counterparts from the entropic point of view. 相似文献
67.
Highly Efficient Three Primary Color Organic Single‐Crystal Light‐Emitting Devices with Balanced Carrier Injection and Transport 下载免费PDF全文
Ran Ding Jing Feng Feng‐Xi Dong Wei Zhou Yang Liu Xu‐Lin Zhang Xue‐Peng Wang Hong‐Hua Fang Bin Xu Xian‐Bin Li Hai‐Yu Wang Shu Hotta Hong‐Bo Sun 《Advanced functional materials》2017,27(13)
Organic single crystals have a great potential in the field of organic optoelectronics because of their advantages of high carrier mobility and high thermal stability. However, the application of the organic single crystals in light‐emitting devices (OLEDs) has been limited by single‐layered structure with unbalanced carrier injection and transport. Here, fabrication of a multilayered‐structure crystal‐based OLED constitutes a major step toward balanced carrier injection and transport by introducing an anodic buffer layer and electron transport layer into the device structure. Three primary color single‐crystal‐based OLEDs based on the multilayered structure and molecular doping exhibit a maximum luminance and current efficiency of 820 cd cm?2 and 0.9 cd A?1, respectively, which are the highest performance to date for organic single‐crystal‐based OLEDs. This work paves the way toward high‐performance organic optoelectronic devices based on the organic single crystals. 相似文献
68.
Qiaomu Wang Kaifei Tang Qiaobo Liao Yang Xu Haocheng Xu Yandong Wang Peng Wang Zhen Meng Kai Xi 《Advanced functional materials》2023,33(6):2211356
Covalent organic frameworks (COFs) with various topologies are typically synthesized by selecting and designing connecting units with rich shapes. However, this process is time-consuming and labour-intensive. Besides, the tight stacking of COFs layers greatly restrict their structural advantages. It is crucial to effectively exploit the high porosity and active sites of COFs by topological design. Herein, for the first time, inducing in situ topological changes in sub-chemometric COFs by adding graphene oxide (GO) without replacing the monomer, is proposed. Surprisingly, GO can slow down the intermolecular stacking and induce rearrangement of COFs nanosheets. The channels of D- [4+3] COFs are significantly altered while the stacking of periodically expanded framework is weakened. This not only maximizes the exposure of pore area and polar groups, but also shortens the channels and increases the redox activity, which enables high loading while enhancing host-guest interactions. This topological transformation to exhibit the structural features of COFs for efficient application is an innovative molecular design strategy. 相似文献
69.
Minhao Jiang Xiangyu Yan Yibo Wang Fang Pu Huiling Liu Yumei Li Chunfeng Yang Jiawei Zhu Xuemeng Liu Jinsong Ren Xiaogang Qu 《Advanced functional materials》2023,33(24):2300091
Hydrogen-bond organic frameworks (HOFs) with excellent structural and luminescent properties have emerged as a promising material for the construction of fluorescence sensors. However, designing a facile, universal and high throughput sensor with multiplex detection capacity still remains challenging. Herein, a one-component sensor array is constructed that mimics natural gustatory system for accurate and high-throughput discrimination and identification of versatile analytes. HOF as a single sensing element greatly simplifies the probe preparation in sensor array and detection procedure. Metal ions, proteins and bacteria as the model targets are rapid and accurately discriminated, presenting the universality of the system. Particularly, the system is successfully used for the classification of antibiotic mechanisms. The study expands the application scope of HOFs and provides a facile and universal system for sensing applications. 相似文献
70.
Louis Frentzel-Beyme Pascal Kolodzeiski Kai Terlinden Sebastian Henke 《Advanced functional materials》2023,33(36):2302033
Porous framework materials are of major importance for a wide range of technologies. Nevertheless, many of these materials lack processibility as they are typically synthesized under rather harsh conditions and obtained as microcrystalline powders that cannot easily be coated or deposited from solution. Herein, a new approach to water-processable metal–organic framework materials is presented. The materials are based on amphiphilic organic building blocks consisting of polar carboxylate groups and non-polar alkyl chains connected to a rigid aromatic core. The amphiphilic building blocks assemble to porous framework structures via bonding to kinetically labile sodium ions from concentrated aqueous solution. The obtained crystalline materials, termed amphiphile salt frameworks , are thermally and mechanically stable (some derivatives up to 365 °C and up to at least 4000 bar hydrostatic pressure), exhibit persistent microporous channels accessible to several gases (N2, CO2, propane, propylene, n-butane), and can be reversibly assembled/disassembled by crystallization from or dissolution in water. Systematic variation of the hydrophobic side chains of the amphiphile building blocks allows extracting structure-property relationships and first design rules for this new class of water-processable microporous framework materials. 相似文献