共查询到20条相似文献,搜索用时 31 毫秒
1.
Dr. Hong Wang Dr. Lu Wang Dr. Qiang Wang Shuyang Ye Dr. Wei Sun Yue Shao Zhiping Jiang Dr. Qiao Qiao Dr. Yimei Zhu Prof. Pengfei Song Dr. Debao Li Prof. Le He Prof. Xiaohong Zhang Prof. Jiayin Yuan Prof. Tom Wu Prof. Geoffrey A. Ozin 《Angewandte Chemie (International ed. in English)》2018,57(38):12360-12364
Ammonia, a key precursor for fertilizer production, convenient hydrogen carrier, and emerging clean fuel, plays a pivotal role in sustaining life on Earth. Currently, the main route for NH3 synthesis is by the heterogeneous catalytic Haber–Bosch process (N2+3 H2→2 NH3), which proceeds under extreme conditions of temperature and pressure with a very large carbon footprint. Herein we report that a pristine nitrogen‐doped nanoporous graphitic carbon membrane (NCM) can electrochemically convert N2 into NH3 in an acidic aqueous solution under ambient conditions. The Faradaic efficiency and rate of production of NH3 on the NCM electrode reach 5.2 % and 0.08 g m?2 h?1, respectively. Functionalization of the NCM with Au nanoparticles dramatically enhances these performance metrics to 22 % and 0.36 g m?2 h?1, respectively. As this system offers the potential to be scaled to industrial levels it is highly likely that it might displace the century‐old Haber–Bosch process. 相似文献
2.
Howard Yi Fan Sim Jaslyn Ru Ting Chen Charlynn Sher Lin Koh Hiang Kwee Lee Xuemei Han Gia Chuong Phan‐Quang Jing Yi Pang Chee Leng Lay Srikanth Pedireddy In Yee Phang Edwin Kok Lee Yeow Xing Yi Ling 《Angewandte Chemie (International ed. in English)》2020,59(39):16997-17003
The electrochemical nitrogen reduction reaction (NRR) offers a sustainable solution towards ammonia production but suffers poor reaction performance owing to preferential catalyst–H formation and the consequential hydrogen evolution reaction (HER). Now, the Pt/Au electrocatalyst d‐band structure is electronically modified using zeolitic imidazole framework (ZIF) to achieve a Faradaic efficiency (FE) of >44 % with high ammonia yield rate of >161 μg mgcat?1 h?1 under ambient conditions. The strategy lowers electrocatalyst d‐band position to weaken H adsorption and concurrently creates electron‐deficient sites to kinetically drive NRR by promoting catalyst–N2 interaction. The ZIF coating on the electrocatalyst doubles as a hydrophobic layer to suppress HER, further improving FE by >44‐fold compared to without ZIF (ca. 1 %). The Pt/Au‐NZIF interaction is key to enable strong N2 adsorption over H atom. 相似文献
3.
Youwen Liu Ming Cheng Zhihai He Bingchuan Gu Chong Xiao Tengfei Zhou Zaiping Guo Jiandang Liu Haiyan He Bangjiao Ye Bicai Pan Yi Xie 《Angewandte Chemie (International ed. in English)》2019,58(3):731-735
Nitrate is a raw ingredient for the production of fertilizer, gunpowder, and explosives. Developing an alternative approach to activate the N≡N bond of naturally abundant nitrogen to form nitrate under ambient conditions will be of importance. Herein, pothole‐rich WO3 was used to catalyse the activation of N≡N covalent triple bonds for the direct nitrate synthesis at room temperature. The pothole‐rich structure endues the WO3 nanosheet more dangling bonds and more easily excited high momentum electrons, which overcome the two major bottlenecks in N≡N bond activation, that is, poor binding of N2 to catalytic materials and the high energy involved in this reaction. The average rate of nitrate production is as high as 1.92 mg g?1 h?1 under ambient conditions, without any sacrificial agent or precious‐metal co‐catalysts. More generally, the concepts will initiate a new pathway for triggering inert catalytic reactions. 相似文献
4.
The direct synthesis of nanostructured electrode materials on three‐dimensional substrates is important for their practical application in electrochemical cells without requiring the use of organic additives or binders. In this study, we present a simple two‐step process to synthesize a stable core–shell structured cobalt sulfide/cobalt aluminum hydroxide nanosheet (LDH‐S) for pseudocapacitor electrode application. The cobalt aluminum layered double hydroxide (CoAl‐LDH) nanoplates were synthesized in basic aqueous solution with a kinetically‐controlled thickness. Owing to the facile diffusion of electrolytes through the nanoplates, thin CoAl‐LDH nanoplates have higher specific capacitance values than thick nanoplates. The as‐grown CoAl‐LDH nanoplates were transformed into core–shell structured LDH‐S nanosheets by a surface modification process in Na2S aqueous solution. The chemically robust cobalt sulfide (CoS) shell increased the electrochemical stability compared to the sulfide‐free CoAl‐LDH electrodes. The LDH‐S electrodes exhibited high electrochemical performance in terms of specific capacitance and rate capability with a galvanostatic discharge of 1503 F g?1 at a current density of 2 A g?1 and a specific capacitance of 91 % at 50 A g?1. 相似文献
5.
Wence Xu Guilan Fan Jialiang Chen Jinhan Li Le Zhang Shengli Zhu Xuncheng Su Fangyi Cheng Jun Chen 《Angewandte Chemie (International ed. in English)》2020,59(9):3511-3516
The electrocatalytic nitrogen reduction reaction (NRR) is an alternative eco‐friendly strategy for sustainable N2 fixation with renewable energy. However, NRR suffers from sluggish kinetics owing to difficult N2 adsorption and N≡N cleavage. Now, nanoporous palladium hydride is reported as electrocatalyst for electrochemical N2 reduction under ambient conditions, achieving a high ammonia yield rate of 20.4 μg h?1 mg?1 with a Faradaic efficiency of 43.6 % at low overpotential of 150 mV. Isotopic hydrogen labeling studies suggest the involvement of lattice hydrogen atoms in the hydride as active hydrogen source. In situ Raman analysis and density functional theory (DFT) calculations further reveal the reduction of energy barrier for the rate‐limiting *N2H formation step. The unique protonation mode of palladium hydride would provide a new insight on designing efficient and robust electrocatalysts for nitrogen fixation. 相似文献
6.
Thermoregulated Phase‐Transition Synthesis of Two‐Dimensional Carbon Nanoplates Rich in sp2 Carbon and Unimodal Ultramicropores for Kinetic Gas Separation
下载免费PDF全文
![点击此处可从《Angewandte Chemie (International ed. in English)》网站下载免费的PDF全文](/ch/ext_images/free.gif)
Lu‐Hua Zhang Prof. Wen‐Cui Li Dr. Hong Liu Quan‐Gao Wang Lei Tang Qing‐Tao Hu Wen‐Jing Xu Prof. Wei‐Hong Qiao Prof. Zhong‐Yuan Lu Prof. An‐Hui Lu 《Angewandte Chemie (International ed. in English)》2018,57(6):1632-1635
The development of highly selective, chemically stable and moisture‐resistant adsorbents is a key milestone for gas separation. Porous carbons featured with random orientation and cross‐linking of turbostratic nanodomains usually have a wide distribution of micropores. Here we have developed a thermoregulated phase‐transition‐assisted synthesis of carbon nanoplates with more than 80 % sp2 carbon, unimodal ultramicropore and a controllable thickness. The thin structure allows oriented growth of carbon crystallites, and stacking of crystallites in nearly parallel orientation are responsible for the single size of the micropores. When used for gas separation from CH4, carbon nanoplates exhibit high uptakes (5.2, 5.3 and 5.1 mmol g?1) and selectivities (7, 71 and 386) for CO2, C2H6 and C3H8 under ambient conditions. The dynamic adsorption capacities are close to equilibrium uptakes of single components, further demonstrating superiority of carbon nanoplates in terms of selectivity and sorption kinetics. 相似文献
7.
K2Mn4O8/Reduced Graphene Oxide Nanocomposites for Excellent Lithium Storage and Adsorption of Lead Ions
下载免费PDF全文
![点击此处可从《Chemistry (Weinheim an der Bergstrasse, Germany)》网站下载免费的PDF全文](/ch/ext_images/free.gif)
Shu‐Meng Hao Prof. Jin Qu Jing Yang Chen‐Xi Gui Qian‐Qian Wang Qian‐Jie Li Prof. Xiaofeng Li Prof. Zhong‐Zhen Yu 《Chemistry (Weinheim an der Bergstrasse, Germany)》2016,22(10):3397-3404
Ion diffusion efficiency at the solid–liquid interface is an important factor for energy storage and adsorption from aqueous solution. Although K2Mn4O8 (KMO) exhibits efficient ion diffusion and ion‐exchange capacities, due to its high interlayer space of 0.70 nm, how to enhance its mass transfer performance is still an issue. Herein, novel layered KMO/reduced graphene oxide (RGO) nanocomposites are fabricated through the anchoring of KMO nanoplates on RGO with a mild solution process. The face‐to‐face structure facilitates fast transfer of lithium and lead ions; thus leading to excellent lithium storage and lead ion adsorption. The anchoring of KMO on RGO not only increases electrical conductivity of the layered nanocomposites, but also effectively prevents aggregation of KMO nanoplates. The KMO/RGO nanocomposite with an optimal RGO content exhibits a first cycle charge capacity of 739 mA h g?1, which is much higher than that of KMO (326 mA h g?1). After 100 charge–discharge cycles, it still retains a charge capacity of 664 mA h g?1. For the adsorption of lead ions, the KMO/RGO nanocomposite exhibits a capacity of 341 mg g?1, which is higher than those of KMO (305 mg g?1) and RGO (63 mg g?1) alone. 相似文献
8.
Defect Engineering Metal‐Free Polymeric Carbon Nitride Electrocatalyst for Effective Nitrogen Fixation under Ambient Conditions
下载免费PDF全文
![点击此处可从《Angewandte Chemie (International ed. in English)》网站下载免费的PDF全文](/ch/ext_images/free.gif)
Chade Lv Yumin Qian Chunshuang Yan Yu Ding Prof. Yuanyue Liu Prof. Gang Chen Prof. Guihua Yu 《Angewandte Chemie (International ed. in English)》2018,57(32):10246-10250
Electrocatalytic nitrogen reduction reaction (NRR) under ambient conditions provides an intriguing picture for the conversion of N2 into NH3. However, electrocatalytic NRR mainly relies on metal‐based catalysts, and it remains a grand challenge in enabling effective N2 activation on metal‐free catalysts. Here we report a defect engineering strategy to realize effective NRR performance (NH3 yield: 8.09 μg h?1 mg?1cat., Faradaic efficiency: 11.59 %) on metal‐free polymeric carbon nitride (PCN) catalyst. Illustrated by density functional theory calculations, dinitrogen molecule can be chemisorbed on as‐engineered nitrogen vacancies of PCN through constructing a dinuclear end‐on bound structure for spatial electron transfer. Furthermore, the N?N bond length of adsorbed N2 increases dramatically, which corresponds to “strong activation” system to reduce N2 into NH3. This work also highlights the significance of defect engineering for improving electrocatalysts with weak N2 adsorption and activation ability. 相似文献
9.
Mariya Edeleva Sylvain R. A. Marque Kuanish Kabytaev Yohann Guillaneuf Didier Gigmes Elena Bagryanskaya 《Journal of polymer science. Part A, Polymer chemistry》2013,51(6):1323-1336
Thermal decomposition of four tertiary N‐(2‐methylpropyl)‐N‐(1‐diethylphosphono‐2,2‐dimethylpropyl)‐N‐oxyl (SG1)‐based alkoxyamines (SG1‐C(Me)2‐C(O)‐OR, R = Me, tBu, Et, H) has been studied at different experimental conditions using 1H and 31P NMR spectroscopies. This experiment represents the initiating step of methyl methacrylate polymerization. It has been shown that H‐transfer reaction occurs during the decomposition of three alkoxyamines in highly degassed solution, whereas no products of H‐transfer are detected during decomposition of SG1‐MAMA alkoxyamine. The value of the rate constant of H‐transfer for alkoxyamines 1 (SG1‐C(Me)2‐C(O)‐OMe) and 2 ( SG1‐C(Me)2‐C(O)‐OtBu) has been estimated as 1.7 × 103 M?1s?1. The high influence of oxygen on decomposition mechanism is found. In particular, in poorly degassed solutions, nearly quantitative formation of oxidation product has been observed, whereas at residual pressure of 10?5 mbar, the main products originate from H‐atom transfer reaction. The acidity of the reaction medium affects the decomposition mechanism suppressing the H‐atom transfer. © 2012 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem, 2013 相似文献
10.
Electrolytic ammonia synthesis from nitrogen at ambient conditions is appearing as a promising alternative to the Haber‐Bosch process which is consuming high energy and emitting CO2. Here, a typical MOF material, HKUST‐1 (Cu?BTC, BTC=benzene‐1,3,5‐tricarboxylate), was selected as an electrocatalyst for the reaction of converting N2 to NH3 under ambient conditions. At ?0.75 V vs. reversible hydrogen electrode, it achieves excellent catalytic performance in the electrochemical synthesis of ammonia with high NH3 yield (46.63 μg h?1 mg?1 cat. or 4.66 μg h?1 cm?2) and good Faraday efficiency (2.45%). It is indicated that the good performance of the HKUST‐1 catalyst may originate from the formation of Cu(I). In addition, the catalyst also has good selectivity for N2 to NH3. 相似文献
11.
A Molecular Copper Catalyst for Electrochemical Water Reduction with a Large Hydrogen‐Generation Rate Constant in Aqueous Solution
下载免费PDF全文
![点击此处可从《Angewandte Chemie (International ed. in English)》网站下载免费的PDF全文](/ch/ext_images/free.gif)
Peili Zhang Prof. Mei Wang Yong Yang Tianyi Yao Prof. Licheng Sun 《Angewandte Chemie (International ed. in English)》2014,53(50):13803-13807
The copper complex [(bztpen)Cu](BF4)2 (bztpen=N‐benzyl‐N,N′,N′‐tris(pyridin‐2‐ylmethyl)ethylenediamine) displays high catalytic activity for electrochemical proton reduction in acidic aqueous solutions, with a calculated hydrogen‐generation rate constant (kobs) of over 10000 s?1. A turnover frequency (TOF) of 7000 h?1 cm?2 and a Faradaic efficiency of 96 % were obtained from a controlled potential electrolysis (CPE) experiment with [(bztpen)Cu]2+ in pH 2.5 buffer solution at ?0.90 V versus the standard hydrogen electrode (SHE) over two hours using a glassy carbon electrode. A mechanism involving two proton‐coupled reduction steps was proposed for the dihydrogen generation reaction catalyzed by [(bztpen)Cu]2+. 相似文献
12.
John Giantsidis Mark M. Turnbull 《Acta Crystallographica. Section C, Structural Chemistry》2000,56(3):334-335
The title compound, 2‐amino‐5‐carboxypyridinium chloride, C6H7N2O2+·Cl?, was isolated from a 1 M HCl aqueous solution containing 2‐amino‐5‐cyanopyridine. The structure is held together by extensive hydrogen bonding between the chloride ions and the carboxylic acid, amino and pyridinium H atoms. The molecules pack as sheets, with the sheets at a distance of 3.21 (3) Å from one another. 相似文献
13.
Lili Zhang Liang‐Xin Ding Gao‐Feng Chen Xianfeng Yang Haihui Wang 《Angewandte Chemie (Weinheim an der Bergstrasse, Germany)》2019,131(9):2638-2642
Constructing efficient catalysts for the N2 reduction reaction (NRR) is a major challenge for artificial nitrogen fixation under ambient conditions. Herein, inspired by the principle of “like dissolves like”, it is demonstrated that a member of the nitrogen family, well‐exfoliated few‐layer black phosphorus nanosheets (FL‐BP NSs), can be used as an efficient nonmetallic catalyst for electrochemical nitrogen reduction. The catalyst can achieve a high ammonia yield of 31.37 μg h?1 mg?1cat. under ambient conditions. Density functional theory calculations reveal that the active orbital and electrons of zigzag and diff‐zigzag type edges of FL‐BP NSs enable selective electrocatalysis of N2 to NH3 via an alternating hydrogenation pathway. This work proves the feasibility of using a nonmetallic simple substance as a nitrogen‐fixing catalyst and thus opening a new avenue towards the development of more efficient metal‐free catalysts. 相似文献
14.
Bi‐doped TiO2 nanotubes with variable Bi/Ti ratios were synthesized by hydrothermal treatment in 10 mol·L?1 NaOH (aq.) through using Bi‐doped TiO2 particles derived from conventional sol‐gel method as starting materials. The effects of Bi content on the morphology, textural properties, photo absorption and photocatalytic activity of TiO2 nanotubes were investigated. The scanning electron microscopy (SEM), transmission electron microscopy (TEM), X‐ray diffraction (XRD) and X‐ray photoelectron spectroscopy (XPS) observations of the obtained samples revealed the formation of titanate nanotube structure doped with Bi, which exists as a higher oxidation state than Bi3+. Bi‐doping TiO2 nanotubes exhibited an extension of light absorption into the visible region and improved photocatalytic activities for hydrogen production from a glycerol/water mixed solution as compared with pure TiO2 nanotubes. There was an optimal Bi‐doped content for the photocatalytic hydrogen production, and high content of Bi would retard the phase transition of titanate to anatase and result in morphology change from nanotube to nanobelt, which in turn decreases the photocatlytic activity for hydrogen evolution. 相似文献
15.
The analysis of 17O NMR transverse relaxation rates and EPR transverse electronic relaxation rates for aqueous solutions of the four DTPA‐like (DTPA = diethylenetriamine‐N,N,N′,N″,N″‐pentaacetic acid) complexes, [Gd(DTPA‐PY)(H2O)]? (DTPA‐PY = N′‐(2‐pyridylmethyl)), [Gd(DTPA‐HP)(H2O)2]? (DTPA‐HP = N′‐(2‐hydroxypropyl)), [Gd(DTPA‐H1P)(H2O)2]? (DTPA‐H1P = N′‐(2‐hydroxy‐1‐phenylethyl)) and [Gd(DTPA‐H2P)(H2O)2] (DTPA‐H2P = N′‐(2‐hydroxy‐2‐phenylethyl)), at various temperatures allows us to understand the water exchange dynamics of these four complexes. The water‐exchange lifetime (τM) parameters for [Gd(DTPA‐PY)(H2O)]?, [Gd(DTPA‐HP)(H2O)2]?, [Gd(DTPA‐H1P)(H2O)2]? and [Gd(DTPA‐H2P)(H2O)2] are of 585, 98, 163, and 69 ns, respectively. Compared with [Gd(DTPA)(H2O)]2? (τM = 303 ns), the τM value of [Gd(DTPA‐PY)(H2O)]? is slightly higher, but the other three complexes values are significantly lower than those of [Gd(DTPA)(H2O)]2?. This difference is explained by the fact that the gadolinium(III) complexes of DTPA‐HP, DTPA‐H1P, and DTPA‐H2P have two inner‐sphere waters. The 2H longitudinal relaxation rates of the labeled diamagnetic lanthanum complex allow the calculation of its rotational correlation time (τR). The τR values calculated for DTPA‐PY, DTPA‐HP, DTPA‐H1P, and DTPA‐H2P are of 127, 110, 142 and 147 ps, respectively. These four values are higher than the value of [La(DTPA)]2? (τR = 103 ps), because the rotational correlation time is related to the magnitude of its molecular weight. 相似文献
16.
Huan Ouyang Dr. Ning Chen Guojing Chang Xiaoliang Zhao Yuanyuan Sun Dr. Shuai Chen Prof. Huawei Zhang Prof. Dongjiang Yang 《Angewandte Chemie (International ed. in English)》2018,57(40):13197-13201
Chemically durable and effective absorbent materials for selenite (SeO32?) remain highly desirable for contamination remediation. Now a bismuth‐based metal–organic framework (Bi‐MOF, CAU‐17) was used as adsorbent to capture SeO32? anions from aqueous solution with ultrahigh adsorption capacity of 255.3 mg g?1 and fast kinetics. Furthermore, the adsorbent showed excellent selectivity for SeO32? and was able to work steadily in a broad pH range of 4–11. Density functional theory (DFT) calculation, XANES modeling, and EXAFS fitting suggested that SeO32? anions were immobilized by forming Bi?O?Se bonds (T‐3 structural model) though splitting the O?Bi?O bond in the crystal structure, leading to a structural transformation of CAU‐17 in the solid state. 相似文献
17.
Linping Mu Zhiqun He Prof. Xiangfei Kong Guanbao Hui Min Xu Chunjun Liang Dr. Xiping Jing Dr. Andrzej Danel Dr. Ewa Kulig Dr. 《Chemphyschem》2010,11(12):2623-2629
Pyrazolo[3,4‐b]quinoline derivatives are reported to be highly efficient organic fluorescent materials suitable for applications in light‐emitting devices. Although their fluorescence remains stable in organic solvents or in aqueous solution even in the presence of H2O, halide salts (LiCl), alkali (NaOH) and weak acid (acetic acid), it suffers an efficient quenching process in the presence of protic acid (HCl) in aqueous or ethanolic solution. This quenching process is accompanied by a change in the UV spectrum, but it is reversible and can be fully recovered. Both steady‐state and transient fluorescence spectra of 1‐phenyl‐3,4‐dimethyl‐1H‐pyrazolo‐[3,4‐b]quinoline (PAQ5) during quenching are measured and analyzed. It is found that a combined dynamic and static quenching mechanism is responsible for the quenching processes. The ground‐state proton‐transfer complex [PAQ5 ??? H+] is responsible for static quenching. It changes linearly with proton concentration [H+] with a bimolecular association constant KS=1.95 M ?1 controlled by the equilibrium dissociation of HCl in ethanol. A dynamic quenching constant KD=22.4 M ?1 is obtained by fitting to the Stern–Volmer equation, with a bimolecular dynamic quenching rate constant kd=1.03×109 s?1 M ?1 under ambient conditions. A change in electron distribution is simulated and explains the experiment results. 相似文献
18.
Bifunctional Electrocatalysts for Overall Water Splitting from an Iron/Nickel‐Based Bimetallic Metal–Organic Framework/Dicyandiamide Composite
下载免费PDF全文
![点击此处可从《Angewandte Chemie (International ed. in English)》网站下载免费的PDF全文](/ch/ext_images/free.gif)
Xiaojia Zhao Dr. Pradip Pachfule Shuang Li Jan Ron Justin Simke Dr. Johannes Schmidt Prof. Dr. Arne Thomas 《Angewandte Chemie (International ed. in English)》2018,57(29):8921-8926
Pyrolysis of a bimetallic metal–organic framework (MIL‐88‐Fe/Ni)‐dicyandiamide composite yield a Fe and Ni containing carbonaceous material, which is an efficient bifunctional electrocatalyst for overall water splitting. FeNi3 and NiFe2O4 are found as metallic and metal oxide compounds closely embedded in an N‐doped carbon–carbon nanotube matrix. This hybrid catalyst (Fe‐Ni@NC‐CNTs) significantly promotes the charge transfer efficiency and restrains the corrosion of the metallic catalysts, which is shown in a high OER and HER activity with an overpotential of 274 and 202 mV, respectively at 10 mA cm?2 in alkaline solution. When this bifunctional catalyst was further used for H2 and O2 production in an electrochemical water‐splitting unit, it can operate in ambient conditions with a competitive gas production rate of 1.15 and 0.57 μL s?1 for hydrogen and oxygen, respectively, showing its potential for practical applications. 相似文献
19.
Dr. Madleen Busse Iman Trinh Prof. Peter C. Junk Assoc. Prof. Richard L. Ferrero Prof. Philip C. Andrews 《Chemistry (Weinheim an der Bergstrasse, Germany)》2013,19(17):5264-5275
The synthesis and characterisation of nine new tris‐substituted bismuth(III) aminoarenesulfonates of the general formula [Bi(O3S‐RN)3] (RN=o‐aminophenyl 1 , m‐aminophenyl 2 , 6‐amino‐3‐methoxyphenyl 3 , p‐aminophenyl 4 , 2‐pyridyl 5 , o‐aminonaphthyl 6 , 5‐aminonaphthyl 7 , 4‐amino‐3‐hydroxynaphthyl 8 and 5‐isoquinolinyl 9 ) is described. Two synthetic strategies, using Ag2O and [Bi(OtBu)3], were explored and compared. The possibility to access heteroleptic bismuth(III) complexes with the new silver(I) metathesis reaction is demonstrated with the synthesis of the heteroleptic bismuth(III) aminoarenesulfonate complexes [PhBi(O3S‐P2)2(dmso)] 10 , [Ph2Bi(O3S‐P2)]∞ 11 and [PhBi(O3S‐P2)2]∞ 12 , of which the solid state structures 10 and 12 are presented (2P‐SO3?=2‐pyridinesulfonate). These complexes offer remarkable in‐vitro activity against three standard laboratory strains of Helicobacter pylori (H. pylori) as demonstrated by their exceptionally low minimum inhibitory concentration (MIC) values of 0.049 μg mL?1 for the strains 251 and B128, which places most MIC values in the nano‐molar region. These results demonstrate the importance of the amino functionality in addition to the sulfonate group on the bactericidal properties against H. pylori. 相似文献
20.
Graphitic Carbon Nitride/Nitrogen‐Rich Carbon Nanofibers: Highly Efficient Photocatalytic Hydrogen Evolution without Cocatalysts
下载免费PDF全文
![点击此处可从《Angewandte Chemie (International ed. in English)》网站下载免费的PDF全文](/ch/ext_images/free.gif)
Qing Han Bing Wang Jian Gao Prof. Liangti Qu 《Angewandte Chemie (International ed. in English)》2016,55(36):10849-10853
An interconnected framework of mesoporous graphitic‐C3N4 nanofibers merged with in situ incorporated nitrogen‐rich carbon has been prepared. The unique composition and structure of the nanofibers as well as strong coupling between the components endow them with efficient light‐harvesting properties, improved charged separation, and a multidimensional electron transport path that enhance the performance of hydrogen production. The as‐obtained catalyst exhibits an extremely high hydrogen‐evolution rate of 16885 μmol h?1 g?1, and a remarkable apparent quantum efficiency of 14.3 % at 420 nm without any cocatalysts, which is much higher than most reported g‐C3N4‐based photocatalysts even in the presence of Pt‐based cocatalysts. 相似文献