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991.
992.
Phase-pure and well-intergrown Cu-LTA membranes are developed through copper ions exchange of sodium ions in Na-LTA framework. For pervaporation of 90.0 wt% ethanol/10.0 wt% water mixtures, the Cu-LTA membrane shows much higher water flux than Na-LTA membranes due to the enhancement of the pore size after ions exchange. 相似文献
993.
Yan‐Tong Xu Zi‐Ming Ye Jia‐Wen Ye Li‐Ming Cao Rui‐Kang Huang Jun‐Xi Wu Dong‐Dong Zhou Xue‐Feng Zhang Chun‐Ting He Jie‐Peng Zhang Xiao‐Ming Chen 《Angewandte Chemie (Weinheim an der Bergstrasse, Germany)》2019,131(1):145-149
Cobalt imidazolate frameworks are classical electrocatalysts for the oxygen evolution reaction (OER) but suffer from the relatively low activity. Here, a non‐3d metal modulation strategy is presented for enhancing the OER activity of cobalt imidazolate frameworks. Two isomorphous frameworks [Co4(MO4)(eim)6] (M=Mo or W, Heim=2‐ethylimidazole) having Co(eim)3(MO4) units and high water stabilities were designed and synthesized. In different neutral media, the Mo‐modulated framework coated on a glassy carbon electrode shows the best OER performances (1 mA cm?2 at an overpotential of 210 mV in CO2‐saturated 0.5 m KHCO3 electrolyte and 2/10/22 mA cm?2 at overpotential of 388/490/570 mV in phosphate buffer solution) among non‐precious metal catalysts and even outperforms RuO2. Spectroscopic measurements and computational simulations revealed that the non‐3d metals modulate the electronic structure of Co for optimum reactant/product adsorption and tailor the energy of rate‐determining step to a more moderate value. 相似文献
994.
Shuning Cai Wenting Deng Feifei Huang Lijue Chen Chun Tang Wenxiang He Shichuan Long Ruihao Li Zhibing Tan Junyang Liu Jia Shi Zitong Liu Zongyuan Xiao Deqing Zhang Wenjing Hong 《Angewandte Chemie (Weinheim an der Bergstrasse, Germany)》2019,131(12):3869-3873
Photoresponsive molecular systems are essential for molecular optoelectronic devices, but most molecular building blocks are non‐photoresponsive. Employed here is a photoinduced proton transfer (PIPT) strategy to control charge transport through single‐molecule azulene junctions with visible light under ambient conditions, which leads to a reversible and controllable photoresponsive molecular device based on non‐photoresponsive molecules and a photoacid. Also demonstrated is the application of PIPT in two single‐molecule AND gate and OR gate devices with electrical signal as outputs. 相似文献
995.
Sharon Hongxia Guan Michelle Wenlin Huang Xiaoping Li Qingsong Cai 《Analytical letters》2018,51(4):613-625
Four commonly found pesticides (alachlor, atrazine, metolachlor, and simazine) in surface water were determined using dispersive pipette extraction followed by gas chromatography–mass spectrometry. The rapid mixing and equilibrium between the dispersive pipette extraction adsorbent and water sample resulted in fast and efficient extraction. Using only 5?mL of water sample, the estimated time consumption for extraction of each sample was less than 5?min. Method validation was performed to evaluate accuracy, precision, linearity, the limits of detection, and the limits of quantitation. Average recovery of above 90% was obtained with relative standard deviations below 10%, which indicated good accuracy and precision of the dispersive pipette extraction method. Coefficients of determination were all above 0.9901 and showed good linearity. For the four pesticides studied using the current method, the limits of detection ranged from 7 to 40?ng?L?1, and limits of quantitation were from 20 to 130?ng?L?1. Method validation results supported the application of the current method for drinking water safety monitoring per National Primary Drinking Water Regulations established by the US Environmental Protection Agency. Water samples from Lake Lanier and Stone Mountain Lake (Georgia, USS) were analyzed with this method as a preliminary work for a larger scale drinking water quality study in the future. Trace amounts of simazine and atrazine were found in lake water samples, but both were below the regulation levels of the US Environmental Protection Agency. 相似文献
996.
A water-soluble polysaccharide TC-DHPA4 with a molecular weight of 8.0 × 105 Da was isolated from tissue-cultured Dendrobium huoshanense by anion exchange and gel permeation chromatography. Monosaccharide analysis revealed that the homogeneous polysaccharide was made up of rhamnose, arabinose, mannose, glucose, galactose and glucuronic acid with a molar ratio of 1.28:1:1.67:4.71:10.43:1.42. The sugar residue sequence analysis based on the GC-MS files and NMR spectra indicated that the backbone of TC-DHPA4 consisted of the repeated units:→6)-β-Galp-(1→6)-β-Galp-(1→4)-β-GlcpA-(1→6)-β-Glcp-(1→6)-β-Glcp-(→. The sugar residue sequences β-Glcp-(1→)-α-Rhap-(1→3)-β-Galp-(1→, β-Glcp-(1→4)-α-Rhap-(1→3)-β-Galp-(1→, β-Galp-(1→6)-β-Manp-(1→3)-β-Galp-(1→, and α-l-Araf-(1→2)-β-Manp-(1→3)-β-Galp-(1→ were identified as the branches attached to the C-3 position of (1→6)-linked galactose in the backbone. 相似文献
997.
The marine fungus Chondrostereum sp. was collected from a soft coral Sarcophyton tortuosum from the South China Sea. This fungus was cultured in glucose-peptone-yeast (GPY) medium and the culture broth was extracted with EtOAc. By the method of 1H NMR pre-screening and tracing the diagnostic proton signals of the methyl groups, two new hirsutane-type sesquiterpenoids, chondrosterins N and O (1 and 2) were isolated from the metabolite extracts. Their structures were elucidated on the basis of MS, 1D and 2D NMR data. 相似文献
998.
Nan Zhang Leigang Li Juan Wang Zhiwei Hu Qi Shao Xiangheng Xiao Xiaoqing Huang 《Angewandte Chemie (International ed. in English)》2020,59(21):8066-8071
Surface regulation is an effective strategy to improve the performance of catalysts, but it has been rarely demonstrated for nitrogen reduction reaction (NRR) to date. Now, surface‐rough Rh2Sb nanorod (RNR) and surface‐smooth Rh2Sb NR (SNR) were selectively created, and their performance for NRR was investigated. The high‐index‐facet bounded Rh2Sb RNRs/C exhibit a high NH3 yield rate of 228.85±12.96 μg h?1 mg?1Rh at ?0.45 V versus reversible hydrogen electrode (RHE), outperforming the Rh2Sb SNRs/C (63.07±4.45 μg h?1 mg?1Rh) and Rh nanoparticles/C (22.82±1.49 μg h?1 mg?1Rh), owing to the enhanced adsorption and activation of N2 on high‐index facets. Rh2Sb RNRs/C also show durable stability with negligible activity decay after 10 h of successive electrolysis. The present work demonstrates that surface regulation plays an important role in promoting NRR activity and provides a new strategy for creating efficient NRR electrocatalysts. 相似文献
999.
David Vila‐Liarte Maximilian W. Feil Aurora Manzi Juan Luis Garcia‐Pomar He Huang Markus Dblinger Luis M Liz‐Marzn Jochen Feldmann Lakshminarayana Polavarapu Agustín Mihi 《Angewandte Chemie (International ed. in English)》2020,59(40):17750-17756
Perovskite nanocrystals (NCs) have revolutionized optoelectronic devices because of their versatile optical properties. However, controlling and extending these functionalities often requires a light‐management strategy involving additional processing steps. Herein, we introduce a simple approach to shape perovskite nanocrystals (NC) into photonic architectures that provide light management by directly shaping the active material. Pre‐patterned polydimethylsiloxane (PDMS) templates are used for the template‐induced self‐assembly of 10 nm CsPbBr3 perovskite NC colloids into large area (1 cm2) 2D photonic crystals with tunable lattice spacing, ranging from 400 nm up to several microns. The photonic crystal arrangement facilitates efficient light coupling to the nanocrystal layer, thereby increasing the electric field intensity within the perovskite film. As a result, CsPbBr3 2D photonic crystals show amplified spontaneous emission (ASE) under lower optical excitation fluences in the near‐IR, in contrast to equivalent flat NC films prepared using the same colloidal ink. This improvement is attributed to the enhanced multi‐photon absorption caused by light trapping in the photonic crystal. 相似文献
1000.
Yanying Lu Tianyu Zhu Wessel van den Bergh Morgan Stefik Kevin Huang 《Angewandte Chemie (International ed. in English)》2020,59(39):17004-17011
Developing high capacity and stable cathodes is a key to successful commercialization of aqueous Zn‐ion batteries (ZIBs). Pure layered V2O5 has a high theoretical capacity (585 mAh g?1), but it suffers severe capacity decay. Pre‐inserting cations into V2O5 can substantially stabilize the performance, but at an expense of lowered capacity. Here we show that an atomic layer deposition derived V2O5 can be an excellent ZIB cathode with high capacity and exceptional cycle stability at once. We report a rapid in situ on‐site transformation of V2O5 atomic layers into Zn3V2O7(OH)2?2 H2O (ZVO) nanoflake clusters, also a known Zn‐ion and proton intercalatable material. High concentration of reactive sites, strong bonding to the conductive substrate, nanosized thickness and binder‐free composition facilitate ionic transport and promote the best utilization of the active material. We also provide new insights into the V2O5‐dissolution mechanisms for different Zn‐salt aqueous electrolytes and their implications to the cycle stability. 相似文献