JOURNAL OF ORGANIC CHEMISTRY
·
2021
·
IF 4.354
Ming Li,Jun-Yang Tao,Liang-Neng Wang,Jia-Wei Li,Yue-Jin Liu,Ming-Hua Zeng
Modification of commercially available biaryl monophosphine ligands via ruthenium(II)-catalyzed P(III)-directed-catalyzed ortho C–H secondary alkylation is described. The use of highly ring-strained norbornene as a secondary alkylating reagent is the key to this transformation. A series of highly bulky ligands with a norbornyl group were obtained in excellent yields. The modified ligands with secondary alkyl group outperformed common substituted phosphines in the Suzuki–Miyaura cross-coupling reaction at a ppm mole level of Pd catalyst.
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高影响因子
CHEMOSPHERE
·
2019
·
IF 5.108
Yusi Tian,Minghua Zhou,Yuwei Pan,Jingju Cai,Gengbo Ren
Pre-magnetized Fe 0 (Pre-Fe 0 ) was for the first time applied as heterogeneous catalyst to enhance the oxidation efficiency of electro-Fenton (EF) for the degradation of p -nitrophenol (PNP). The parameters including current, initial pH and pre-Fe 0 dosage of Pre-Fe 0 /EF process were optimized and compared with other two processes (conventional Fe 0 /EF and electro-oxidation) to confirm its advantage. The rate constants of PNP removal were 1.40–3.82 folds of those by Fe 0 /EF process under various experimental conditions. The application of pre-Fe 0 as catalyst could extend the working pH range from 3.0 to neutral conditions for PNP removal and reduce the Fe 0 dosage from 2 to 0.5 mM corresponding to Fe 0 /EF, avoiding the second pollution of iron sludge . The superiority of Pre-Fe 0 /EF process was also verified to improve the degradation and mineralization of other phenols and antibiotics. Furthermore, a possible pathway of PNP degradation was revealed by the identification of intermediates and organic acids, and the possible mechanism of pre-Fe 0 efficiently enhanced the EF efficiency was proposed. This work demonstrated that such a novel heterogeneous EF process using pre-Fe 0 catalyst was clean and promising for the degradation of refractory organic pollutants .
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SENSORS AND ACTUATORS B-CHEMICAL
·
2021
·
IF 7.46
Chaoge Zhou,Fanqi Meng,Ke Chen,Xueli Yang,Tianshuang Wang,Peng Sun,Fangmeng Liu,Xu Yan,Kengo Shimanoe,Geyu Lu
In this work, we successfully prepare the octahedral NiO/Zn 2 SnO 4 p-n heterostructure by a simple hydrothermal synthesis and subsequent wet impregnation process. The microscopic morphology characterization results show that the as-prepared composites are uniformly dispersed and have an octahedral structure with a size of 3−5 μm. The gas devices are fabricated and their sensing performances are investigated systematically. The response and selectivity of NiO/Zn 2 SnO 4 composites to acetone have been significantly improved than that of pure Zn 2 SnO 4 . Moreover, the response of the sensor to 100 ppb acetone is 1.4 at 300 °C, indicating that the detection limit is less than 100 ppb. The enhancement in sensing properties of composites is largely due to the p-n heterojunction formed by NiO and Zn 2 SnO 4 , which causes the transfer of carriers and the catalytic effect of NiO.
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ACS Nano
·
2011
·
IF 9.865
Kui Wang,Dong-Sheng Guo,Xiang Wang,Yu Liu
We report the novel construction of nanosupramolecular binary vesicles based on host−guest complex formation between p-sulfonatocalix[4]arene and asymmetric viologen, which was identified by UV−vis and fluorescence spectroscopy, dynamic laser scattering, transmission electron microscopy, scanning electron microscopy, and surface tension experiments. The critical aggregation concentration of asymmetric viologen decreases pronouncedly by a factor of ca. 1000 owing to the complexation of p-sulfonatocalix[4]arene. Furthermore, we have demonstrated that the resulting vesicles can respond to multiple external stimuli, including temperature, host−guest inclusion, and redox. Methods of warming and inclusion of cyclodextrins were then employed to disrupt the vesicle architecture to release hydrophilic doxorubicin from the interior of the vesicle. Finally, cell experiments were performed to evaluate the cellular toxicity of the supramolecular binary vesicle and the anticancer efficiency of doxorubicin-loaded vesicle.
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SURFACE & COATINGS TECHNOLOGY
·
2016
·
IF 2.139
Yun Chen,Yali Hao,Wei Huang,Yan Ji,Wenzhong Yang,Xiaoshuang Yin,Ying Liu,Xiang Ling
Ni-P-nano-Al 2 O 3 composite coatings on the mild steel were obtained by adding Al 2 O 3 nanoparticles into the traditional electroless Ni-P bath. Cationic and anionic surfactants were used to prevent the agglomeration of the incorporated nano-Al 2 O 3 . Surface morphology , compositions and microstructures of the coating were studied using scanning electron microscopy (SEM), energy dispersive spectrometer (EDS), and X-ray diffraction (XRD) as well. Corrosion resistances of the modified mild steel samples were evaluated in 3.5 wt.% NaCl solution by electrochemical impedance spectroscopy (EIS). The results showed that compared to the pure Ni-P coating on the mild steel, the coating formed in the bath with 6 g/L nano-Al 2 O 3 performed the highest resistance. Under the optimal conditions, the adding of anionic surfactant (SDBS) improved the anti-corrosion performance of the samples further, while the addition of cationic surfactant led to a worse corrosion resistance. The potential mechanism was that anionic surfactant molecules would contact with active sites of Ni-P composite coating and nano-Al 2 O 3 in the bath, which would improve the dispersion of nano-Al 2 O 3 , thus leading to a homogeneous coating with better corrosion resistance.
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Journal of Materials Chemistry C
·
2017
·Vol. 5
·期 8
·2107-2113
·
IF 5.256
Xiwei Zhang,Jie Mao,Zhibin Shao,Senlin Diao,Dan Hu,Zhenjie Tang,Haihua Wu,Jiansheng Jie
For solar cells, high open circuit voltage is necessary for their high output voltage. Usually, two methods are used to increase the open circuit voltage: using suitable and matched large band-gap materials and reduction of saturation current. Herein, large band-gap p-type ZnSe nanowires and n-type CdS films are used to construct core–shell p–n heterojunctions with high open circuit voltage. Furthermore, a 4 nm Si3N4 layer is inserted between the ZnSe core and the CdS shell in order to passivate the interface defects and to reduce recombination and the saturation current. Additionally, a fast annealing process is employed to reduce the series resistance for improved performance. For a typical device, an optimum high open circuit voltage of ∼1.3 V and an energy conversion efficiency of ∼5.27% were achieved for its photovoltaic operation. Moreover, tens of devices were fabricated to demonstrate their stable and consistent performance.
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Journal of Materials Chemistry C
·
2019
·Vol. 7
·期 30
·9308-9315
·
IF 6.641
Ningwei Sun,Kaixin Su,Ziwei Zhou,Xuzhou Tian,Daming Wang,Nicole Vilbrandt,Andreas Fery,Franziska Lissel,Xiaogang Zhao,Chunhai Chen
Switchable fluorescent materials have gained great attention due to their promising applications in sensors, memory devices and displays. However, further progress is hindered by the low fluorescence contrast, modest response speed and inferior long-term cycling stability. Based on a rational design strategy by combining a highly conjugated tetraphenyl-p-phenylenediamine (TPPA) unit and an aggregation induced emission (AIE)-active tetraphenylethylene (TPE) unit, we synthesized a novel diamine “N,N′-bis(4-aminophenyl)-N,N′-di(4-(1,2,2-triphenylethenyl)phenyl)-1,4-phenylenediamine” to construct an electro- and AIE-active polymer. In addition to the high efficiency solid-state fluorescence and the extremely stable redox properties, the resulting polymer TPE-TPPA-PA realized highly integrated emission/color dual-switchable properties, including multistage color-changing, high fluorescence on/off contrast up to 252, impressively rapid response rate (1.3/0.5 s for EC and 0.7/2.1 s for EFC processes) and excellent cycling stability over 10 000 s. The demonstrated synergistic effect between stable electroactive TPPA and AIE-active TPE may provide a new pathway for further molecular design to realize high-performance emission/color dual-switchable materials.
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CANADIAN JOURNAL OF CHEMICAL ENGINEERING
·
2021
·Vol. 100
·期 11
·3381-3394
·
IF 2.007
Lin Li,Shizhan Sheng,Huihua Wang,Tianpeng Qu,Dong Hou,Deyong Wang,Minqi Sheng
Ni-P alloys have been successfully electrodeposited in the choline chloride and ethylene glycol with a molar proportion of 1:2(CE) electrolyte and their activities toward hydrogen evolution reaction (HER) have been also evaluated. The electrodeposition of Ni-P alloy follows a co-deposition process, and the bulk growth of which depends on an instantaneous nucleation under diffusion control. The morphologies of Ni-P alloys are significantly influenced by the P content, and low P content can lead to a smooth surface. As expected, Ni-9.0 wt.% P alloy shows an impressive HER catalytic performance with a Tafel slope (b) of 72.9 mV dec −1 and an overpotential of 105 mV at 50 mA, in agreement with its large ECSA ( C dl = 3.25 mF cm −2 ) and small interface charge-transfer resistance. More interestingly, Ni-9.0 wt.% P alloy exhibits a sustainable catalytic activity toward HER after 1000 cycling test with a tiny potential decline of ~10 mV at 100 mA cm −2 . Such a striking HER activity of Ni-9.0 wt.% P alloy can be attributed to the synergistic effect among the induced active sites from lattice contraction, negatively charged P incorporation, and a mixed nanometre crystal and amorphous structure. Thus, Ni-P alloy electrodeposited in a CE-based electrolyte can be used as a promising electrode material with high HER activity in alkaline solutions for hydrogen production.
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ELECTROCHEMISTRY COMMUNICATIONS
·
2008
·Vol. 10
·期 7
·1052-1055
·
IF 4.186
P. Zhang,H.P. Zhang,G.C. Li,Z.H. Li,Y.P. Wu
We have successfully developed a new process to prepare porous poly(methyl methacrylate-co-acrylonitrile) (P(MMA-AN)) copolymer based gel electrolyte. The porous structure in the polymer matrix is achieved by adding SnO 2 nanoparticles which are mostly used as gas sensor materials. The quasi-aromatic solvent, NMP, has an electron-repulsion effect with the space charge layer on the surface of SnO 2 nanoparticles and forms a special gas–liquid phase interface . Once the cast polymer solution is stored at an elevated temperature to evaporate the solvent, gas–liquid phase separation happens and spherical pores are obtained. The ionic conductivity at room temperature of the prepared gel polymer electrolyte based on the porous membrane is as high as 1.54 × 10 −3 S cm −1 with the electrochemical stability up to 5.10 V (vs. Li/Li + ). This method presents another promising way to prepare porous polymer electrolyte for practical use.
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APPLIED SURFACE SCIENCE
·
2015
·
IF 2.711
Xiwei Zhang,Dan Hu,Zhenjie Tang,Dongwei Ma
Single ZnSe–ZnO nanowire axial p–n junction was fabricated by regioselectively oxidizing the p-type ZnSe NW in air. Pronounced current rectification behavior with on/off ratio of ∼50 and ideality factor of ∼1.7 were presented. The axial p–n junction also exhibited high sensitivity to UV light . A high performance UV light photodetector with a responsibility of ∼0.67 × 10 4 A W −1 , a gain of ∼2.3 × 10 4 and a detectivity of ∼4.1 × 10 13 cm Hz 1/2 W −1 were elucidated based on this axial p–n junction. This new method is expected to construct more nano-devices based on one-dimensional semiconductor nanostructures.
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Small
·
2025
·
IF 12.1
Yuyan Dong,Ligang Yuan,Linhui Tang,Zheng Zhang,Shibing Zou,Jianwei Chen,Xin Cui,Ning Li,Lei Shi,Keyou Yan
Perovskite's surface defects trigger deep level traps and energy misalignment, resulting in substantial interface recombination and energy loss in perovskite solar cells (PSCs). Herein, 9-fluoreneacetic acid (FAA), a self-assembled molecule (SAM), is employed to passivate the interface defects and modulate energy alignment. SAM modification reduces the defect density from 6.37 × 10 15 to 3.11 × 10 15 cm −3 and produces a p-type surface with an upward band bending, thus constructing a well-defined n-i-p heterojunction for efficient charge separation. Accordingly, the target PSC realizes 24.75% power conversion efficiency (PCE) and retains 92% for 1100 h during maximum power point tracking (MPPT) at room temperature. Furthermore, over 80% of initial PCE has been reserved after 2500 h aging in 25–30% relative humidity (RH). This SAM strategy is expected to enhance the efficiency and stability for n-i-p PSCs.
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产品关联
DOI
PubMed
高影响因子
ACS Applied Materials & Interfaces
·
2025
·
IF 8.2
Boyuan Di,Xinlu Li,Xiaokun Wen,Wenyu Lei,Xinyue Xu,Wenchao Kong,Haixin Chang,Jia Zhang,Wenfeng Zhang
High-performance p-type atomically thin transistors are fundamental components in CMOS-based digital logic circuits for beyond-silicon electronics. Compared with the recent breakthrough in high-quality semimetal contacts approaching the quantum limit on n-type atomically thin channel transistors, achieving high-performance p-type analogues with high-quality contacts remains challenging, which was mainly hindered by the lack of proper high-work-function metallic electrodes with Fermi level unpinning capacity. Herein, we demonstrate that semimetal TiS2 electrodes prepared with a damage-free transfer process can be a feasible option for p-type atomically thin MoTe2 transistors. Owing to its intrinsic large work function (∼5.3 eV) and high-quality contacts with negligible Schottky barrier at the TiS2/MoTe2 interface, the scaled p-type bilayer MoTe2 transistor with 500 nm channel length and the monolayer transistor with 800 nm channel length exhibit a high on-state current (Ion) of 100 μA/μm with the on/off ratio (Ion/off) over 106 and an Ion of 68 μA/μm with the Ion/off ratio over 107, respectively. Such a demonstration will enable monolithic atomically thin MoTe2-based beyond-silicon electronics via the common CMOS technology.
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DOI
PubMed
高影响因子
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