RSC Advances
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2014
·Vol. 5
·期 8
·5674-5679
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IF 3.708
Gang Wang,Li Peng,Yaochen Zheng,Yanqin Gao,Xuedong Wu,Tianhui Ren,Chao Gao,Jin Han
We describe a novel triethylamine catalyzed S → O acetyl migration reaction for yielding thiol compounds under mild conditions through the formation of a transitional 5-membered ring. A series of epoxy compounds have been transformed into their thiol counterparts which could be used for construction of topological and functional sulfur-containing polymers. The one-pot two-step processes including the S → O acetyl migration and the following thiol-click reactions avoided separation of thiol intermediates. Applying these processes on a new-type latent polythiols overcomes crosslinking problem usually met in preparation of multithiol compounds due to the formation of disulfide bonds.
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COMPOSITES PART B-ENGINEERING
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2020
·
IF 7.635
Jiahao Zou,Huajun Duan,Yongsheng Chen,Sa Ji,Jianfan Cao,Huiru Ma
In order to improve the flame retardancy while maintaining the excellent mechanical properties and heat resistance of epoxy resin, a novel P/N/S-containing high efficiency flame retardant named TAP was designed and synthesized by a simple one-pot reaction among 2-thenaldehyde, 2-aminobenzothiazole (ABZ) and 9,10-dihydro-9-oxa-10-phosphaphenanthrene-10-oxide (DOPO). The chemical structure of TAP was characterized by Fourier transform infrared (FTIR) spectroscopy, 1 H and 31 P nuclear magnetic resonance (NMR) spectroscopy. Compared to pure EP, the introduction of TAP can reduce the thermal decomposition rate of epoxy resin and increase the char residue . Meantime, when the phosphorus content was only 0.48%, EP/7.5%TAP passed the vertical burning V-0 rating, obtaining a high flame-retardant efficiency. With the addition of 10 wt% TAP, the limiting oxygen index (LOI) value increased from 22.8% of pure EP to 31.5%, while the peak heat release rate (PHRR), total heat release (THR) and total smoke production (TSP) values decreased by 41.26%, 35.70% and 24.03%, respectively. In addition, the glass transition temperature (T g ) of the epoxy resin decreased from 185 °C to 177 °C, while the storage modulus at 30 °C increased. Subsequently, the flexural tests of the samples revealed that the mechanical properties were well maintained. All these results demonstrated that the TAP was a novel high efficiency flame retardant for EP, which enabled the cured EP to maintain excellent heat resistance and mechanical properties.
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CHINESE JOURNAL OF CATALYSIS
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2022
·
IF 12.92
Yue Huang,Kai Dai,Jinfeng Zhang,Graham Dawson
Non-stoichiometric W 18 O 49 (WO) prepared by solvothermal method has excellent NIR absorption due to the localized surface plasmon resonance effect caused by oxygen vacancies. This has great potential in the field of using sunlight to convert carbon dioxide into organic fuels. In addition, through the amination of CdSe, the one-dimensional/two-dimensional step-scheme (S-scheme) WO/CdSe-diethylenetriamine (WO/CdSe-D) photocatalyst with electron transmission channels driven by visible light to NIR light is constructed by microwave solvothermal method. The LSPR of WO and the synergistic effect of coupling semiconductors to construct S-scheme heterojunctions can improve light utilization and achieve efficient charge carrier transfer efficiency. The optimized photocatalyst of 35%WO/CdSe-D has the best CO 2 reduction performance compared to WO and CdSe-D, and the yield is 25.37 µmol h –1 g –1 . X-ray photoelectron spectroscopy was used to verify the charge transfer path of the S-scheme WO/CdSe-D heterojunction. This work provides a possibility for the application of non-stoichiometric oxides rich in oxygen vacancies in the field of photocatalytic CO 2 reduction.
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Journal of Materials Chemistry A
·
2021
·Vol. 10
·期 2
·779-788
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IF 12.732
Kang Yin,Xiao Xu,Muyu Wang,Jiazheng Zhou,Biwen Duan,Jiangjian Shi,Dongmei Li,Huijue Wu,Yanhong Luo,Qingbo Meng
Crystallization growth plays a crucial role in influencing the film quality and final photoelectric conversion performance of a kesterite Cu2ZnSn(S,Se)4 (CZTSSe) solar cell. Herein, an exploration of a two-step selenization strategy to control the growth kinetics of an aqueous solution derived CZTSSe film for high solar cell efficiency is reported. By synergistically exploiting the benefits of high and low temperature selenization in facilitating the CZTSSe phase formation, introducing beneficial point defect states, configuring the interfacial energy band structure, and sustaining excellent surface microstructure, a total-area cell efficiency of 12.5% has been achieved. These results demonstrate the significance of controlling the crystallization growth of CZTSSe to improve the device performance. The high cell performance achieved here is comparable to that of hydrazine or dimethyl sulfoxide solution-based cells and thus would help facilitate the development of CZTSSe solar cells toward more diversified film fabrication technologies.
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Sustainable Energy & Fuels
·
2022
·Vol. 6
·期 14
·3383-3393
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IF 6.813
Jiawei Wei,Ping Li,Jing Shi,Minghua Huang,Weiqian Tian,Huanlei Wang
Designing high-performance carbon-based oxygen reduction catalysts using a facile strategy is an attractive research direction in the field of energy conversion and storage. Herein, N/S co-doped carbon was prepared using κ-carrageenan and melamine as precursors, in which melamine can be decomposed into nitrogen-containing gas for realizing nitrogen doping, and the sulfate groups in κ-carrageenan can be converted for sulfur doping. Such an N/S doping strategy enables a carbon catalyst with a large specific surface area, hierarchical porous structure, and rich defective sites to be achieved, displaying a high positive onset potential (Eonset = 0.98 V) and half wave potential (E1/2 = 0.89 V), excellent stability, and methanol tolerance. More importantly, S doping could increase the positive charge density of the carbon adjacent to the nitrogen, which is favorable for enhancing the chemisorption of O2 and weakening the O–O bond, thereby promoting the reaction from O2 to OH− and improving electron transfer. Furthermore, with this catalyst as the air cathode, the assembled aqueous Zn–air battery exhibits a high open-circuit potential of 1.53 V and a remarkable peak power density of 166.05 mW cm−2, outperforming the Pt/C catalyst. This work gives a facile and effective strategy to construct high-performance ORR catalysts with four electron transfer for Zn–air batteries.
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Polymer Chemistry
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2013
·Vol. 5
·期 6
·1857-1862
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IF 5.231
Yaling Zhang,Yuan Zhao,Bin Yang,Chongyu Zhu,Yen Wei,Lei Tao
A multicomponent reaction (MCR) has been carried out on the platform of controlled radical polymerization (CRP) to construct a ‘one pot’ MCR-CRP system for the facile preparation of well-defined functional polymers. In the current work, a novel ‘one pot’ system has been built through a combination of the Kabachnik–Fields (KF) reaction and reversible addition fragmentation chain transfer (RAFT) polymerization. Compared to a traditional stepwise method and polymer post-polymerization modification, this novel ‘one pot’ system exhibited distinct advantages to much more facilely and efficiently prepared well-defined poly(aminophosphonate)s (polyAPPs). A series of unique polyAPPs have also been successfully prepared through this KF–RAFT system, suggesting this novel method is a general and versatile approach to prepare well-defined organophosphorous polymers.
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CHEMICAL ENGINEERING JOURNAL
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2024
·
IF 13.3
Qianqian Wang,Xiaoyan Ma,Wei You,Pengcheng Ma,Ran Bi,Senyang Song,Fang Chen,Fengjin Qu,Xinli Wang,Pengfei Liu
The construction of cost-effective and high-performance metal organic framework (MOF) derived metal phosphides as multifunctional electrode materials for self-powered overall water splitting (OWS) is considerable promising. Herein, the trimetallic phosphides embedded in sulfur-containing carbon matrix (SC-FeNiCeP/NF) derived from high-valence metal engineered MOF are grown on nickel foam by hydrothermal and chemical vapor deposition for achieving self-powered OWS. Based on the electron coupling between the metal phosphide interface by high-valent Ce as “electronic storage” to accelerate electron transfer, the SC-FeNiCeP/NF as electrocatalysts present low overpotential with 208 mV and 107 mV at 10 mA cm −2 in oxygen evolution reaction (OER) and hydrogen evolution reaction (HER), respectively. For supercapacitor, the SC-FeNiCeP/NF nanoarray exhibits high specific capacitance with 2290 F g −1 at 1 A g −1 . Combined with excellent SC-FeNiCeP/NF-based asymmetric supercapacitor (ASC) and OWS devices, the self-powered OWS are assembled to produce H 2 and O 2 simultaneously in alkaline water for up to ∼ 120 s, creating new possibilities for the energy storage and conversion systems based on the designable and multifunctional MOF-derived materials.
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INTERNATIONAL JOURNAL OF HYDROGEN ENERGY
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2021
·
IF 5.816
Kexin Huang,Wanqing Zhang,Rajkumar Devasenathipathy,Zhongyun Yang,Xiaoxia Zhang,Xiaoqu Wang,Du-Hong Chen,Youjun Fan,Wei Chen
The economical, efficient and durable oxygen reduction catalysts facilitate the enhancement of electrochemical energy devices competitiveness towards widespread applications. In view of this, we provide an innovative sulfuration inducing method for the synthesis of ZnS and cobalt nanoparticles decorated N, S co-doped CNTs (ZnS/Co-NSCNTs) catalyst. S introduced into the zinc-based zeolitic imidazolate frameworks (ZIF-8) and cobalt-based zeolitic imidazolate frameworks (ZIF-67) precursors via pyrolysis , and induced the generation of ZnS/Co-NSCNTs have been confirmed by XRD , SEM, TEM, and XPS techniques . The key features including activity sites, transfer channels and adsorption energy back up the excellent electrocatalytic activity of the as-prepared ZnS/Co-NSCNTs towards oxygen reduction reactions (ORR). ZnS/Co-NSCNTs additionally exhibited a positive half-wave potential of 0.871 V (vs. RHE) with improved current density towards ORR. In alkaline medium , ZnS/Co-NSCNTs catalyst displayed a high tolerance towards methanol and an excellent long-term cycling stability. The observed onset potential for our prepared ZnS/Co-NSCNTs catalyst is analogous with the commercially available noble metal catalysts . Also, ZnS/Co-NSCNTs catalyst as a cathode in zinc-air battery displayed an enhanced electrochemical performance with a highly specific capacity of 750.1 mAh g −1 , outstanding cycling stability, and high rate behavior. This work provides a new approach for the construction of stable low-cost alternative air-cathode catalysts for other energy conversion and storage applications.
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Journal of Energy Chemistry
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2020
·
IF 7.216
Xuedong Jing,Na Lu,Jindou Huang,Peng Zhang,Zhenyi Zhang
Engineering lattice defects in two-dimensional (2D) sulfide semiconductors has been accepted as an effective strategy to enhance the efficiency of the solar-to-fuels conversion. Although many researches have proven the lattice defect-mediated photocatalytic activity of ZnIn 2 S 4 , the artificial control of S-defects for optimizing the charge-carrier kinetics process in ZnIn 2 S 4 has long been a challenging task. Herein, we report a facile one-step method to modulate the lattice S-content of ZnIn 2 S 4 microflowers (MFs) only through adjusting the used amount of S-precursor in the hydrothermal solution that contains the metal precursors with a fixed Zn/In stoichiometric ratio at 1:2. We also demonstrated that the S-vacancies at the In facets were the main type of lattice defects in the formed ZnIn 2 S 4 MFs, which could enhance both the separation and migration processes of the photoinduced charge-carriers due to the existence of discrete defect energy-levels (DELs) and the reduced effective mass of electrons, as evidenced by the first-principles calculations and the electron spectra analyses. The ZnIn 2 S 4 MFs with the optimal content of S-vacancy obtained by a hydrothermal treatment of the precursors with the Zn/In/S stoichiometric ratio of 1:2:8 possessed the long-lived photoinduced electron (~94.64 ns) for contributing to the photo-physical and -chemical processes. Thus, upon visible light irradiation, the H 2 -evolution rate of this sample reached ~ 2.40 mmol h −1 g −1 with an apparent quantum efficiency of ~ 0.16% at 420 nm even though only using 5 mg of photocatalysts without any cocatalysts .
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MATERIALS SCIENCE IN SEMICONDUCTOR PROCESSING
·
2025
·
IF 4.6
Rui Wang,Yanchun Yang,Guonan Cui,Lulu Bai,Zhihui Gong,Chengjun Zhu
CuSb(S, Se) 2 (CASSe) is known to have great potential for copper-based low-cost thin-film solar cells due to its excellent stability, earth-abundant raw materials, and suitability for the low-temperature preparation process. In this work, CASSe thin-film solar cells were prepared using the green n-butylammonium butyrate ionic solution-based method for the first time. The phase purity, crystallinity , morphology, and electrical properties of films prepared at different conditions (sintering and selenization conditions) were studied. With the help of the XRD , Raman spectra , SEM, and c-AFM measurements, the optimal preparation of CASSe thin film is confirmed at 230 °C for 3 min (sintering condition) and 390 °C for 20 min (selenization condition). Using glass/Mo/CuSb(S, Se) 2 /CdS/i-ZnO/ITO/Al as the structure of the device, the corresponding thin film solar cell can be fabricated, which presents a photoelectric conversion efficiency (PCE) of 0.14 %. Although the performance of the device is poor, our conclusions are meaningful in the development of CASSe material, supplementing the blank of preparing CASSe thin film solar cells by the green solution-based method.
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产品关联
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高影响因子
Journal of Integrative Agriculture
·
2025
·
IF 4.4
Pei Yu,Qian Luan,Jing Wang,Fei Lao,Haiming Shi,Xuebing Xu,Chunming Liu,Jihong Wu
The occurrence of fruity and fermented off-flavors significantly diminishes the quality and consumer acceptance of cold-pressed peanut oil (CPO). This study investigated the effects of freeze-thaw stress (0, 3, and 6 cycles) on the flavor of cold-pressed peanut oil and found that fruity and fermented off-flavors were significantly increased. Quantitative analysis and odor activity value (OAV) calculations confirmed ethyl 3-methylbutanoate (OAV=248) and ethyl 2-methylbutanoate (OAV=195) for fruity off-flavors, while butanoic acid (OAV=93) and 3-methylbutanoic acid (OAV=81) were key drivers of the fermented off-flavors. Crucially, the S-curve method revealed a synergistic interaction between ethyl 3-methylbutanoate and butanoic acid. Molecular docking revealed a preferential binding of ethyl 3-methylbutanoate to olfactory receptor OR11G2 (-7.2 kcal mol −1 ) driven by hydrophobic interactions. Butanoic acid was preferentially anchored in OR52E1 (-6.5 kcal mol −1 ), stabilized by a hydrogen bond to the receptor backbone and complementary hydrophobic interactions. These findings provide a scientific basis for improving the quality of cold-pressed peanut oil and preventing off-flavors.
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产品关联
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高影响因子
APPLIED SURFACE SCIENCE
·
2025
·
IF 6.9
Caicai Ran,Mang Lu,Linli Hou,Huanggen Yang,Limin Liu
Heterogeneous interface regulation acts a significant role in tailoring the intrinsic physicochemical property for achieving excellent photocatalytic H 2 evolution performance, which still faces a huge challenge. In this work, by comparing H 2 evolution property of various cadmium zinc sulphide (Cd x Zn 1−x S) solid solutions, 1-D Cd 0.9 Zn0 .1 S nanorods possessing the optimum photocatalytic H 2 evolution performance were obtained. Additionally, bimetallic metal organic framework (MOF)-derived NiFe 2 O 4 @C (NFO@C) microspheres with custom-built heterogeneous interface were successfully prepared via a solvothermal/pyrolysis strategy. Moreover, NFO@C microspheres were assembled on Cd 0.9 Zn0 .1 S surface to fabricate a series of NFO@C/Cd 0.9 Zn 0.1 S heterojunction photocatalysts with varied contents of NFO@C. The NFO@C/Cd 0.9 Zn 0.1 S heterojunction with a NFO@C content of 20 wt% (abbreviated as NC20) exhibited the highest H 2 production rate of 96.25 mmol g –1 h −1 , which was 3.8 times that of Cd 0.9 Zn 0.1 S. Under a light wavelength of 420 and 450 nm, the apparent quantum efficiency of NC20 reached 34.8 % and 65.1 %, respectively. The photocatalytic H 2 evolution activity of NC20 remained stable after the 16-h cycle experiment, whereas the severe photocorrosion of Cd 0.9 Zn 0.1 S was encountered. Furthermore, the easy recyclability of NC20 should not be overlooked. The results of a series of material characterization clearly demonstrate that the introduction of NFO@C could efficiently improve light absorption and the photoinduced carrier separation capability of the composite photocatalysts. This study not only opens up a facile and controllable preparation way for the synthesis of heterojunction structures with tailored heterogeneous interfaces, but also offers a new sight to ameliorate the H 2 evolution capability, stability and recyclability of Cd x Zn 1−x S solid solutions.
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