International Journal of Polymeric Materials and Polymeric Biomaterials
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2017
·
IF 1.515
Ping Jiang,Jinlong Zhang,Shan Shan Jia,Yiqiang Wu,Qinlin Wu
First, ethyl cellulose-g-poly(2-(dimethylamino) ethyl methacrylate) (EC-g-PDMAEMA) was synthesized through atom transfer radical polymerization. Second, the polymer was used to prepare self-supporting microporous membranes through nonsolvent-induced phase separation process. The chemical structures of EC0.2-g-PDMAEMA15 was confirmed by 1H NMR and FTIR. And the copolymer micelles were characterized by UV, laser particle-size analysis, and TEM. The results indicated that the copolymer had pH- and temperature-responsive behaviors. Furthermore, the morphology study of microporous membranes indicated that the pores became smaller and more uniform with the increase of tetrahydrofuran (THF) content and “open time”, and the most optimal preparation conditions were using 75% THF/25% DMF (v/v) as solvents with the “open time” 30 s. What’s more, the membranes were responsive to pH and temperature stimulus in terms of water flux.
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高影响因子
Environmental Science-Nano
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2019
·Vol. 6
·期 9
·2850-2862
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IF 7.704
Xiaoyu Bai,Yi Li,Liangbo Xie,Xiaohui Liu,Sihui Zhan,Wenping Hu
Antibiotics accumulate because of their extensive use and difficult degradation, which can lead to the formation of novel antibiotic resistant genes and bacteria, which can cause damage to human health and the ecological environment. Here, we designed a novel photo-electro-Fenton-like (PEF-like) system with bifunctional Z-scheme WO3/g-C3N4 for accelerated decomposition and enhanced mineralization of stubborn ciprofloxacin (CIP). This PEF-like system, accompanied by visible light activation, with the optimal WO3/g-C3N4 (1 : 6) composite exhibited outstanding removal efficiency of CIP compared with a single photocatalysis system and electro-Fenton-like (EF-like) system, and the elimination rate reached 100% within 2 h under visible light irradiation. The WO3/g-C3N4 (1 : 6) composite displayed the strongest visible light absorption, the weakest recombination of electron–hole pairs, the highest photocurrent response and the lowest electrochemical impedance compared with pristine WO3 and g-C3N4. Significantly, WO3/g-C3N4 (1 : 6) played a dual role in the PEF-like system which could not only produce ˙OH, ˙O2− and h+ during photocatalysis, but could also generate ˙OH through the reactions of W5+ and photoexcited electrons of g-C3N4 for the decomposition of H2O2. It was worth noting that this bifunctional PEF-like catalyst with photoelectric synergy could replace Fe2+ in a conventional electro-Fenton reaction and the pH range was broadened while still maintaining efficient degradation efficiency in the range of 2–9. The PEF-like system maintained a high elimination rate of CIP after five consecutive runs which revealed that it possessed prominent stability and feasibility.
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高影响因子
APPLIED SURFACE SCIENCE
·
2018
·
IF 4.439
Lianying Lu,Guohong Wang,Min Zou,Juan Wang,Jun Li
Hierarchical TiO 2 /g-C 3 N 4 heterojunction photocatalysts with well-defined multiscale porous TiO 2 framework are synthesized by simply calcinating tetrabutyl titanate and melamine precursors. The samples have been characterized by XRD, XPS, SEM, TEM, FTIR, nitrogen absorption-desorption equipment and TGA. The photocatalytic activity of these samples has been investigated in photo-degradation of Rhodamine B (RhB). The results show that calcining temperature critically affects the microstructure, surface area, interface structure and catalytic properties of the prepared samples. At the optimal calcining temperature of 550 °C, the apparent reaction rate constant of the catalyst is 55.0 × 10 −3 min −1 , which is 16.2 fold of pure TiO 2 (3.4 × 10 −3 min −1 ) and 3.4 fold of pure g-C 3 N 4 (16.4 × 10 −3 min −1 ), respectively. The strengthened visible-light-driven photocatalytic activity is attributed to the formation of a unique Z-scheme TiO 2 /g-C 3 N 4 heterojunction due to C- or N-doping at the surface of the porous TiO 2 framework. This mechanism explains the observation in a series of radical trapping experiments that superoxide ions and photo-generated holes play major roles in the photo-decolorizing process while hydroxyl radicals are also involved with a minor role.
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高影响因子
MATERIALS SCIENCE IN SEMICONDUCTOR PROCESSING
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2020
·
IF 3.085
Junnan Qu,Yi Du,Yibing Feng,Jianyong Wang,Bo He,Minxing Du,Yang Liu,Nan Jiang
A visible-light-responsive hybrid photocatalyst , K-doped g-C 3 N 4 /BiOBr, has been synthesized by K-doped g-C 3 N 4 (K–CN) and BiOBr. The property of photocatalysts was characterized by XRD , FT-IR, TEM, SEM , DRS , PL , EIS and HPLC. The photocatalytic activity of K-doped g-C 3 N 4 /BiOBr was evaluated by degradation of Rhodamine B (RhB) and tetracycline hydrochloride under visible-light irradiation. The K-doped g-C 3 N 4 /BiOBr hybrid photocatalyst which contains K–CN with mass fraction of 20% (20K–CN/BiOBr) shows the best degradation efficiency of RhB. The degradation efficiency of RhB (20 mg/L) can be achieved to 99% and the degradation efficiency of tetracycline hydrochloride by BiOBr decreased with the increase of K-doped g-C 3 N 4 doping. The results of photocurrent and EIS assumed that the tight coupling between K–CN and BiOBr can enhance the separating efficiency of photo-generated carrier. In addition, the capture experiment proof that h + is the primary active substance in the system of reaction and ·OH is the auxiliary active substance. After five degradation experiments, the efficiency of the degradation of Rhodamine B by the sample can still reach 90%, which proves that the samples are stable. A new and efficient method is provided in this work to solve the pollution of organic dyes and antibiotics.
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高影响因子
NEW JOURNAL OF CHEMISTRY
·
2019
·Vol. 43
·期 17
·6753-6764
·
IF 3.069
Qiannan Li,Yuguo Xia,Kangliang Wei,Xiaotong Ding,Shun Dong,Xiuling Jiao,Dairong Chen
Utilizing surface polarization to improve the separation efficiency of photoinduced carriers is considered to be an effective strategy to enhance the photocatalytic activity. Herein, a novel nonprecious metal-based P-doped g-C3N4 (PCN)/polyaniline (PANI)/BaTiO3 (BTO) (PPB) ternary photocatalyst with a hollow architecture was rationally designed and prepared by a combined wet-chemical and thermal treatment strategy. Except for the Z-scheme involved in PCN and PANI, the vertical polarization provided by ferroelectric BTO further improved the separation efficiency of the photoinduced charge carrier, resulting in an enhanced visible-light photocatalytic hydrogen production activity of 602 μmol h−1 g−1, which was 21-fold higher than that of pristine g-C3N4, and an apparent quantum efficiency of 4.16% at 420 nm. In addition, benefitting from this ternary heterojunction, the photoinduced electrons were concentrated on the intermediate p-type PANI while holes were left on the lateral n-type PCN involved in the Z-scheme, resulting in the retention of high oxidation–reduction potentials. Moreover, this approach to enhance the photocatalytic activity by constructing a Z-scheme heterojunction and surface polarization could expand to other photosystems, which provides a new avenue for the rational design and the synthesis of novel photocatalysts.
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高影响因子
ACS Sustainable Chemistry & Engineering
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2020
·
IF 7.632
Yong-Ting Li,Xiao-Li Zhang,Zhi-Kun Peng,Pu Liu,Xiu-Cheng Zheng
It is a crucial and urgent task to develop high performance catalysts for the hydrolysis of ammonia borane (NH3BH3, AB), which is presently thought to be an effective strategy for hydrogen generation. In this work, we immobilize the ultrafine RuNi alloy nanoparticles in the network of hierarchical porous g-C3N4 thin sheets with a facile adsorption–in situ reduction method. The structural and physicochemical properties of the as-prepared catalysts are studied using various techniques. The influence of different molar ratios of Ru to Ni in the catalysts on the hydrolytic dehydrogenation rate of AB is investigated to optimize the best one. The detailed reaction kinetics and the enhancing effect of NaOH with different dosages on the hydrolysis rate are studied through a series of experiments. Catalyzed by the optimal catalysts (denoted as Ru0.5Ni0.5/p-g-C3N4), the hydrolysis reaction is first-order and near zero-order relative to the Ru and AB concentrations, respectively. The corresponding turnover frequency reaches 840.3 min–1, and the apparent activation energy is as low as 14.1 kJ mol–1, which are greatly superior to many similar or counterpart catalysts previously reported. The results indicate the potential of the bimetallic alloy catalysts for the hydrolytic dehydrogenation of hydrogen storage materials.
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高影响因子
JOURNAL OF ALLOYS AND COMPOUNDS
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2022
·
IF 6.371
Chunli Cui,Genrui Zhang,Yu Yang,Tingting Wu,Lei Wang
Constructing heterojunction has been proved to be an efficient strategy for enhancing the photocatalytic performance of g-C 3 N 4 by prohibiting charge recombination and providing surface active sites. Herein, a novel structure of ultra-thin carbon bridged MoC quantum dots/g-C 3 N 4 nanosheets was constructed for the first time to facilitate carrier transfer and accelerate surface reactions. In our designed composites, a surface-to-surface contact has been formed between conductive carbon layer and g-C 3 N 4 nanosheet via ultrasonic assembly process. Moreover, there exist strong interfaces between MoC QDs and carbon layer because of the in-situ conversion method. As to this unique structure, the ultra-thin carbon layer functions as charge separation and migration high ways while the MoC QDs perform as noble-metal-free co-catalysts consuming the surface electrons promptly. Significantly, an optimal 40 wt% MoC QDs-C/g-C 3 N 4 photocatalyst (MCCN) is synthesized with a hydrogen evolution rate of 2989 μmol h −1 g −1 , which is 69.6 and 1.7 times higher than that of pure g-C 3 N 4 and Pt/g-C 3 N 4 , respectively. Our work provides new insights on designing highly efficient heterojunction photocatalysts for water splitting.
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高影响因子
JOURNAL OF HAZARDOUS MATERIALS
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2019
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IF 7.65
Ming Wu,Xin He,Binghua Jing,Teng Wang,Chengyin Wang,Yanlin Qin,Zhimin Ao,Shaobin Wang,Taicheng An
Graphite carbon nitride ( g -C 3 N 4 , CN) is considered as a promising semiconductor for environmental catalysis. However, pure CN can not meet the requirements for actual applications due to its high recombination rate of photogenerated electron-hole pairs and a relatively large band gap preventing full utilization of solar energy. In this work, we report synthesis of a novel carbon and defects co-modified g -C 3 N 4 (C x CN) by calcination of melamine activated by oxalic. This new catalyst C x CN has porous structure with much higher surface areas compared with pristine CN. UV–vis analysis and DFT calculations show that C x CN has a lower bandgap for enhancing visible light adsorption compared with CN. Photoluminescence (PL) and photoelectrochemical analyses show that C x CN has a low recombination rate of photogenerated electron-hole pairs, which improves the utilization of solar energy. As a result, C x CN samples show high efficiency for the degradation of bisphenol A (BPA) under visible light irradiation, where the best catalyst of C x CN (C 1.0 CN) samples shows about 22 times higher photocatalytic degradation rate than that of CN. Moreover, C 1.0 CN shows high mineralization rate and can degrade BPA into CO 2 and H 2 O by the generated active species, like superoxide radicals ( O 2 − ) and holes (h + ).
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高影响因子
APPLIED SURFACE SCIENCE
·
2022
·
IF 7.392
Xiaoqi Jiang,Qing Li,Wenjie Xia,Zhiwei Huang,Xiaomin Wu,Huawang Zhao,Zhilei Guo,Weixin Kong,Chung-shin Yuan,Guohua Jing,Huazhen Shen
Elemental mercury (Hg 0 ) is the most difficult mercury species to remove from the flue gas. Photocatalysts of transition metal oxide modified TiO 2 can effectively remove Hg 0 . However, the metal oxide easily aggregates into large nanoparticles, reducing the atom utilization efficiency and photocatalytic activity. We presented a facile strategy of employing g-C 3 N 4 as an anchor to successfully load highly dispersed ultrasmall CeO 2 clusters on g-C 3 N 4 /TiO 2 . Moreover, the mechanism of anchoring CeO 2 clusters and charge transfer of the ternary photocatalyst were explored in-depth. The results demonstrated that at 250 °C, the photooxidation efficiency of Hg 0 by CeO 2 -g-C 3 N 4 /TiO 2 was several times higher than that of CeO 2 /TiO 2 , TiO 2 , and g-C 3 N 4 . The cavity of the tri-s-triazine ring anchored small CeO 2 clusters via strong Ce-N coordination bonds. A combined type II and Z-scheme transport paths accelerated the separation of photogenerated electron holes. This research offers valuable surface engineering strategy for highly dispersed ultrasmall cluster decorated TiO 2 .
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高影响因子
Nano Research
·
2018
·Vol. 12
·期 2
·457-462
·
IF 7.994
Tang Shangfeng,Yin Xuepeng,Wang Guanyu,Lu Xiuli,Lu Tongbu
A visible-light-response, efficient and robust photo-catalyst for CO 2 reduction is highly desirable. Herein, we demonstrate that single titanium-oxide species implanted in two-dimensional (2D) graphitic carbon nitride (g-C3N4) matrix (2D TiO-CN) can efficiently photo-catalyze the reduction of CO 2 to CO under the irradiation of visible light. The synergistic interaction between single titanium oxide species and g-C3N4 in 2D TiO-CN not only enhances the separation of photo-excited charges, but also results in visible light response of single titanium-oxide species, realizing high activity of CO 2 photo-reduction with extremely high CO generation rate of 283.9 μmol·h −1 ·g −1 , 5.7, 6.8 and 292.2 times larger than those of TiO 2 /CN hybrid material, CN and commercial TiO 2 , respectively. Time-resolved fluorescence and electron spin resonance spectroscopy revealed the catalytic mechanism of the fabricated 2D TiO-CN photocatalysts for CO 2 reduction.
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高影响因子
JOURNAL OF COLLOID AND INTERFACE SCIENCE
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2020
·
IF 7.489
Suci Meng,Pengfei An,Lijie Chen,Shichao Sun,Zhongkai Xie,Min Chen,Deli Jiang
Developing high-efficient and low-cost photocatalysts is of great significance yet challenging for photocatalytic hydrogen evolution. Herein, we report a 2D/2D Ru-modulated CoP nanosheets (Ru-CoP -x , where x refers the Ru-to-Co molar ratio)/g-C 3 N 4 nanosheets (GCN NSs) ternary hybrid as a photocatalyst for hydrogen evolution under visible light. The optimal photocatalyst 25% Ru-CoP-1:8/GCN NSs exhibits an excellent hydrogen evolution rate of 1172.5 µmol g −1 h −1 under visible light with a high apparent quantum efficiency (AQE) of 3.49% at 420 nm, which is close to Pt/g-C 3 N 4 photocatalytic system and higher than most reported transition metal phosphides (TMP)/g-C 3 N 4 photocatalytic system. Experimental results indicate that the higher photocatalytic hydrogen evolution performance can be mainly attributed to the binary Ru-CoP -x co-catalyst with efficient charge separation and promoted surface water reduction kinetics, and the 2D/2D self-assembly structure with strong interface Schottky effect and short charge transport distance. This study provides a new approach to develop cost-effective Pt-alternative co-catalysts for photocatalytic hydrogen evolution by incorporating a small amount of ruthenium into the transition metal phosphides.
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高影响因子
EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY
·
2024
·
IF 6
Yuxin Feng,Xuan Xuan,Yuemiao Hu,Jiaguo Lu,Zhiwen Dong,Ziqiang Sun,Hongying Yao,Lei Hu,Qikun Yin,Yi Liu,Hongbo Wang
Murine double minute 2 (MDM2) and homologous protein murine double minute X (MDMX) are p53 negative regulators that perform significant driving effects in tumorigenesis, and targeting these oncoproteins has became an efficient strategy in treating cancers. However, the definite antitumor activity and significance ordering of each protein in MDM family is still unclear due to the similar structure and complicated regulation. Herein, we identified two G-rich sequences ( G 1 and G 5 ) located in the promoter that could assemble the G-quadruplex to respectively inhibit and promote the transcription of the MDM2 and MDMX. Based on this target, we designed and synthesized a novel G-quadruplex ligand A3f and achieved the differentiated regulation of MDM protein. In triple-negative breast cancer (TNBC) cells, A3f could induce MDM2-dependent proliferation arrest and exhibit additive therapeutic effect with MDMX inhibitors. Overall, this study provided a novel strategy to regulate the transcription of MDM genes by targeting certain G-rich sequences, and discovered an active antitumor molecule for use in TNBC treatment.
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PubMed
高影响因子
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