APPLIED CATALYSIS B-ENVIRONMENTAL
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2017
·
IF 9.446
Mei Ming,Yanlin Ren,Min Hu,Yun Zhang,Ting Sun,Yuling Ma,Xiaojing Li,Weidong Jiang,Daojiang Gao,Jian Bi,Guangyin Fan
Exploring MXenes as supports for synthesis of highly efficient catalysts are extremely important for hydrodechlorination of chlorophenols because of the acute toxicity and strong potential bioaccumulation of chlorophenols. We reported a facile strategy to synthesize Rh nanoparticles deposited on 2D alk-Ti 3 C 2 X 2 (X = O, F) (alk-Ti 3 C 2 X 2 for short) MXene, which was prepared through the removal of the Al layers of Ti 3 AlC 2 and post-treatment by alkalization. Modifying the Ti 3 C 2 X 2 support by alkalization triggered the substitution of surface fluorine groups with surface oxygen species. The changes in the surface chemistry of alk-Ti 3 C 2 X 2 effectively prevented particle aggregation to form well-dispersed Rh nanoparticles in small sizes with relative high metal dispersion, thereafter improving the hydrogen uptake capacity of the catalyst. Consequently, the Rh/alk-Ti 3 C 2 X 2 catalyst significantly enhanced the catalytic performance for the HDC reaction, which could be assigned to the large number of active components from small Rh nanoparticles. This strategy provides a basis for investigating the use of MXenes as supports to synthesize well-defined metal nanoparticles in 2D layered structures for potential applications.
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DOI
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BIOCHEMICAL ENGINEERING JOURNAL
·
2017
·
IF 2.892
Yumin Fang,Zhuoni Hou,Xiaodan Zhang,Dongfeng Yang,Zongsuo Liang
Salvia miltiorrhiza Bunge ( S. miltiorrhiza ) and Salvia castanea Diels f. t omentosa Stib ( S. castanea ) are both important medicinal plants which have been widely used to treat cardiovascular diseases. Tanshinone and phenolic acid are active and specialized metabolites in the two species. However, the divergent mechanism of specialized metabolism in the two species is yet unknown. We found that S. castanea produced higher levels of cryptotanshinone, tanshinone IIA, caffeic acid, and rosmarinic acid, but lower levels of dihydrotanshinone I and salvianolic acid B than S. miltiorrhiza . Some key genes involved in specialized metabolism were potentially associated with the diverse metabolism between the two species. LH with 1 g l −1 contributed more to tanshinone accumulation in S. castanea than that in S. miltiorrhiza . Genes involved in tanshinone biosynthesis in S. castanea were also more sensitive to LH than those in S. miltiorrhiza . Knowledge about diverse specialized metabolism in the two species will help us understand mechanism of tanshinone and phenolic acid biosynthesis.
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JOURNAL OF COLLOID AND INTERFACE SCIENCE
·
2025
·
IF 9.7
Xiaowei Li,Jianmin Gou,Lili Bo,Tian Fang,Chengzhuo Li,Jiangping Ma,Xiaolin Guan,Jinhui Tong
The development of highly efficient non-precious electrocatalysts for the oxygen evolution reaction (OER) remains a significant challenge. In this work, we introduce a highly effective OER electrocatalyst, Cu-F-Co 3 O 4 , synthesized by doping copper (Cu) and fluorine (F) into Co 3 O 4 using a quenching method. Both experimental and theoretical calculations reveal that Cu and F incorporation significantly shifts the d-band center closer to the Fermi level, creates abundant oxygen vacancies, and facilitates the reconstruction of the catalyst to form the CuCo 2 O 4-y F y /CuO heterojunction. This structural modification enhances the OER performance of the catalyst. Additionally, the multi-dimensional architecture exposes more active sites and accelerates mass and charge transfer kinetics. The optimal catalyst, Cu-F-Co 3 O 4 -0.7, demonstrates a low overpotential of 290 mV at 10 mA·cm −2 , along with remarkable stability exceeding 100 h, significantly outperforming both pristine Co 3 O 4 and benchmark RuO 2 electrocatalysts. These findings offer new insights into activating surface reconstruction in spinel oxides by engineering both anion and cation defects for water oxidation.
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DOI
PubMed
高影响因子
CERAMICS INTERNATIONAL
·
2025
·
IF 5.6
Kai Ma,Yao Luo,Jietao Wang,Xu Chang,Tong Liu,Yao Wang,Mingyue Ding
Developing robust fuel electrodes with high catalytic activity and stability under CO/CO 2 atmospheres is critical for reversible solid oxide fuel cells (RSOFCs). Here, we report a novel A-site-deficient perovskite Sr 1.95 Fe 1.5 Mo 0.3 Ni 0.2 F 0.1 O 6-δ (SFMNF) synthesized via electrospinning, combining Ni 2+ (B-site cation) and F - (anion) co-doping to enhance CO 2 electrolysis and syngas oxidation performance. Physicochemical characterization reveals that F-doping lowers the crystallization temperature, increases oxygen vacancy concentration, and strengthens CO 2 chemisorption. Reduction under H 2 induces exsolution of Ni 3 Fe alloy nanoparticles. The SFMNF electrode achieves a current density of 233 mA cm -2 at 1.3 V and 750°C in CO:CO 2 =2:1 atmosphere, with 36.2% higher activity than the pre-reduced state. Electrochemical impedance and distribution of relaxation time analyses identify CO 2 adsorption/dissociation as the rate-limiting step. The cell demonstrates exceptional durability over 50 redox cycles and 85-hour of operation without carbon deposition. This work highlights dual doping as an effective strategy to tailor perovskite properties for efficient CO 2 utilization in RSOFCs.
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APPLIED SURFACE SCIENCE
·
2020
·
IF 6.182
Mingquan Liu,Yingying Jiao,Junchao Qin,Zhongjun Li,Jianshe Wang
Nonmetals doping are effective for adjusting the electronic and molecular structures of C 3 N 4 nanosheets (CN), which could broaden the range of visible light response and improve the photo-induced electron-hole separation. Here a series of nonmetals (S, P, F and Br) doped C 3 N 4 nanosheets (x-CN) decorated with boron doped C 3 N 4 nanodots (BCNDs) was prepared for the first time. Compared with the pristine nonmetals doped CN, the integrating of BCNDs with x-CN can effectively facilitates the charge separation and transfer in the photocatalytic process, and endows enhanced photocatalytic activity for hydrogen production. The maximum photocatalytic hydrogen production rate of the BCNDs/S-CN, BCNDs/P-CN, BCNDs/F-CN and BCNDs/Br-CN composite can reach 3924.81 μmol·g −1 ·h −1 , 2387.62 μmol·g −1 ·h −1 , 2374.06 μmol·g −1 ·h −1 and 3471.56 μmol·g −1 ·h −1 respectively, which is about 3.3, 4.3, 4.0 and 3.1 times that of their counterparts, respectively. This work demonstrates that BCNDs plays an important role to improve the photocatalytic properties by forming 0D/2D isotype heterojunction with nonmetals doped C 3 N 4 nanosheets and provides new members for heterojunction photocatalysts, which is conductive to further fundamental and applied research.
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SEPARATION AND PURIFICATION TECHNOLOGY
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2022
·
IF 9.136
Zheng Kong,Lun Lu,Chao Zhu,Junjie Xu,Qile Fang,Renlan Liu,Yi Shen
PFOA has caused enormous environmental risks with recalcitrance, toxicity, and bioaccumulation, while the degradation of PFOA is still a challenging topic related to the high energy of C F bonds. However, the conventional methods such as biological oxidation, electrochemical oxidation and membrane separation have their own drawbacks. Actually, adsorption-photocatalysis is considered a potential treatment due to effectiveness and thoroughness. Instead of preparing the composite material by adding TiO 2 , the method to in-situ grow TiO 2 in the MOF (MIL-125(Ti)) was carried out, which achieved narrowed band gap and improved the photoresponse ability, simultaneously. Furthermore, the surface F-functionalized MOF provided more available special adsorption sites for PFOA enrichment. Linked fluorine groups not only improved the adsorption capacity (185.151 μmol/g) but also enhanced the photocatalytic rate (1.221 E −4 /s) by altering the electronic density of VB and CB. The constructed F-TiO 2 @MIL-125 stepwise degraded PFOA through a dominant ·OH attack pathway and maintained the oxidize ability of h + to PFOA. As a bifunctional material for adsorption and photocatalysis , F-TiO 2 @MIL-125 was able to be applied in various water environments repeatedly, which has unlimited environmental application potential.
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JOURNAL OF NATURAL PRODUCTS
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2024
·
IF 3.3
Weihong Wang,Jiaxu Shang,Shupeng Yin,Kunyu Xia,Rui Ma,Weiming Zhu,Peng Fu
Metabolites with high chemical reactivity serve important roles in chemical defenses of organisms. Formaldehyde, as a simple and highly reactive small molecule, can be produced by microorganisms, plants, and animals. Its toxicity is well known, but information about its other biological functions remains scarce. Here, we report that the natural product SEK34b produced by Streptomyces species can react nonenzymatically with formaldehyde in water to yield the methylene-bridged dimer phaeochromycin F. This process can eliminate the toxic substance formaldehyde produced by Staphylococcus aureus. Furthermore, there is a substantial inhibitory impact of phaeochromycin F on S. aureus. We hypothesize that these constitute an integrated system of defense and attack of Streptomyces species against competitors. Our study indicates that formaldehyde can react with vancomycin and tigecycline under mild conditions to generate the derivatives bearing an imidazolidin-4-one moiety, thereby reducing the antibacterial activity of these antibiotics. These data provide a possible chemical interaction mechanism of bacteria involving the nonenzymatic reactions of formaldehyde with highly reactive natural products.
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DOI
PubMed
高影响因子
TALANTA
·
2016
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IF 4.035
Haiyang Liu,Bibo Zhang,Chunyan Tan,Feng Liu,Jiakun Cao,Ying Tan,Yuyang Jiang
A simple Schiff base (BMSA) prepared from salicylaldehyde and 2-(1H-benzo[ d ]imidazol-2-yl)aniline was evaluated as an efficient fluorescent chemosensor for the selective recognition of Al 3+ and Cu 2+ over other common metal ions . This sensor could detect Al3 + in CH 3 OH/PBS with distinct emission red-shift (the detection limit 0.31 μM)and Cu 2+ in CH 3 OH/Tris-HCL (the detection limit 0.54 μM) with obvious fluorescence quenching . The obtained BMSA-Al 3+ and BMSA-Cu 2+ complexes could act as cascade sensors for detecting F − and S 2− , respectively. The recognizing behavior of BMSA toward Al 3+ and Cu 2+ has been investigated in detail through Job's Plot, FT-IR NMR , and HRMS analysis. Moreover, this chemosensor was verified to be of low cytotoxicity and good imaging characteristics for the detection of Al 3 + and Cu 2+ , and further for the recognition of F − and S 2− in living cells, suggesting that BMSA was proved to be a useful tool for tracking Al3 + /Cu 2+ and F − /S 2− ions in vivo .
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JOURNAL OF ELECTROANALYTICAL CHEMISTRY
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2023
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IF 4.5
Wenhao Yu,Wenruo Li,Luzheng Zhao,Weiqiang Kong,Shaofeng Xu,Xu Han,Haoyuan Zhu,Shun Liu,Jiancong Guo,Zhongsheng Wen
CuF 2 is a promising candidate of electrode materials for lithium-ion batteries due to its high specific capacity, high power density and environmental friendliness. However, the irreversible phase conversion and sluggish kinetics caused by serious copper dissolution and low conductivity make CuF 2 difficult to achieve long cycling life. A facile strategy to incorporate CoPPc into CuF 2 was proposed firstly to regulate the Cu-F bonding force to realize the high reversibility of CuF 2 for lithium-ion storage. The results of DFT calculation, differential charge density simulation, work function calculation and COHP bond level calculation show that the existence of CoPPc can improve the surface charge distribution of CuF 2 and thus improve the reversibility for durable lithium-ion storage. The cycle life performance of the CuF 2 @CoPPc composite electrode obtained by this method reached staggering 500 cycles and the capacity remained at 594.8 mAh/g.
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JOURNAL OF MATERIALS SCIENCE-MATERIALS IN ELECTRONICS
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2018
·Vol. 30
·期 1
·647-657
·
IF 2.324
Xiao Tai,Huang Zu-Sheng,Wang Lingyun,Cao Derong
Three novel dithieno[3,2- f :2′,3′- h ]quinoxaline-based organic dyes ( IQ-C, IQ-D and IQ-F ) with three π-spacers were synthesized and developed for dye sensitized solar cells, where dithieno[3,2- f :2′,3′- h ]quinoxaline was used as electron-withdrawing π-spacers, and 2,3-diphenylquinoxaline or dibenzo[ a,c ]phenazine as auxiliary electron-withdrawing π-spacers. The dye IQ-D with 2,3-diphenylquinoxaline as auxiliary electron-withdrawing π-spacer exhibited higher photocurrent ( J sc ) and photovoltage ( V oc ) than that of the dye IQ-C with 2,3-bis(4-(octyloxy)phenyl)quinoxaline as the additional electron-withdrawing π-spacer, due to the larger adsorption amount of IQ-D . The dye IQ-F with a rigid conjugated dibenzo[ a,c ]phenazine as additional electron-withdrawing π-spacer showed the highest efficiency of 6.54% under AM 1.5 G irradiation. It was demonstrated that the π-spacers influence the photovoltaic performance of the dithieno[3,2- f :2′,3′- h ]quinoxaline-based organic dyes significantly. The results indicated that the dyes with three π-spacers are promising candidates for efficient dye-sensitized solar cells.
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JOURNAL OF ALLOYS AND COMPOUNDS
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2020
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IF 4.65
Zhihao Wang,Mengxiao Zhang,Jiao He,Yongan Tang,Tingchao He,Qiang Sun,Dianyuan Fan,Yu Wang
The development of emitting materials that present both photoluminescence (PL) and X-ray excited optical luminescence has recently been attracting rising research interest for visualization applications. We introduced in this study the hydrothermally crystallized (Sr 1- x Mn x ) 5 (PO 4 ) 3 F 1- y Cl y ( x = 0–0.05, y = 0–0.40) nanorods with favorable PL and X-ray excited optical luminescence properties after composition modulating. The effects of solution pH and Cl − incorporation on structure and morphology of the products were firstly unveiled. (Sr 1- x Mn x ) 5 (PO 4 ) 3 F gives green emission at ∼548 nm ( 4 T 1 ( 4 G) → 6 A 1 ( 6 S)) under either 402 nm excitation or X-ray irradiation, and the optimal PL and X-ray excited optical luminescence were observed at x = 0.03. The replacement of F − by larger Cl − led to the generation of an amount of Frenkel defects (the dislocated F − and anion vacancies V F . ) along the c -axis, benefit from which the (Sr 0.97 Mn 0.03 ) 5 (PO 4 ) 3 F 1- y Cl y samples present enhanced PL and X-ray excited optical luminescence intensities by factors of 1.6 and 7.4, respectively, and the corresponding optimal y values are determined to be 0.20 and 0.30. Fluorescence decay analysis found steadily shortened fluorescent lifetime for Mn 2+ at higher Mn 2+ and Cl − concentrations, and the underlying mechanism was discussed. The (Sr,Mn) 5 (PO 4 ) 3 (F,Cl) apatite material, with enhanced PL and X-ray excited optical luminescence, may find novel applications for both lighting and scintillating.
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INORGANICA CHIMICA ACTA
·
2023
·
IF 2.8
Shun-Ping Zhao,Xu-lin Cui,Qiang-hong Yu,Yu Guo,Jie Wang,Heng Xu
Hybrid materials of lead halide have numerous structural variations and superior optoelectronic capabilities. The hybrid crystal 1 prepared by the hybrid halogen method has the chemical formula [ p -F-Bz-1-APy][Pb 2 Br 3.2 I 2.8 ] (C 24 H 20 F 2 N 4 Br 3.2 I 2.8 Pb 2 ) ( p -F-Bz-1-APy = p -fluoro-phenyl-1-aminopyridinium) with a space group of P 2 1 / c , two unequal [F1/F2-Bz-1-APy] + cations, and a heterogeneous double-chain inorganic layer made of edge-sharing Pb 2 Br 3.2 I 2.8 octahedron. The two cations adopt a lower-energy and more stable structural configuration, according to potential energy scans of the dihedral angles of the benzene and pyridine rings. The stacked structures are held together by a variety of intermolecular interactions, including hydrogen bonds (anion-cation, cation-cation), stacking (cation-cation), and the rare C-F2…π halo-bond. Hirshfeld surface analysis quantifies intermolecular interactions, revealing that interactions involving Br atoms and [F2-Bz-1-APy] + cations contribute more to the formation of stacking structures than interactions involving I atoms and [F1-Bz-1-APy] + cations. The logarithmic derivative method clearly reveals two dielectric relaxation processes, one in the low frequency region (<10 2 Hz) masked by the DC conductance and one in the high frequency region (10 2 -10 7 Hz), which were then fitted by the Arrhenius formula to obtain their corresponding activation energies of 77.75 KJ/mol and 144.14 KJ/mol, respectively. Our research offers inspiration and a framework for the development of novel lead halide-based optoelectronic materials and dielectric analyses.
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