INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH
·
2019
·
IF 3.375
Qun Li,Tareque Odoom-Wubah,Yaping Zhou,Rafal Mulka,Yanmei Zheng,Jiale Huang,Daohua Sun,Qingbiao Li
The search for efficient and durable catalysts for volatile organic compounds oxidation is essential for environmental remediation. Herein, porous coral-like cobalt–manganese oxide (CoMnOx) catalyst was synthesized through annealing Co–Mn–1,3-propanediol precursors at 300 °C in air and applied for the catalytic oxidation of benzene. The as-prepared CoMnOx exhibited uniform porous coral-like structure, with an improved benzene catalytic abatement performance as compared to those of Mn3O4 and Co3O4 samples prepared by the same method, respectively. According to BET, H2-TPR, O2-TPD, and XPS analysis, the as-obtained CoMnOx catalyst showed the highest BET surface area, better low-reducibility temperature, and high content of absorbed oxygen groups when compared to Mn3O4 and Co3O4, which makes significant contribution to its catalytic benzene oxidation activity. Moreover, a plausible surface reaction mechanism for benzene oxidation over CoMnOx catalyst was also proposed through the in situ DRIFTS study.
研究领域:
环境科学
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催化
·
材料科学
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产品关联
DOI
高影响因子
JOURNAL OF POWER SOURCES
·
2022
·
IF 9.794
Jiahao Chen,Hong Zhang,Hongzhu Chen,Enjie Xia,Yanmei Wu,Zhicheng Li
Solid-state Li-ion batteries (LIBs) have recently attracted much attention for their high safety and energy density . Polyvinylidene fluoride (PVDF) is as a potential electrolyte for solid-state LIBs due to its high permittivity, wide voltage window and excellent thermal stability. Here, Y 3+ -doped Li 29 Zr 9 Nb 3 O 40 (LZNO) Li-ionic conductor with room temperature conductivity (σ 25 ) of 1.26 × 10 −4 S cm −1 is prepared. LZNO decorated PVDF-based composite solid electrolytes (CSEs) are fabricated. The PVDF-based CSE with 10% (mass ratio) of LZNO shows σ 25 of 2.34 × 10 −4 S cm −1 , and has thermal stability with melting temperature up to 332 °C and voltage window of 4.8 V. The assembled Li ( Ni 0.8 Co 0.1 Mn 0.1 ) O 2 |CSE|Li cells show initial specific discharge capacity of 216.7 mAh g −1 at 0.1 C, and exhibit high capacity and cycle performance. LiFePO 4 |CSE|Li cells display initial specific discharge capacity of 137.4 mAh g −1 at 0.5 C and high cycle performance. Addition of LZNO powder in CSEs can inhibit the dehydrofluorination of PVDF during the charge-discharge of cells, alleviate the deterioration of interface resistance, and greatly improve the specific discharge capacity of cells at high rates.
研究领域:
材料科学
·
电化学
·
能源存储
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DOI
高影响因子
MICROCHEMICAL JOURNAL
·
2023
·
IF 4.8
Ziyue Sun,Hongli Zhao,Kaicha Chen,Fangfang Zhou,Minbo Lan
In this work, the carbon fiber microelectrode (CFME) coated by ERGO-CNT network was used as a substrate to support dendrite PtPd nanoclusters. An enzyme-free O 2 − electrochemical sensor (PtPd@ERGO-CNT-CFME) was prepared based on this strategy. Due to the brilliant loading and dispersing abilities of the substrate and the excellent electrochemical activity of the dendrite PtPd alloy, PtPd@ERGO-CNT-CFME demonstrated outstanding detection ability towards O 2 − . The as-constructed sensor showed a wide-linear range of 16–744 μM and 744–3064 μM with high sensitivity of 6967.3 μA mM −1 cm −2 and 4124.3 μA mM −1 cm −2 , and the detection limit was 5.07 μM. Furthermore, PtPd@ERGO-CNT-CFME was successfully applied to monitor O 2 − released from living cells. This phenomenon indicated the application potential for O 2 − detection in biological samples.
研究领域:
电化学
·
纳米材料
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生物传感器
·
分析化学
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DOI
高影响因子
NEW JOURNAL OF CHEMISTRY
·
2024
·Vol. 48
·期 6
·2558-2568
·
IF 2.7
Shiman Zhou,Qianqian Zhu,Denan Li,Lifeng Zhang,Yanshuo Li,Zhenxin Zhang
Tetrabromobisphenol A (TBBPA), a prevalent brominated flame retardant, poses significant environmental and health risks, necessitating its removal. In this study, WO3 with different structures was synthesized for TBBPA photodegradation under visible light using H2O2 and O2 as oxidants. The catalyst exhibited robust stability and reusability, rendering it suitable for practical applications. The crystalline structure and surface structure of WO3 controlled its catalytic activity towards TBBPA photodegradation. Monoclinic WO3 with the (022) plane was found to be the most active for ˙O2− active species generation from H2O2 and thus active for TBBPA degradation. Degradation product analysis showed that the catalyst was active not only for the removal of TBBPA, but also for the debromination of TBBPA. Nearly 100% debromination was achieved.
研究领域:
环境科学
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材料科学
·
化学工程
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产品关联
DOI
高影响因子
JOURNAL OF THE AMERICAN CERAMIC SOCIETY
·
2025
·Vol. 109
·期 1
·e70407
·
IF 3.8
Yuwei Zhang,Cuiwei Li,Guangjin Chen,Chenran Zhao,Zhikun Song,Kepi Chen,Haoran Sun,Linghao Wu,Junhui Xiang
A series of (Y, Yb, Zr, Hf, Sn, W)O 2−δ high-entropy ceramics with varying mole fraction of main elements were synthesized for the first time through the solid-state reaction synthesis method. The microstructure, phase composition, and properties of the prepared materials were thoroughly analyzed and tested. The results indicate that the phase composition transformed from a single-phase fluorite structure to a single-phase C-type rare earth sesquioxide structure as the mole fraction of +3 cations increases. The thermal conductivity of the prepared high-entropy ceramics with porosity of 49.8%–50.1% is very low ranging from 0.33 to 0.37 W·m −1 ·K −1 . Among them, the single-phase C-type rare earth sesquioxide with a higher oxygen vacancy concentration was employed as a catalyst in the CO 2 hydrogenation reaction, attaining a high CO 2 conversion rate of 82.0%. The obtained results have deepened understanding of the role of oxygen vacancies and have important guiding significance for the study of high-entropy oxides with fluorite derived structures.
研究领域:
材料科学
·
陶瓷
·
催化
·
能源材料
·
固态化学
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产品关联
DOI
高影响因子
APPLIED CATALYSIS B-ENVIRONMENTAL
·
2018
·
IF 11.698
Meichao Gao,Jinxiang Yang,Tao Sun,Zizhong Zhang,Dafeng Zhang,Huijuan Huang,Huaxiang Lin,Yi Fang,Xuxu Wang
The photocatalytic overall conversion of CO 2 with H 2 O to chemical fuel and oxygen mimicking natural photosynthesis is a huge challenge in photocatalysis. This work shows the achievement of the solar-driven photocatalytic overall CO 2 reduction with H 2 O to CO and O 2 over a Persian buttercup-like BiOBr x Cl 1-x solid solution. A CO generation rate of 15.86 μmol g −1 h −1 with the approximate stoichiometric O 2 evolution is yielded on BiOBr 0.6 Cl 0.4 solid solution under simulated solar light irradiation, which was about 7.5 and 10.2 times higher than that of pure BiOCl (2.11 μmol g −1 h −1 ) and BiOBr (1.55 μmol g −1 h −1 ), respectively. The enhanced photoactivity is contributed to the mediate band gap and energy level tuned by the formation of BiOBr x Cl 1-x solid solution to facilitate the separation of photogenerated charges. Besides the unique electron structure, the photoinduced oxygen vacancy (O V ) formed on BiOBr x Cl 1-x solid solution also plays an important role in the CO 2 reduction.
研究领域:
化学
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材料科学
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环境科学
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DOI
高影响因子
AICHE JOURNAL
·
2026
·
IF 4
Zhiheng Wang,Ningning Wu,Jiali Huang,Tuo Ji,Han Lin,Liwen Mu,Xiaohua Lu,Jiahua Zhu
Direct synthesis of hydrogen peroxide (DSHP) from H 2 and O 2 is indeed a promising sustainable alternative to the conventional anthraquinone oxidation process, yet achieving high H 2 O 2 productivity and selectivity simultaneously remains a significant challenge. Herein, we designed a diode-inspired interfacial microenvironment to address this challenge by synchronizing the kinetic relay of the key transport and reaction steps in DSHP. Specifically, this microenvironment was fabricated by grafting hydrophobic silane molecules onto the carbon surface followed by loading palladium nanoparticles. Results indicate that the interfacial microenvironment enables an efficient relay of H 2 dissociation, H 2 O 2 formation and desorption, shutting down the reverse path of the side reaction. Benefiting from this diode-inspired interfacial design, high H 2 O 2 productivity of 21,647.1 mol kg Pd −1 h −1 and H 2 O 2 selectivity of 93.3% were successfully achieved under ambient conditions. This work demonstrated the critical role of the interfacial microenvironment in regulating the synergy between mass transfer and reaction in heterogeneous reaction.
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DOI
高影响因子
CHINESE JOURNAL OF CHEMICAL ENGINEERING
·
2020
·
IF 2.627
Yingfei Hou,Lin Jiang,Yaoyao Zhang,Zhiwen Qin,Chi Jiang,Ming Wang
Lithium-air (also known as lithium-oxygen) batteries have attracted considerable global attention in recent years due to their extremely high energy density (11,140 W·h·kg −1 ). The electrolyte is a key element in lithium-air batteries and the traditional organic electrolyte has great safety risk due to leakage. On the contrary, the polymer electrolyte has the advantages of high safety, high stability and easy processing comparing with the organic liquid electrolytes. In this paper, a new idea was proposed to coat the Nafion membrane on a layer of polymer for blocking the oxidation reduction electric (RM) and Li based on the selective permeability on lithium ion of the Nafion membrane. Self-made thickness-controllable Nafion membrane, polyvinylidene fluoride-hexafluoropropylene copolymer (PVDF-HFP) and 2,2,6,6-tetramethylpiperidinooxy (TEMPO) were used to prepare a quasi solid polymer electrolyte (NSPE). Electrochemical workstation and LAND battery testing system were used to perform a galvanostatic charge/discharge test on Li-O 2 . The ionic conductivity of NSPE was 4.3 × 10 −4 S·cm −1 at room temperature and the discharge platform was 2.6 V and the charging voltage was 3.7 V after 50 cycles with the cut-off capacity of 500 mA·h·g −1 .
研究领域:
材料科学
·
电化学
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DOI
高影响因子
CATALYSIS TODAY
·
2018
·
IF 4.667
Miao Lai,Jie Zhao,Qingcai Chen,Shuaijun Feng,Yujie Bai,Yingxuan Li,Chuanyi Wang
In the photocatalytic volatile organic compounds (VOCs) degradation, the accumulation of intermediate products on the surface of catalysts could cause a decrease in activity through retarding reactant (e.g. O 2 ) supply to surface active sites. Herein, Bi decorated TiO 2 photocatalysts (Bi/TiO 2 ) for photocatalytic toluene degradation were prepared and systematically studied. It is found that metallic Bi modification improves the ability of photocatalysts to capture O 2 . As a result, the activities of the Bi/TiO 2 photocatalysts are obviously higher than that of the TiO 2 for photocatalytic toluene degradation, and the productions of photogenerated reactive oxygen species ( O 2 − and H 2 O 2 ) over the Bi/TiO 2 photocatalysts are almost equal to that over the TiO 2 despite the fact that the separation efficiency of photoinduced charge carriers is decreased after the addition of Bi. Adsorbed benzaldehyde is the main surface intermediate on the surface of the Bi/TiO 2 photocatalysts, whereas plenty of more readily oxidized aliphatic carboxylate species was monitored on the surface of the TiO 2 , which can be attributed to insufficient O 2 supply to the TiO 2 surface. This further indicates the positive role of the promoted O 2 supply by Bi in the photocatalytic toluene degradation. The present work offers a new window for addressing the catalyst deactivation in the photocatalytic VOCs degradation.
研究领域:
环境催化
·
大气污染控制
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材料化学
·
表面科学
·
光化学
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DOI
高影响因子
ChemSusChem
·
2017
·Vol. 10
·期 7
·1385-1389
·
IF 7.226
Hao Wan,Ya Mao,Zixuan Liu,Qingyou Bai,Zhe Peng,Jingjing Bao,Gang Wu,Yang Liu,Deyu Wang,Jingying Xie
As the first step during discharge, the mass transfer of oxygen should play a crucial role in Li–air batteries to tailor the growth of discharge products, however, not enough attention has been paid to this issue. Herein, we introduce an oxygen-enriching cosolvent, 1,2-(1,1,2,2-tetrafluoroethoxy) ethane (FE1), into the electrolyte, and investigate its influence on the discharge performance. The incorporation of this novel cosolvent consistently enhances the oxygen solubility of the electrolyte, and improves the oxygen diffusivity following a volcano-shape trend peaking at 50 % FE1. It is interesting that the discharge capacities obtained with the investigated electrolytes share the similar volcano trends as the oxygen transport under 50 mA g carbon −1 and higher current densities. The improved oxygen diffusion could benefit the volumetric utilization of the air cathode, especially at the separator side, probably owing to the fast oxygen transport to moderate its concentration gradient. Our results demonstrate the importance of oxygen provision, which easily becomes the capacity-determining factor. Graphical Got Oxygen? The enhancement of oxygen provision is achieved by incorporating 1,2-(1,1,2,2-tetrafluoroethoxy) ethane as the cosolvent in the electrolyte. The oxygen's diffusivity, rather than solubility, exerts the principal effect on discharge performance of the Li–air battery, especially at higher current density, owing to the ameliorated oxygen's accessibility, which improves the utilization ratio of the whole air cathode.
研究领域:
电化学
·
能源材料
·
电池技术
·
纳米材料
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物理化学
·
先进储能系统
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DOI
高影响因子
ACS Sustainable Chemistry & Engineering
·
2019
·
IF 6.97
Tingshuai Yang,Chaozhu Shu,Ruixin Zheng,Minglu Li,Zhiqian Hou,Peng Hei,Qiang Zhang,Dexin Mei,Jianping Long
Gel polymer electrolytes (GPEs) have received extensive attention due to their excellent nonflammability, leak prevention, and low cost. However, low ionic conductivity at room temperature and poor interfacial stability hinder the further application of GPEs. Here, a novel GPE based on PVDF-HFP/PMMA/SiO2 (PPSE-X, X represents the mass percentage of SiO2 in the GPE) is designed and fabricated. The synthesized PPSE-15 demonstrates an organic–inorganic double complexation structure, in which two kinds of polymer cross-link, leading to the increase of lithium-ion migration amount (tli+) in PPSE-15. Moreover, polar functional group (Si–O) in the nanometer SiO2 promotes the lithium salt dissociation, regulates the Li+ deposition and thus inhibits the production of lithium dendrite. The Li/PPSE-15/Li symmetric cell can run steadily for more than 750 h at a current density of 0.5 mA cm–2. Not only that, the Li–O2 battery assembled with PPSE-15 as an electrolyte can operate over 300 cycles at room temperature. After full charge and discharge for 5 cycles, the capacity retention reaches 48.3%. In addition, the existing PPSE-15 demonstrates excellent safety and flexibility and shows great potential in high-performance Li–O2 batteries.
研究领域:
储能
·
材料科学
·
电化学
·
聚合物纳米复合材料
·
电池技术
✓ 已验证
DOI
高影响因子
CHEMICAL ENGINEERING JOURNAL
·
2026
·
IF 13.2
Akkammagari Putta Rangappa,Wei Xiong,Wenhua Xue,Xinxin Lu,Yiqi Geng,Yuchao Shao,Guohan Sun,Jun Zhao
Activation of molecular O 2 on catalytic surfaces to form reactive oxygen species (ROS) is a pivotal step in catalytic reactions. In this study, we synthesized a bimetallic Zn 3 In 2 S₆ (ZIS) catalyst enriched with Pd S interfaces via a straightforward cation exchange process between Pd 2+ and Zn 2+ . These interfaces function as electron reservoirs, and Pd incorporation significantly enhances photocatalytic performance by reorganizing the electronic structure of the ZIS matrix, thereby improving charge carrier dynamics and reaction kinetics. Additionally, Pd modification optimizes O 2 adsorption strength, preventing excessive population of the π* antibonding orbital that can lead to O O bond cleavage and reduce ROS generation. Theoretical calculations reveal that monodentate adsorption of O 2 on Pd-ZIS surfaces promotes efficient photo induced electron transfer across all excited states, enabling effective ROS activation. The combination of experimental findings and theoretical analysis identified the mechanisms underlying the improved selectivity of Pd-modified ZIS catalysts. As a result, the optimized Pd-ZIS-5 photocatalyst demonstrates a high photo-oxidation performance for HMF oxidation, achieving 92.4 % conversion, 86.3 % yield, and 93.4 % selectivity–representing a 1.7-fold improvement over prismatic ZIS. Overall, this work demonstrates how Pd doping and tailored O 2 adsorption strength enhance photocatalytic processes, offering valuable insights for advanced biomass conversion and sustainable chemical production.
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产品关联
DOI
高影响因子
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