ChemistrySelect
·
2024
·Vol. 9
·期 44
·e202403927
·
IF 1.9
Hui Han,He Cui,Jiabo Wang,Kai Ge,Yongfang Yang
Graphical In this paper, 2D MOF-Co, 2D MOF-Co/Cu, and 2D MOF-Co/Cu/Fe are designed and prepared using 1,4-benzendicarboxylic acid (1,4-BDC) as organic ligands. Their charge transfer, separation efficiency, and effects on photocatalytic CO 2 reduction are studied. The results show that 2D multimetallic MOF-Co/Cu/Fe has better photocatalytic CO 2 reduction activity, so it has higher research value and development prospect in the field of photocatalytic CO 2 reduction. In this study, 2D multimetallic MOFs combined with the advantages of 2D nanosheets, with the synergetic effect of multimetallic nodes, exhibited good photocatalytic activity for reduction of CO 2 . Herein, a 2D MOF-Co/Cu/Fe were successfully prepared via one-pot stirring of the solutions of multimetal salts and organic ligands at room temperature. Introduction of the second and third metal (Cu and Fe) into MOF-Co does not change the 2D morphology of MOFs, although it improved the photocatalytic CO 2 reduction performance by broadening the light absorption range of 2D MOF-Co, accelerating the separation efficiency and transfer rate of photogenerated carriers. Upon irradiation with full-spectrum light, the average CO yield of 2D MOF-Co/Cu/Fe achieved 17.06 µmol·g −1 ·h −1 , being about 1.8 and 1.2 times that of 2D MOF-Co and 2D MOF-Co/Cu. This work provides an insight into 2D multimetallic MOFs-based photocatalysts in catalytic CO 2 reduction.
研究领域:
材料科学
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环境科学
·
化学
✓ 已验证
产品关联
DOI
高影响因子
SEPARATION AND PURIFICATION TECHNOLOGY
·
2016
·
IF 3.299
Qizhou Dai,Jiazhong Zhou,Mili Weng,Xubiao Luo,Daolun Feng,Jianmeng Chen
This study presents an electrochemical method for the degradation of metronidazole (MNZ) in aqueous solution with novel PbO 2 electrode, which was prepared via electrodeposition in nitrate solution. The influencing factors on electrochemical decomposition of pollutants were evaluated and the removal of MNZ and chemical oxygen demand (COD) reached 78.09% and 21.77% after 120 min treatment under the optimal conditions with the concentration of supporting electrolyte, the initial concentration of MNZ, the pH and the current density were 0.10 mol/L, 100 mg/L, 6.4 and 10 mA/cm 2 , respectively. Then, the Co doped PbO 2 electrodes were prepared and used to degrade MNZ under the optimal conditions. Relatively good performance was achieved when the molar ratio of Pb and Co was 100:1. Compared to pure PbO 2 electrode, the steady-state polarization curves and cyclic voltammetry analysis showed that 1.0% Co-PbO 2 electrode had a higher oxygen evolution potential and greater current of reduction and oxidation peaks, which increased the electrochemical activity and decreased the energy consumption. Finally, based on the intermediate products identified by IC and GC/MS, the main degradation pathway of MNZ was proposed including ring open, denitrification and radical reactions.
研究领域:
环境科学
·
电化学工程
✓ 已验证
DOI
高影响因子
APPLIED SURFACE SCIENCE
·
2022
·
IF 7.392
Bingcai Chen,Pengpeng Li,Bing Wang,Yingde Wang
CO sensor is helpful to monitor the working state of combustion equipment, such as industrial boilers and engines, and to ensure the production process and human life safety. However, balancing fast response/recovery and high response value for metal oxide CO sensors remains a challenge. In this work, based on band gap engineering, porous TiO 2 /CeO 2 NSs with different TiO 2 coupling amounts were prepared by hydrothermal method combined with flame annealing. The heterojunction composed of TiO 2 and CeO 2 narrowed the energy band width of the composite system and made the electron transmission more efficient, which endowed TiO 2 /CeO 2 NSs with good gas sensing properties. The results indicated that the response value of TiO 2 /CeO 2 NSs is 9.78 time that of CeO 2 NSs. Its ultrafast response/recovery time (2 s/6 s), good CO selectivity and wide CO monitoring range (500 ppb-5000 ppm) are also impressive. The TiO 2 /CeO 2 NSs sensor has great potential for rapid CO monitoring.
研究领域:
材料科学
·
传感器技术
✓ 已验证
产品关联
DOI
高影响因子
RENEWABLE ENERGY
·
2022
·
IF 8.634
Zhuoheng Tu,Ping Zhang,Mingzhen Shi,Xiaomin Zhang,Youting Wu,Xingbang Hu
Efficient recovery of CO and H 2 from offgas streams is environmentally and economically meaningful from the view point of the wide use of syngas (CO/H 2 ) in the chemical industry. This work reports selective and simultaneous separation of CO and H 2 from N 2 using protic chlorocuprate ionic liquids (PCILs)-based membranes. The chemical structures of the prepared PCILs were characterized using FTIR , NMR and ESI-MS, and the thermal stability, melting points, viscosity and density of PCILs were determined. The morphology and elemental distribution of PCIL-based membranes were characterized by SEM and EDS. Facilitated transport of CO is observed in these membranes, and the CO permeability is up to 178.3 barrers (0.1 bar, 40 °C) in [TEAH][CuCl 2 ], with a CO/N 2 selectivity of 26.2. H 2 permeability and H 2 /N 2 selectivity are also found to reach 198.2 barrers (0.5 bar, 40 °C) and 29.1, respectively. The permeability of CO and the selectivity of CO/N 2 can be further optimized to 405.9 barrers and 69.9 by altering the Cu(I) content, respectively. In addition, the selectivity of CO/H 2 can be tuned drastically via varying the Cu(I) content (from 0.77 to 12.0) and the operating temperature (from 2.14 to 0.42), which may be applied to the composition adjustment of syngas. In a word, this work offers a new strategy for designing IL-based membranes that used for CO and H 2 capture.
研究领域:
化学工程
·
环境科学
✓ 已验证
产品关联
DOI
高影响因子
JOURNAL OF CATALYSIS
·
2021
·
IF 7.92
Huiyuan Cheng,Zihao Fan,Xuemei Wu,Manman Feng,Wentao Zheng,Guangping Lei,Xiangcun Li,Fujun Cui,Gaohong He
Single-atom catalysts (SACs) with well-defined active sites provide an efficient route for catalyzing CO 2 reduction reaction (CO 2 RR). Although enormous attention has been focused on metal-N x moieties, understanding the effect of metal-C coordination and engineering of the hybrid metal-N/C sites have rarely been reported. Herein, we fabricated Co SACs with tunable isolated Co-N 5-x C x ( x = 1, 2, 3) sites supported on porous carbon frameworks. Benefiting from the difference in electronegativity of the coordinated N and C atoms, the CO Faradaic efficiency (FE CO ) enhanced considerably from 54% to 76% and 92% at −0.8 V vs . RHE for Co-N 4 C 1 , Co-N 3 C 2 , and Co-N 2 C 3 , respectively. Further density functional theory (DFT) calculations uncover that the increased ratio of Co-C coordination induced electron enrichment of Co atoms and upper-shift the d -band center to near Fermi level, and thus favorably promotes the electron-donating ability of Co centers and strengthens the adsorption of *COOH.
研究领域:
材料科学
·
催化化学
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环境科学
✓ 已验证
产品关联
DOI
高影响因子
JOURNAL OF ALLOYS AND COMPOUNDS
·
2021
·
IF 5.316
Xiaoming Fan,Yuyin Fan,Xiao Zhang,Lin Tang,Jinxue Guo
Heterostructured materials favoring synergism, efficient charge transfer, and abundant active sites have aroused enormous interests for water electrolysis. Here heterogeneous Co@CoO encapsulated in P, N co-doped carbon nanofibers supported on carbon cloth (Co@CoO-PNC/CC) has been prepared to pursue attractive synergism for the application of pH-tolerant catalyst for oxygen evolution reaction (OER) in both alkaline and neutral solutions. The prepared Co@CoO-PNC/CC exhibits advanced OER performances, generating a current density of 10 mA cm −2 at overpotential of 289 mV in alkaline media and 371 mV in neutral media. The high OER activity can be assigned to the synergistic effect of abundant active sites and enhanced charge transfer between Co and CoO, as well as the specific P, N co-doped carbon nanofiber architecture.
研究领域:
材料科学
·
电化学
✓ 已验证
产品关联
DOI
高影响因子
ULTRASONICS SONOCHEMISTRY
·
2021
·
IF 7.491
Yang Yang,Yiqing Feng,Kejian Li,Saira Ajmal,Hanyun Cheng,Kedong Gong,Liwu Zhang
Among the possible products of CO 2 electrochemical reduction, CO plays a unique and vital role, which can be an ideal feedstock for further reduction to C 2+ products, and also the important component of syngas that can be used as feedstock for value-added chemicals and fuels. However, it is still a challenge to tune the CO selectivity on Cu electrode. Here we newly construct an ultrasound-assisted electrochemical method for CO 2 reduction, which can tune the selectivity of CO 2 to CO from less than 10% to >80% at −1.18 V versus (vs.) reversible hydrogen electrode (RHE). The partial current density of CO production is significantly improved by 15 times. By in-situ Raman study, the dominating factor for the improved CO production is attributed to the accelerated desorption of *CO intermediate. This work provides a facile method to tune the product selectivity in CO 2 electrochemical reduction.
研究领域:
电化学
·
材料科学
✓ 已验证
DOI
高影响因子
IONICS
·
2019
·Vol. 25
·期 11
·5485-5494
·
IF 2.289
Wang Xiaoqing,Tian Songran,Zhang Xiaoqing,Li Guoyan,Liu Ying,Chen Botao,Cheng Bowen
A 3D Ni 3 S 2 @Mn-Co-OH/NF cross-linked nanosheet heterostructure composite electrode has been successfully fabricated by a facile two-step hydrothermal method. The as-prepared Ni 3 S 2 @Mn-Co-OH/NF composite electrode exhibits a high capacitance (3163 F g −1 at a current density of 3 mA cm −2 ), a superior rate performance (2071 F g −1 at a current rate of 30 mA cm −2 ), and stable cycling property (maintaining 96.6% of the initial capacitance after 4000 cycles at a current rate of 10 mA cm −2 ). This excellent electrochemical performance can be ascribed to the unique cross-linked nanosheet heterostructure formed directly on Ni foam current collector and the synergistic effect between Mn-Co-OH and Ni 3 S 2 of the composite electrode.
研究领域:
材料科学
·
能源存储
✓ 已验证
产品关联
DOI
高影响因子
ACS Applied Materials & Interfaces
·
2023
·
IF 9.5
Mengyi Zhang,Xiaohui Sun,Xudong Cai,Xiaolu Zhan,Yufei Wu,Xuyang Zhang,Guohua Wu,Xiangwei Wang
In the field of electromagnetic wave (EMW) absorption, carbon matrix materials based on metal–organic frameworks (MOFs) have drawn more interest as a result of their outstanding advantages, such as porous structure, lightweight, controlled morphology, etc. However, how to broaden the effective absorption bandwidth [EAB; reflection loss (RL) ≤ −10 dB] is still a challenge. In this paper, large microsphere structures of a Co/C composite composed of small particle clusters were successfully prepared by the solvothermal method and annealing treatment. At a filling ratio of 40 wt %, the Co/C composite shows attractive microwave absorption (MA) performance after being annealed at 600 °C in an atmosphere of argon. With an EAB of 6.32 GHz (9.92–16.24 GHz) and a thickness of just 2.57 mm, the minimum RL can be attained at −54.55 dB. Most importantly, the EAB can attain 7.12 GHz (10.88–18.0 GHz) when the thickness is 2.38 mm, which is larger than that of the majority of MOF-derived composites. The superior MA performance is strongly related to excellent impedance matching and a higher attenuation constant. This study provides a simple strategy for synthesizing a MOF-derived Co/C composite with a wide EAB.
研究领域:
材料科学
·
电磁学
✓ 已验证
产品关联
DOI
PubMed
高影响因子
INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH
·
2020
·
IF 3.573
Benyong Yang,Wentao Mu,Benedict Tsz Woon Lo,Sijie Liu,Zhihang Chen,Liam John France,Xuehui Li
NOx and CO formation is, at present, a consequence arising from fuel production, but their emission need not be. In this study, a series of novel Ir-containing TiO2-nanobelt catalysts were designed and prepared for the simultaneous removal of NOx and CO. Activity data demonstrates that the TiO2(B) support promotes NO reduction compared to anatase. Furthermore, reaction efficiency (RE), a measure of NOx consumption vis-à-vis that of CO, reveals that catalysts containing anatase promote CO oxidation more so than their TiO2(B) counterparts. Increasing Ir concentration over the latter promotes low-temperature catalytic performance, an effect believed to be linked to the formation of Ir0–IrO2 composites. In situ DRIFTS experiments reveal the relevance of nitrite/nitrate formation and consumption at 250 °C, a mechanism insinuated by the RE value. However, at 300 °C, both TOF and RE increase, signifying the participation of a faster and more-selective reaction, which appears consistent with the isocyanate-mediated pathway.
研究领域:
环境科学
·
催化化学
✓ 已验证
产品关联
DOI
高影响因子
SN Applied Sciences
·
2020
·Vol. 2
·期 3
·1-10
·
IF 0
Sun Xueying,Liu Xinjie,Wang Jie,Jiang Xusheng,Liu Rongmei,Li Anran,Li Wen
In this work, we first successfully loaded the MOF structure Co-HKUST nanobundles on a foamed nickel without adding any binder. The Co-HKUST is a pseudo-capacitive material with excellent electrochemical performance as a unique energy storage material. As an electro-active material, such cobalt-based MOF exhibits superior pseudo-capacitive behavior in the KOH aqueous electrolyte with a high specific capacitance of 578.6 F g −1 at 1 A g −1 , and the specific capacitance remains 452.3 F g −1 when the current density increased to 10 A g −1 with a good rate performance (78.2%). Meanwhile, the cycle retention rate of the Co-HKUST is 88.7% after 1000 cycles at 7.5 A g −1 . The two-electrode asymmetric supercapacitor (ASC) device is also assembled in this work. The specific capacitance of Co-HKUST//AC ASC is 200.5 F g −1 at 1 A g −1 . Though 5000 cycles at 5 A g −1 , only 8.2% of the capacitance is lost. Energy density of asymmetric Co-HKUST//AC device can reach 71.35 Wh kg −1 at 1 A g −1 with a power of 809.9 W kg −1 . More interestingly, even if the current density increased to 10 A g −1 , the energy density maintains 44 Wh kg −1 at power density of 8.5 kW kg −1 . The above test results can fully show that the synthesized Co-HKUST material is a promising energy storage material.
研究领域:
材料科学
·
电化学
✓ 已验证
DOI
Nano Research
·
2022
·Vol. 16
·期 6
·8405-8410
·
IF 10.269
Cao Renfei,Cui Yangfeng,Huang Gang,Liu Wanqiang,Liu Jianwei,Zhang Xinbo
Li-O 2 batteries with extremely high specific energy density have been regarded as a kind of promising successor to current Li-ion batteries. However, the high charge overpotential for the decomposition of Li 2 O 2 discharge product reduces the energy efficiency and triggers a series of side reactions that cause the Li-O 2 batteries to have a limited lifetime. Herein, Co-doped C 3 N 4 (Co-C 3 N 4 ) photocatalysts were designed by an in situ thermal evaporation method to take advantage of the photo-assisted charging technology to conquer the shortcomings of Li-O 2 batteries encountered in the charge process. Different from the commonly used photocatalysts, the Co-C 3 N 4 photocatalysts perform well no matter with and without illumination, owing to the Co doping induced conductivity and electrocatalytic ability enhancement. This makes the Co-C 3 N 4 reduce the charge and discharge overpotentials and improve the cycling performance of Li-O 2 batteries (from 20 to 106 cycles) without illumination. While introducing illumination, the performance can be further improved: Charge voltage reduces to 3.3 V, and the energy efficiency increases to 84.84%, indicating that the Co-C 3 N 4 could behave as a suitable photocathode for Li-O 2 batteries. Besides, the low charge voltage and the continuous illumination together weaken the corrosion of the Li anode, making the long-term high-efficiency operation of Li-O 2 batteries no longer just extravagant hope.
研究领域:
材料科学
·
电化学
·
能源技术
✓ 已验证
产品关联
DOI
高影响因子
危险品化学品经营许可证（带存储）