Surfaces and Interfaces
·
2024
·
IF 5.7
Yong Shi,Xin Lan Ma,Jin Suo Gao,Feng Yun Yu,Chun Yan Li,Wei Xiong,Li Ping Huang
The catalytic activity, adsorption and synergistic effect over bimetallic MOF derivatives with different dopant metal were systemically compared. A series of Me-Cu/TiO 2 (Me=Fe, Co, Ni) derived from bimetallic Me/Cu-BTC MOFs were fabricated via a sacrificing template method and applied for CO-SCR. Among the bimetallic catalysts, Fe-Cu/TiO 2 presented the best low-temperature of nearly 100% NO conversion from 150 °C to 350 °C with good NO selectivity. For Me-Cu/TiO 2 (Me=Fe, Co, Ni), the productions of crucial Cu + intermediate were determined to be 51.17%, 50.45%,49.4% by XPS, which were consistent with their catalytic activity results. The superior redox behavior of Fe-Cu/TiO 2 can be attributed to its higher Oβ / (Oα +Oβ) ratio of 32.90% and the higher Me 2+ / Me 3+ ratio of 1.79. In situ infrared analysis revealed that the Fe doping not only improved the formation and stability of nitrate species, but also enhanced the quantity of Lewis acid sites by forming Cu + -CO. Furthermore, a possible low-temperature Langmuir-Hinshelwood (L-H) mechanism over Me-Cu /TiO 2 (Me=Fe, Co, Ni) was proposed.
研究领域:
材料科学
·
环境催化
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产品关联
DOI
高影响因子
COLLOIDS AND SURFACES A-PHYSICOCHEMICAL AND ENGINEERING ASPECTS
·
2024
·
IF 4.9
Rui Gou,Yong Li,Qilong Chen,Sha Wang,Dan Sun,Changhua Li,Xianmin Gong,Yi He
Metal corrosion causes a lot of waste of resources, and the protection of metals from corrosion is becoming increasingly important. In this study, zeolite-imidazole (ZIF-67) was grown on the surface of Co-MOF for the first time by a one-step (complexation) method. 2-Mercaptobenzimidazole (MBI) was then loaded into the inner cavity of ZIF-67, resulting in the formation of a new composite material, Co-MOF@ZIF-67@MBI. The modified Co-MOF exhibits excellent interfacial compatibility with the water-based epoxy resin, and the Co-MOF@ZIF-67@MBI composite coating demonstrates robust anti-corrosion properties. Following a 60-day immersion period, the electrochemical experiment demonstrated that the corrosion resistance modulus of the Co-MOF@ZIF-67@MBI composite coating reached 10 8 Ω cm², indicating that the coating effectively enhanced the corrosion resistance of the coating and significantly extended the service life of the coating.
研究领域:
材料科学
·
腐蚀与防护
·
复合材料
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产品关联
DOI
高影响因子
JOURNAL OF NANOPARTICLE RESEARCH
·
2017
·Vol. 19
·期 8
·1-7
·
IF 2.02
Li Nannan,Liu Jian,Duan Xiulan,Yu Fapeng,Jiang Huaidong
This report discusses the preparation and microstructure of Co/Ni co-doped MgGa 2 O 4 nanoparticles. The nanoparticles with the size of 20–55 nm were synthesized by sol-gel method. The phase and crystallinity were confirmed by X-ray powder diffraction (XRD) pattern. The particle size was estimated according to XRD data and transmission electron microscopy. The electronic structure was studied using X-ray photoelectron spectroscopy (XPS). The XPS studies showed that Ga 3+ ions possess tetrahedral and octahedral sites of spinel structure and the inverse degree (two times of the fraction of tetrahedral Ga 3+ ions) has increased with the increase of the doping concentration of Co 2+ and Ni 2+ ions. For Co/Ni co-doped MgGa 2 O 4 , two broad absorption bands of 350~500 and 550~700 nm were observed in the absorption spectra. The broad band at 350~500 nm was assigned to the combination of the absorption of octahedral Co 2+ and Ni 2+ ions, whereas the absorption band at 550~700 nm is mainly due to tetrahedrally coordinated Co 2+ ions and octahedrally coordinated Ni 2+ ions.
研究领域:
材料科学
·
纳米技术
✓ 已验证
DOI
高影响因子
SPECTROCHIMICA ACTA PART A-MOLECULAR AND BIOMOLECULAR SPECTROSCOPY
·
2021
·
IF 4.098
Xiao-Lan Zhao,Jia-Li Liu,Fa-Ting Xie,Tong Yang,Rong Hu,Yun-Hui Yang
In this paper, a simple, rapid, and low-cost colorimetric method was designed based on Co/Fe-MOFs-iodide composite for the quantitative detection of H 2 S. It is know that iodide can improve the catalytic activity of bimetallic porous material Co/Fe-MOFs via adsorption into the framework of MOFs. Herein, we demonstrate a novel strategy to enhance the peroxidase-like activity of MOFs. Compared to horseradish peroxidase (HRP), the kinetic measurement results show that Co/Fe-MOFs-iodide exhibits excellent affinity to substrates, promoting electron transfer. Due to the synergetic effect of Co/Fe-MOFs and iodide, and rapid electron transfer process, Co/Fe-MOFs-iodide demonstrates improved peroxidase-like activity. As a proof-of-concept application, a novel, highly sensitive H 2 S colorimetric method is established with a detection limit (LOD) of 0.33 nM. In the absence of iodide, LOD is approx. 200-fold higher than that of the amplified colorimetric assay. The proposed method can also accurately detect traces of H 2 S in serum samples.
研究领域:
生物化学
·
分析化学
✓ 已验证
DOI
PubMed
高影响因子
ChemPlusChem
·
2025
·
IF 2.8
Chunqiu Zhao,Qiang Chang,Fu Yin,Guowei Niu,Chenghua Zhang,Dan Liu,Bhekie B. Mamba,Alex T. Kuvarega
Graphical To enhance the catalytic performance of Zn−NC in the hydrogenation of CO to dimethyl ether, highly dispersed bimetallic catalysts are synthesized through the pyrolysis different metal-doped ZIF. The incorporation of secondary metals (Mn, Fe, Co, Ni, Cu) leads to distinct variations in catalytic performance. Among them, the introduction of Cu significantly improves catalytic activity. Highly dispersed bimetallic atomic-scale catalysts have garnered significant attention in syngas conversion filed due to the synergistic effects of the precisely structured bimetallic site, which facilitate the effective activation of CO. Despite their potential, synthesizing these catalysts to meet the specific application requirements remains challenging. Herein, various bimetallic catalysts were synthesized through the pyrolysis of the bimetallic ZIF precursors which were prepared by in situ doping of different metals (Mn, Fe, Co, Ni and Cu) into the ZIF-8 structure. In the presence of a highly dispersed and highly loaded Zn, the doping content in the ultimate second metallic catalysts varied between 0.15–1.20 wt % for different metals. The catalysts were systematically characterized using XRD, BET, TEM, XPS, Raman, ICP, and H 2 -TPD techniques. Among them, the Zn−NC regulated with Cu or Ni exhibited superior catalytic performance. Notably, the Cu−Zn−NC catalyst showed the highest activity, achieving a CO conversion of 32.8 % and optimal DME selectivity approaching 95.2 % in CO hydrogenation reactions. These enhanced performance metrics were attributed to the synergetic effects of bimetallic components. The incorporation of Cu not only preserved the original Zn−N structure but also preserved the catalytic performance unchanged. This preparation strategy is expected to filter out new research targets to use in diverse catalytic applications.
研究领域:
催化化学
·
材料科学
·
能源化学
✓ 已验证
产品关联
DOI
PubMed
高影响因子
CHEMICAL ENGINEERING JOURNAL
·
2024
·
IF 13.3
Xiaoqian Hao,Shengjun Xu,Yan Huang,Shuanglong Ma,Boqiang Gao,Jia Song,Jingzhen Wang,Sihui Zhan
Molybdenum disulfide serves as an ideal support for single atom catalysts (SACs), offering not only coordination elements but also abundant active sites, such as surface defects and vacancies. Herein, a novel Co-SAC (MoSO-Co-C) containing a four-coordinated configuration (Mo-Co-C 3 ) is designed and synthesized, in which the carbon intercalation is utilized to regulate sulfur vacancies for anchoring the Co atom. The introduction of Co atoms and C intercalation significantly enhances the E ads between catalyst and peroxymonosulfate (PMS), favoring the formation of metastable intermediates. The k obs of sulfamethoxazole (SMX) removal for MoSO-Co-C is 9.2 times and 1.8 times higher than those of catalysts without Co or C intercalation. SMX is removed mainly by electron transfer pathway, wherein SMX and PMS act on the same Co site of MoSO-Co-C, and electrons are transferred from SMX to MoSO-Co-C and eventually to PMS. The MoSO-Co-C demonstrated excellent SMX degradation in the diverse water matrices, and the removal efficiency of SMX maintained above 95 % after 72 h of continuous degradation. This study provides new insights into the design of transition metal-based SAC and in-depth understanding of PMS activation mechanism.
研究领域:
环境科学
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催化
·
水处理
·
材料科学
✓ 已验证
产品关联
DOI
高影响因子
Chem Catalysis
·
2022
·
IF 0
Zhe Zhang,Min Wang,Feng Wang
Summary Heterojunction is promising to promote the spatial charge separation while the poor lattice mismatches and the bulk size of semiconductors constrain the photocarrier separation and migration to the surface. Herein, we report the surface oxidative reconstruction of CdS to form CdO quantum dots (QDs)/CdS intimate heterojunction. We developed a plasma-assisted method to prepare CdO-QDs/CdS heterojunction where CdS(200) and CdO(111) are tilted with a dihedral angel of 159° to form a semi-coherent interface, maximally reducing the interface dangling bonds. The semi-coherent interface and the quantum size of CdO-QDs efficiently promotes charge separation and migration to the surface, accelerating the photocatalytic bio-CO evolution. With glycerol as feedstock, the CO generation rate over CdO-QDs/CdS reaches 2.37 mmol g −1 ·h −1 , which is 4-fold of that over CdS. The present work reports a new method for the preparation of CdO-QDs/CdS intimate heterojunction and gives insight into tuning lattice coherency to promote photocarrier separation.
研究领域:
材料科学
·
能源科学
✓ 已验证
DOI
Journal of Materials Chemistry A
·
2016
·Vol. 4
·期 27
·10609-10617
·
IF 8.262
Dewei Liang,Shouliang Wu,Jun Liu,Zhenfei Tian,Changhao Liang
Morphology control and impurity doping are two widely applied strategies to improve the electrochemical performance of nanomaterials. Herein, we report an environmentally friendly approach to obtain Co-doped Ni(OH)2 nanosheet networks using a laser-induced cobalt colloid as a doping precursor followed by an aging treatment in a hybrid medium of nickel ions. The shape and specific surface area of the doped Ni(OH)2 can be successfully adjusted by changing the concentration of sodium thiosulfate. Furthermore, a Co-doped Ni(OH)2 nanosheet network was further converted into Co-doped NiO with its pristine morphology retained via facile thermal decomposition in air. The structure and electrochemical performance of the as-prepared samples are investigated with scanning and transmission electron microscopy, energy dispersive X-ray analysis, X-ray diffraction, Fourier transform infrared spectroscopy, the nitrogen adsorption–desorption isotherm technique, and electrochemical measurements. The Co-doped Ni(OH)2 electrode shows an ultrahigh specific capacitance of 1421 F g−1 at a current density of 6 A g−1, and a good retention level of 76% after 1000 cycles, in sharp contrast with only a 47% retention level of the pure Ni(OH)2 electrode at the same current density. In addition, the Co-doped NiO electrode exhibits a capacitance of 720 F g−1 at 6 A g−1 and 92% retention after 1000 cycles, which is also superior to the corresponding values of relevant pure NiO electrodes. The Co2+ partially substitutes for Ni2+ in the metal hydroxide and oxide, resulting in an increase of free holes in the valence band, and, therefore, enhancement of the p-type conductivity of Ni(OH)2 and NiO. Moreover, such novel mesoporous nanosheet network structures are also able to enlarge the electrode–electrolyte contact area and shorten the path length for ion transport. The synergetic effect of these two results is responsible for the observed ultrahigh pseudocapacitor performance.
研究领域:
材料科学
·
电化学
✓ 已验证
产品关联
DOI
高影响因子
Catalysts
·
2025
·Vol. 15
·期 3
·219
·
IF 4
Xuan Han,Chao Guo,Hui Wang,Weijuan Xu,Qinlian Liu,Qingshan Zhao,Mingbo Wu
Hydrogen production from water electrolysis offers a highly promising and sustainable route to solve the energy crisis. However, it is severely limited by the sluggish kinetics of the oxygen evolution reaction (OER) occurring on the anode. Herein, employing carbon dots functionalized with benzene sulfonate groups (BS-CDs) as a distinctive inductor, a Co(OH)2catalyst featuring abundant defects was synthesized for an enhanced OER. The highly hydrophilic nature of BS-CDs exerts a significant interfacial induction effect on the growth dynamics of Co(OH)2, fostering the formation of elevated crystal defects and a substantial quantity of oxygen vacancies. The resulting BS-CDs/Co(OH)2catalyst requires an overpotential of only 340 mV to achieve a current density of 10 mA cm−2in alkaline media, demonstrating markedly improved OER activity compared to pristine Co(OH)2and N-CDs/Co(OH)2induced by amine-modified CDs. Furthermore, the structural integrity of the catalyst is maintained, with a current retention rate of 92% observed following a 20 h stability assessment. This work provides a novel approach for developing cost-effective transition metal catalysts that exhibit exceptional catalytic efficiency and excellent stability for the OER.
研究领域:
材料科学
·
催化化学
·
能源化学
✓ 已验证
产品关联
DOI
高影响因子
CERAMICS INTERNATIONAL
·
2016
·
IF 2.758
Haiyan He,Ping Yang,Jia Li,Ruixia Shi,Ling Chen,Aiyu Zhang,Yuanna Zhu
CeO 2 nanostructures with various morphologies were prepared through controlling preparation conditions via a hydrothermal method without any surfactants and templates. Cerium acetate, cerium chloride and cerium nitrate were used as cerium precursors to investigate the influence of anions on the growth process of CeO 2 nanostructures. The morphology evolution of CeO 2 and Ce(OH) 3 nanostructures indicates that the anions play an important role for the growth kinetics of resulting samples. Cl − and Ac − ions promoted the formation of one dementional (1D) CeO 2 nanostructures such as nanowires, nanorods and nano hexagonal prisms, while the oxidizing anion NO 3 - facilitated the synthesis of CeO 2 nanocubes. The hydrothermal reaction temperature is another key to govern the morphologies of CeO 2 nanostructures. The formation process of the nanostructures was explored and the possible growth mechanism was discussed. The variety of CeO 2 nanostructures represented inequable catalytic performance for CO oxidation . Because of different surface areas and structures, CeO 2 nanowires revealed the best catalysis performance while that of the nanocubes is the worst.
研究领域:
材料科学
·
化学
✓ 已验证
DOI
高影响因子
COLLOIDS AND SURFACES A-PHYSICOCHEMICAL AND ENGINEERING ASPECTS
·
2021
·
IF 4.539
Xu Ouyang,Lan Zhou,Xinliang Xu,Zhangyan Yang,Lei Wang,Lizhe Lu,Guojin Liu,Guoqing Zhang
In order to improve the encapsulation efficiency and shell properties of PMMA capsules, poly(MMA-co-TMPTA)/fragrance microcapsules were fabricated by in-situ polymerization with Trimethylolpropane Triacrylate (TMPTA) as the co-monomer. The poly (MMA-co-TMPTA)/fragrance microcapsules were characterized by scanning electron microscopy (SEM), thermogravimetric analyzer (TGA), pyrolysis gas chromatography-mass spectrometer (PGC-MS) and electronic nose (PEN-3). The results indicate that the poly(MMA-co-TMPTA)/fragrance microcapsules present pomegranate shape with rough and sunk surface and have the particle size in the range of 10−20 μm. poly(MMA-co-TMPTA)/fragrance microcapsules has good thermal stability, high encapsulation efficiency of 91.6 % and good slow-release property, and the fragrance on the fabric can be retained for more than 3 months.
研究领域:
材料科学
·
化学工程
✓ 已验证
DOI
高影响因子
Nature Communications
·
2025
·Vol. 16
·期 1
·1-10
·
IF 15.7
Wang Qiyou,Luo Tao,Cao Xueying,Gong Yujie,Liu Yuxiang,Xiao Yusen,Li Hongmei,Gröbmeyer Franz,Lu Ying-Rui,Chan Ting-Shan,Ma Chao,Liu Kang,Fu Junwei,Zhang Shiguo,Liu Changxu,Lin Zhang,Chai Liyuan,Cortes Emiliano,Liu Min
Single-atom catalysts (SACs) have received increasing attention due to their 100% atomic utilization efficiency. The electrochemical CO 2 reduction reaction (CO 2 RR) to CO using SAC offers a promising approach for CO 2 utilization, but achieving facile CO 2 adsorption and CO desorption remains challenging for traditional SACs. Instead of singling out specific atoms, we propose a strategy utilizing atoms from the entire lanthanide (Ln) group to facilitate the CO 2 RR. Density functional theory calculations, operando spectroscopy, and X-ray absorption spectroscopy elucidate the bridging adsorption mechanism for a representative erbium (Er) single-atom catalyst. As a result, we realize a series of Ln SACs spanning 14 elements that exhibit CO Faradaic efficiencies exceeding 90%. The Er catalyst achieves a high turnover frequency of ~130,000 h − 1 at 500 mA cm − 2 . Moreover, 34.7% full-cell energy efficiency and 70.4% single-pass CO 2 conversion efficiency are obtained at 200 mA cm − 2 with acidic electrolyte. This catalytic platform leverages the collective potential of the lanthanide group, introducing new possibilities for efficient CO 2 -to-CO conversion and beyond through the exploration of unique bonding motifs in single-atom catalysts.
研究领域:
材料科学
·
环境科学
·
化学工程
✓ 已验证
产品关联
DOI
PubMed
高影响因子
危险品化学品经营许可证（带存储）