Journal of Cleaner Production
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2023
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IF 11.1
Dong Wang,Yumeng Wang,Luheng Jing,Lei Wang,Tonghui Zhang,Xuefen Wang
In this work, a flower-like Fe(OH) 3 @Co 2 (OH) 2 CO 3 catalyst was prepared via the confinement effects provided by L-phenylalanine, which favored the heterostructure construction of active iron centers (Fe(OH) 3 ) anchored on the Co 2 (OH) 2 CO 3 nanosheet supports. Benefiting from the created electron-transfer interface and dual metal active sites, the limitation of redox cycling was broken and exhibited highly efficient catalytic activities , the optimal Fe(OH) 3 @Co 2 (OH) 2 CO 3 catalyst showed comparable catalytic performance for the degradation of dye (degradation degree of 99% methylene blue and orange II within 18 min). In addition, the prepared catalysts were employed for the efficient removal of antibiotics (tetracycline (98.9%), norfloxacin (92.5%) and doxycycline hyclate (90.2%). Besides, the preferred nanofibrous composite membranes prepared by combination of nanofibrous membranes (NFMs) with Fe(OH) 3 @Co 2 (OH) 2 CO 3 catalysts possessed considerable potential for large-scale MB removal (treatment capacity of 238.5 L m −2 and permeability of 191.8 L m −2 h − 1 driven by gravity) and stability (182.7 L m −2 of treatment capacity was achieved in the third run). The strategy of construction of rapid interface-redox on the heterogenous catalysts was designed to enhance catalytic performance, which provided a promising chance for the efficiently large-scale removal of dyes and antibiotics.
研究领域:
材料科学
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环境科学
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催化化学
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DOI
高影响因子
CHEMICAL ENGINEERING JOURNAL
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2022
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IF 16.744
Le Gao,Yawen Li,Guifang Li,Jiaqi Huo,Lishan Jia
Interface engineering as an effective material modification method can regulate local corresponding interfacial geometry and electronic structures, thus enabling a higher intrinsic activity for the oxygen evolution reaction (OER). Herein, we carefully designed p-p heterojunction precursor Co4-MOF@La(HCO 2 ) 3 with internal electric field through electrostatic adherence, which then in-situ transformed into p-p type heterojunction electrocatalyst (Co(OH) 2 )4@La(OH) 3 under KOH activation strategy. The one-step in-situ conversion of (Co(OH) 2 )4@La(OH) 3 generated the interface with significant difference in metal atomic radius and exhibits fascinating nanostructures, which enhances the specific surface area and increases the number of active sites compared with the parent material. Impressively, the obtained material (Co(OH) 2 )4@La(OH) 3 demonstrates satisfying electrocatalytic activity in OER with a low overpotential of only 233 mV to reach a current density of 20 mA cm −2 , and excellent stability for 50 h at 10 mA cm −2 in alkaline medium. In-situ Raman technique indicates that multivalent Co centers are the true active sites during the OER process. Based on density functional theory (DFT) calculation results, La atoms possess empty d orbitals, which are beneficial to facilitate charge transfer from Co to La at the heterojunction interface. Meanwhile, the introduction of La atoms changes the coordinated environment around the adjacent atoms at the interface, which induces the upshift of the d-band center for Co atoms and increases the binding strength of the adsorbed oxygen intermediate.
研究领域:
材料科学
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电化学
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能源转换与存储
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产品关联
DOI
高影响因子
JOURNAL OF CHEMICAL THERMODYNAMICS
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2020
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IF 2.888
Kaiyu Zhao,Kangrui Sun,Yafei Guo,Lingzong Meng,Tianlong Deng
The isopiestic equilibria for the systems {Li 2 B 4 O 5 (OH) 4 + H 2 O}, {LiB 5 O 6 (OH) 4 + H 2 O} and {Li 2 B 4 O 5 (OH) 4 + LiB 5 O 6 (OH) 4 + H 2 O} at 288.15 K and ambient pressure were measured by the isopiestic method using a modified gravimetric isopiestic apparatus. The water activities and osmotic coefficients were determined based on the sodium chloride standard reference solution. On the basis of Pitzer model, an extended Pitzer model was developed to describe the thermodynamic properties of the aqueous systems containing different forms of lithium borates, then the Pitzer single salt parameters β (0) , β (1) , β (2) and C ϕ for the binary systems {Li 2 B 4 O 5 (OH) 4 + H 2 O} and {(LiB 5 O 6 (OH) 4 + H 2 O} and mixing ion-interaction parameters θ B 4 O 5 OH 4 , B 5 O 6 OH 4 and ψ Li , B 4 O 5 OH 4 , B 5 O 6 OH 4 for the ternary system {Li 2 B 4 O 5 (OH) 4 + LiB 5 O 6 (OH) 4 + H 2 O} were fitted with the experimental osmotic coefficients using the Fortran 97 program. Meanwhile, the water activities were calculated by the Pitzer parameters, and the good agreement between the calculated water activities and experimental results of this ternary system indicated that the Pitzer parameters obtained in this work were reliable.
研究领域:
物理化学
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热力学
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无机化学
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DOI
高影响因子
Molecular Catalysis
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2021
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IF 5.062
Zijing Wang,Changjuan Mo,Sixuan Xu,Shanshuai Chen,Tiansheng Deng,Wanbin Zhu,Hongliang Wang
The catalytic conversion of carbohydrate to platform chemicals, e.g. lactic acid (LA), is the key to unlock the potential of biomass. In this study, we report that the combination of Ba(OH) 2 and Ca(OH) 2 can efficiently catalyse high-concentration (> 0.5 M) of glucose to relatively high yield of LA (> 40 %) under mild conditions (60 °C). Both glucose conversion and LA yield were sensitive to the pH of the catalytic system. A high loading of Ba(OH) 2 led to a high initial pH of the reaction solution, resulting in serious side reactions. While, a low loading of Ba(OH) 2 led to a quike decrease of OH − and Ba 2+ both of which were continuously consumpted by the formed LA. The combination of Ca(OH) 2 with Ba(OH) 2 could significantly improve LA yield, since Ca(OH) 2 , with limited solubility, could act as a controlled-release catalyst for the real-time supply of OH − and Ca 2+ . OH − was indispensable for glucose isomerization to fructose as well as for fructose retro-aldol reaction to C 3 intermediates. Ca 2+ could combine with LA to form stable calcium lactate, liberating Ba 2+ to catalyse the conversion of C 3 intermediates to LA. Under the preliminary optimized reaction conditions, the yield of LA could be reached to 42.55 % and 38.32 % from 0.5 M and 1 M glucose, respectively. This catalytic system has advantages of mild reaction condition, short reaction time, and capable of conversion of high-concentration substrates, enabling it with a great potential for practical applications.
研究领域:
生物化学
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可再生资源化学
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产品关联
DOI
高影响因子
APPLIED SURFACE SCIENCE
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2024
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IF 6.3
Yulan Song,Cuilan Tang,Tao Wang,Yansong Liu,Xiaoshan He,Chunping Xie,Guo Chen,Chengfu Deng,Zhibing He,Jinglin Huang
Constructing electronic structures with abundant surface/interface structures and effective regulation of catalytic active centers is an effective strategy to improve electrocatalytic performance, but designing efficient bifunctional non-noble metal oxygen evolution reaction (OER) and urea oxidation reaction (UOR) electrocatalysts remains challenging. Studies have shown that p-n heterojunctions can effectively regulate the electronic structure of catalytic active sites while having abundant surface/interface structure, which plays an important role in improving the native catalytic activity. Herein, FeNi-OH/Co(OH) 2 /NF p-n heterojunction structure was constructed by a simple electrochemical deposition method, and the effects of content, deposition time, and number of cycles on catalytic performance were investigated. The results show that Fe(0.02 M)Ni(0.07 M)–OH(100 s)/Co(OH) 2 (5)/NF composite material has the best OER and UOR catalytic performance. For OER, the electrocatalyst only requires an overpotential of 271 mV to obtain a current density of 50 mA cm −2 , and an applied voltage of 1.56 V to obtain a total water decomposition of 10 mA cm −2 (FeNi-OH/Co(OH) 2 /NF||Pt). For UOR, a voltage of only 1.314 V ( vs. RHE) is required to achieve a current density of 10 mA cm −2 , and an applied voltage of 1.44 V can achieve a current density of 10 mA cm −2 . Experimental, in situ measurements and theoretical results indicate that the improvement in catalytic activity is mainly due to the potential difference between FeNi-OH and Co(OH) 2 , which induces self-driven charge transfer at the interface, promoting the adsorption of reactant molecules, optimizing reaction barriers, accelerating chemical bond cleavage, and thus promoting catalytic reactions.
研究领域:
材料科学
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电化学
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催化
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产品关联
DOI
高影响因子
Nature Communications
·
2024
·Vol. 15
·期 1
·1-10
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IF 14.7
Lv Jiabao,Cao Ang,Zhong Yunhao,Lin Qingyang,Li Xiaodong,Wu Hao Bin,Yan Jianhua,Wu Angjian
Renewable-driven electrocatalytic nitrate conversion offers a promising alternative to alleviate nitrate pollution and simultaneously harvest green ammonia. However, due to the complex proton-electron transfer processes, the reaction mechanism remains elusive, thereby limiting energy efficiency. Here, we adopt Ni(OH)₂ as a model catalyst to investigate the dynamic evolution of the reaction interface. A proposed OH cycle mechanism involves the formation of a locally OH-enriched microenvironment to promote the hydrogenation process, which is identified through in-situ spectroscopy and isotopic labelling. By further activating the dynamic state through the implementation of surface vacancies via plasma, we achieve a high Faradaic efficiency of almost 100%. The activated interface accelerates the OH cycle by enhancing dehydroxylation, water dissociation, and OH adsorption, thereby promoting nitrate electroreduction and inhibiting hydrogen evolution. We anticipate that rational activation of the dynamic interfacial state can facilitate electrocatalytic interface activity and improve reaction efficiency.
研究领域:
电化学
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催化
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环境科学
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材料科学
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DOI
高影响因子
JOURNAL OF SOLID STATE ELECTROCHEMISTRY
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2024
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IF 2.6
Li Gang,Ren Haifang,Geng Chunping,Wu Xiang
Electrical energy storage devices (EES) play an important role in the development of portable electronic devices, power grids, and electric vehicles. Supercapacitors (SCs) become the focus of the EES field due to their high power density and high energy density. ZnCo 2 O 4 ternary metal oxides show considerable potential as electrodes for SCs. In this work, Ni(OH) 2 and PPy materials are combined on the surface of ZnCo 2 O 4 samples. The synthesized products possess a specific capacitance of 1256 C/g at 1 A/g and an energy density of 69 Wh/kg at 1350 W/kg. Moreover, the assembled device retains 81% of its capacity after being fully charged and discharged 10,000 times.
研究领域:
材料科学
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能源存储
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产品关联
DOI
高影响因子
NANOTECHNOLOGY
·
2021
·Vol. 32
·期 34
·345706
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IF 3.874
Leqiu He,Yan Wang,Yajie Guo,Guobing Li,Xubin Zhang,Wangfeng Cai
Novel core−shell nanostructure electrodes benefit from the excellent properties of their constituent materials, as well as the synergy between them. However, it is challenging to fabricate such structures efficiently. In this study, NiSe nanorods were fabricated using Ni foam as the conductive substrate and reactant via a one-step hydrothermal process, and Ni(OH)2 nanosheets were coated on the surface of the nanorods via one-step electrodeposition. The effect of the structure and morphology on the properties of the material was explored using scanning electron microscopy, x-ray diffraction, and electrochemical technology. The obtained core−shell NiSe/Ni(OH)2 exhibited an areal capacity of 1.89 mAh cm−2 at a current density of 5 mA cm−2. The assembled NiSe/Ni(OH)2//AC hybrid supercapacitor exhibited excellent energy and power densities, indicating that NiSe/Ni(OH)2 has great potential for use as a battery-type electrode in energy storage systems.
研究领域:
材料科学
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电化学
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纳米技术
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产品关联
DOI
PubMed
高影响因子
JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY
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2025
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IF 6.2
Xisong Feng,Mengjian Gao,Wanqing Wei,Wei Song,Jian Wen,Hongyu Wang,Guipeng Hu,Xiaomin Li,Cong Gao,Jing Wu
25-hydroxyvitamin D3 (25(OH)VD3) is an important daily nutritional supplement, and direct enzymatic C25 hydroxylation of vitamin D3 (VD3) to 25(OH)VD3 is a green and sustainable method. However, the low catalytic activity and electron transfer efficiency of redox partners of cytochrome P450 limited its production. Here, structure-guided semirational design of CYP109E1 led to the mutant CYP109E1M2, which showed a 2-fold increase in 25(OH)VD3 production compared to the wild-type. Furthermore, the novel reductase domain BmRD was first employed to construct a fusion protein with CYP109E1M2. Notably, truncating only two amino acids at the N-terminus of BmRD generated a fusion protein Chimera-2, resulting in a 38.5% increase in 25(OH)VD3 production. Under optimized conditions, the engineered strain Escherichia coli 03-2 produced 491.3 mg/L 25(OH)VD3 with a conversion of 49.0% and a space-time yield of 61.4 mg/(L·h). This work demonstrates the modification and optimization potential of P450 and lays a theoretical foundation for the industrialization of the 25(OH)VD3 biosynthesis.
研究领域:
生物化学
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分子生物学
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酶工程
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DOI
PubMed
高影响因子
CRYSTAL GROWTH & DESIGN
·
2024
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IF 3.2
Huiqin Ma,Zhuxiang Mao,Wen Liu,Yahao Zhao,Peng Liu,Difu Zhan,Qian Fu,Yizhong Huang,Changcun Han
ZnIn2S4 (ZIS) is an N-type direct bandgap semiconductor material with a visible light response, which exhibits excellent photocatalytic water-splitting performance. To enhance ZIS-based photocatalysts, heterojunction construction and cocatalyst loading methods have been explored extensively. In this research, a Co9S8/ZnIn2S4 (CS/ZIS) heterojunction was successfully synthesized via a solvothermal method, and then Ni(OH)2 nanoparticles were successfully loaded on CS/ZIS by photodeposition, yielding the Ni(OH)2/CS/ZIS photocatalyst. Our findings reveal tight coupling of ZIS nanosheets with the CS surface, establishing an effectively constructed heterojunction structure that enhances interface charge transfer and light absorption. The synergistic effect of CS and Ni(OH)2 significantly boosts the photocatalytic hydrogen production of ZIS composites. The optimum hydrogen production rate of CS/ZIS is 10.06 mmol·h–1·g–1 and that of Ni(OH)2/CS/ZIS reaches 12.92 mmol·h–1·g–1, a 11.9-fold increase over pure ZIS, with exceptional light stability. Furthermore, we discuss the photocatalytic reaction mechanism based on the experimental and characterization results. This work presents a novel approach to designing highly efficient photocatalysts using ZnIn2S4, aimed at enhancing the conversion of solar energy into chemical energy.
研究领域:
材料科学
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能源化学
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纳米技术
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产品关联
DOI
高影响因子
IEEE TRANSACTIONS ON DIELECTRICS AND ELECTRICAL INSULATION
·
2022
·Vol. 30
·期 1
·230-237
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IF 2.509
Bin Du,Yuxiang Mai,Nanqing Chen,Yushun Zhao
The interfacial effect of nanoparticles can effectively regulate electron migration in epoxy composites. In this article, hydroxylated C60 [C60(OH)] was prepared and added to epoxy resin (EP). The inhibition of electron motion in epoxy composites was realized, and the dielectric strength of the epoxy composites was improved. The results of dynamic mechanical analysis (DMA) showed that C60(OH) regulated the structure of the crosslinked EP network and increased the crosslink density by 16.5%. The results of a density functional theory (DFT) simulation showed that the doping of C60(OH) formed a potential energy barrier at the C60(OH)-EP interface, which was conducive to the directional migration and capture of electrons driven to C60(OH). Electrostatic force microscopy (EFM) and pulsed electroacoustic (PEA) experiments showed that C60(OH) had a strong ability to capture charge, and the charge migration rate of C60(OH)/EP was 43% lower than that of pure EP in the presence of 10 kV/mm when the EP was doped with 0.1wt% C60(OH). The breakdown strength and volume resistivity increased by 17.87% and 222%, respectively. Thus, this article provides a new method to improve the dielectric strength of epoxy composites.
研究领域:
材料科学
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化学工程
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DOI
高影响因子
INORGANIC CHEMISTRY
·
2022
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IF 5.436
Min Chen,Zhengli Liang,Xiaoxiao Wang,Jiehua Li,Xingguo Chen,Xingxing Jiang,Zheshuai Lin,Zhen Ma,Hongming Liu
A series of lanthanide-containing water-resistant nitrates, namely RE(OH)2NO3 (RE = Tb(1), Dy(2), Ho(3), and Er(4)), was obtained through the hydrothermal process. As possible nonlinear optical materials, they feature a layered isomorph composed of an [REO3(OH)6] polyhedron and an [NO3] triangle, and the synergistic arrangement of the [REO3(OH)6] and [NO3] groups in their structures leads to their obvious second-order nonlinear optical effect. Nevertheless, the unique optical absorption caused by the electronic transitions on 4f–4f orbitals of lanthanides results in their second harmonic generation responses of different strengths, with 1 exhibiting 5.07 times that of KDP, but 2–4 showing less than half of KDP. In addition, 1 possesses an outstanding water-resistant capacity and a transparent cut-off edge around 300 nm, foreshadowing its potential value as a nonlinear optical crystal. Moreover, 1 is found to emit characteristic green fluorescence due to the typical 5D4 → 7F5 transitions of the excited Tb3+ ions
研究领域:
材料科学
·
光学
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化学
✓ 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）