APPLIED CATALYSIS B-ENVIRONMENTAL
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2018
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IF 11.698
He Xiao,Wenyao Zhang,Qiushi Yao,Liulian Huang,Lihui Chen,Bruno Boury,Zhongwei Chen
Metal organic frameworks (MOFs) are exploited in many applications of materials science and very recently were investigated as precursors or reagents for material synthesis. In a new way different from previous approaches, here we introduce for the first time the synthesis of metal oxide M x O y in the presence of M-free MOF acting partially as a sacrificial template and as a provider of doping metal atom. We demonstrate this approach in the case of ZnO prepared by a simple hydrothermal method in the presence of a Zn-free MOF like MIL-53(Al) or MIL-125(Ti). The resulting ZnO show low content of Al or Ti < 2% and properties are significantly different depending on whether MIL-53(Al) or MIL-125(Ti) are used or if no MOF is present. The nature and presence of MOF has different major effects on the morphology, the specific surface area of as prepared ZnO and also on the oxygen defects in its crystal structure. Corroborating the XPS, UV–vis DRS, PL, EPR and DFT studies evidence the role of such O-defects on band gap narrowing for samples calcined at 400 °C. These exhibit high efficiency in photodegradation of methyl orange (MO) compared to ZnO prepared in MOF-free conditions or previous literatures. The kinetics of MO degradation is different depending on the morphology, the specific surface and oxygen defects. The present data open the door to a new approach of the synthesis of metal oxides and a control of their properties.
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高影响因子
FUEL
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2025
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IF 7.5
Jianping Ding,Xiaoyan Zhou,Zhengzheng Yang,Changgeng Liu,Mingchao Sun,Congling Yang,Lu Fan
In this study, a novel strategy was proposed for synthesizing dual single-atom Ce-Ti catalysts supported on γ-Fe 2 O 3 via ball milling and calcination. Compared to γ-Fe 2 O 3 and single-atom Ce/γ-Fe 2 O 3 and Ti/γ-Fe 2 O 3 catalysts, the Ce-Ti/γ-Fe 2 O 3 catalyst exhibits superior NO conversion rates and significantly enhanced tolerance to H 2 O and SO 2 at 200–240 °C. These advancements are attributed to the synergistic interactions between Ce and Ti, which enhance redox properties, increase Lewis acid site density, and facilitate the Langmuir-Hinshelwood reaction pathway. In-situ DRIFTS and density functional theory (DFT) analyses revealed the mechanistic role of surface-active oxygen species and intermediate formation in promoting the SCR reaction. The findings provide valuable mechanistic insights and establish a scalable approach for the development of high-performance, environmentally friendly catalysts for industrial NO x removal.
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Desalination and Water Treatment
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2024
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IF 1
Xiaoxia Chen,Yu Ma,Zhengjie Su,Xinxin Zhang,Jinguo Lin,Xiaoyun Chen
Herrin, the lignin extracted from Rice hull , Phyllostachys edulis , Cunninghamia lanceolata, and Populus tomentosa Carrière were used as a soft support to grow Ti-doped Bi 2 (O,S) 3 bimetal oxysulfide catalysts, labeled BT-Rh, BT-Pe, BT-Cl, and BT-Ptc, respectively. The catalytic reduction activity was investigated through the decolorization of methyl orange (MO), methylene blue (MB), and reduction of Cr(VI) solutions under dark. The lignin-supported BiTiOS improved crystallinity, decreased aggregate size, increased specific surface area, and enhanced electrochemical active sites, leading to improve electron transfer and accelerated reduction rates. The catalytic reduction activity of organic dyes and Cr(VI) was significantly improved with lignin-supported BiTiOS. The 5 mg BT-Pe catalyst completely reduced 100 mL of 50 ppm MO, MB, and Cr(VI) solutions in 6, 6, and 18 min, respectively, with the reaction kinetic rate of 0.6782, 1.090, and 0.1189 min −1 , and demonstrated good durability, maintaining a reduction rate of 95 % after six cycles. This work provides a feasible approach combining biomass/inorganic materials to treat industrial wastewater.
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JOURNAL OF THE AMERICAN CERAMIC SOCIETY
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2024
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IF 3.5
Hongbin An,Ruoyu Chen,Saisai Li,Lingfeng Huang,Wenbao Jia,Qianfang Wu,Aiqing Mao
Powder synthesis is crucial for achieving the densification and facilitating widespread applications of high entropy carbide (HEC). Specifically, the production of fine particle-size powders is essential to enhance the densification of HECs. Consequently, this paper proposes the molten salt method for synthesizing HEC powders. The synthesis process successfully yielded (Ta Nb Ti V) C powders with a particle size of only 0.44 µm at 1400°C, exhibiting a uniform distribution of each element. Subsequent densification of (Ta Nb Ti V) C within the 1700–1900°C temperature range was carried out using spark plasma sintering. It was observed that as the densification temperature increased, the densification and mechanical properties of HEC significantly improved. This study presents innovative ideas for the preparation of HEC at lower temperatures.
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ACS Applied Nano Materials
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2024
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IF 5.3
Yue Liu,Dongdong Wang,Heng Zhang,Lili Liu,Liu Pei,Shaobo Huang,Xindong Wang
Nowadays, Ti-based materials are used as the construction materials of anode porous transport layers (PTLs) in proton exchange membrane water electrolysis (PEM WE). The major limiting factors of Ti anodes include passivation and corrosion. Herein, the challenges are addressed by using selective pulsed electrodeposition (PE), preparing orientated Au nanoparticles (AuNPs) and a degradable polypyrrole (PPy) composite coating (PE-Au/PPy coating) on Ti-based PTLs. The PTL treatment consists of four steps: electropolymerizing of PPy, mechanical polishing of PPy outside the pores of Ti felts, acid etching, and final electrodepositing AuNPs. Testing results show that etched Ti enables AuNPs to be preferentially deposited on the active surface to make the PE-Au/PPy coating highly conductive, effectively inhibiting Ti passivation. PPy formed a conductivity difference with highly active acid-etched Ti, promoting the preferential deposition of AuNPs on the active Ti surface, which improves noble metal utilization. The PE-Au/PPy coating presents a low interfacial contact resistance (ICR) (ca. 0.9 mΩ cm2 at 140 N cm–2) and excellent corrosion resistance (0.17 μA cm–2) in the simulated PEM WE environments. Significantly, the PE-Au/PPy coating exhibits high electrochemical properties and ultralong lifespans of over 1000 h, still with a low ICR (1.5 mΩ cm2), further validating the usefulness of the protective layer. In addition, here the preferential deposition process of AuNPs on the Ti surface is analyzed using X-ray photoelectron spectroscopy (XPS) and Fourier transform infrared (FT-IR), clarifying the protective mechanisms in PE-Au/PPy coating. Overall, this work not only shows the great potential of PE-Au/PPy coating as PTL anode materials but also optimizes noble metal utilization.
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CERAMICS INTERNATIONAL
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2024
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IF 5.1
Gulizhabaier Abulipizi,Yuxin Wang,Yanlun Fang,Yicheng Xu,Chaomin Qu,Ziang Zong,Leping Ding,Zimin Yu,Juanjuan Zhou,Zhanjun Li
Most of near-infrared (NIR) persistent luminescence (PersL) materials can only be activated by ultra violet-visible light illumination or X-ray irradiation, which hinders their advanced biomedical applications. Herein, NaYTi 2 O 6 : Cr, with a typical double-metal perovskite structure, is developed with ∼758 nm emission after being excited by 700 nm light within the NIR bio-imaging window. This NIR-to-NIR PersL property can be repeatedly charged by 700 nm NIR illumination in situ and in vivo . The anti-cite disorder of Na + -Y 3+ pair and relatively low bandgap of NaYTi 2 O 6 matrix are the vital factors of this property. NaYTi 2 O 6 : Cr has great potential to be applied as a functional ceramic coating in designing self-luminescent medical Ti-implants, so that it can be imaged in vivo by using NIR PersL imaging rather than conducting risky X-ray fluoroscopy imaging. This conceptual work not only provides a NIR-to-NIR PersL biomaterial but also is significant in designing visible medical implants.
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JOURNAL OF MOLECULAR STRUCTURE
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2024
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IF 4
Hanlu Zeng,Yunlan Xu,Dengjie Zhong,Qingmei Qiao,Yuqin Yang
The performance of a photocatalytic fuel cell (PFC) depends on its photoelectrode. In this work, a novel three-dimensional flower-like hierarchical photoanode Zn Zr MOF/FeWO 4 /BiOBr/Ti was synthesized, characterized and applied in PFC to degrade rhodamine B and generate electricity simultaneously. The characterization results of XRD, SEM, EDS, FI-IR, DRS, and XPS show that the photoanode was successfully prepared. The loading of FeWO 4 and Zn Zr MOF widened the nanosheet spacing of BiOBr, which enhanced the light absorption intensity, broadened the light absorption band edge from 467.6 nm to 490.2 nm, and increased the photocurrent density from 0.0149 mA/cm 2 to 0.156 mA/cm 2 . The maximum photocurrent density, maximum power density, degradation rate , and FF of the PFC with the prepared photoanode were respectively 0.256 mA·cm −2 , 22.65 μW·cm −2 90.48 % (1 h), and 0.216, which were far higher than those of PFCs with mono and binary photoanodes. The strong photocatalytic performance of the photoanode is attributed to the type II heterojunction formed between BiOBr and FeWO 4 , which helps to separate electron-hole pairs. The main reactive materials responsible for degrading rhodamine B are h + and ·O 2 - . This research provides a new idea for developing an efficient visible light response photoanode.
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高影响因子
MATERIALS RESEARCH BULLETIN
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2024
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IF 5.3
Qingmei Qiao,Yunlan Xu,Dengjie Zhong,Xihong Ke,Yuqin Yang,Hanlu Zeng
In order to enhance the carrier separation efficiency and redox ability of photoanode, a dual Z-scheme heterojunction Ce-UiO-66/g-C 3 N 4 /Bi 2 WO 6 /Ti photoanode was prepared and assembled with Cu cathode to form PFC. The characterization results show that Ce-UiO-66/g-C 3 N 4 /Bi 2 WO 6 uniformly distributed on the Ti substrate, with average crystallite size of 9.04 nm and average particle size of 33.05 nm, which provides sufficient reactive active sites for RhB degradation. The RhB degradation rate, P max , J sc , V oc and FF of the PFC were 90.9 % (90 min), 7.53 µW cm -2 , 0.152 mA cm -2 , 0.37 V and 0.134, respectively. The turnover frequency (TOF) for RhB degradation by the PFC reached 0.98 h -1 . Fermi energy level analysis shows that a double-Z heterojunction is formed between Bi 2 WO 6 and g-C 3 N 4 , and between Bi 2 WO 6 and Ce-UiO-66, which not only effectively separates photogenerated e - - h + , but also retains the high redox ability of the composite. Moreover, with the introduction of Ce-UiO-66, the composite photoanode has larger specific surface area and wider visible light absorption range. In addition, because of the built-in electric field, the photogenerated electrons can migrate to the surface of composite particles more easily and react with dissolved oxygen to generate more •O 2 - to participate in the degradation of RhB. This work provides a valuable reference for developing PFC photoanode with high efficiency and visible light response.
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BIOSENSORS & BIOELECTRONICS
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2021
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IF 10.618
Yukun Yang,Wenyan Yan,Xiaomin Wang,Ligang Yu,Jinhua Zhang,Baoqing Bai,Caixia Guo,Sanhong Fan
In this work, a molecularly imprinted photoelectrochemical (MIP-PEC) sensor based on a novel PEC composite of metal-organic frameworks (MOFs) and TiO 2 (NH 2 -MIL-125(Ti)–TiO 2 ) was established for the ultrasensitive and selective detection of oxytetracycline (OTC). This is the first attempt of applying MOFs in the construction of MIP-PEC sensor. The NH 2 -MIL-125(Ti)–TiO 2 was synthesized by a simple one-step solvothermal method and modified onto the surface of indium tin oxide (ITO) electrode as the photosensitive layer. Subsequently, molecularly imprinted polymer (MIP) was modified as recognition element by electropolymerization . The NH 2 -MIL-125(Ti)–TiO 2 showed an enhanced photocurrent response due to stronger light absorption capacity and matched energy band. Furthermore, MIP greatly improved the selectivity and sensitivity of the constructed PEC sensor. The photocurrent response of the MIP-PEC sensor was reduced after OTC recognition because the specific binding of OTC to the imprinted cavities blocked the electron transfer of the electrode. Under optimal experimental conditions, the MIP-PEC sensor exhibited a wide detection range from 0.1 nM to 10 μM with a low limit of detection (LOD) of 60 pM, as well as certain reproducibility, stability and good applicability in real samples. The proposed sensor provides ideas for the application of MOFs in the construction of PEC sensors and will offer an alternative method for the detection of other pollutants in the field of food safety.
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PubMed
高影响因子
PROCESS SAFETY AND ENVIRONMENTAL PROTECTION
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2025
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IF 7.8
Jia Guo,Yongqi Zhao,Junjie Jiang,Xiaolong Liu,Yongqiang Wang,Huazhen Chang,Tingyu Zhu
Selective catalytic reduction (SCR) with ammonia (NH 3 ) is an established method for NO x elimination. However, the catalytic activity of conventional VW/Ti catalysts declines sharply at ultra-high temperatures (above 700 °C). To address this limitation, this study employed machine learning (ML) to optimize high-temperature SCR catalysts. A gradient boosting decision tree (GBDT) model with Shapley Additive Explanations (SHAP) identified calcination temperature, crystal phase, and surface acidity as the key factors influencing catalytic performance. Based on these insights, a designstrategy was developed for VW/Ti catalysts under ultra-high temperature conditions and successfully identified a catalyst exhibiting excellent resistance to high-temperature degradation through evaluation and characterization. Experimental validation confirmed that Si doping significantly improves catalytic activity and thermal stability, with the VW/5Ti1Si-800 catalyst demonstrating superior performance. This study highlights the effectiveness of combining ML and experimental approaches to mitigate high-temperature deactivation in SCR catalysts.
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MICROCHIMICA ACTA
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2020
·Vol. 187
·期 8
·1-9
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IF 6.232
Li Jingxian,Jiang Ding,Shan Xueling,Wang Wenchang,Chen Zhidong
A novel “off-on” electrochemiluminescence (ECL) aptasensor based on ECL resonance energy transfer (RET) system from 3,4,9,10-perylenetetracar-boxylic acid/the metal-organic frameworks NH 2 -MIL-125(Ti) (PTCA/NH 2 -MIL-125) to Au nanoparticles (Au NPs) was put forward for microcystin-LR (MC-LR) assay. The electrochemiluminescence (ECL) emission spectra of PTCA/NH 2 -MIL-125 show excellent spectral overlap with the UV-vis absorption spectrum of Au NPs. A linear response ranging from 10 fM (9.95 × 10 −6 μg L −1 ) to 0.1 μM (99.5 μg L −1 ) was obtained, and the detection limit was 3.6 fM (3.58 × 10 −6 μg L −1 ) under optimal conditions at a potential of − 1.6 V ( S/N = 3). Besides, the prepared ECL-RET MC-LR aptasensor exhibited good selectivity and stability.
Graphical abstract
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高影响因子
Journal of Energy Chemistry
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2022
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IF 13.599
Fan Peng,Youqi Chu,Yu Li,Qichang Pan,Guangchang Yang,Lixuan Zhang,Sijiang Hu,Fenghua Zheng,Hongqiang Wang,Qingyu Li
The Nickel-rich layered cathode materials charged to 4.5 V can obtain a specific capacity of more than 200 mAh g −1 . However, the nickel-rich layered cathode materials suffer from the severe capacity fade during high-voltage cycling, which is related to the phase transformation and the surface sides reactions caused by the lattice oxygen evolution. Here, the simultaneous construction of a Mg, Ti-based surface integrated layer and bulk doping through Mg, Ti surface treatment could suppress the lattice oxygen evolution of Ni-rich material at deep charging. More importantly, Mg and Ti are co-doped into the particles surface to form an Mg 2 TiO 4 and Mg 0.5– x Ti 2– y (PO 4 ) 3 outer layer with Mg and Ti vacancies. In the constructed surface integrated layer, the reverse electric field in the Mg 2 TiO 4 effectively suppressed the outward migration of the lattice oxygen anions, while Mg 0.5– x Ti 2– y (PO 4 ) 3 outer layer with high electronic conductivity and good lithium ion conductor could effectively maintained the stability of the reaction interface during high-voltage cycling. Meanwhile, bulk Mg and Ti co-doping can mitigate the migration of Ni ions in the bulk to keep the stability of transition metal–oxygen (M−O) bond at deep charging. As a result, the NCM@MTP cathode shows excellent long cycle stability at high-voltage charging, which keep high capacity retention of 89.3% and 84.3% at 1C after 200 and 100 cycles under room and elevated temperature of 25 and 55 °C, respectively. This work provides new insights for manipulating the surface chemistry of electrode materials to suppress the lattice oxygen evolution at high charging voltage.
研究领域:
材料科学
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电化学
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