APPLIED SURFACE SCIENCE
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2020
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IF 6.182
Bin Sun,Furong Tao,Zixuan Huang,Wei Yan,Yuxin Zhang,Xusheng Dong,Yue Wu,Guowei Zhou
As a novel transition metal carbides and/or carbonitrides, MXene possess two-dimensional characteristic, abundant surface hydrophilic functional groups, and excellent electrical conductivity that bestow a possibility to building MXene-based photocatalysts. Inspired by this, an emerging Ti 3 C 2 MXene cocatalyst bridged Ag/Ag 3 PO 4 to induce a highly visible-light-driven photocatalytic activity, synthesized by electrostatic self-assembly method and the partial reduction of Ag + ions to Ag 0 in MXene solution is reported. The resultant hybrids reveal a well-defined hybrid structures with Ag/Ag 3 PO 4 anchoring on the layer structured Ti 3 C 2 nanosheets. Benefiting from the unique structural features, the Ag/Ag 3 PO 4 /Ti 3 C 2 hybrids present Ti 3 C 2 content-dependent photocatalytic activity toward the methyl orange (MO) degradation and Cr(VI) reduction under visible-light irradiation. Remarkably, the Ag/Ag 3 PO 4 /Ti 3 C 2 hybrid with 3 wt% Ti 3 C 2 content achieves the greatest MO degradation efficiency and Cr(VI) reduction efficiency after irradiation for 1 h, which are increased to 1.72 and 1.46 times higher than that obtained on pristine Ag 3 PO 4 nanoparticles, respectively. Such impressive photocatalytic activity is related to the synergeric effects derived from Ag, Ag 3 PO 4 , and Ti 3 C 2 , which greatly enhance visible light absorption, promote separation and transfer of photo-generated electron-hole pairs. This work highlights that the MXene-based photocatalysts would be desirable candidates for environmental purification of organic pollutants and heavy metal ions.
研究领域:
材料科学
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环境科学
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化学
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DOI
高影响因子
Journal of Environmental Chemical Engineering
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2017
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IF 0
Jun Liu,Qingyong Tian,Zhaohui Wu,Weijing Yao,Xiangheng Xiao,Wei Wu
Trinary g-C 3 N 4 /Ag/Ag 3 PO 4 heterostructures with different Ag content were designed and synthesized by in situ deposition and reduction routes. The photocatalytic performances of these heterostructures were investigated under visible light (λ > 450 nm) and simulated sunlight. Moreover, the influence of Ag content and ratio of each component on the photocatalytic performance of g-C 3 N 4 /Ag/Ag 3 PO 4 was also studied. As a result, the photocatalytic activities of all these g-C 3 N 4 /Ag/Ag 3 PO 4 samples were higher than commercial P25 (TiO 2 ). Moreover, sample S1 (the ratio of g-C 3 N 4 , Ag 3 PO 4 and Ag is 1: 2.52: 0.12) showed the better photocatalytic activities than other g-C 3 N 4 /Ag/Ag 3 PO 4 samples (S2 and S3) and g-C 3 N 4 /Ag 3 PO 4 (1: 3) under the same light irradiation. It indicated that small amount of Ag nanoparticles could improve the photocatalytic performances by compared with g-C 3 N 4 /Ag 3 PO 4 sample. And S1 showed a stable photodegradation after 6 times of cycle experiments under simulated sunlight. The stable and significant superior photocatalytic performance of g-C 3 N 4 /Ag/Ag 3 PO 4 could be attributed to the fast charge separation among g-C 3 N 4 , Ag and Ag 3 PO 4 during the Z -scheme charge transfer and recombination process.
研究领域:
材料科学
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环境科学
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DOI
ACTA PHYSICO-CHIMICA SINICA
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2023
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IF 10.9
Kexin Dong,Chuqi Shen,Ruyu Yan,Yanping Liu,Chunqiang Zhuang,Shijie Li
The escalating presence of pharmaceutical antibiotics in natural water poses an overwhelming threat to the sustainable development of society. Photocatalysis technology stands out as a promising and cutting-edge environmental purification alternative. C 3 N 5 , identified as a distinctive nonprecious nonmetal photocatalyst, holds potential for environmental protection. However, challenges persist originating from the sluggish photoreaction kinetics and severe photo-carrier reunion. Currently, the design of a special S-scheme photosystem proves to be a reliable strategy for obtaining outstanding photocatalysts. In this context, a plasmonic S-scheme photosystem involving Ag/Ag 3 PO 4 /C 3 N 5 was developed through a feasible route. The compactly connected 0D/0D/2D Ag/Ag 3 PO 4 /C 3 N 5 heterostructure, benefitting from the synergy between the plasmonic effect and the S-scheme junction, facilitates the efficient utilization of appreciably reinforced sunlight absorption, effective photo-carrier disassociation, and notable photoredox capacity. Consequently, this system generates •OH and
⋅ O 2 - effectively. Ag/Ag 3 PO 4 /C 3 N 5 demonstrates a superb photocatalytic levofloxacin eradication rate of 0.0362 min −1 , marking a substantial advancement of 24.8, 1.1, and 0.7 folds compared to C 3 N 5 , Ag 3 PO 4 , and Ag 3 PO 4 /C 3 N 5 , respectively. Impressively, Ag/Ag 3 PO 4 /C 3 N 5 delivers remarkable anti-interference performance and reusability. This achievement signifies a significant step toward developing potent C 3 N 5 -involved photosystems for environmental purification. Download: Download high-res image (106KB) Download: Download full-size image
研究领域:
环境科学
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材料科学
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DOI
高影响因子
Materials Science and Engineering B-Advanced Functional Solid-State Materials
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2024
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IF 3.9
Congzhi Hu,Yuye Li,Tingting Du,Youyong Pang,Yongping Liu,Botian Liu,Ling Li,Huidan Lu,Bin Huang
In this paper, a new supramolecular Z-scheme heterojunction photocatalyst, designated as Ag/Ag 3 PO 4 /Perylene diimide organic molecules after secondary acid-base self-assembly (PDI-2), was synthesized through precipitation and photoreduction techniques. Ag/Ag 3 PO 4 /60 %PDI-2 (APP-6) exhibited the best photocatalytic activity due to the synergistic effect of Z-scheme heterojunction and surface plasmon resonance (SPR) effect of Ag nanoparticles (Ag NPs). Under visible light (λ > 420 nm), the degradation efficiency of APP-6 for Rhodamine B (RhB) and Bisphenol A (BPA) was 99.7 % and 90.7 %, respectively. Additionally, PDI-2 was transformed into smaller nanoclusters, which increased the specific surface area of the photocatalyst, and reduced the charge transport distance. Moreover, APP-6 exhibited the smallest electrochemical impedance, the largest photocurrent, the smallest fluorescence lifetime. Free radical trapping experiments showed that •O 2 − was the main reactive group and a possible photocatalytic mechanism was proposed by combining the Ultraviolet–visible diffuse reflectance spectrophotometer (UV–vis DRS) and the Mott-Schottky plots.
研究领域:
材料科学
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环境科学
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产品关联
DOI
高影响因子
JOURNAL OF COLLOID AND INTERFACE SCIENCE
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2017
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IF 4.233
Qingyong Li,Fulei Wang,Yuxiang Hua,Yuting Luo,Xiaoheng Liu,Guorong Duan,Xujie Yang
A series of novel visible-light-driven Ag/Ag 3 PO 4 /WO 3 (AAPW) Z-scheme heterostructures were fabricated using a facile deposition-precipitation method followed by photo-reduction without adding any surfactant . To explore more deeply about the photocatalytic activity of AAPW nanocomposites under neutral and strongly acidic/alkaline conditions, we investigated their photocatalytic rhodamine B (RhB) efficiency at different pH value that was controlled by adding HNO 3 or NaOH aqueous solution. It was found that as-prepared AAPW photocatalysts showed enhanced photocatalytic RhB efficiency under neutral and even strongly acidic/alkaline environment. The process of charge carrier separation and transfer in the AAPW nanocomposites and Z-scheme mechanism for RhB degradation were described in sufficient detail based on systematical characterizations and measurements. The silver particles introduced to build AAPW Z-scheme structure should contribute to more efficient charge separation, resulting in enhanced photocurrent response and photocatalytic activity . We expect that this work will provide systematic study concerning Z-scheme Ag/Ag 3 PO 4 /WO 3 structure, and fulfill the research about photodegrade activity of catalyst under strongly acidic/alkaline conditions.
研究领域:
材料科学
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环境科学
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DOI
高影响因子
APPLIED CATALYSIS B-ENVIRONMENTAL
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2017
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IF 9.446
Chenxi Zhang,Kai Yu,Yajun Feng,Yue Chang,Ting Yang,Ying Xuan,Da Lei,Lan-Lan Lou,Shuangxi Liu
The novel visible-light-driven 3DOM-SrTiO 3 /Ag/Ag 3 PO 4 ternary composites were fabricated and used as photocatalysts in the degradation of organic contaminants, including RhB, phenol , and MB. Through the XRD, SEM, TEM, DR UV–vis, XPS, PL spectroscopy, N 2 sorption , and photoelectrochemical measurement, the obtained 3DOM-SrTiO 3 /Ag/Ag 3 PO 4 ternary composites were well characterized. The effects of SrTiO 3 :Ag 3 PO 4 molar ratio and stop-bands of 3DOM-SrTiO 3 on the catalytic performance were systemically investigated. 3DOM-SrTiO 3 /Ag/Ag 3 PO 4 ternary composite photocatalysts exhibited notably enhanced activity compared with single 3DOM-SrTiO 3 and Ag 3 PO 4 catalyst. Among these ternary photocatalysts, S35A65(300) exhibited the most excellent photocatalytic performance under visible light irradiation, which could be mainly attributed to synergy effect of the notably improved separate efficiency of photogenerated electron-hole pairs and the suitable stop-bands of 3DOM-SrTiO 3 (300) material. Although the gradually reduced activity in cycling tests was obtained over S35A65(300) under visible light irradiation, an excellent durability could be achieved for S35A65(300) under UV–vis light irradiation. No obvious loss in photocatalytic efficiency was observed after six cycles for RhB degradation. The notably improved enhanced durability of 3DOM-SrTiO 3 /Ag/Ag 3 PO 4 ternary composites under UV–vis light irradiation could be mainly attributed to the Z-scheme mechanism of this ternary composite photocatalyst.
研究领域:
材料科学
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环境科学
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光催化
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DOI
高影响因子
SEPARATION AND PURIFICATION TECHNOLOGY
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2023
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IF 8.6
Huarong Liao,Miaomiao Li,Yuxiang Wang,Guan Wang,Liujun Yang,Junxia Shao,Cheng Zhang,Hua Li,Jianmei Lu
Refining the visible light absorption and optimizing the separation of photogenerated electron-hole pairs are pivotal in enhancing the photocatalytic activity of composites. A novel Z-scheme plasma photocatalyst, Ag/Ag 3 PO 4 /In-MOF (A/AP/In), was developed in this study. Experimental results demonstrated that A/AP/In exhibited the highest photocatalytic activity for BPA among all samples tested, achieving complete degradation of 50 ppm BPA within 30 min, as well as its apparent degradation rate was about 11 times higher than that of pure Ag 3 PO 4 and 4 times higher than that of pure In-MOF. The enhanced photocatalytic activity can be mainly attributed to the existence of Z-type heterojunctions and the surface plasmon resonance (SPR) effect induced by Ag nanoparticles , which facilitate efficient migration and separation of photogenerated carriers. Meanwhile, the incorporation of Ag nanoparticles enhances visible light absorption and protects Ag 3 PO 4 from photocorrosion in the composites. Moreover, A/AP/In maintains the large specific surface area of In-MOF and provides abundant reactive active sites. In addition, the photocatalytic performance of A/AP/In was above 90 % after five consecutive cycles confirming its good stability. Overall, this study proposes a novel approach for constructing bifunctional composites with efficient adsorption/catalytic degradation.
研究领域:
材料科学
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环境化学
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光催化
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DOI
高影响因子
JOURNAL OF MATERIALS SCIENCE & TECHNOLOGY
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2021
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IF 8.067
Feihu Mu,Benlin Dai,Wei Zhao,Shijian Zhou,Haibao Huang,Gang Yang,Dehua Xia,Yan Kong,Dennis Y.C. Leung
To boost the visible light catalytic performance of typical metal-organic frameworks (MOFs) materials (MIL-68(In)-NH 2 ), a novel stable Z-scheme Ag/Ag 3 PO 4 /MIL-68(In)-NH 2 plasmonic photocatalyst was constructed by electrostatic attraction, co-precipitation reaction, and in-situ photoreduction reaction methods for the first time. The photocatalytic activities of the photocatalysts are systematically explored by the photocatalytic degradation of bisphenol A (BPA) and reduction of Cr(VI) under visible light. Ag/Ag 3 PO 4 /MIL-68(In)-NH 2 displays the best photocatalytic performance among the as-prepared photocatalysts. The rate constant of BPA degradation on Ag/Ag 3 PO 4 /MIL-68(In)-NH 2 is 0.09655 min −1 , which is better than many reported photocatalytic materials. It also achieved a maximum rate constant of 0.02074 min −1 for Cr(VI) reduction. The boosted photocatalytic performance is due to the improved absorption caused by localized surface plasmon resonance (LSPR), effective interface charge transfer and separation, and more reactive sites provided by the large specific surface area. Besides, the photocatalytic degradation pathway of BPA is concluded according to GC-MS analysis. Finally, a more reasonable Z -scheme mechanism is speculated and verified through a series of characterizations and simulations, such as time-resolved photoluminescence spectroscopy (TRPL), electron spin resonance (ESR), and finite difference time domain (FDTD) method.
研究领域:
材料科学
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环境科学
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化学
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光催化
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产品关联
DOI
高影响因子
JOURNAL OF COLLOID AND INTERFACE SCIENCE
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2015
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IF 3.368
Chao Jin,Guanglei Liu,Lianhai Zu,Yao Qin,Jinhu Yang
In this article, we report a novel Ag@Ag 3 PO 4 @ZnO ternary heterostructures synthesized through a three-step approach. Firstly, single-crystalline Ag nanorods are fabricated and served as the templates for subsequent Ag 3 PO 4 deposition. Secondly, Ag 3 PO 4 crystals are grown around Ag core nanorods through a solution co-precipitation process, leading to the Ag@Ag 3 PO 4 binary heterostructures. Finally, ZnO nanorod arrays on the surface of the Ag@Ag 3 PO 4 heterostructures are realized via a seeded growth strategy, forming the typical Ag@Ag 3 PO 4 @ZnO ternary heterostructures. The photodegradation of rhodamine B under ultraviolet–visible light irradiation indicates that the Ag@Ag 3 PO 4 @ZnO ternary heterostructures exhibit much higher activities than pure Ag 3 PO 4 and binary heterostructures of Ag@Ag 3 PO 4 . The higher photocatalytic activity of the Ag@Ag 3 PO 4 @ZnO composites may be attributed to the effective photogenerated charge separation at heterointerfaces of Ag/Ag 3 PO 4 and Ag 3 PO 4 /ZnO, and the rapid electron transport along one-dimensional Ag and ZnO nanorods.
研究领域:
材料科学
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环境科学
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产品关联
DOI
PubMed
高影响因子
JOURNAL OF MEMBRANE SCIENCE
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2025
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IF 9
Boyang Xu,Xuefei Zhou,Yifan Zhang,Yalei Zhang,Qipeng Zhao,Tai-Shung Chung
Photocatalytic membranes have emerged as promising catalytic oxidation materials to mitigate fouling with self-cleaning capacity, yet their visible-light activity and charge recombination remain challenging. In this work, hydrophilic Ag/Ag 3 PO 4 -PDA-n@PES ultrafiltration (UF) membranes were fabricated via polydopamine-assisted surface modification of polyethersulfone (PES) substrates followed by in-situ mineralization of Ag/Ag 3 PO 4 nanoparticles. The membranes were systematically characterized, and the optimized Ag/Ag 3 PO 4 -PDA-5@PES exhibited a water flux of 125 L m −2 h −1 (LMH) and 89.0 % bovine serum albumin (BSA) rejection, outperforming the pristine PES (98 LMH, 66 %). Under visible light, the membrane achieved 87–89 % degradation of organic dyes with a kinetic constant of 0.0254 min −1 for Rhodamine B (RhB), retaining >80 % efficiency after five cycles. In cyclic filtration with RhB, only a 13 % flux decline occurred after three backwashing/self-cleaning cycles, with a flux recovery of 98 %, confirming its strong antifouling and self-cleaning capacity. Moreover, a continuous operation with synthetic urine wastewater achieved 80–95 % chemical oxygen demand (COD) and 90–95 % chroma removal, demonstrating the membrane's practical potential in wastewater treatment.
研究领域:
环境科学
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材料科学
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化学工程
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光催化
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水处理技术
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产品关联
DOI
高影响因子
APPLIED SURFACE SCIENCE
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2021
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IF 6.707
Yuxuan Dai,Yuting Wang,Gancheng Zuo,Jijie Kong,Yang Guo,Cheng Sun,Qiming Xian
We report a simple strategy to synthesize the Ag 3 PO 4 nanopolyhedrons with regular morphology and uniform size under mild conditions. The photocatalytic properties of the composite were optimized by adjusting the content of Ag nanoparticles. The as-prepared photocatalysts were characterized and the photocatalytic performances were evaluated by the degradation of acenaphthylene (ANY) under visible-light illumination. The surface plasmon resonance (SPR) of appropriate Ag nanoparticles was generated on surface under visible light irradiation, which enhanced the absorption and utilization of visible light. At the same time, the conductivity of Ag promoted the separation and transfer of photogenerated carriers, provided active sites for the reaction, and enhanced the photocatalytic degradation efficiency through the generation of active species. As a result, the optimized composite exhibited enhanced visible-light photocatalytic activity of 0.03512 min −1 and higher removal rate of 97.3% for ANY (4 times and 1.8 times higher than that of pristine Ag 3 PO 4 , respectively), more photogenerated active species (h + and •O 2 – ) and relatively high stability (4 times of cycle experiments). In addition, the possible degradation pathway of ANY was proposed. The work of this paper has a crucial guiding significance for the working principle and design direction of silver semiconductor composite photocatalysts with surface plasmon effect.
研究领域:
环境科学
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材料科学
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产品关联
DOI
高影响因子
CHEMICAL ENGINEERING JOURNAL
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2019
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IF 8.355
Yaxin Liu,Dongzhi Yang,Ting Xu,Yongzheng Shi,Linna Song,Zhong-Zhen Yu
Although silver phosphate (Ag 3 PO 4 ) exhibits high quantum efficiency and intriguing photocatalytic ability, its poor light stability limits its wide application. Herein, structurally stable and porous Ag/Ag 3 PO 4 /reduced graphene oxide microspheres are fabricated with electrostatic spraying, freezing, lyophilizing and crosslinking and used for the first time to remove toxic Cr(VI) ions with high efficiency and durability. Polydopamine serves as both moderate reductant and effective linker for Ag/Ag 3 PO 4 components to distribute well on reduced graphene oxide (rGO) sheets with controlled Ag/Ag 3 PO 4 ratios, endowing the porous microspheres with fast transfer of electrons and enhanced structural stability. Both the heterogeneous junctions of Ag/Ag 3 PO 4 and the conductive rGO sheets accelerate the electron transfer from Ag 3 PO 4 to Ag and rGO, decrease the recombination of electrons and holes and enhance the light stability of Ag 3 PO 4 . In addition, both the photogenerated electrons of Ag 3 PO 4 and the π electrons on rGO sheets reduce Cr(VI). The resulting porous microspheres deliver an excellent visible light photocatalytic efficiency of 0.62 mg min −1 g −1 (quantum yield of 2.37%) for reduction of Cr(VI) under the light intensity of 800 mW cm −2 , and a high removal efficiency of more than 90% of Cr(VI) over 30 h under a continuous photocatalytic removal system. These outstanding performances make the structurally stable and porous microspheres promising for continuous removal of Cr(VI) ions.
研究领域:
环境科学
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材料科学
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DOI
高影响因子