INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH
·
2021
·
IF 3.764
Like Ouyang,Yan Zhang,Yuan Wang,Xinlong Wang,Shaojun Yuan
The coupled adsorption–photocatalytic oxidation process provides a great potential scenario to enhance the removal efficiency of arsenite contaminants by converting As(III) to As(V) and simultaneous adsorption. In this study, the boron-doped black TiO2/g-C3N4 nanocomposite is synthesized by combination of sol–gel and in situ decomposition-thermal polymerization methods as a photocatalyst for the photocatalytic oxidation and adsorption of As(III). Under dark conditions, the boron-doped samples (B-TiO2 and B-TiO2/g-C3N4) display an increase in the As(III) adsorption capacity by one order of magnitude up to circa 3.2 mg g–1 with an initial As(III) concentration of 2 mg L–1 at 298.15 K and pH 5. The adsorption kinetics of As(III) on B-TiO2/g-C3N4 conform to the pseudo-second-order kinetic model, revealing the chemical adsorption mechanism. Under visible light irradiation, the total arsenic removal capacity is substantially improved by 20% with a removal capacity of 3.9 mg g–1. The enhancement of arsenic adsorption is attributed to the chemical complexation and hydrogen bond, in which B–OH bonds play a dominant role. The photocatalytic oxidation mechanism of the as-synthesized B-TiO2/g-C3N4 is attributed to the synergism of superoxide radicals, hydroxyl radicals, and photogenerated holes.
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高影响因子
JOURNAL OF MOLECULAR LIQUIDS
·
2021
·
IF 6.165
Pengfei Wang,Yao Liu,Ning Jiang,Ruisen Jing,Shutao Li,Qian Zhang,Huiqiang Liu,Junshan Xiu,Zhao Li,Yunyan Liu
A ternary heterojunction composite photocatalyst g-C 3 N 4 /AgBr/black phosphorus was constructed by co-modifying AgBr with g-C 3 N 4 (CN) and black phosphorus nanosheets (BPNs). The photoluminescence (PL), photocurrent intensity and electrochemical impedance spectroscopy (EIS) results proved that, compared with bare AgBr and binary CN/AgBr and AgBr/BPNs, ternary CN/AgBr/BPNs effectively promoted the separation and suppresses the recombination of electron-hole pair. The photocatalytic experiment proved that the CN/AgBr/BPNs photocatalyst exhibited almost 8 times for degradation rate of MO，and well above those of binary CN/AgBr and AgBr/BPNs. According to trapping experiments of the active species, the analysis of the energy band , we proposed the double S-scheme to explain the charge transfer and the boosting of photocatalytic activity in ternary CN/AgBr/BPNs. Impressively, this double S-scheme facilitated the transmittance of electrons at the CB position of AgBr to the VB of CN and BPNs, and greatly overcome the light corrosion and enhance the stability of AgBr. This work designed a novel S-scheme mechanism heterojunction photocatalytic material, which provides a convenient way for efficient wastewater treatment.
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CHEMICAL ENGINEERING JOURNAL
·
2021
·
IF 13.273
Rongdi Tang,Daoxin Gong,Yaocheng Deng,Sheng Xiong,Jie Deng,Ling Li,Zhanpeng Zhou,Jiangfu Zheng,Long Su,Lihua Yang
In this study, a novel π-π stacked PDI/g-C 3 N 4 /TiO 2 @Ti 3 C 2 photocatalyst with step-scheme (S-scheme) heterojunction was constructed to boost the atrazine (ATZ) photocatalytic degradation by activating peroxymonosulfate (PMS). The π-π interaction in the PDI/g-C 3 N 4 induced the delocalization of the photoelectrons, therefore promoted their migration. Meanwhile, the intimate contact and the staggered band configurations between the PDI/g-C 3 N 4 and TiO 2 @Ti 3 C 2 results in the S-scheme heterojunction thus declined the recombination of photocarriers. The π-π interaction and S-scheme heterojunction synergistically promoted the ATZ removal rate to 75% within one hour and can be well-adapted in a variety of environments. It was found that 1 O 2 domain the photocatalysis, and the H 2 O 2 generated during the reaction may also be helpful for the process. The transformation of ATZ, intermediates, and three pathways during the process were also investigated via LC-MS. Moreover, the total organic carbon analysis shows that the mineralization of ATZ reached 46.08%.
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SEPARATION AND PURIFICATION TECHNOLOGY
·
2021
·
IF 7.312
Runyu Zhou,Yongsheng Fu,Gaofeng Zhou,Shixiang Wang,Yiqing Liu
In this study, a novel Fe/Co bimetallic spinel sulfide (FeCo 2 S 4 ) modified g-C 3 N 4 composite (FeCo 2 S 4 -CN) was prepared by a hydrothermal method and firstly applied as a catalyst for the activation of peracetic acid (PAA) at neutral pH. The efficient rhodamine B (RhB) degradation in FeCo 2 S 4 -CN/PAA system indicated that PAA was successfully activated by FeCo 2 S 4 -CN. The scanning electron microscopy (SEM) and X-ray diffraction (XRD) results indicated that g-C 3 N 4 carrier could anchor FeCo 2 S 4 particles with good dispersion. The X-ray photoelectron spectroscopy (XPS) analysis suggested that the surface ≡Co(II) and ≡Fe(II) could activate PAA to form CH 3 C(O)O • and • OH, synchronously yielding ≡Co(III) and ≡Fe(III). Meanwhile, the surface ≡Co(III) and ≡Fe(III) could also react with PAA to generate CH 3 C(O)OO • as well as ≡Co(II) and ≡Fe(II), resulting in the redox cycles of ≡Co(II)/≡Co(III) and ≡Fe(II)/≡Fe(III). Besides, the presence of S 2- in FeCo 2 S 4 -CN was favorable to these redox cycles. Radical scavenging experiments confirmed that organic radicals (i.e., CH 3 C(O)O • and CH 3 C(O)OO • ) were the primary reactive species for RhB degradation in FeCo 2 S 4 -CN/PAA system. This system also exhibited a high removal efficiency for various organic contaminants, suggesting its potential application in degrading refractory pollutants.
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Catalysis Science & Technology
·
2018
·Vol. 8
·期 14
·3484-3492
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IF 5.365
Xing Ding,Dong Xiao,Lei Ji,Ding Jin,Ke Dai,Zixin Yang,Shengyao Wang,Hao Chen
The construction of a multifunctional two-dimensional (2D) composite photocatalyst is of great significance because such a composite can exhibit enhanced catalytic performance and improved practical usability in contrast to a single component catalyst. Herein, a ternary photocatalyst composed of g-C3N4, a carbon layer (C), and Fe3O4 nanoparticles was successfully synthesized by a facile one-pot hydrothermal carbonization (HTC) method from g-C3N4, glucose, and FeCl3. The resultant composite, Fe3O4/C/g-C3N4, had an ordered 2D heterostructure and exhibited enhanced visible-light-driven photocatalytic performances and good magnetic recyclability. The kobs for Cr(VI) photoreduction (or dimethoate photodegradation) over Fe3O4/C/g-C3N4 was 20.9-fold (or 2.1-fold) of that over g-C3N4. Comparative study of Fe3O4/C/g-C3N4, C/g-C3N4, and g-C3N4 on their optoelectronic properties revealed that this enhanced photocatalytic activity was mainly due to rapid photogenerated electron transport from the g-C3N4 component to carbon and/or Fe3O4, which effectively suppressed the recombination of photogenerated electrons and holes. In addition, the good surface adsorption capacity of the carbon component towards Cr(VI) also contributed to Cr(VI) photoreduction over Fe3O4/C/g-C3N4. Finally, a reasonable photocatalytic reaction mechanism of Fe3O4/C/g-C3N4 was proposed based on the results of trapping experiments. This study is not only limited to developing a high-performance g-C3N4 based photocatalyst, but also expected to provide a green, facile, and cost-efficient strategy to combine 2D materials with a carbonaceous layer and other functional components for a multifunctional system.
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COLLOIDS AND SURFACES A-PHYSICOCHEMICAL AND ENGINEERING ASPECTS
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2022
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IF 5.518
Jinge Du,Shuanglong Ma,Na Zhang,Wenjing Liu,Mengdi Lv,Tianjun Ni,Zhen An,Kai Li,Yichun Bai
A novel porous Z-scheme Ag/AgFeO 2 /g-C 3 N 4 (AAF/UPCN) photocatalyst was successfully prepared via a facile hydrothermal, precipitation and photo-deposition–method. Under visible light irradiation, AAF/UPCN exhibited excellent bisphenol A degradation effect and Staphylococcus aureus inactivation effect compared with porous g-C 3 N 4 (UPCN) and AgFeO 2 . The •O 2 ‾ was the major active species during the photocatalytic degradation process. For the photocatalytic mechanism, the photoexcited electrons of UPCN transferred to AgFeO 2 mediated by Ag nanoparticles . This charge migration and separation route was verified collectively by the PL spectra, photoelectrochemical characterizations, chemical scavenger experiments and ESR measurements. Furthermore, the band distribution of catalysts was obtained by DFT calculation. This Ag nanoparticles mediated electron transfer pathway could promote the effective segregation of photoexcited carriers. The synergistic effect of UPCN, AgFeO 2 and Ag in heterostructure could promote the efficient separation of photogenerated charge carriers. This study provides a new strategy for rational design of high-efficient g-C 3 N 4 -based photocatalysts for environmental remediation.
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高影响因子
JOURNAL OF PHYSICS AND CHEMISTRY OF SOLIDS
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2024
·
IF 4.3
Jin Chen,Suqing Qin,Xiaofeng Yang,Yueying Wang,Tai Yang,Meidan Que,Yuzhao Ma,Yanjun Li
BiOBr can effectively mitigate the ecological and environmental problems caused by pollution with antibiotics, and its photocatalytic properties can be improved by utilizing heterojunction structures and cocatalysts. In this study, the Z-scheme heterojunction ternary photocatalyst BiOBr/g-C 3 N 4 /CQDs (BCC x ) was obtained by using an uncomplicated electrostatic self-assembly process. The incorporation of carbon quantum dots (CQDs) with high conductivity provided a conduit for charge transfer between g-C 3 N 4 and BiOBr. The loading density of CQDs on BiOBr/g-C 3 N 4 could be rapidly adjusted by changing the concentration of the CQDs precursor in solution. The presence of CQDs enhanced the absorption of visible light and inhibited the synthesis of photogenerated charge carriers, thereby resulting in a synergistic effect on the Z-scheme heterojunction and improving the photocatalytic properties under visible light. In particular, BCC50 had the highest catalytic performance, with a tetracycline pollutant degradation efficiency of 100% within 60 min. The degradation efficiency remained above 95% even after repeated use in five cycles. The principles of semiconductor energy bands and internal electrostatic field generation are applied to explain the photocatalytic mechanism responsible for tetracycline degradation using BiOBr/g-C 3 N 4 /CQDs.
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JOURNAL OF COLLOID AND INTERFACE SCIENCE
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2018
·
IF 5.091
Haitao Li,Ming Wang,Yiping Wei,Fei Long
A series of noble-metal-free NiS 2 -loaded g-C 3 N 4 hybrid composites were prepared via simple hydrothermal method. Benefited from the wider spectral response range and the effective separation of photoelectron-holes of g-C 3 N 4 -NiS 2 heterojunction catalysts, as well as the rich unsaturated active S atoms on the NiS 2 with S 2 2− , the composite catalysts has prominent photocatalytic performance for H 2 evolution. Remarkably, the optimal composite photocatalysts achieved an average hydrogen production rate as high as 715.83 μmol/h/g in 3 h under visible-light irradiation, which is 2.75 times as high as that of precious metal Pt (259.5 μmol/h/g) as a co-catalyst. Besides, the composite catalyst still shows prominent photocatalytic performance for H 2 evolution after three continuous photocatalytic reaction cycles for 9 h. This study provided a facile method to build a low-cost but effective metal sulfide co-catalyst for hydrogen production under visible light irradiation.
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PubMed
高影响因子
ECOTOXICOLOGY AND ENVIRONMENTAL SAFETY
·
2021
·
IF 6.291
Qingguo Chen,Yan Hao,Zhao Song,Mei Liu,Dongzhi Chen,Baikang Zhu,Jianmeng Chen,Zhi Chen
Degradation of norfloxacin (NFX) by zinc oxide (ZnO)/g-C 3 N 4 , a magnetic sheet ZnO with g-C 3 N 4 on its surface was studied. Through a new preparation system method, hydrothermal reaction provides a solid-layered magnetic ZnO material basis, and the simple thermal condensation method was used to transform the urea into g-C 3 N 4 on the magnetic sheet ZnO in a uniform and orderly manner to increase the stability and photocatalytic performance of the material. Compared with previous studies, the pore volume and photocatalytic performance of the material are improved, and became more stable. By studying the degradation effect of basic and photocatalytic materials prepared in different proportions, the kinetic constant of ZGF is 0.01446 (min −1 ). The response surface methodology (RSM) was used to study the optimization and effect of solution pH (4−12), photocatalyst concentration (0.2–1.8 g/L), and NFX concentration (3–15 mg/L) on the degradation rate of NFX during photocatalytic degradation. The R 2 value of the RSM model was 0.9656. The NFX removal rate is higher than 90% when the amount of catalyst is 1.43 g/L, the solution pH is 7.12, and the NFX concentration is less than 8.61 mg/L. After 5 cycles, the degradation rate of magnetic materials decreased to 92.8% of the first time. The capture experiment showed that the photocatalytic machine Toxicities was mainly hole action. The TOC removal rate within 2 h was 30%, a special intermediate toxicity analysis method was adopted according to the characteristics of NFX's inhibitory effect on Escherichia coli community. The toxicity of degraded NFX solution disappeared, and the possibility of non-toxic harm of by-products was verified. LC-Q-TOF method was used to detect and analyze various intermediate products converted from NFX after photocatalytic degradation, and the photocatalytic degradation pathway of NFX was proposed.
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高影响因子
JOURNAL OF PHOTOCHEMISTRY AND PHOTOBIOLOGY A-CHEMISTRY
·
2024
·
IF 4.1
Xian-De Zhou,Yong-Hui Tian
Biomass is a natural and renewable carbon resource. One of the possible green approaches to “carbon neutrality” is catalytic conversion of biomass resources into high value-added chemicals. As a result, photocatalytic selective oxidation of the biomass product 5-hydroxymethylfurfural (5-HMF) to 2,5-dicarbonylfuran (DFF) is an ecologically benign and energy efficient method. In this study, 2D g-C 3 N 4 /BiOCl heterostructures composites were prepared by easy ultrasonication-assisted stirring method for the first application of photocatalytic oxidation of 5-HMF to DFF. The physicochemical properties of the synthesized materials were characterized by SEM, XRD, FT-IR, XPS, UV–vis, BET surface area, PL and EPR analysis. The experimental results show that the g-C 3 N 4 /BiOCl composite is superior to pure g-C 3 N 4 and BiOCl in the oxidation of 5-HMF to DFF. The improved photocatalytic performance of the g-C 3 N 4 /BiOCl composites can be attributed to the improved visible light absorption, the creation of compact and intact Z-type heterojunction, increased surface area and enhanced separation efficiency of photogenerated electron-hole pairs. In addition, the photocatalyst has high stability and reusability. A putative photocatalytic process is proposed based on the respective energy band locations of these two semiconductors.
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高影响因子
Inorganic Chemistry Frontiers
·
2025
·
IF 6.4
Kexin Yang,Zhijia Song,XiaoXiao Fu,Wei Yan,Tao Zhang,Yiwei Hua,Haixin Lin,Qin Kuang,Zhaoxiong Xie
The photocatalytic direct one-step two-electron (2e-) oxygen reduction reaction (ORR) holds great potential in efficient H2O2 synthesis. However, it is still a significant challenge to design photocatalysts for achieving high-efficiency H2O2 production via this direct one-step 2e- ORR pathway. To address this, we have constructed a Z-scheme BAIO/C3N4 heterojunction by in situ growing Ba2AgIO6 (BAIO) on the surface of C3N4 nanosheets. Under visible light irradiation, the optimal sample, with a BAIO:C3N4 mass ratio of 1:1.5, exhibited a remarkable H2O2 yield of up to 535.9 μmol g-1 h-1, which is 8.8 times higher than that of pure C3N4. This enhancement is attributed to the improved charge separation and migration efficiency facilitated by the enhanced internal electric field (IEF) in BAIO/C3N4 heterojunction. Furthermore, the heterojunction altered the O2 adsorption configuration to the Yeager-type, promoting a more efficient and selective direct one-step 2e- ORR for H2O2 production. This study highlights the importance of regulating the reaction pathway to enhance photocatalytic H2O2 production activity and offers a new insight for designing highly active photocatalysts.
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高影响因子
CHEMICAL ENGINEERING JOURNAL
·
2025
·
IF 13.2
Chunxia Yao,Wei Song,Xuesheng Wang,Sai Huang,Yangyang Lu,Jiaxin Zhou,Weiguo Song,Zhijie Zhang
This study presents an innovative nanocomposite film with multiple synergistic sterilization modes, which aims to enhance the freshness of fruits and reduce wastage by capitalizing on the availability of sunlight. In detail, α-Fe 2 O 3 /g-C 3 N 4 (FOCN) nanocomposite with excellent visible-light-harvesting ability and photodynamic antibacterial activity was fabricated, which was then filled within a chitosan (CS) matrix, resulting in a novel antibacterial film for food preservation. The obtained α-Fe 2 O 3 /g-C 3 N 4 /chitosan (FOCN/CS) film exhibited impressive antibacterial activities, with sterilizing rate of 99.7 % ± 0.6 % against Escherichia coli ( E. coli ) and 97.6 % ± 0.4 % against Staphylococcus aureus ( S. aureus ) with short processing time (10 min) under visible light illumination. Based on this, the FOCN/CS film demonstrated excellent food preservation performance, which significantly prolonged the shelf life of strawberries, baby bok choy and pork. Such satisfactory preservation ability originates from the synergistic effect of α-Fe 2 O 3 and g-C 3 N 4 , which formed S-type heterojunction and bestow the FOCN/CS film with superior photodynamic antibacterial activity. Therefore, the film provides a novel microbiological control barrier for food preservation, with the potential to effectively reduce microbiologically induced food spoilage problems.
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