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Journal of Materiomics · 2015 · IF 0

Dual Z-scheme charge transfer in TiO2–Ag–Cu2O composite for enhanced photocatalytic hydrogen generation

Junwei Fu,Shaowen Cao,Jiaguo Yu

Photocatalytic hydrogen generation is one of the most promising solutions to convert solar power into green chemical energy. In this work, a multi-component TiO 2 –Ag–Cu 2 O composite was obtained through simple impregnation-calcination of Cu 2 O and subsequent photodeposition of Ag onto electrospun TiO 2 nanotubes. The resulting TiO 2 –Ag–Cu 2 O photocatalyst exhibits excellent photocatalytic H 2 evolution activity due to the synergetic effect of Ag and Cu 2 O on electrospun TiO 2 nanotubes. A dual Z-scheme charge transfer pathway for photocatalytic reactions over TiO 2 –Ag–Cu 2 O composite was proposed and discussed. This work provides a prototype for designing Z-scheme photocatalyst with Ag as an electron mediator.

研究领域: 材料科学 · 能源科学
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CHEMICAL ENGINEERING JOURNAL · 2017 · IF 6.216

Fabrication of magnetically recoverable photocatalysts using g-C3N4 for effective separation of charge carriers through like-Z-scheme mechanism with Fe3O4 mediator

Zhi Zhu,Pengwei Huo,Ziyang Lu,Yongsheng Yan,Zhi Liu,Weidong Shi,Chunxiang Li,Hongjun Dong

A novel efficient magnetic oxidation-reduction like-Z-scheme structure photocatalyst composed of g-C 3 N 4 , CdS and the oxidation-reduction mediators of Fe 3 O 4 is successfully synthesized by heat treatment methods. The like-Z-scheme CdS/Fe 3 O 4 /g-C 3 N 4 photocatalyst exhibits universal degradation property on removing kinds of antibiotics, and the photocatalytic activity is better than that of CdS/g-C 3 N 4 and pure g-C 3 N 4 . The excellent photocatalytic performance is originated from the unique like-Z-scheme structure and oxidation–reduction function of Fe 3 O 4 , which effectively separates the hole-electron and sufficiently utilizes the photogenerated carriers for generating more active radicals. The results showed that when the content of Fe 3 O 4 is 10%, the CdS/Fe 3 O 4 /g-C 3 N 4 exhibited superior activity. The best degradation rate constant K in the like-Z-scheme photocatalyst is approximately 26 times of pure g-C 3 N 4 . The important role of Fe 3 O 4 and the photocatalytic mechanism are also discussed in detail. This work not only puts forward a novel design idea of the like-Z-scheme material, but also is expected to be widely applied to the universal removal of kinds of antibiotics according to the practical requirement.

研究领域: 材料科学 · 环境科学
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APPLIED SURFACE SCIENCE · 2020 · IF 6.182

Synergy of charge pre-separation and direct Z-scheme bridge in BiVO4{0 4 0}/Ag6Si2O7 photocatalyst boosting organic pollutant degradation

Di Zhang,Juanyuan Hao,Peng Wan,Dan Zhang,Quan Sun,Zongjun Liu,Fei Li,Haitao Fang,You Wang

The rapid recombination and poor redox capability of photoinduced charge carriers seriously impede the photocatalytic activity . Herein, a direct Z-scheme photocatalyst was fabricated by selectively depositing Ag 6 Si 2 O 7 nanoparticles (NPs) on the {0 4 0} facets of BiVO 4 . Owing to the facet-dependent band structure of BiVO 4 , the photoinduced electrons and holes can be pre-separated upon photoillumination and transfer to {0 4 0} and {1 1 0} facets of BiVO 4 , respectively. A rapid combination of the separated electrons at the {0 4 0} facets of BiVO 4 with holes of the Ag 6 Si 2 O 7 NPs then takes place triggering a direct Z-scheme photocatalysis. Such a charge pre-separation triggered by the faceted BiVO 4 , together with Z-scheme at the interface warrants not only effective photoinduced charge separation but also excellent redox capability owing to the increased redox potential. The photocatalytic rate constant of the optimum BiVO 4 {0 4 0}/Ag 6 Si 2 O 7 heterostructure is 28.2 and 17.2 times higher than those of pristine BiVO 4 and Ag 6 Si 2 O 7 , respectively. This study offers a new insight for constructing direct Z-scheme photocatalysts with high degradation efficiency based on facet-controlled crystals.

研究领域: 材料科学 · 环境科学
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OPTICAL MATERIALS · 2024 · IF 3.8

Construction of Cu2O ternary composite comprising SiC and g-C3N4 for improved photocatalytic degradation of methyl orange via synergetic Z-scheme effect

Mengyao Xue,Jingwei Han,Xing Dai,Yucai Ge,Yunhua Zhang,Zibin Hai

Cu 2 O–SiC/g-C 3 N 4 composite photocatalysts with excellent photocatalytic performance under visible light were synthesized for the first time via a facile approach combining calcination with hydrothermal reaction. Comprehensive characterization of the synthesized samples encompassing composition, morphology, structure and photoelectric properties was conducted utilizing techniques such as X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), scanning electron microscopy (SEM), transmission electron microscopy (TEM), diffuse reflectance spectroscopy (DRS), photoluminescence spectroscopy (PL), and electrochemical impedance spectroscopy (EIS). Results unequivocally demonstrate successful preparation of the ternary composite through Cu 2 O loading onto SiC/g-C 3 N 4 , evincing markedly elevated activity compared to individual counterparts and binary composites. Notably, in the presence of the prepared Cu 2 O–SiC/g-C 3 N 4 , the degradation rate of methyl orange reached 93.70 % under illumination with a visible LED light rated at 5 W. The notable enhancement in photocatalytic performance of the ternary composites is primarily ascribed to the synergistic effects stemming from the formation of p-n junctions between Cu 2 O and g-C 3 N 4 , alongside the Z-scheme configuration established between Cu 2 O and SiC. Free radical quenching experiments corroborated •O 2 − and h + as the principal redox species mediating the visible light quenching process. This study not only presents a feasible strategy for the fabrication of Cu 2 O-based ternary composites with significantly augmented photocatalytic performance but also delineates a novel avenue for the design and construction of composite photocatalysts facilitating enhanced charge-carrier generation and separation concomitantly.

CAS / MDL: 547-58-0 409-21-2
研究领域: 材料科学 · 环境科学
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Materials Science and Engineering B-Advanced Functional Solid-State Materials · 2022 · IF 3.407

High efficient and stable Z-scheme g-C3N4/Zn0.5Cd0.5S photocatalyst driven by visible light for hydrogen evolution

Lianqing Yu,Xingyu Zhao,Jiandong He,Lijie Duan,Yankun Wang,Yaping Zhang,Haifeng Zhu

It is extremely desirable to develop efficient and cheap water splitting photocatalysts. An ultrahigh performance and stable photocatalyst g-C 3 N 4 /Zn 0.5 Cd 0.5 S was prepared by simple sintering method. g-C 3 N 4   nanosheets are evenly distributed around 20–30 nm ZnCdS nanoparticles, which can accelerate carriers separation and transfer, and increase the carriers life-time from 4.1 ns to 5.5 ns. UV–vis absorption spectra demonstrate that their absorption range can reach to visible light edge of 539 nm. The photocatalyst has a high photocatalytic hydrogen evolution rate of 16.66 mmol•h −1 •g −1 under visible light illumination (λ = 400–780 nm). Furthermore, after six recycles of photocatalyst, the hydrogen evolution stability still remains 94%. The excellent photocatalytic performance is attributed to the Z-scheme energy band structure formed between g-C 3 N 4 and Zn 0.5 Cd 0.5 S by simple sintering method. This work provides significant progress toward the synthesis of cheap Z-scheme photocatalysts for practical applications.

研究领域: 材料科学 · 能源化学
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APPLIED CATALYSIS B-ENVIRONMENTAL · 2016 · IF 8.328

Photocorrosion inhibition and high-efficiency photoactivity of porous g-C3N4/Ag2CrO4 composites by simple microemulsion-assisted co-precipitation method

Yanyang Shang,Xi Chen,Wenwen Liu,Pengfei Tan,Haoyun Chen,Laidi Wu,Cheng Ma,Xiang Xiong,Jun Pan

A facile microemulsion-assisted co-precipitation method was carried out to synthesize nano-sized Ag 2 CrO 4 highly dispersed on the surface of porous g-C 3 N 4 as high-efficiency visible-light-driven composite photocatalysts for the first time. The structure and morphology of the composites were systematically characterized by various techniques. Compared with Ag 2 CrO 4 and g-C 3 N 4 , g-C 3 N 4 /Ag 2 CrO 4 composites showed a dramatically increased photocatalytic activity in degradation of rhodamine B (RhB) and methylene blue (MB). The optimum mass ratio of the Ag 2 CrO 4 to g-C 3 N 4 was about 30   wt%, the degradation rate of which were 6.1 (7.9) and 9.7 (15.2) times higher than pure Ag 2 CrO 4 and g-C 3 N 4 in RhB (MB) degradation, respectively. The excellent photocatalytic activity and stability mainly benefited from the synergistic effect including smaller Ag 2 CrO 4 particle size, high specific surface area of the composites and matched band potentials which not only promoted the separation of photon-generated charge carriers, but also inhibited the photocorrosion of Ag 2 CrO 4 . Further study revealed that the photocatalytic mechanism followed a Z-scheme which provided an efficient transfer pathway for charge carriers meanwhile endowed the composites with strong oxidation and reduction ability. Hence the porous g-C 3 N 4 /Ag 2 CrO 4 composites are potential in environmental purification.

研究领域: 材料科学 · 环境科学 · 化学
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APPLIED SURFACE SCIENCE · 2018 · IF 4.439

Highly efficient direct Z-scheme WO3/CdS-diethylenetriamine photocatalyst and its enhanced photocatalytic H2 evolution under visible light irradiation

Taiping Hu,Pengfei Li,Jinfeng Zhang,Changhao Liang,Kai Dai

Cadmium sulfide (CdS) has demonstrated great promise in artificial photocataytic hydrogen (H 2 ) production. However, the serious photocorrosion hinders its effective interaction and real-life application. In this work, a typical direct Z-scheme WO 3 /CdS-diethylenetriamine (CdS-DETA) composite has been designed via facile in-situ solvothermal method, which exhibits excellent H 2 production properties in visible light region. In this system, the inorganic–organic CdS-DETA nanobelts (NBs) possess enough active sites and large surface area for the encouraging nanojunction structure information. Furthermore, we also systematically calculated energy band structure and investigated charge transfer of the WO 3 /CdS-DETA by PL and photocurrent test, the results demonstrated that the suitable band gap matching between CdS-DETA and WO 3 and high redox potential improve the separation of photogenerated holes and electrons, restraining intrinsic photocorrosion of CdS as well as improving the photocatalytic activity. 5%WO 3 /CdS-DETA presented the most outstanding H 2 evolution rate (15522 μmol g −1  h −1 ), which is twice higher than that of pure CdS-DETA. WO 3 /CdS-DETA composites also presented high stability after three recycle H 2 production experiment. Finally, direct Z-scheme photocatalytic mechanism is calculated.

研究领域: 材料科学 · 能源化学
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JOURNAL OF COLLOID AND INTERFACE SCIENCE · 2020 · IF 7.489

Synthesis of EDTA-bridged CdS/g-C3N4 heterostructure photocatalyst with enhanced performance for photoredox reactions

Yi Xiao,Ting Wang,Ganhua Qiu,Kun Zhang,Changguo Xue,Benxia Li

Photocatalytic reactions represent a kind of green and sustainable chemical processes for organic transformations, but the efficiency is limited by the severe recombination and/or inadequate redox potentials of photoinduced charge carriers in photocatalysts . To address these issues, herein, the CdS-EDTA/g-C 3 N 4 heterostructures were designed according to Z-scheme photocatalytic mechanism and synthesized by the hydrothermal growth of CdS on g-C 3 N 4 nanoflakes with assistance of EDTA chelating agent. EDTA played multiple roles in the formation of CdS-EDTA/g-C 3 N 4 heterostructure photocatalysts, such as controlling the morphology of CdS nanostructures , linking CdS and g-C 3 N 4 together, and boosting the charge transfer between two semiconductors. The optimized CdS-EDTA/g-C 3 N 4 (10%) photocatalyst exhibited much higher activities toward the selective reduction of nitrophenol and the selective oxidation of benzyl alcohol , than those of CdS/g-C 3 N 4 heterostructures without EDTA. The enhanced photocatalysis of CdS-EDTA/g-C 3 N 4 can be ascribed to the efficient separation and suitable photoredox potentials of photoexcited charge carriers in the EDTA-bridged Z-scheme system. This work provides the inspiration for exploring inexpensive organic electron mediators for constructing all-solid-state Z-scheme photocatalysts and demonstrates the enhanced performance of Z-scheme photocatalysts for photoredox reactions of organic transformations.

研究领域: 材料科学 · 光化学
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APPLIED CATALYSIS A-GENERAL · 2017 · IF 4.339

Fabrication of an all solid Z-scheme photocatalyst g-C3N4/GO/AgBr with enhanced visible light photocatalytic activity

Xuli Miao,Xiaoping Shen,Jiajia Wu,Zhenyuan Ji,Jiheng Wang,Lirong Kong,Miaomiao Liu,Chunsen Song

In this work, an excellent ternary visible-light all solid Z-scheme photocatalytic heterojunction of g-C 3 N 4 /GO/AgBr has been prepared by the attachment of graphene oxide (GO) to the surface of g-C 3 N 4 , followed by in-situ growth of AgBr nanoparticles on GO sheets. The g-C 3 N 4 /GO/AgBr heterojunction exhibits excellent photocatalytic efficiency for RhB degradation, which is about 17.5, 7.9, 3.5, 4.0 and 2.2 times as high as that of P25, g-C 3 N 4 , AgBr, g-C 3 N 4 /GO and g-C 3 N 4 /AgBr heterojunction, indicating the introduction of GO into the system largely improved the capability of the photocatalysis since GO acted as the charge transmission bridge between g-C 3 N 4 and AgBr. Moreover, the photocatalytic performance of g-C 3 N 4 /GO/AgBr just showed a slight decrease after 4 degradation cycles, demonstrating a high stability of the g-C 3 N 4 /GO/AgBr photocatalyst. The photocatalytic mechanism investigation indicated that O 2 − and h + are the major active species in the photocatalytic process. It is expected that the GO-inserted Z-scheme photocatalytic heterojunction could be applied to practical pollutant degradation.

CAS / MDL: 7782-42-5
研究领域: 材料科学 · 环境科学
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OPTICAL MATERIALS · 2022 · IF 3.754

Novel Z-scheme Bi3O4Br/NH2-MIL-125(Ti) composite for efficient photocatalytic degradation of tetracycline

Hao Hu,Jiacheng Jin,Mingchen Xu,Chengdong Xu,Yue Cheng,Weiwei Ji,Zhencen Ding,Min Shao,Yushan Wan

The present work demonstrates the synthesis of the microsphere composite photocatalyst Bi 3 O 4 Br/NH 2 -MIL-125(Ti) (BOB/NMILT) system, and the physicochemical properties of the material were analyzed by various characterization means. Further, the photocatalytic performance of the BOB/NMILT system was evaluated by degrading tetracycline (TC) under simulated sunlight. The degradation rate of TC using BOB/NMILT-5 reached 88.5% within 90 min. The degradation rate is 6.5 times and 3 times higher than that of individual catalysts NH 2 -MIL-125(Ti) (NMILT) and Bi 3 O 4 Br, respectively. The improvement in photocatalytic activity of composites mainly benefited from the construction of heterojunctions , which effectively inhibited the recombination of carriers. Importantly, the role of h + and •O 2 − was found to be significant in the reaction of TC. Cumulatively, a Z-scheme photocatalytic degradation mechanism of tetracycline on the BOB/NMILT composite system was proposed. The proposal of this system is of great significance for the future development of photocatalytic materials that can degrade tetracycline.

CAS / MDL: 10312-55-7 60-54-8
研究领域: 环境科学 · 材料科学
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RSC Advances · 2016 ·Vol. 6 ·期 34 ·28263-28269 · IF 3.289

Fabrication of g-C3N4/Au/CdZnS Z-scheme photocatalyst to enhance photocatalysis performance

Xiumin Ma,Quantong Jiang,Weimin Guo,Meng Zheng,Weichen Xu,Fubin Ma,Baorong Hou

In this study, a sandwich-structured C3N4/Au/CdZnS photocatalyst with Au nanoparticles sandwiched between C3N4 and CdZnS was fabricated. The results showed that there was a 6.3 mmol g−1 increase of hydrogen production for C3N4/Au/CdZnS photocatalyst compared to C3N4/CdZnS in 4 h. The photoinduced I–t curve, electrochemical impedance spectrum (EIS), photogenerated electron lifetime and photoluminescence spectra showed that the photocatalytic ability of the composite was enhanced by anchoring Au as the electron transfer mediator between C3N4 and CdZnS through the Z-scheme charge-carrier transfer mechanism. Au functioned as an electron transition mediator, which could induce a combination between photogenerated electrons and holes in the CdZnS and C3N4, respectively. These photogenerated holes of CdZnS can be involved in the S2−/SO32− oxidation process and the electrons from the C3N4 surface might be involved in the water to hydrogen reduction reaction, thus enhancing the photocatalysis performance of C3N4/Au/CdZnS photocatalyst.

研究领域: 材料科学 · 环境科学 · 化学
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JOURNAL OF COLLOID AND INTERFACE SCIENCE · 2025 · IF 9.7

In-situ generated metallic Bi accelerating Z-scheme charge transfer in Bi2O3/Bi/PCN heterojunction for highly efficient photocatalytic NO oxidation

Zixun Fang,Yao Zhou,Yang Yang,Yidong Hou,Can Yang,Jinshui Zhang

Artificial Z-scheme photocatalytic systems, inspired by natural photosynthesis, have been widely employed for pollutant removal. In this study, we fabricated a ternary Z-scheme Bi 2 O 3 /Bi/porous carbon nitride (PCN) heterojunction with an intimately coupled interface through a simple EG-assisted solvothermal approach to improving photocatalytic performance of NO oxidation. The in-situ generated metallic Bi acts as an electron mediator, effectively accelerating the separation and transfer of photoexcited carriers. The unique Z-scheme charge transfer mechanism provides the strong redox abilities and isolates the active sites for specific reactions, thus promoting photocatalytic NO oxidation activity. As a result, the optimized Bi 2 O 3 /Bi/PCN sample achieved a NO removal efficiency of 94.6%, outperforming single-component catalysts and most previously reported heterojunction-based photocatalysts. Additionally, in-situ Fourier transform infrared spectroscopy was employed to propose the NO removal mechanism, offering valuable insight into the conversion pathway. Such a heterogeneous Z-scheme photocatalytic system with a strong redox ability, high charge-separation efficiency, and long-term stability, demonstrates significantly enhanced photoactivity for pollutant removal and is expected to attract increasing interest for other photocatalytic applications.

CAS / MDL: 1304-76-3 3317-61-1
研究领域: 环境科学 · 材料科学 · 光催化技术
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