ACTA PHYSICO-CHIMICA SINICA
·
2024
·
IF 10.8
Asif Hassan Raza,Shumail Farhan,Zhixian Yu,Yan Wu
This work illustrates the novelty of double S-scheme ZnS/ZnO/CdS ternary heterojunction photocatalyst with efficient photocatalytic activity. The sample with optimal CdS content, ZnS/ZnO/CdS-14% (ZZC14%), displayed the maximum H 2 evolution rate of 4.1 mmol·g ‒1 ·h ‒1 . The maximum photocatalytic performance was approximately 2 and 13 times higher than their corresponding counterparts, ZnS/CdS and ZnO/ZnS, respectively. A high AQE of 19.8% under 420 nm was obtained. Additionally, the slight changes in H 2 evolution activities and retentions of crystal structures after six successive cycles indicate the stability of the photocatalyst. In accordance with the theoretical calculations and experimental results, the remarkable enhancement in photocatalytic activity is attributed to fast electron transfer and separation as well as the intimate contact due to mutual interaction between S-scheme. This work highlights an innovative approach to constructing a dual S-scheme photocatalytic system with high separation and fast migration capabilities of photogenerated charge carriers for splitting water to produce hydrogen. Download: Download high-res image (131KB) Download: Download full-size image
研究领域:
材料科学
·
能源科学
·
环境科学
✓ 已验证
产品关联
DOI
高影响因子
FUEL
·
2024
·
IF 6.7
Yan Wang,Xi Wu,Qiaoling Yang,Yuqi Zhao,Hengliang Wang,Arturo Pajares,Jinying Zhang,Jiahong Wang,Wai-Yeung Wong,Xin Wang
Designing ternary heterojunction photocatalysts is regarded as a compelling approach to attain exceptional photocatalytic activity. However, they always suffer from poor interfacial contact and unclear charge transfer pathways. Herein, a metal-free dual S-scheme heterojunction photocatalyst comprised of black phosphorus (BP), carbon nitride (CN), violet phosphorus (VP) was designed by electrostatic self-assembly. The non-metallic feature of the BPCNVP heterostructure facilitates to form strong interfacial contact by coordinating active P sites in VP and BP with N atoms in CN. Notably, a definite dual S-scheme heterojunction configuration is achieved by rational band alignment of VP and BP, respectively, which significantly boosts the driving force for charge separation. The BPCNVP heterostructure exhibited a hydrogen evolution rate of 1669μmol h -1 g −1 with excellent stability, surpassing most reported metal-free photocatalysts. This work demonstrates that the design of dual S-scheme heterojunction by metal-free materials provides valuable insights into the intricate reaction mechanism of ternary heterojunction photocatalysts.
研究领域:
材料科学
·
能源科学
·
环境科学
✓ 已验证
产品关联
DOI
高影响因子
Nanoscale
·
2024
·Vol. 16
·期 36
·17009-17023
·
IF 5.8
Congcong Wang,Suili Shi,Boya Liu,Guorong Wang,Zhiliang Jin
Rational design and synthesis of a unique heterojunction photocatalyst structure is an important strategy to enhance its performance and structural stability. Herein, Co9S8/MnCdS/Co3O4 photocatalysts with double S-scheme heterojunctions were successfully prepared by coupling Co9S8 and Co3O4 sheet structures with n-type MnCdS nanoparticles through a simple solvothermal and mechanical mixing method. The construction of the dual S-scheme heterostructure offers the possibility to expand the light absorption range, extend the carrier lifetime and maximise the redox capacity. In addition, the mechanism of charge transfer and the reason for the improvement of photocatalytic activity were explored through photoelectrochemical characterization. The lamellar structures of Co9S8 and Co3O4 not only provide excellent dispersion and slow down the agglomeration of MnCdS nanoparticles, but also promote charge transfer, which improves the photocatalytic hydrogen production effect. Under simulated solar irradiation, the evolution rate of H2 after 5 h was as high as 46.44 μmol, which was 3.49 and 1.49 times higher than those of pristine MnCdS and MnCdS/Co3O4, respectively. Meanwhile, it has good stability under 20 h irradiation. This work demonstrates a novel idea for the rational design of double S-scheme photocatalysts with efficient space separation.
研究领域:
材料科学
·
光催化
✓ 已验证
产品关联
DOI
PubMed
高影响因子
JOURNAL OF PHOTOCHEMISTRY AND PHOTOBIOLOGY A-CHEMISTRY
·
2024
·
IF 4.1
Xupeng Chen,Jun Yu,Yong Jin,Yunzhao Zhang,Jie He,Xingang Li,Chun Zhang
In this paper, C/ZnO/ZnFe 2 O 4 @ZnIn 2 S 4 ternary heterojunctions were prepared using Zn-Fe bimetal-organic frameworks (Zn-Fe MOFs) as precursors and applied to the photocatalytic degradation of tetracycline hydrochloride (TC). The experimental results show that 30 mg of the composite (FS-2) showed 96 % removal of 20 mg/L TC. The improved photocatalytic performance was attributed to the synergistic effect of the double S-scheme heterojunction and the carbon layer, which greatly facilitated the separation of electron-hole pairs by the reverse motion of electrons and holes driven by the difference of work functions and the built-in electric field at the interface. The carbon layer acts as an electronic bridge can further improve the charge transfer between the interfaces of different photocatalysts, allowing more useful electrons and holes with strong redox capabilities to participate in the surface reactions. Combining the experimental results and density functional theory (DFT) calculations, the photocatalytic mechanism of the dual S-scheme system is proposed. This study provides a theoretical basis for the design of novel photocatalytic materials with dual S-scheme heterojunctions and efficient photocatalytic degradation.
研究领域:
环境科学
·
材料科学
✓ 已验证
产品关联
DOI
高影响因子
JOURNAL OF ALLOYS AND COMPOUNDS
·
2024
·
IF 5.8
Xiao-hu Ma,Si-yuan He,Zhe-rui Zhang,Zhe Meng
Persistent light-emitting materials (PLMs), which have the potential to store and release light energy after light irradiation, are receiving increasing attention for their role in prolonging the lifetime of photogenerated electrons for the development of photocatalysts with round-the-clock applications. In this paper, a double S-scheme Sr 2 MgSi 2 O 7 :Eu 2+ ,Dy 3+ /ZnIn 2 S 4 /UiO-66-NH 2 (SZU) heterojunction with round-the-clock catalytic activity was prepared by hydrothermal self-assembly method. The photocatalytic performance of the SZU heterojunction for RhB(MB) degradation was significantly improved compared with the pristine ZnIn 2 S 4 and UiO-66-NH 2 . The SZU heterojunction has excellent catalytic degradation performance for RhB (MB), and the removal rate of RhB (MB) reaches 72.2 % (81.7 %) after visible light irradiation for 40 (60) minutes. After the end of light, the total removal rate of RhB (MB) reached 86.7 % (96.8 %) when the catalysis continued for several hours under dark conditions, which was 14 % and 15 % higher than that under visible light irradiation, respectively. Based on the characteristics of SMS photoluminescence, combined with a large number of photocatalytic experiments, The sustained photocatalytic activity was enhanced under both daytime and darkness conditions, not only because of the production of SZU complexes, which prolonged the visible light response of ZnIn 2 S 4 , but also because of the construction of double S-scheme heterojunctions, which facilitates the light storage capacity, charge transfer, and the separation of photo-induced charge carriers and effectively promoted the photocatalytic activity of the photocatalysts. This work contributes to a deeper understanding of the design of round-the-clock photocatalysts, and provides a useful exploration for the practical application of photocatalytic technology.
研究领域:
材料科学
·
环境科学
·
光催化技术
✓ 已验证
产品关联
DOI
高影响因子
危险品化学品经营许可证（带存储）