scholarly journals Metallic 1T-TiS2 nanodots anchored on a 2D graphitic C3N4 nanosheet nanostructure with high electron transfer capability for enhanced photocatalytic performance

RSC Advances ◽  
2017 ◽  
Vol 7 (87) ◽  
pp. 55269-55275 ◽  
Author(s):  
Yang Liu ◽  
Xiaojie She ◽  
Xiaoni Zhang ◽  
Chenglu Liang ◽  
Jingjie Wu ◽  
...  

The introduction of metallic TiS2 nanodots in 2D-C3N4 nanosheets improved the photocatalytic activity due to the suppression of e–h recombination.

2019 ◽  
Vol 8 (1) ◽  
pp. 56-61
Author(s):  
Aneeya K. Samantara ◽  
Debasrita Dash ◽  
Dipti L. Bhuyan ◽  
Namita Dalai ◽  
Bijayalaxmi Jena

: In this article, we explored the possibility of controlling the reactivity of ZnO nanostructures by modifying its surface with gold nanoparticles (Au NPs). By varying the concentration of Au with different wt% (x = 0.01, 0.05, 0.08, 1 and 2), we have synthesized a series of (ZnO/Aux) nanocomposites (NCs). A thorough investigation of the photocatalytic performance of different wt% of Au NPs on ZnO nanosurface has been carried out. It was observed that ZnO/Au0.08 nanocomposite showed the highest photocatalytic activity among all concentrations of Au on the ZnO surface, which degrades the dye concentration within 2 minutes of visible light exposure. It was further revealed that with an increase in the size of plasmonic nanoparticles beyond 0.08%, the accessible surface area of the Au nanoparticle decreases. The photon absorption capacity of Au nanoparticle decreases beyond 0.08% resulting in a decrease in electron transfer rate from Au to ZnO and a decrease of photocatalytic activity. Background: Due to the industrialization process, most of the toxic materials go into the water bodies, affecting the water and our ecological system. The conventional techniques to remove dyes are expensive and inefficient. Recently, heterogeneous semiconductor materials like TiO2 and ZnO have been regarded as potential candidates for the removal of dye from the water system. Objective: To investigate the photocatalytic performance of different wt% of Au NPs on ZnO nanosurface and the effect of the size of Au NPs for photocatalytic performance in the degradation process. Methods: A facile microwave method has been adopted for the synthesis of ZnO nanostructure followed by a reduction of gold salt in the presence of ZnO nanostructure to form the composite. Results: ZnO/Au0.08 nanocomposite showed the highest photocatalytic activity which degrades the dye concentration within 2 minutes of visible light exposure. The schematic mechanism of electron transfer rate was discussed. Conclusion: Raspberry shaped ZnO nanoparticles modified with different percentages of Au NPs showed good photocatalytic behavior in the degradation of dye molecules. The synergetic effect of unique morphology of ZnO and well anchored Au nanostructures plays a crucial role.


2018 ◽  
Vol 22 (09n10) ◽  
pp. 877-885 ◽  
Author(s):  
Qiang Luo ◽  
Kun Zhu ◽  
Shi-Zhao Kang ◽  
Lixia Qin ◽  
Sheng Han ◽  
...  

By facilely pre-implanting Co[Formula: see text] ions in the graphene oxide, a novel 5,15-diphenyl-10,20-di(4-pyridyl)porphyrin pillared graphene oxide was fabricated by means of electrostatic interaction and coordination interaction. It was shown that the morphology and the structure of graphene oxide and pyridylporphyrin nanocomposite were modified by introducing Co[Formula: see text] ions on the interface between graphene oxide and pyridylporphyrin. Furthermore, it was found that the photocatalytic hydrogen evolution activity over the Co[Formula: see text] ions implanted in the graphene oxide and pyridylporphyrin nanocomposite was evidently higher than in the graphene oxide and pyridylporphyrin nanocomposite without Co[Formula: see text]. This confirmed that strong interaction and efficient electron transfer between pyridylporphyrin and graphene oxide are the important reasons for the enhanced photocatalytic activity for hydrogen evolution. Subsequently, this technique will be a simple and efficient approach to optimize the transfer pathway of photogenerated electrons and to improve photocatalytic performance by implanting metal ions in the interface of nanocomposites.


NANO ◽  
2018 ◽  
Vol 13 (03) ◽  
pp. 1850029
Author(s):  
Bin Zeng ◽  
Wanfeng Liu ◽  
Wujun Zeng ◽  
Can Jin

Graphene decorated with hierarchical CuS nanoplates (CuS NP-G) was synthesized using a microwave method to be used as a photocatalytic material. The incorporation of graphene into hierarchical CuS nanoplates was confirmed by structural, morphological and optical characterizations. The photocatalytic performance of the nanocomposite was evaluated. This study confirmed that the introduction of graphene was an effective way not only to improve the structural stability and service durability of the composite, but also to improve its solar photocatalytic activity by promoting the electron transfer and charge separation of hierarchical CuS nanoplates.


2015 ◽  
Vol 287 ◽  
pp. 126-132 ◽  
Author(s):  
Xianjie Chen ◽  
Fenglin Liu ◽  
Bing Liu ◽  
Lihong Tian ◽  
Wei Hu ◽  
...  

2020 ◽  
pp. 129677
Author(s):  
Rıza Bayrak ◽  
Seçil Kırlangıç Ataşen ◽  
Ismail Yılmaz ◽  
İzzet Yalçın ◽  
Murat Erman ◽  
...  

Materials ◽  
2019 ◽  
Vol 12 (23) ◽  
pp. 3948
Author(s):  
Lingfang Qiu ◽  
Zhiwei Zhou ◽  
Mengfan Ma ◽  
Ping Li ◽  
Jinyong Lu ◽  
...  

Novel visible-light responded aluminosilicophosphate-5 (SAPO-5)/g-C3N4 composite has been easily constructed by thermal polymerization for the mixture of SAPO-5, NH4Cl, and dicyandiamide. The photocatalytic activity of SAPO-5/g-C3N4 is evaluated by degrading RhB (30 mg/L) under visible light illumination (λ > 420 nm). The effects of SAPO-5 incorporation proportion and initial RhB concentration on the photocatalytic performance have been discussed in detail. The optimized SAPO-5/g-C3N4 composite shows promising degradation efficiency which is 40.6% higher than that of pure g-C3N4. The degradation rate improves from 0.007 min−1 to 0.022 min−1, which is a comparable photocatalytic performance compared with other g-C3N4-based heterojunctions for dye degradation. The migration of photo-induced electrons from g-C3N4 to the Al site of SAPO-5 should promote the photo-induced electron-hole pairs separation rate of g-C3N4 efficiently. Furthermore, the redox reactions for RhB degradation occur on the photo-induced holes in the g-C3N4 and Al sites in SAPO-5, respectively. This achievement not only improves the photocatalytic activity of g-C3N4 efficiently, but also broadens the application of SAPOs in the photocatalytic field.


2021 ◽  
Vol 50 (9) ◽  
pp. 3253-3260 ◽  
Author(s):  
Shan Zhao ◽  
Junbiao Wu ◽  
Yan Xu ◽  
Xia Zhang ◽  
Yide Han ◽  
...  

CdS/Ag2S/g-C3N4 ternary composites showed excellent photocatalytic performance toward H2 evolution. Their improved photocatalytic activity could be attributed not only to the synergic effect, but also to the introduction of Ag2S.


Molecules ◽  
2021 ◽  
Vol 26 (4) ◽  
pp. 1092
Author(s):  
Ban Chen ◽  
Xican Li ◽  
Xiaojian Ouyang ◽  
Jie Liu ◽  
Yangping Liu ◽  
...  

Synthetic arylamines and dietary phytophenolics could inhibit ferroptosis, a recently discovered regulated cell death process. However, no study indicates whether their inhibitory mechanisms are inherently different. Herein, the ferroptosis-inhibitory mechanisms of selected ferrostatin-1 (Fer-1) and two dietary stilbenes (piceatannol and astringin) were compared. Cellular assays suggested that the ferroptosis-inhibitory and electron-transfer potential levels decreased as follows: Fer-1 >> piceatannol > astringin; however, the hydrogen-donating potential had an order different from that observed by the antioxidant experiments and quantum chemistry calculations. Quantum calculations suggested that Fer-1 has a much lower ionization potential than the two stilbenes, and the aromatic N-atoms were surrounded by the largest electron clouds. By comparison, the C4′O-H groups in the two stilbenes exhibited the lowest bond disassociation enthalpies. Finally, the three were found to produce corresponding dimer peaks through ultra-performance liquid chromatography coupled with electrospray ionization quadrupole time-of-flight tandem mass spectrometry analysis. In conclusion, Fer-1 mainly depends on the electron transfer of aromatic N-atoms to construct a redox recycle. However, piceatannol and astringin preferentially donate hydrogen atoms at the 4′-OH position to mediate the conventional antioxidant mechanism that inhibits ferroptosis, and to ultimately form dimers. These results suggest that dietary phytophenols may be safer ferroptosis inhibitors for balancing normal and ferroptotic cells than arylamines with high electron-transfer potential.


Sign in / Sign up

Export Citation Format

Share Document