In situ chemical reduction of the Ta3N5 quantum dots coupled TaON hollow spheres heterojunction photocatalyst for water oxidation

2012 ◽  
Vol 22 (41) ◽  
pp. 21972 ◽  
Author(s):  
Zheng Wang ◽  
Jungang Hou ◽  
Shuqiang Jiao ◽  
Kai Huang ◽  
Hongmin Zhu
2018 ◽  
Vol 90 (14) ◽  
pp. 8635-8641 ◽  
Author(s):  
Ying Chen ◽  
Jiaju Fu ◽  
Chen Cui ◽  
Dechen Jiang ◽  
Zixuan Chen ◽  
...  

2018 ◽  
Vol 6 (48) ◽  
pp. 24686-24692 ◽  
Author(s):  
Zhiping Zeng ◽  
Tao Li ◽  
Yu-Bing Li ◽  
Xiao-Cheng Dai ◽  
Ming-Hui Huang ◽  
...  

Cascade charge transfer between graphene quantum dots and Ag nanocrystals in photoelectrochemical water splitting was finely regulated by layer-by-layer (LbL) assembly.


2019 ◽  
Vol 7 (15) ◽  
pp. 9289-9296 ◽  
Author(s):  
Jun Yuan ◽  
Xiang Hu ◽  
Junxiang Chen ◽  
Yangjie Liu ◽  
Taizhong Huang ◽  
...  

Vanadium nitride quantum dots within N-doped carbon hollow spheres exhibit excellent storage performance.


2021 ◽  
Author(s):  
Di Liu ◽  
Liping CHEN ◽  
Wenbin Chen ◽  
Mengtao Qin ◽  
Siqi Wei

Well-dispersed Pt quantum dots (QDs) was first to be successfully deposited on PDI supramolecular nanorods surface via a simple in situ chemical reduction. Under visible light irradiation, Pt QDs/PDI composites...


Author(s):  
Ain Uddin ◽  
Weifan Sang ◽  
Yong Gao ◽  
Kyle Plunkett

The synthesis of poly(p-xylylene)s (PPXs) with sidechains containing alkyl bromide functionality, and their post-polymer modification, is described. The PPXs were prepared by a diimide hydrogenation of poly(p-phenylene vinylene)s (PPVs) that were originally synthesized by a Gilch polymerization. The polymer backbone reduction was carried out with hydrazine hydrate in toluene at 80 °C to provide polymers with the sidechain-containing bromide functionality intact. To demonstrate post-polymer modification of the sidechains, the resulting PPX polymers were modified with trimethylamine to form tetraalkylammonium ion functionality and were evaluated as anion conducting membranes. While PPX homopolymers containing tetralkylammonium ions were completely water soluble and not able to form valuable films, PPX copolymers containing mixed tetraalkylammonium ions and hydrophobic chains were capable of film formation and alkaline stability. In addition, an in situ crosslinking process that used N,N,N',N'-tetramethyl-1,6-hexanediamine during the tetraalkylammonium formation of brominated PPX polymers was also evaluated and gave reasonable films with conductivities of ~10 mS-cm-1.


2019 ◽  
Author(s):  
Ain Uddin ◽  
Weifan Sang ◽  
Yong Gao ◽  
Kyle Plunkett

The synthesis of poly(p-xylylene)s (PPXs) with sidechains containing alkyl bromide functionality, and their post-polymer modification, is described. The PPXs were prepared by a diimide hydrogenation of poly(p-phenylene vinylene)s (PPVs) that were originally synthesized by a Gilch polymerization. The polymer backbone reduction was carried out with hydrazine hydrate in toluene at 80 °C to provide polymers with the sidechain-containing bromide functionality intact. To demonstrate post-polymer modification of the sidechains, the resulting PPX polymers were modified with trimethylamine to form tetraalkylammonium ion functionality and were evaluated as anion conducting membranes. While PPX homopolymers containing tetralkylammonium ions were completely water soluble and not able to form valuable films, PPX copolymers containing mixed tetraalkylammonium ions and hydrophobic chains were capable of film formation and alkaline stability. In addition, an in situ crosslinking process that used N,N,N',N'-tetramethyl-1,6-hexanediamine during the tetraalkylammonium formation of brominated PPX polymers was also evaluated and gave reasonable films with conductivities of ~10 mS-cm-1.


Catalysts ◽  
2021 ◽  
Vol 11 (4) ◽  
pp. 464
Author(s):  
Jie Yu ◽  
Angel Caravaca ◽  
Chantal Guillard ◽  
Philippe Vernoux ◽  
Liang Zhou ◽  
...  

Indoor toxic volatile organic compounds (VOCs) pollution is a serious threat to people’s health and toluene is a typical representative. In this study, we developed a composite photocatalyst of carbon nitride quantum dots (CNQDs) in situ-doped TiO2 inverse opal TiO2 IO for efficient degradation of toluene. The catalyst was fabricated using a sol-gel method with colloidal photonic crystals as the template. The as-prepared catalyst exhibited excellent photocatalytic performance for degradation of toluene. After 6 h of simulated sunlight irradiation, 93% of toluene can be converted into non-toxic products CO2 and H2O, while only 37% of toluene is degraded over commercial P25 in the same condition. This greatly enhanced photocatalytic activity results from two aspects: (i) the inverse opal structure enhances the light harvesting while providing adequate surface area for effective oxidation reactions; (ii) the incorporation of CNQDs in the framework of TiO2 increases visible light absorption and promotes the separation of photo-generated charges. Collectively, highly efficient photocatalytic degradation of toluene has been achieved. In addition, it can be expanded to efficient degradation of organic pollutants in liquid phase such as phenol and Rhodamine B. This study provides a green, energy saving solution for indoor toxic VOCs removal as well as for the treatment of organic wastewater.


2021 ◽  
Vol 42 (7) ◽  
pp. 1096-1101 ◽  
Author(s):  
Jinxiu Zhao ◽  
Xiang Ren ◽  
Xu Sun ◽  
Yong Zhang ◽  
Qin Wei ◽  
...  

2011 ◽  
Vol 363 (2) ◽  
pp. 703-706 ◽  
Author(s):  
Hyunki Kim ◽  
Minwon Suh ◽  
Byung-Hwa Kwon ◽  
Dong Seon Jang ◽  
Sung Wook Kim ◽  
...  

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