ChemInform ◽  
2006 ◽  
Vol 37 (9) ◽  
Author(s):  
H. Kadowaki ◽  
J. Sato ◽  
H. Kobayashi ◽  
N. Saito ◽  
H. Nishiyama ◽  
...  

Nanoscale ◽  
2019 ◽  
Vol 11 (14) ◽  
pp. 6876-6885 ◽  
Author(s):  
Yuan-Yuan Li ◽  
Bing-Xin Zhou ◽  
Hua-Wei Zhang ◽  
Shao-Fang Ma ◽  
Wei-Qing Huang ◽  
...  

Structural defects can greatly inhibit electron transfer in two-dimensional (2D) layered polymeric carbon nitride (CN), seriously lowering its utilization ratio of photogenerated charges during photocatalysis.


CrystEngComm ◽  
2019 ◽  
Vol 21 (22) ◽  
pp. 3439-3450 ◽  
Author(s):  
Yi Lin ◽  
Pinyun Ren ◽  
Chengyang Wei

Two-dimensional nanophotocatalysts MoS2/TiO2 with a tunable decoration amount of MoS2 nanosheets were fabricated through a hydrothermal route.


2017 ◽  
Vol 16 (02) ◽  
pp. 1750013 ◽  
Author(s):  
Guoyan Nie ◽  
Peng Li ◽  
Jin-Xia Liang ◽  
Chun Zhu

Two-dimensional optical catalysis materials have a wonderful potential application. Here, a new two-dimensional material consisting of the supported single-atom Au on a graphite carbon nitride (g-C3N[Formula: see text] single layer has been designed and its electronic and optical properties have been characterized by density functional calculations. The bandgap of 1.82[Formula: see text]eV calculated by the hybrid functional HSE06 shows that the Au/g-C3N4 is an indirect semiconductor, and the electron can easily be excited from the single-atom Au to the bottom of the conduction band. This material therefore has relatively strong optical properties in the visible region. Moreover, the process of Au insertion into the cavity of g-C3N4 single layer is energy-favorable. This work may provide insights and a new avenue for fabricating supported Au catalysts with high stability.


2016 ◽  
Vol 6 (4) ◽  
pp. 1064-1069 ◽  
Author(s):  
Kazuhiko Maeda ◽  
Miharu Eguchi

Photocatalytic activity of restacked ACa2Nb2TaO10 (A = H, Li, Na, K, Rb, Cs) nanosheets for H2 evolution under band-gap irradiation (λ > 300 nm) was enhanced not upon hydration of the interlayer nanospace, but by protonation.


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