Synergistic effect of 2D Ti2C and g-C3N4 for efficient photocatalytic hydrogen production

2017 ◽  
Vol 5 (32) ◽  
pp. 16748-16756 ◽  
Author(s):  
Mengmeng Shao ◽  
Yangfan Shao ◽  
Jianwei Chai ◽  
Yuanju Qu ◽  
Mingyang Yang ◽  
...  

The novel photocatalyst Ti2C/g-C3N4 exhibits substantially enhanced water splitting activities due to its improved light absorbance, efficient separation of photoinduced carriers and large surface area.

2015 ◽  
Vol 3 (18) ◽  
pp. 10060-10068 ◽  
Author(s):  
Yijun Yang ◽  
Ye Yao ◽  
Liu He ◽  
Yeteng Zhong ◽  
Ying Ma ◽  
...  

Enhanced and stable photocatalytic activity upon water splitting was demonstrated in a series of TiO2–carbon hybrid nanomaterials, which were derived from oleylamine wrapped ultrathin TiO2 nanosheets.


Author(s):  
Franklin J. DiBartolomeo ◽  
Christine A. Trinkle

Rapid creation of devices with microscale features is a vital step in the commercialization of a wide variety of technologies, such as microfluidics, fuel cells and self-healing materials. The current standard for creating many of these microstructured devices utilizes the inexpensive, flexible material poly-dimethylsiloxane (PDMS) to replicate microstructured molds. This process is inexpensive and fast for small batches of devices, but lacks scalability and the ability to produce large surface-area materials. The novel fabrication process presented in this paper uses a cylindrical mold with microscale surface patterns to cure liquid PDMS prepolymer into continuous microstructured films. Results show that this process can create continuous sheets of micropatterned devices at a rate of 3.94 in2/sec (100 mm2/sec), almost an order of magnitude faster than soft lithography, while still retaining submicron patterning accuracy.


NANO ◽  
2020 ◽  
Vol 15 (10) ◽  
pp. 2050125
Author(s):  
Hui’e Wang

Here, a novel material consisting of black phosphorus (BP) and nickel-dimethylglyoxime nanorods was successfully prepared via a facile in situ calcination strategy, which possesses efficient catalytic activity for hydrogen production from water splitting. The reason for this phenomenon was explained by a series of characterization technologies such as SEM, TEM, XRD, UV–Vis, XPS and photoelectrochemical. We demonstrated that the fast e− transport channels were provided by the formed hollow structure of C@Ni-D nanorods, the highly exposed active sites on C@Ni-BP nanorods benefiting from the direct in situ growth of BP, the resulted synergetic effects of C@Ni-D-2 nanorods and BP achieved a better performance of photocatalytic hydrogen production from water splitting. The optimal hydrogen generation of C@Ni-BP-2 nanorods could reach up to 600[Formula: see text][Formula: see text]mol within 180[Formula: see text]min and the rate of hydrogen production did not decrease significantly after four repeated reaction cycles. This work may offer new direction in situ growth of novel catalysts for achieving highly efficient hydrogen production.


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