Size effect of Pt co-catalyst on photocatalytic efficiency of g-C3N4 for hydrogen evolution
By Yunqing Zhu, T. Wang, Tao Xu, Yingxuan Li, Chuanyi Wang. Applications of Surface Science, 2019
209 citations recorded by the source corpus.
Abstract Graphitic carbon nitride (g-C3N4) with Pt co-catalyst was synthesized by in-situ photoreduction and used as a visible light photocatalyst. The size of Pt co-catalyst can be controlled form single atoms to nano-clusters by the induced amount of Pt precursor. The results indicated that compared with nano-clusters, the Pt0.1-CN (with 0.1 wt% Pt loading amount) which is characterized as single-atom Pt exhibits a pronounced photocatalytic hydrogen evolution capability. For Pt0.1-CN with single-atom Pt as co-catalyst, the H2 generation is up to 473.82 µmol mg−1pt under visible light irradiation (λ > 420 nm). The enhanced photocatalytic performance is mainly attributed to the synergistic effect of high light adsorption efficiency, effective charge separation, and high dispersed active sites of Pt atoms. The results of this work highlighted that loading g-C3N4 with Pt single atoms will achieve a maximum utilization efficiency of Pt atoms and an improvement photocatalytic performance.
Subfields: Electrical and Electronic Engineering, Materials Chemistry, Renewable Energy, Sustainability and the Environment
View Paper: https://www.semanticscholar.org/paper/46e4232c1178e02eb360367a669ad3b2d52b001e
How researchers see this paper
The researchers whose trusted networks rank it highest, strongest advocate first. Every researcher gets a different order.
In Materials Chemistry
In Renewable Energy, Sustainability and the Environment
Citations in the corpus
- Size effect, mutual inhibition and oxidation mechanism of the catalytic removal of a toluene and acetone mixture over TiO2 nanosheet-supported Pt nanocatalysts (2020, background): “In recent years, many researchers have performed many studies to investigate the size effect of Pt in the field of electrocatalysis [25–30], photocatalysis [31,32], and dehydrogenation/ hydrogenation [33–35].”