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  5. Black Phosphorus/Platinum Heterostructure: A Highly Efficient Photocatalyst for Solar‐Driven Chemical Reactions

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Article
en
2018

Black Phosphorus/Platinum Heterostructure: A Highly Efficient Photocatalyst for Solar‐Driven Chemical Reactions

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en
2018
Vol 30 (40)
Vol. 30
DOI: 10.1002/adma.201803641

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Paul Kim Ho Chu
Paul Kim Ho Chu

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Licheng Bai
Xin Wang
Shaobin Tang
+9 more

Abstract

A 2D black phosphorus/platinum heterostructure (Pt/BP) is developed as a highly efficient photocatalyst for solar-driven chemical reactions. The heterostructure, synthesized by depositing BP nanosheets with ultrasmall (≈1.1 nm) Pt nanoparticles, shows strong Pt-P interactions and excellent stability. The Pt/BP heterostructure exhibits obvious P-type semiconducting characteristics and efficient absorption of solar energy extending into the infrared region. Furthermore, during light illumination, accelerated charge separation is observed from Pt/BP as manifested by the ultrafast electron migration (0.11 ps) detected by a femtosecond pump-probe microscopic optical system as well as efficient electron accumulation on Pt revealed by in situ X-ray photoelectron spectroscopy. These unique properties result in remarkable performance of Pt/BP in typical hydrogenation and oxidation reactions under simulated solar light illumination, and its efficiency is much higher than that of other common Pt catalysts and even much superior to that of conventional thermal catalysis. The 2D Pt/BP heterostructure has enormous potential in photochemical reactions involving solar light and the results of this study provide insights into the design of next-generation high-efficiency photocatalysts.

How to cite this publication

Licheng Bai, Xin Wang, Shaobin Tang, Yihong Kang, Jiahong Wang, Ying Yu, Zhang‐Kai Zhou, Chao Ma, Xue Zhang, Jun Jiang, Paul Kim Ho Chu, Xue‐Feng Yu (2018). Black Phosphorus/Platinum Heterostructure: A Highly Efficient Photocatalyst for Solar‐Driven Chemical Reactions. , 30(40), DOI: https://doi.org/10.1002/adma.201803641.

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Publication Details

Type

Article

Year

2018

Authors

12

Datasets

0

Total Files

0

Language

en

DOI

https://doi.org/10.1002/adma.201803641

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