Promoting photocatalytic hydrogen evolution over the perovskite oxide Pr0.5(Ba0.5Sr0.5)0.5Co0.8Fe0.2O3 by plasmon-induced hot electron injection

Nanoscale ◽  
2020 ◽  
Vol 12 (36) ◽  
pp. 18710-18720
Author(s):  
Zhishan Li ◽  
Qimeng Zhang ◽  
Jian-Gang Li ◽  
Huachuan Sun ◽  
Muk-Fung Yuen ◽  
...  

Exploration of highly efficient and stable photocatalysts for water splitting has attracted much attention.

2017 ◽  
Vol 5 (37) ◽  
pp. 19649-19655 ◽  
Author(s):  
Weiren Cheng ◽  
Hui Su ◽  
Fumin Tang ◽  
Wei Che ◽  
Yuanyuan Huang ◽  
...  

We report a newly designed Au cluster-nanoparticle/C3N4 photocatalyst for realizing efficient plasmonic hot-electron injection, which could effectively improve the hydrogen production rate by 6–20 times in the 400–900 nm range.


2019 ◽  
Vol 58 (31) ◽  
pp. 10713-10717 ◽  
Author(s):  
Shan‐Shan Wang ◽  
Long Jiao ◽  
Yunyang Qian ◽  
Wen‐Chao Hu ◽  
Gui‐Yin Xu ◽  
...  

2018 ◽  
Vol 9 (1) ◽  
Author(s):  
Ying-Chu Chen ◽  
Yu-Kuei Hsu ◽  
Radian Popescu ◽  
Dagmar Gerthsen ◽  
Yan-Gu Lin ◽  
...  

2021 ◽  
Author(s):  
Jiaquan Huang ◽  
Xinyi Zhao ◽  
Xunkun Huang ◽  
Wanzhen Liang

Utilizing plasmon-generated hot carriers to drive chemical reactions has currently become an active area of research in solar photocatalysis at the nanoscale. However, the mechanism underlying exact transfer and the generation dynamics of hot carriers, and the strategies used to further improve the quantum efficiency of the photocatalytic reaction still deserve a further look. In this work, we perform a nonadiabatic excited-state dynamics study to depict the correlation between the reaction rate of plasmon-driven water splitting (PDWS) and the sizes of gold particles, the incident light frequency and intensity, and the near-field's spatial distribution. Four model systems, \ce{H2O} and \ce{Au20}@\ce{H2O} separately interacting with the laser field and the near field generated by the Au nanoparticle (NP) with a few nanometers in size, have been investigated. Our simulated results clearly unveil the mechanism of PDWS and hot-electron injection in a Schottky-free junction: the electrons populated on the antibonding orbitals of \ce{H2O} are mandatory to drive the \ce{OH} bond breaking and the strong orbital hybridization between \ce{Au20} and \ce{H2O} creates the condition for direct electron injection. We further find that the linear dependence of the reaction rate and the field amplitude only holds at a relatively weak field and it breaks down when the second {\ce{OH}} bond begins to dissociate and field-induced water fragmenting at a very intensive field, and that with the guarantee of electron injection, the water splitting rate increases with the increase of NP's size. This study will be helpful for further improving the efficiency of the photochemical reactions involving the plasmon-generated hot carriers and expanding the applications of hot carriers in varieties of chemical reactions.


2019 ◽  
Vol 131 (31) ◽  
pp. 10823-10827 ◽  
Author(s):  
Shan‐Shan Wang ◽  
Long Jiao ◽  
Yunyang Qian ◽  
Wen‐Chao Hu ◽  
Gui‐Yin Xu ◽  
...  

2017 ◽  
Vol 219 ◽  
pp. 432-438 ◽  
Author(s):  
Bo-Tao Zhang ◽  
Jun Liu ◽  
Shizhong Yue ◽  
Yanguo Teng ◽  
Zhijie Wang ◽  
...  

2020 ◽  
Vol 56 (10) ◽  
pp. 1601-1604 ◽  
Author(s):  
Jinlong Wang ◽  
Guangcheng Ouyang ◽  
Yang Wang ◽  
Xiaolan Qiao ◽  
Wei-Shi Li ◽  
...  

Conjugated porous polymers based on 1,3,5-triazine and dibenzo[b,d]thiophene sulfone (DBTSO) units show excellent solar water splitting ability. A high hydrogen evolution rate of 16 287 μmol g−1 h−1 is achieved.


2020 ◽  
Vol 16 ◽  
Author(s):  
Yuxue Wei ◽  
Honglin Qin ◽  
Jinxin Deng ◽  
Xiaomeng Cheng ◽  
Mengdie Cai ◽  
...  

Introduction: Solar-driven photocatalytic hydrogen production from water splitting is one of the most promising solutions to satisfy the increasing demands of a rapidly developing society. CdS has emerged as a representative semiconductor photocatalyst due to its suitable band gap and band position. However, the poor stability and rapid charge recombination of CdS restrict its application for hydrogen production. The strategy of using a cocatalyst is typically recognized as an effective approach for improving the activity, stability, and selectivity of photocatalysts. In this review, recent developments in CdS cocatalysts for hydrogen production from water splitting under visible-light irradiation are summarized. In particular, the factors affecting the photocatalytic performance and new cocatalyst design, as well as the general classification of cocatalysts, are discussed, which includes a single cocatalyst containing noble-metal cocatalysts, non-noble metals, metal-complex cocatalysts, metal-free cocatalysts, and multi-cocatalysts. Finally, future opportunities and challenges with respect to the optimization and theoretical design of cocatalysts toward the CdS photocatalytic hydrogen evolution are described. Background: Photocatalytic hydrogen evolution from water splitting using photocatalyst semiconductors is one of the most promising solutions to satisfy the increasing demands of a rapidly developing society. CdS has emerged as a representative semiconductor photocatalyst due to its suitable band gap and band position. However, the poor stability and rapid charge recombination of CdS restrict its application for hydrogen production. The strategy of using a cocatalyst is typically recognized as an effective approach for improving the activity, stability, and selectivity of photocatalysts. Methods: This review summarizes the recent developments in CdS cocatalysts for hydrogen production from water splitting under visible-light irradiation. Results: Recent developments in CdS cocatalysts for hydrogen production from water splitting under visible-light irradiation are summarized. The factors affecting the photocatalytic performance and new cocatalyst design, as well as the general classification of cocatalysts, are discussed, which includes a single cocatalyst containing noble-metal cocatalysts, non-noble metals, metal-complex cocatalysts, metal-free cocatalysts, and multi-cocatalysts. Finally, future opportunities and challenges with respect to the optimization and theoretical design of cocatalysts toward the CdS photocatalytic hydrogen evolution are described. Conclusion: The state-of-the-art CdS for producing hydrogen from photocatalytic water splitting under visible light is discussed. The future opportunities and challenges with respect to the optimization and theoretical design of cocatalysts toward the CdS photocatalytic hydrogen evolution are also described.


2020 ◽  
Vol 131 (3) ◽  
pp. 456-459
Author(s):  
S. S. Abukari ◽  
R. Musah ◽  
M. Amekpewu ◽  
S. Y. Mensah ◽  
N. G. Mensah ◽  
...  

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