Photocatalytic oxidation of arylalcohols to aromatic aldehydes promoted by hydroxyl radicals over a CoP/CdS photocatalyst in water with hydrogen evolution

2018 ◽  
Vol 8 (10) ◽  
pp. 2540-2545 ◽  
Author(s):  
Yong Xu ◽  
Ling-Zhen Zeng ◽  
Zi-Cheng Fu ◽  
Cong Li ◽  
Zhi Yang ◽  
...  

Hydroxyl free radicals generated by visible-light-catalyzed water splitting over CoP/CdS drive the oxidation of arylalcohols with hydrogen evolution.

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.


2017 ◽  
Vol 46 (34) ◽  
pp. 11335-11343 ◽  
Author(s):  
Jiali Lv ◽  
Jinfeng Zhang ◽  
Kai Dai ◽  
Changhao Liang ◽  
Guangping Zhu ◽  
...  

Sustainable photocatalytic hydrogen evolution (PHE) of water splitting has been utilized to solve the serious environmental pollution and energy shortage problems over the last decade.


RSC Advances ◽  
2016 ◽  
Vol 6 (29) ◽  
pp. 24361-24365 ◽  
Author(s):  
Weiming Wu ◽  
Xianyang Yue ◽  
Xiao-Yuan Wu ◽  
Can-Zhong Lu

Nanocrystalline Ni12P5 was synthesized by a simple hydrothermal method. It showed high catalytic activity (10 760 μmol h−1 g−1, TOF = 9.3 h−1) and good stability (15 h) for the hydrogen evolution from water under visible light irradiation.


2016 ◽  
Vol 51 (14) ◽  
pp. 6987-6997 ◽  
Author(s):  
Tianyu Liu ◽  
Wei Chen ◽  
Ting Huang ◽  
Guorong Duan ◽  
Xujie Yang ◽  
...  

2017 ◽  
Vol 7 (2) ◽  
pp. 452-458 ◽  
Author(s):  
Mei Zhang ◽  
Yanyan Duan ◽  
Hanzhong Jia ◽  
Fu Wang ◽  
Lan Wang ◽  
...  

Schematic illustration of modified g-C3N4for visible-light photocatalytic water splitting to hydrogen. The CN-DPT shows remarkably enhanced hydrogen evolution performance.


2018 ◽  
Author(s):  
Wolfgang Domcke ◽  
Johannes Ehrmaier ◽  
Andrzej L. Sobolewski

The photocatalytic splitting of water into molecular hydrogen and molecular oxygen with sunlight is the dream reaction for solar energy conversion. Since decades, transition-metal-oxide semiconductors and supramolecular organometallic structures have been extensively explored as photocatalysts for solar water splitting. More recently, polymeric carbon nitride materials consisting of triazine or heptazine building blocks have attracted considerable attention as hydrogen-evolution photocatalysts. The mechanism of hydrogen evolution with polymeric carbon nitrides is discussed throughout the current literature in terms of the familiar concepts developed for photoelectrochemical water splitting with semiconductors since the 1970s. We discuss in this perspective an alternative mechanistic paradigm for photoinduced water splitting with carbon nitrides, which focusses on the specific features of the photochemistry of aromatic N-heterocycles in aqueous environments. It is shown that a water molecule which is hydrogen-bonded to an N-heterocycle can be decomposed into hydrogen and hydroxyl radicals by two simple sequential photochemical reactions. This concept is illustrated by first-principles calculations of excited-state reaction paths and their energy profiles for hydrogen-bonded complexes of pyridine, triazine and heptazine with a water molecule. It is shown that the excited-state hydrogen-transfer and hydrogen-detachment reactions are essentially barrierless, in sharp contrast to water oxidation in the electronic ground state, where high barriers prevail. We also discuss in some detail the products of possible reactions of the highly reactive hydroxyl radicals with the chromophores. We hypothesize that the challenge of efficient solar hydrogen generation with carbon-nitride materials is less the decomposition of water as such, but rather the controlled recombination of the photogenerated radicals to the closed-shell products H2 and H2O2.


2019 ◽  
Vol 7 (45) ◽  
pp. 25908-25914 ◽  
Author(s):  
Yunxiong Zeng ◽  
Yingchun Xia ◽  
Wenjia Song ◽  
Shenglian Luo

Solar-driven hydrogen evolution reaction (HER) via water splitting is an attractive technology to address the growing demand for clean fuels.


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