Integrating Catalysis of Methane Decomposition and Electrocatalytic Hydrogen Evolution with Ni/CeO 2 for Improved Hydrogen Production Efficiency

ChemSusChem ◽  
2019 ◽  
Vol 12 (5) ◽  
pp. 1000-1010 ◽  
Author(s):  
Cai Zhang ◽  
Wei Zhang ◽  
Nicholas E. Drewett ◽  
Xiyang Wang ◽  
Seung Jo Yoo ◽  
...  
Nanoscale ◽  
2019 ◽  
Vol 11 (17) ◽  
pp. 8138-8149 ◽  
Author(s):  
Tongming Su ◽  
Zachary D. Hood ◽  
Michael Naguib ◽  
Lei Bai ◽  
Si Luo ◽  
...  

The separation of photogenerated carriers and photocatalytic hydrogen production efficiency was greatly enhanced by the 2D/2D heterojunction of Ti3C2/g-C3N4.


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.


Author(s):  
Parul Verma ◽  
Ashish Singh ◽  
Faruk Ahamed Rahimi ◽  
Tapas Kumar Maji

Colocalization of essential molecular components in the solvated soft supramolecular assembly towards realizing visible-light-driven hydrogen evolution would be an exciting approach for sustainable energy by generating clean solar fuel. In...


2006 ◽  
Vol 3 (3) ◽  
pp. 346-350 ◽  
Author(s):  
Antonio Carlos Caetano de Souza ◽  
José Luz-Silveira ◽  
Maria Isabel Sosa

Steam reforming is the most usual method of hydrogen production due to its high production efficiency and technological maturity. The use of ethanol for this purpose is an interesting option because it is a renewable and environmentally friendly fuel. The objective of this article is to present the physical-chemical, thermodynamic, and exergetic analysis of a steam reformer of ethanol, in order to produce 0.7Nm3∕h of hydrogen as feedstock of a 1kW PEMFC. The global reaction of ethanol is considered. Superheated ethanol reacts with steam at high temperatures producing hydrogen and carbon dioxide, depending strongly on the thermodynamic conditions of reforming, as well as on the technical features of the reformer system and catalysts. The thermodynamic analysis shows the feasibility of this reaction in temperatures about 206°C. Below this temperature, the reaction trends to the reactants. The advance degree increases with temperature and decreases with pressure. Optimal temperatures range between 600 and 700°C. However, when the temperature attains 700°C, the reaction stability occurs, that is, the hydrogen production attains the limit. For temperatures above 700°C, the heat use is very high, involving high costs of production due to the higher volume of fuel or electricity used. The optimal pressure is 1atm., e.g., at atmospheric pressure. The exergetic analysis shows that the lower irreversibility is attained for lower pressures. However, the temperature changes do not affect significantly the irreversibilities. This analysis shows that the best thermodynamic conditions for steam reforming of ethanol are the same conditions suggested in the physical-chemical analysis.


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