Band gap-tunable (CuIn)xZn2(1−x)S2 solid solutions: preparation and efficient photocatalytic hydrogen production from water under visible light without noble metals

2012 ◽  
Vol 22 (45) ◽  
pp. 23929 ◽  
Author(s):  
Miao Xu ◽  
Jiantao Zai ◽  
Yanping Yuan ◽  
Xuefeng Qian
2019 ◽  
Vol 9 (13) ◽  
pp. 2741 ◽  
Author(s):  
Vincenzo Vaiano ◽  
Giuseppina Iervolino

Cu-doped ZnO photocatalysts at different Cu loadings were prepared by a precipitation method. The presence of Cu in the ZnO crystal lattice led to significant enhancement in photocatalytic activity for H2 production from an aqueous glycerol solution under visible light irradiation. The best Cu loading was found to be 1.08 mol %, which allowed achieving hydrogen production equal to 2600 μmol/L with an aqueous glycerol solution at 5 wt % initial concentration, the photocatalyst dosage equal to 1.5 g/L, and at the spontaneous pH of the solution (pH = 6). The hydrogen production rate was increased to about 4770 μmol/L by increasing the initial glycerol concentration up to 10 wt %. The obtained results evidenced that the optimized Cu-doped ZnO could be considered a suitable visible-light-active photocatalyst to be used in photocatalytic hydrogen production without the presence of noble metals in sample formulation.


Nanoscale ◽  
2015 ◽  
Vol 7 (19) ◽  
pp. 8955-8961 ◽  
Author(s):  
Tao Yang ◽  
Xiwang Chang ◽  
Junhong Chen ◽  
Kuo-Chih Chou ◽  
Xinmei Hou

B-doped 3C-SiC nanowires with a finned microstructure have been synthesized. Due to the smaller band gap, the finned microstructure, and the single crystalline nature, the B-doped 3C-SiC nanowires demonstrate efficient activity as high as 108.4 μmol h−1g−1for H2production.


2014 ◽  
Vol 925 ◽  
pp. 200-204
Author(s):  
Leny Yuliati ◽  
Melody Kimi ◽  
Mustaffa Shamsuddin

Zinc sulfide (ZnS) has been reported to act as a photocatalyts to reduce water to hydrogen. However, ZnS could not work under visible light irradiation due to its large band gap energy. In order to improve the performance of ZnS, Ga and Sn were doped to ZnS. The series of Ga (0.1),Sn (x)-ZnS with various amounts of Sn (x) was prepared by hydrothermal method. XRD patterns suggested that the addition of Ga might reduce the crystallinity of ZnS, suggesting that Ga might inhibit the crystal growth or agglomeration of ZnS. On the other hand addition of Sn did not much affect the structure of the Ga (0.1)-ZnS. The DR UU-visible spectra confirmed the red shift of the absorption edge with the addition of Ga due to the reduced band gap energy, while the addition of Sn did not much shift the absorption edge of the Ga (0.1)-ZnS to longer wavelength. FESEM images showed that all the prepared samples have sphere-shaped particles and no remarkable change was observed with the addition of Ga or Sn. The photocatalytic hydrogen production from water was carried out at room temperature in the presence of sacrificial agent under visible light irradiation. While ZnS did not show activity under visible light, all the prepared Ga (0.1)-ZnS and Ga (0.1),Sn (x)-ZnS samples exhibited photocatalytic activity for hydrogen production. The highest hydrogen production was achieved on Ga (0.1),Sn (0.01)-ZnS, which activity was ca. three times higher than that of the single doped Ga (0.1)-ZnS. This study clearly showed that Sn acted as a good co-dopant to increase the photocatalytic activity of Ga (0.1)-ZnS for hydrogen production from water under visible light irradiation.


2010 ◽  
Vol 49 (15) ◽  
pp. 6854-6861 ◽  
Author(s):  
J. A. Villoria ◽  
Rufino M. Navarro Yerga ◽  
S. M. Al-Zahrani ◽  
Jose Luis G. Fierro

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.


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