Gold nanoparticles embedded in Ta2O5/Ta3N5 as active visible-light plasmonic photocatalysts for solar hydrogen evolution

2014 ◽  
Vol 2 (36) ◽  
pp. 14927-14939 ◽  
Author(s):  
Yujing Luo ◽  
Xiaoming Liu ◽  
Xinghua Tang ◽  
Yan Luo ◽  
Qianyao Zeng ◽  
...  

A Nano Au/Ta2O5 composite shows a new recreating photocatalytic activity for hydrogen evolution from water in response to visible light irradiation.

2021 ◽  
Vol 50 (9) ◽  
pp. 3253-3260 ◽  
Author(s):  
Shan Zhao ◽  
Junbiao Wu ◽  
Yan Xu ◽  
Xia Zhang ◽  
Yide Han ◽  
...  

CdS/Ag2S/g-C3N4 ternary composites showed excellent photocatalytic performance toward H2 evolution. Their improved photocatalytic activity could be attributed not only to the synergic effect, but also to the introduction of Ag2S.


2014 ◽  
Vol 1024 ◽  
pp. 368-371 ◽  
Author(s):  
Melody Kimi ◽  
Leny Yuliati ◽  
Mustaffa Shamsuddin

In and Ag co-doped ZnS photocatalysts were successfully prepared by hydrothermal method to extend the light absorption of ZnS to the visible light region. The concentration of In was constant while for Ag was varied to optimize the photocatalytic activity. The In and Ag co-doped ZnS photocatalysts showed smaller band gap energy compared to single doped In (0.1)-ZnS and undoped ZnS. The photocatalytic activity of In and Ag co-doped ZnS photocatalysts was evaluated from the amount of hydrogen produced. The hydrogen evolution rate from aqueous solution containing Na2SO3 and Na2S as sacrificial reagent under visible light irradiation obtained from In and Ag co-doped ZnS is higher compared to the single doped In (0.1)-ZnS when optimum amount of Ag dopant was added. The highest photocatalytic activity is observed for In (0.1),Ag (0.01)-ZnS with hydrogen production rate of 26.82 μmol/h. The higher performance of this photocatalyst is ascribed to the extended visible light absorption, efficient charge separation as well as improved electron transfer associated with synergistic effect of appropriate amount of In and Ag co-doped ZnS.


RSC Advances ◽  
2015 ◽  
Vol 5 (124) ◽  
pp. 102700-102706 ◽  
Author(s):  
Zhijun Huang ◽  
Fengbo Li ◽  
Bingfeng Chen ◽  
Guoqing Yuan

Porous and low-defected g-C3N4 nanotubes with high SBET and optimized optical and electronic properties exhibit enhanced photocatalytic activity.


2020 ◽  
Vol 7 (9) ◽  
pp. 2809-2822
Author(s):  
Dan You ◽  
Dajun Shi ◽  
Qingrong Cheng ◽  
Yanling Chen ◽  
Zhiquan Pan

CdS@Mn-ZIF-67 heterojunction photocatalyst exhibited excellent photocatalytic activity for TC degradation and hydrogen evolution under visible light irradiation and are more effective than the single Mn-ZIF-67 or the hollow CdS nanospheres.


2015 ◽  
Vol 659 ◽  
pp. 231-236 ◽  
Author(s):  
Husni Husin ◽  
Mahidin ◽  
Zuhra ◽  
Fikri Hasfita ◽  
Yunardi

Lanthanum and carbon co-doped sodium tantalum oxide, La-C-NaTaO3, are prepared by incorporating lanthanum and carbon into NaTaO3 cluster via a sol-gel technique using a sucrose as carbon source. The La-C-NaTaO3 prepared sample is calcined at a temperature of 700 °C. Effects of carbon contents on the crystal, shape, optical absorption response and activity of hydrogen production of the sample are evaluated. The crystal of La-C-NaTaO3 is characterized by XRD analysis. The results show that the XRD pattern of the La C co-doped NaTaO3 is found to be crystalline phase with monoclinic structure. From the analysis of SEM images, the particle size of the prepared powder is about 40-200 nm. The optical response is examined by diffuse reflectance spectra (DRS). It is depicted that the absorption edge of La-C-NaTaO3 crystalline shift to higher wavelength. The extension to the visible light absorption edge became drastic with increasing carbon content in the sample. The photocatalytic activity of La-C-NaTaO3 is examined from water-methanol aqueous solution under visible light irradiation. It is found that the photocatalytic activity of La-C-NaTaO3 depend strongly on the doping content of C, and sample La-C-NaTaO3 shows the highest photocatalytic activity for the water reduction. The optimum amounts of carbon to maximize the hydrogen evolution rate is to be 2.5 mol %. The La-C-NaTaO3 catalyst has high activity of H2 evolution of 40.0 [μmol h-1] and long time stability under visible-light irradiation, suggesting a promising utilization of such photocatalyst. La C co-doped NaTaO3 photocatalyst can be developed further in order to produce hydrogen as a green energy.


2015 ◽  
Vol 8 (9) ◽  
pp. 2668-2676 ◽  
Author(s):  
Zijun Sun ◽  
Huafei Zheng ◽  
Jingshi Li ◽  
Pingwu Du

A hybrid structure constructed by uniformly anchoring crystalline Ni2P cocatalyst on 1D CdS nanorods exhibits extraordinarily efficient photocatalytic activity for H2 evolution in water (rate of 1,200 μmol h−1 mg−1 and TOF of 36,400 h−1 per mol Ni2P) under visible light irradiation.


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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