Amino group promoted photocatalytic hydrogen evolution activity observed in two copper(ii)-based layered complexes

2018 ◽  
Vol 47 (36) ◽  
pp. 12726-12733 ◽  
Author(s):  
Lei Li ◽  
Shuang Zhu ◽  
Rui Hao ◽  
Jia-Jun Wang ◽  
En-Cui Yang ◽  
...  

The amino group effect of the photocatalyst on the catalytic activity of water splitting was investigated under visible light irradiation. The hydrogen production rate of the amino group modified layered complex is almost double that without the amino group.

2015 ◽  
Vol 73 (7) ◽  
pp. 1667-1672 ◽  
Author(s):  
Yi-Lin Chen ◽  
Shang-Lien Lo ◽  
Hsiang-Ling Chang ◽  
Hsiao-Mei Yeh ◽  
Liping Sun ◽  
...  

An attractive and effective method for converting solar energy into clean and renewable hydrogen energy is photocatalytic water splitting over semiconductors. The study aimed at utilizing organic sacrificial agents in water, modeled by formic acid, in combination with visible light driven photocatalysts to produce hydrogen with high efficiencies. The photocatalytic hydrogen production of cadmium sulfide (CdS)/titanate nanotubes (TNTs) binary hybrid with specific CdS content was investigated. After visible light irradiation for 3 h, the hydrogen production rate of 25 wt% CdS/TNT achieved 179.35 μmol·h−1. Thanks to the two-step process, CdS/TNTs-WO3 ternary hybrid can better promote the efficiency of water splitting compared with CdS/TNTs binary hybrid. The hydrogen production of 25 wt% CdS/TNTs-WO3 achieved 212.68 μmol·h−1, under the same condition. Coating of platinum metal onto the WO3 could further promote the reaction. Results showed that 0.2 g 0.1 wt% Pt/WO3 + 0.2 g 25 wt% CdS/TNTs had the best hydrogen production rate of 428.43 μmol·h−1. The resultant materials were well characterized by high-resolution transmission electron microscope, X-ray diffraction, scanning electron microscopy, and UV-Vis spectra.


2015 ◽  
Vol 2015 ◽  
pp. 1-9 ◽  
Author(s):  
Melody Kimi ◽  
Leny Yuliati ◽  
Mustaffa Shamsuddin

Ga(0.1),Cu(x)-ZnS (x=0.01, 0.03, 0.05) photocatalysts were successfully synthesized by hydrothermal method. The synthesized Ga and Cu codoped ZnS photocatalysts showed photocatalytic property effective for hydrogen production from aqueous solution containing Na2SO3and Na2S as sacrificial reagent under visible light irradiation. The rate of hydrogen production was found to be strongly dependent on Cu doping content. The highest photocatalytic activity is observed for Ga(0.1),Cu(0.01)-ZnS with hydrogen production rate of 114 µmol/h. The addition of Ga as codoped increased the photocatalytic activity to 58 times as compared to single doped Cu-ZnS. The Ga and Cu codoped ZnS photocatalysts are also stable under long irradiation. The enhancement in the photocatalytic activity of Ga and Cu codoped photocatalyst can be attributed to the synergistic effect between Ga and Cu. The photocatalytic activity was greatly enhanced with the addition of 0.5 wt% Ru as cocatalyst with a hydrogen production rate of 744 µmol/h.


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.


2015 ◽  
Vol 1776 ◽  
pp. 7-12 ◽  
Author(s):  
Yu-Shiuan Lai ◽  
Tao-Wei Yang ◽  
Ming-Show Wong ◽  
Yi-Hao Pai ◽  
Su-Hua Chen

ABSTRACTTitanium oxide photoelectrodes have been used for water splitting for a few decades, but have low solar-to-hydrogen efficiencies. Perovskite halides (e.g., CH3NH3PbI3) have recently emerged as an efficient light absorber system. We try to combine the two materials to create new photoelectrodes to achieve a higher efficiency for hydrogen production. The photoelectrodes are investigated for water-splitting hydrogen production under Xe light irradiation by photoelectrochemical (PEC) reaction. Since perovskite halides are favorable light harvesters under UV and visible light irradiation, the composite films of titania and perovskite halide would achieve efficient water splitting. The hydrogen production rate using the composite films is higher than that using anatase TiO2 electrode. However, the composite films are not stable in water under light irradiation and the perovskite halide gradually decomposes into lead halide.


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.


2014 ◽  
Vol 50 (14) ◽  
pp. 1731-1734 ◽  
Author(s):  
Zheng Wang ◽  
Jungang Hou ◽  
Chao Yang ◽  
Shuqiang Jiao ◽  
Hongmin Zhu

Three-dimensional MoS2–CdS–γ-TaON hollow nanostructures as novel photocatalysts were firstly synthesized via a facile hydrothermal method and they exhibit a high photocatalytic hydrogen production rate without a noble metal.


2022 ◽  
Author(s):  
Xiyu Deng ◽  
Xinya Kuang ◽  
Jiyang Zeng ◽  
Baoye Zi ◽  
Yiwen Ma ◽  
...  

Abstract Photocatalytic water splitting is considered to be a feasible method to replace traditional energy. However, most of the catalysts have unsatisfactory performance. In this work, we used a hydrothermal process to grow Ag nanoparticles in situ on g-C3N4 nanosheets, and then a high performance catalyst (Ag- g-C3N4) under visible light was obtained. The Ag nanoparticles obtained by this process are amorphous and exhibit excellent catalytic activity. At the same time, the local plasmon resonance effect of Ag can effectively enhance the absorption intensity of visible light by the catalyst. The hydrogen production rate promote to 1035 μmol g-1h-1 after loaded 0.6 wt% of Ag under the visible light, which was 313 times higher than that of pure g-C3N4 (3.3μmol g-1h-1). This hydrogen production rate is higher than most previously reported catalysts which loaded with Ag or Pt. The excellent activity of Ag- g-C3N4 is benefited from the Ag nanoparticles and special interaction in each other. Through various analysis and characterization methods, it is shown that the synergy between Ag and g-C3N4 can effectively promote the separation of carriers and the transfer of electrons. Our work proves that Ag- g-C3N4 is a promising catalyst to make full use of solar energy.


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