Potential Co-catalyst application of novel M3P2 (M=Zn, Cd) in photocatalytic hydrogen evolution reaction from water splitting

Author(s):  
Elham Karamian ◽  
Shahram Sharifnia
2020 ◽  
Vol 400 ◽  
pp. 125931 ◽  
Author(s):  
Deng Ding ◽  
Zhuo Jiang ◽  
Dong Ji ◽  
Myung Nosang Vincent ◽  
Ling Zan

2006 ◽  
Vol 974 ◽  
Author(s):  
Jaturong Jitputti ◽  
Sorapong Pavasupree ◽  
Yoshikazu Suzuki ◽  
Susumu Yoshikawa

ABSTRACTTantalate and titanate photocatalysts were prepared by solid-state reaction at 1273 K using various ratios of SrCO3, Ta2O5, and TiO2 as starting materials. The prepared solid photocatalysts were characterized using XRD and SEM analysis. These prepared tantalate and titanate photocatalysts showed high photocatalytic H2 evolution activity by water splitting without co-catalyst loading. The highest H2 evolution rate of prepared photocatalysts was found to be 138 μmolh−1 with the starting materials ratio of 2/0.5/1.5 (Sr/Ta/Ti; mol). Furthermore, this photocatalyst showed photocatalytic activity for H2 evolution from distilled water.


Catalysts ◽  
2021 ◽  
Vol 11 (4) ◽  
pp. 417
Author(s):  
Pablo Ayala ◽  
Ariane Giesriegl ◽  
Sreejith P. Nandan ◽  
Stephen Nagaraju Myakala ◽  
Peter Wobrauschek ◽  
...  

Achieving efficient photocatalytic water splitting remains one of the most vital challenges in the photocatalysis field, as the performance of contemporary heterogeneous catalysts is still limited by their insufficient activity and low predictability. To address this challenge, this work takes inspiration from the concept of heterogeneous single-metal-site catalysts (HSMSCs) and follows the idea of site-isolation, aiming towards single-site co-catalyst species and a higher atom-utilization efficiency. We synthesized a set of photocatalysts through an adsorption-limited wet impregnation process using bare and phosphate-modified TiO2 as model supports and earth-abundant metals (Cu and Ni) with various loadings (0.008–5 wt.%) as co-catalyst species. The catalysts are characterized by TXRF for the determination of the real co-catalyst loadings, UV-vis and FTIR spectroscopes for semi-quantitative analysis of the metal state and binding modes to the substrate, and HRTEM for resolving the morphology of the sample’s surface. All samples were then evaluated towards the photocatalytic hydrogen evolution reaction (HER). We show that much higher turnover frequencies (TOFs) are obtained for both Cu- and Ni-based systems when lower co-catalyst loadings are used, which indicates an improved atom-utilization efficiency that reaches performances comparable to the noble Au co-catalyst. We also introduce a structural model to explain the observed TOF trends, which confirms that both earth-abundant systems undergo a strong structural reconstruction upon site-isolation towards smaller, perhaps even single-site-like species.


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.


2021 ◽  
Author(s):  
Zihao Liu ◽  
Shifeng Li ◽  
Fangfang Wang ◽  
Mingxia Li ◽  
Yonghong Ni

FeNi-layered double hydroxide (LDH) is thought to be an excellent electrocatalyst for oxygen evolution reaction (OER), but it always shows extremely poor electrocatalytic activity toward hydrogen evolution reaction (HER) in...


Author(s):  
Adem Sarilmaz ◽  
Eminegul Genc ◽  
Emre Aslan ◽  
Abdurrahman Ozen ◽  
Gizem Yanalak ◽  
...  

2021 ◽  
Vol 12 (1) ◽  
Author(s):  
Panlong Zhai ◽  
Mingyue Xia ◽  
Yunzhen Wu ◽  
Guanghui Zhang ◽  
Junfeng Gao ◽  
...  

AbstractRational design of single atom catalyst is critical for efficient sustainable energy conversion. However, the atomic-level control of active sites is essential for electrocatalytic materials in alkaline electrolyte. Moreover, well-defined surface structures lead to in-depth understanding of catalytic mechanisms. Herein, we report a single-atomic-site ruthenium stabilized on defective nickel-iron layered double hydroxide nanosheets (Ru1/D-NiFe LDH). Under precise regulation of local coordination environments of catalytically active sites and the existence of the defects, Ru1/D-NiFe LDH delivers an ultralow overpotential of 18 mV at 10 mA cm−2 for hydrogen evolution reaction, surpassing the commercial Pt/C catalyst. Density functional theory calculations reveal that Ru1/D-NiFe LDH optimizes the adsorption energies of intermediates for hydrogen evolution reaction and promotes the O–O coupling at a Ru–O active site for oxygen evolution reaction. The Ru1/D-NiFe LDH as an ideal model reveals superior water splitting performance with potential for the development of promising water-alkali electrocatalysts.


2016 ◽  
Vol 4 (17) ◽  
pp. 6577-6584 ◽  
Author(s):  
Huihui Li ◽  
Liulun Jie ◽  
Jiannan Pan ◽  
Longtian Kang ◽  
Jiannian Yao

Direct photocatalytic hydrogen evolution of an organic small-molecule nanostructure was achieved by constructing a heterostructure of hydrate rubrene/ZnP nanosheets.


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