Structural features of p-type semiconducting NiO as a co-catalyst for photocatalytic water splitting

2010 ◽  
Vol 272 (1) ◽  
pp. 1-8 ◽  
Author(s):  
Che-Chia Hu ◽  
Hsisheng Teng
Nanoscale ◽  
2018 ◽  
Vol 10 (30) ◽  
pp. 14448-14454 ◽  
Author(s):  
Cheng Shi ◽  
Min Zhang ◽  
Xinxin Hang ◽  
Yanfeng Bi ◽  
Liangliang Huang ◽  
...  

A high-nuclearity Cd24 cluster built from Cd4-thiacalix[4]arene SBUs and in situ generated peroxyphosphate PO53− exhibited significant photocatalytic water splitting activity in absence of a co-catalyst.


2019 ◽  
Vol 7 (12) ◽  
pp. 6708-6719 ◽  
Author(s):  
Kyoung-Won Park ◽  
Alexie M. Kolpak

Overall photocatalytic water splitting with a high efficiency has recently been observed for CoO nanoparticle suspensions in the absence of an applied bias or co-catalyst. This study clarifies the mechanism of spontaneous overall water splitting with the prominent efficiency observed on the CoO nanoparticle.


2015 ◽  
Vol 1738 ◽  
Author(s):  
Jyothirmayee Aravind.S.S ◽  
Kandalam Ramanujachary ◽  
Timothy D. Vaden ◽  
Amos Mugweru

ABSTRACTSemiconductor photocatalysis has emerged as an interesting area of research since the discovery of Honda-Fujishima effect. In this study, TiO2/MoO2/graphene composites have been prepared by a solar radiation-assisted co-reduction method, wherein ammonium tetrathiomolybdate salt and graphite oxide are reduced to MoO2 and graphene respectively along with TiO2. The method involved the utilization of focused pulses of natural sunlight using a simple convex lens, thereby eliminating the need for harmful reducing agents. The compound was characterized by XRD and SEM for phase identification and morphology. The TiO2/MoO2/graphene composite exhibits superior photocatalytic water splitting activity without using a co-catalyst. In addition, we demonstrate the electrocatalytic hydrogen production using this earth abundant catalyst, which shows high current density (60 mA/cm2) and low Tafel slope (47 mV/dec). The hydrogen evolved during photocatalysis was detected by gas chromatography.


2020 ◽  
Vol 8 (39) ◽  
pp. 20493-20502
Author(s):  
Stefano Falletta ◽  
Patrick Gono ◽  
Zhendong Guo ◽  
Stavroula Kampouri ◽  
Kyriakos C. Stylianou ◽  
...  

Theoretical methodologies for the band alignment at MOF/co-catalyst/water systems revealing the electronic and atomistic mechanisms underlying their photocatalytic performance.


Author(s):  
Syed Saad Ahsan ◽  
David Erickson

In this work, we present a novel microfluidic photocatalytic water-splitting reactor. Optofluidics offers advantages over conventional reactors in terms of improved photon transfer efficiency and mass transfer efficiency and are therefore the ideal platform for photocatalytic reactions. Our device is a planar optofluidic device which we used to study the kinetics of Platinum-Impregnated Titanium Oxide as the oxygen and hydrogen producing photocatalyst redox mediated by Iodide/Iodate species. We deposit our catalysts via a sol-gel method while the platinum co-catalyst is added by wet impregnation via reduction in Sodium Borohydride. The reactions are performed under a 100W Hg lamp and reaction rates are inferred by measuring the depletion of the two Iodine species via UV-vis absorption spectrophotometry. Our results indicate that reaction rates and efficiencies can be enhanced by using an optofluidic platform as opposed to the conventional slurry reactor used in previous experiments for this class of reaction. We believe that the micro-optofluidic platform of our device offers the benefit of measuring the kinetic properties of these class of reactions quickly and cheaply for the goals of further optimization.


Nanomaterials ◽  
2021 ◽  
Vol 11 (12) ◽  
pp. 3341
Author(s):  
Yuan Guo ◽  
Wanqing Liu ◽  
Wei Duan ◽  
Siyu Wang ◽  
Liqun Jia ◽  
...  

Photocatalytic water splitting for hydrogen generation is a significant pathway for sustainable energy conversion and production. The photocatalysts with a Z-scheme water splitting charge transfer pathway is superior due to the good separation and migration ability of photoexcited charge carriers. Herein, Co3O4/g-C3N4 photocatalysts with Z-scheme charge transfer pathway were successfully constructed by an electrostatic interaction-annealing method. The as-prepared Co3O4/g-C3N4 ultra-thin nanosheets were tested and analyzed by XRD, EA, ICP, SEM, TEM, AFM, XPS, UV-Vis DRS, PL and photoelectrochemical measurements. Moreover, the influences of fabrication parameters on performance of Co3O4/g-C3N4 catalysts were investigated, and 0.5% Co3O4/g-C3N4 exhibited the optimal activity. Based on the characterization and catalytic performance, the Z-scheme charge transfer pathway of Co3O4/g-C3N4 was established and put forward. To further improve the catalytic performance of Co3O4/g-C3N4, 0.5% Pt was added as a co-catalyst. The obtained Pt/0.5% Co3O4/g-C3N4 was recyclable and remained the original catalytic water splitting performance within 20 h. The modification of Co3O4 and Pt improved the separation and migration of e− and h+, and induced the increased hydrogen evolution rate of g-C3N4.


MRS Advances ◽  
2016 ◽  
Vol 1 (59) ◽  
pp. 3923-3927
Author(s):  
Philip Kalisman ◽  
Lilac Amirav

ABSTRACTThe production of hydrogen by photocatalytic water splitting is a potentially clean and renewable source for hydrogen fuel. Cadmium chalcogenides are attractive photocatalysts because they have the potential to convert water into hydrogen and oxygen using photons in the visible spectrum. Cadmium sulfide rods with embedded cadmium selenide quantum dots (CdSe@CdS) are particularly attractive because of their high molar absorptivity in the UV-blue spectral region, and their energy bands can be tuned; however, two crucial drawbacks hinder the implementation of these materials in wide spread use: poor charge transfer and photochemical instability.Utilizing photochemical deposition of co-catalysts onto CdSe@CdS substrates we can address each of these weaknesses. We report how novel co-catalyst morphologies can greatly increase efficiency for the water reduction half-reaction. We also report photostability for CdSe@CdS under high intensity 455nm light (a wavelength at which photocatalytic water splitting by CdSe@CdS is possible) by growing metal oxide co-catalysts on the surface of our rods.


2018 ◽  
Vol 8 (15) ◽  
pp. 3883-3893 ◽  
Author(s):  
Yajun Zou ◽  
Jian-Wen Shi ◽  
Dandan Ma ◽  
Zhaoyang Fan ◽  
Chi He ◽  
...  

Cu2MoS4 was employed as a promising non-noble metal co-catalyst to couple with g-C3N4 for highly efficient water splitting.


2020 ◽  
Vol 8 (40) ◽  
pp. 20963-20969 ◽  
Author(s):  
Wei Chen ◽  
Guo-Bo Huang ◽  
Hao Song ◽  
Jian Zhang

An efficient charge transfer channel for improving the photocatalytic water splitting activity and durability of CdS without sacrificial agents.


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