Inkjet Printing of Functionalized TiO2 Catalytic Layer for Water Oxidation Reaction

2015 ◽  
Vol 1776 ◽  
pp. 13-17 ◽  
Author(s):  
Y. Treekamol ◽  
D. Lehmann ◽  
M. Schieda ◽  
I. Herrmann-Geppert ◽  
T. Klassen

ABSTRACTOur investigations with silane-modified TiO2 have revealed a beneficial effect of functionalization on the photoelectrochemical performance on spin-coated electrodes. However, in order to produce large area photoelectrodes, a more scalable manufacturing technology is required. Inkjet printing can fulfil this role and furthermore allow a finer control over coating morphologies. In this work, inkjet-printed photoelectrodes were prepared with silane-functionalized TiO2 nanoparticles, and investigated as electrodes for photoactivated water splitting. The catalyst layers, having thickness around 700 nm, were printed on FTO-coated glass supports, from cellulose stabilized dispersions. For comparison, electrodes of similar thicknesses were also prepared by spin-coating. After removing the stabilizer at 300 °C under air atmosphere, the electrodes were characterized in photoelectrochemical cells containing 0.5 M H2SO4 as electrolyte and a platinum ring as counter electrode. Under simulated sunlight, the best photocurrent densities for the oxygen evolution reaction were obtained for the inkjet-printed electrodes prepared with functionalized particles (up to 0.26 mA cm-2 at 1.2 V against the standard hydrogen electrode (SHE), compared to 0.18 mA cm-2 for spin coated). Microscopy of the printed electrodes shows structurally homogenous coatings with evenly distributed roughness. Under continuous illumination at 0.7 V (SHE), the electrodes showed no significant drop in photocurrent within five hours.

Energies ◽  
2020 ◽  
Vol 13 (4) ◽  
pp. 974 ◽  
Author(s):  
Swetha S. M. Bhat ◽  
Sang Eon Jun ◽  
Sol A Lee ◽  
Tae Hyung Lee ◽  
Ho Won Jang

Photoelectrochemical water splitting is considered as a long-term solution for the ever-increasing energy demands. Various strategies have been employed to improve the traditional TiO2 photoanode. In this study, TiO2 nanorods were decorated by graphitic carbon nitride (C3N4) derived from different precursors such as thiourea, melamine, and a mixture of thiourea and melamine. Photoelectrochemical activity of TiO2/C3N4 photoanode can be modified by tuning the number of precursors used to synthesize C3N4. C3N4 derived from the mixture of melamine and thiourea in TiO2/C3N4 photoanode showed photocurrent density as high as 2.74 mA/cm2 at 1.23 V vs. RHE. C3N4 synthesized by thiourea showed particle-like morphology, while melamine and melamine with thiourea derived C3N4 yielded two dimensional (2D) nanosheets. Nanosheet-like C3N4 showed higher photoelectrochemical performance than that of particle-like nanostructures as specific surface area, and the redox ability of nanosheets are believed to be superior to particle-like nanostructures. TiO2/C3N4 displayed excellent photostability up to 20 h under continuous illumination. Thiourea plays an important role in enhancing the photoelectrochemical performance of TiO2/C3N4. This study emphasizes the fact that the improved photoelectrochemical performance can be achieved by varying the precursors of C3N4 in TiO2/C3N4 heterojunction. This is the first report to show the influence of C3N4 precursors on photoelectrochemical performance in TiO2/C3N4 systems. This would pave the way to explore different precursors influence on C3N4 with respect to the photoelectrochemical response of TiO2/C3N4 heterojunction photoanode.


2017 ◽  
Vol 53 (30) ◽  
pp. 4278-4281 ◽  
Author(s):  
Pravin S. Shinde ◽  
Su Yong Lee ◽  
Jungho Ryu ◽  
Sun Hee Choi ◽  
Jum Suk Jang

We report CTAB-mediated synthesis of internally porous Au-embedded hematite photoanode with enhanced photoelectrochemical water oxidation performance.


Author(s):  
Rhys J. Williams ◽  
Patrick J. Smith ◽  
Candice Majewski

AbstractHigh Speed Sintering (HSS) is a novel polymer additive manufacturing process which utilises inkjet printing of an infrared-absorbing pigment onto a heated polymer powder bed to create 2D cross-sections which can be selectively sintered using an infrared lamp. Understanding and improving the accuracy and repeatability of part manufacture by HSS are important, ongoing areas of research. In particular, the role of the ink is poorly understood; the inks typically used in HSS have not been optimised for it, and it is unknown whether they perform in a consistent manner in the process. Notably, the ambient temperature inside a HSS machine increases as a side effect of the sintering process, and the unintentional heating to which the ink is exposed is expected to cause changes in its fluid properties. However, neither the extent of ink heating during the HSS process nor the subsequent changes in its fluid properties have ever been investigated. Such investigation is important, since significant changes in ink properties at different temperatures would be expected to lead to inconsistent printing and subsequently variations in part accuracy and even the degree of sintering during a single build. For the first time, we have quantified the ink temperature rise caused by unintentional, ambient heating during the HSS process, and subsequently measured several of the ink’s fluid properties across the ink temperature range which is expected to be encountered in normal machine operation (25 to 45 ∘C). We observed only small changes in the ink’s density and surface tension due to this heating, but a significant drop (36%) in its viscosity was seen. By inspection of the ink’s Z number throughout printing, it is concluded that these changes would not be expected to change the manner in which droplets are delivered to the powder bed surface. In contrast, the viscosity decrease during printing is such that it is expected that the printed droplet sizes do change in a single build, which may indeed be a cause for concern with regard to the accuracy and repeatability of the inkjet printing used in HSS, and subsequently to the properties of the polymer parts obtained from the process.


2019 ◽  
Vol 7 (11) ◽  
pp. 6294-6303 ◽  
Author(s):  
Xiaohu Cao ◽  
Yifan Wang ◽  
Junqi Lin ◽  
Yong Ding

A CoOx nanolayer derived from Co8POM by photodeposition effectively passivates the surface states of hematite, thereby improving the water oxidation kinetics.


2020 ◽  
Vol 45 (16) ◽  
pp. 9380-9385
Author(s):  
J. Pfrommer ◽  
A. Steigert ◽  
C. Goebel ◽  
I. Lauermann ◽  
W. Calvet ◽  
...  
Keyword(s):  

2020 ◽  
Vol 8 (7) ◽  
pp. 3845-3850 ◽  
Author(s):  
Meirong Huang ◽  
Wenhai Lei ◽  
Min Wang ◽  
Shuji Zhao ◽  
Changli Li ◽  
...  

Large-scale BiVO4 photoanodes were prepared for solar water splitting. A photocurrent density of water oxidation of ∼2.23 mA cm−2 at 1.23 VRHE and ∼0.83% conversion efficiency at 0.65 VRHE were achieved, with <4% decay after 5 h of operation under harsh conditions.


RSC Advances ◽  
2015 ◽  
Vol 5 (77) ◽  
pp. 62611-62618 ◽  
Author(s):  
Lianwen Jia ◽  
Jiale Xie ◽  
Chunxian Guo ◽  
Chang Ming Li

A largely voided TiO2 nanorod array was modified with Fe2O3 thin layers to deliver ∼3.3 times higher the applied bias photon-to-current efficiency than that of a plain TiO2 nanorod array.


2014 ◽  
Vol 176 ◽  
pp. 199-211 ◽  
Author(s):  
Yi-Hsuan Lai ◽  
Masaru Kato ◽  
Dirk Mersch ◽  
Erwin Reisner

This discussion describes a direct comparison of photoelectrochemical (PEC) water oxidation activity between a photosystem II (PSII)-functionalised photoanode and a synthetic nanocomposite photoanode. The semi-biological photoanode is composed of PSII from the thermophilic cyanobacterium Thermosynechococcus elongatus on a mesoporous indium tin oxide electrode (mesoITO|PSII). PSII embeds all of the required functionalities for light absorption, charge separation and water oxidation and ITO serves solely as the electron collector. The synthetic photoanode consists of a TiO2 and NiOx coated nanosheet-structured WO3 electrode (nanoWO3|TiO2|NiOx). The composite structure of the synthetic electrode allows mimicry of the functional key features in PSII: visible light is absorbed by WO3, TiO2 serves as a protection and charge separation layer and NiOx serves as the water oxidation electrocatalyst. MesoITO|PSII uses low energy red light, whereas nanoWO3|TiO2|NiOx requires high energy photons of blue-end visible and UV regions to oxidise water. The electrodes have a comparable onset potential at approximately 0.6 V vs. reversible hydrogen electrode (RHE). MesoITO|PSII reaches its saturation photocurrent at 0.84 V vs. RHE, whereas nanoWO3|TiO2|NiOx requires more than 1.34 V vs. RHE. This suggests that mesoITO|PSII suffers from fewer limitations from charge recombination and slow water oxidation catalysis than the synthetic electrode. MesoITO|PSII displays a higher ‘per active’ site activity, but is less photostable and displays a much lower photocurrent per geometrical surface area and incident photon to current conversion efficiency (IPCE) than nanoWO3|TiO2|NiOx.


2021 ◽  
Vol 16 (1) ◽  
Author(s):  
Elfatih Mustafa ◽  
Rania E. Adam ◽  
Polla Rouf ◽  
Magnus Willander ◽  
Omer Nur

Abstract Highly efficient photoelectrochemical (PEC) water oxidation under solar visible light is crucial for water splitting to produce hydrogen as a source of sustainable energy. Particularly, silver-based nanomaterials are important for PEC performance due to their surface plasmon resonance which can enhance the photoelectrochemical efficiency. However, the PEC of ZnO/Ag2WO4/AgBr with enhanced visible-light water oxidation has not been studied so far. Herein, we present a novel photoelectrodes based on ZnO/Ag2WO4/AgBr nanorods (NRs) for PEC application, which is prepared by the low-temperature chemical growth method and then by successive ionic layer adsorption and reaction (SILAR) method. The synthesized photoelectrodes were investigated by several characterization techniques, emphasizing a successful synthesis of the ZnO/Ag2WO4/AgBr heterostructure NRs with excellent photocatalysis performance compared to pure ZnO NRs photoelectrode. The significantly enhanced PEC was due to improved photogeneration and transportation of electrons in the heterojunction due to the synergistic effect of the heterostructure. This study is significant for basic understanding of the photocatalytic mechanism of the heterojunction which can prompt further development of novel efficient photoelectrochemical-catalytic materials. Graphic Abstract


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