MRS Meetings and Events

 

EN03.04.02 2022 MRS Spring Meeting

Enhancing the Photocatalytic Activity of TiO2 Through the Use of Selective Contacts Based on Photovoltaic Solar Cells

When and Where

May 9, 2022
5:00pm - 7:00pm

Hawai'i Convention Center, Level 1, Kamehameha Exhibit Hall 2 & 3

Presenter

Co-Author(s)

Lluis Soler1,Joaquim Puigdollers1,Miquel Anglada1,Eloi Costals1,David Rovira1,Maykel Jiménez Guerra1,Cristobal Voz1,Pablo Ortega1,Edgardo Saucedo1,Jordi Llorca1

University of Politecnica-Catalunya1

Abstract

Lluis Soler1,Joaquim Puigdollers1,Miquel Anglada1,Eloi Costals1,David Rovira1,Maykel Jiménez Guerra1,Cristobal Voz1,Pablo Ortega1,Edgardo Saucedo1,Jordi Llorca1

University of Politecnica-Catalunya1
Photocatalysis is defined as the acceleration of chemical reactions under illumination and in the presence of a catalyst, which absorbs light and is involved in the chemical transformation of the reaction partners. Photocatalytic activity is highly dependent on the ability of the catalyst to efficiently create and separate photogenerated charge carriers. The electrochemical energies of photogenerated electrons and holes are used to oxidize or reduce compounds to make useful materials, including hydrogen and hydrocarbons, and to remove contaminants on wall surfaces and water. Since the illumination source is from the sun, photocatalysis is considered a green technology for converting solar energy into chemical energy.<br/>The working principles behind the operation of photocatalysis and the photovoltaic solar cell are similar. In both cases, the objective is to generate energetically separated electrons and holes, preventing them from recombining before accessing the external circuit. In the solar cell, the photogenerated electrons and holes recombine through the external circuit through metallic cables connected to an electrical load, while in photocatalysis electrons and holes participate in reduction and oxidation reactions. In both cases, avoiding recombination of the carriers before reaching the external circuit (solar cell) or the active surface (photocatalysis) is of paramount importance.<br/>In this work we optimize the generation of hydrogen from TiO<sub>2</sub> using an approach widely used in solar cells, that is, using selective contacts of holes and electrons. In particular, the generation of hydrogen has been studied using three different systems, all of them based on TiO<sub>2</sub> sol-gel. These have been: TiO<sub>2</sub> alone, TiO<sub>2</sub>/Au and a-Si:H(n)/c-Si/MoO<sub>3-x</sub>/TiO<sub>2</sub>/Au. In the latter case, the a-Si:H(n)/c-Si/MoO<sub>3-x</sub> structure corresponds to a crystalline silicon solar cell, without electrical contacts.<br/>The overall mean hydrogen production was 1.6 <i>mmol/h g<sub>titania</sub></i> for the TiO<sub>2</sub> absorber alone, whereas in sample with Au the overall mean production increases to 4.3 <i>mmol/h g<sub>titania</sub></i> due to the catalytic effect of the Au nanoparticles. However, for the sample deposited on top of the electrodeless silicon solar cell the generation of hydrogen increased an extra 33 % with respect to the TiO<sub>2</sub>/Au sample, with a mean overall hydrogen production of 5.7 <i>mmol/h g<sub>titania</sub></i>.<br/>This experimental result can be explained by taking into account the energy diagram of the different layers. The final conclusion is that the TiO2/Au interface acts as a selective contact of holes, and the a-Si (n)/c-Si/MoO3-x structure acts as a selective contact of electrons.<br/>Additional characterization of the samples was performed by HRTEM, SEM and EDX.

Symposium Organizers

Sage Bauers, National Renewable Energy Laboratory
Jeffrey Neaton, University of California, Berkeley
Lydia Wong, Nanyang Technological University
Kazuhiko Maeda, Tokyo Inst of Technology

Symposium Support

Bronze
University of Pennsylvania’s Master of Chemical Sciences
MilliporeSigma
MRS-Singapore

Session Chairs

Jeffrey Neaton
Lydia Wong

In this Session

EN03.04.01
A First-Principles Analysis of Hydrogen Evolution Reaction Using an AgTe Catalyst

EN03.04.02
Enhancing the Photocatalytic Activity of TiO2 Through the Use of Selective Contacts Based on Photovoltaic Solar Cells

EN03.04.03
Tailoring Metal-Insulator-Semiconductor Junctions for Photoelectrochemical Water and Urea Oxidation

EN03.04.04
Effects of 1D/2D Heterostructure Formation on the Charge Carrier Recombination Dynamics of TiO2 Nanotube Photoanodes for Solar Photoelectrochemical Water Splitting

EN03.04.05
High-Quality Ta3N5 Photoelectrodes for Photoelectrochemical Energy Conversion

EN03.04.06
Tandem PEC Device with Perovskite/g-C3N4 and Phosphorene/g-C3N4 as the Electrodes for Hydrogen Evolution and Ciprofloxacin Photodegradation

EN03.04.08
Unbiased Photoelectrochemical Solar Fuel Generation Enabled by Antimony Trisulfide Photoanode Based on Iodide Oxidation Reaction

EN03.04.09
Band Edge Engineering in Metal Oxide Heterostructures for Efficient Charge Separation for Solar Water Oxidation in Photoelectrochemical Cell

EN03.04.13
Preparation of p-p Heterojunction and Its Photocatalytic H2 Production by CuO-Mn3O4 Nanocomposite

EN03.04.14
Boosted Photoelectrochemical Water Splitting by BiVO4 Nanodots on In2O3 Nanorods

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