Metal oxides are a promising catalyst for photoelectrochemical (PEC) water splitting to produce hydrogen as an alternative fuel. However, their effectiveness is restricted at low voltage. Adding phosphorus reduced energy losses during water splitting.
BiVO4 is a metal oxide semiconductor and a top-performing photocatalyst for the photoelectrochemical (PEC) water-splitting process, which generates hydrogen as a form of an alternative fuel. Image Credit: City University of Hong Kong. Click the press release link for the largest view.
The research was co-led by Professor Ng Yun-hau of CityU’s School of Energy and Environment (SEE) and researchers from Australia and Germany.
Bismuth vanadate (BiVO4) is a metal oxide semiconductor, which is responsive to both ultraviolet and visible light, and is regarded as a top-performing photocatalyst for PEC water splitting.
Dr Ng, an expert in PEC research explained, “In the PEC water-splitting process, hydrogen and oxygen are produced from water, using sunlight and specialized semiconductors as photocatalysts, such as BiVO4. With light energy and an additional small voltage supply, the photocatalysts directly dissociate water molecules into hydrogen and oxygen. However, if the voltage supply is too low, a large fraction of the photo-excited charge carriers cannot be extracted efficiently, leading to energy loss and affecting the water-splitting efficiency. This poor charge transport is due mainly to the trap states of charge carriers and small polaron formation.”
Native defects and polaron formation hinder charge carrier transport
With solar energy, the electrons in the semiconductor are excited, and can bounce up and across the band gap from the valence band to the conduction band to make an electric current flow. But the native defects of the semiconductor introduce “trap states,” which trap the photo-induced electrons and the positively charged holes until they recombine, preventing them from moving freely to become an electric current.
Moreover, when an electron is excited within a semiconductor, its charge can induce lattice expansion, confining the electron within the lattice unit, and forming a small polaron, which can be regarded as a deep trap state that strongly traps the electron. It requires thermal vibration energy (known as polaron hopping activation energy) to hop from one site to another. Hence, the small polaron formation has a detrimental effect on charge mobility, which is common in transition metal oxides.
The research team took on this challenge to find ways to enhance charge mobility. They found that by modifying the BiVO4 photoanodes with phosphorus doping, the charge mobility is 2.8 times higher than that of the pristine one. This also greatly increased the charge separation efficiency, up to 80% at 0.6V, which is about 1.43 times stronger than the pristine one, and up to 99% at 1.0V.
Dr Wu Hao, the first author of the paper, then-postdoc in Professor Ng’s group, and now an Assistant Professor in the Macao Institute of Materials Science and Engineering at Macau University of Science and Technology, shared one of the highlights of the study: “We discovered that the polaron hopping activation barriers of BiVO4 photoanodes were reduced upon incorporating phosphorus. This was proven by our combined theoretical and experimental studies.”
Synergistic effects of phosphorus doping
The team’s experiments and measurements also confirm that phosphorus doping passivated the trap states that are intrinsically formed on the BiVO4 surface, thereby increasing the open-circuit photovoltage for splitting water molecules.
They showed that the charge transport in phosphorus-doped BiVO4 was improved by concurrently mediating the polaron hopping barrier and trap state, thus introducing efficient PEC water splitting for hydrogen production at low voltage. The synergistic effects allowed the phosphorus-doped BiVO4 to exhibit a record-high photon-to-current conversion efficiency of 2.21% at 0.6V.
Professor Ng noted, “We hope the mechanistic understanding of the enhancement of BiVO4 properties will provide key insights into trap state passivation and polaron hopping for many photoactive metal oxides, and more importantly, will offer a potential option for efficient hydrogen production to help achieve carbon neutrality.”
The first author of the research is Dr Wu, and the corresponding author is Professor Ng. Other collaborators included researchers from the Institute for Solar Fuels of Helmholtz-Zentrum Berlin für Materialien und Energie (HZB) and Queensland University of Technology.
What stands out about this work is the combined power input of both solar energy and electrical power to free the hydrogen from water.
As a technology that is very young the progress is impressive. And there are lots more metal oxides to examine, innovations to come and ideas to be tested.
To date water splitting is quite some way from being a competitive source for hydrogen. It is still more sensible economically to use the existing processes for supplies. Those sources are not going to reduce the dependency on fossil fuels.
Yet, this is major progress. There isn’t any super expensive precious metals involved. Considering the conflict threatened state of the world economy, that is a very good thing, indeed.
By Brian Westenhaus via Newenergyandfuel.com
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