New Materials Could Turn Water into the Fuel of the Future and puts chemical fuels from sunlight on the fast track to commercial viability

Scientists at the Department of Energy’s Lawrence Berkeley National Laboratory (Berkeley Lab) and the California Institute of Technology (Caltech) have—in just two years—nearly doubled the number of materials known to have potential for use in solar fuels.

They did so by developing a process that promises to speed the discovery of commercially viable generation of solar fuels that could replace coal, oil, and other fossil fuels.

Solar fuels, a dream of clean-energy research, are created using only sunlight, water, and carbon dioxide. Researchers are exploring a range of possible target fuels, but one possibility is to produce hydrogen by splitting water.

Each water molecule is comprised of an oxygen atom and two hydrogen atoms. Pure hydrogen is highly flammable, making it an ideal fuel. If you could find a way to extract that hydrogen from water using sunlight, then, you would have a plentiful and renewable energy source. The problem, however, is that water molecules do not simply break down when sunlight shines on them—if they did, the oceans would not cover three-fourths of the planet. Instead, they need a little help from a solar-powered catalyst.

To create practical solar fuels, scientists have been trying to develop low-cost and efficient materials that perform the necessary chemistry using only visible light as an energy source.

Over the past four decades, researchers identified only 16 of these “photoanode” materials. Now, using a new high-throughput method of identifying new materials, a team of researchers led by Caltech’s John Gregoire and Berkeley Lab’s Jeffrey Neaton, Kristin Persson, and Qimin Yan have found 12 promising new photoanodes.

PNAS – Solar fuels photoanode materials discovery by integrating high-throughput theory and experiment

“What is particularly significant about this study, which combines experiment and theory, is that in addition to identifying several new compounds for solar fuel applications, we were also able to learn something new about the underlying electronic structure of the materials themselves,” says Neaton, the director of the Molecular Foundry.

Gregoire, JCAP coordinator for Photoelectrocatalysis and leader of the High Throughput Experimentation group, adds “It’s exciting to find 12 new potential photoanodes for making solar fuels, but even more so to have a new materials discovery pipeline going forward.”

Previous materials discovery processes relied on cumbersome testing of individual compounds to assess their potential for use in specific applications. Instead, the scientists combined computational and experimental approaches by first mining a materials database for potentially useful compounds, and then rapidly test the most promising candidates using high-throughput experimentation.

In the work described in the PNAS paper, they explored 174 metal vanadates—compounds containing the elements vanadium and oxygen along with one other element from the periodic table. The research reveals how different choices for this third element can produce materials with different properties, and reveals how to “tune” those properties to make a better photoanode.

Computational resources at NERSC performed hundreds of comprehensive high-throughput theoretical calculations, and software and expertise at the Molecular Foundry enabled the scientists to analyze and understand the most promising photoanode materials candidates.

Through analysis of nearly 200 compounds in the Materials Project database, the scientists found that compounds composed of vanadium, oxygen, and a third element possess a highly tunable electronic structure with band gaps in the visible light range that is uniquely favorable for water oxidation.

“Importantly, we were able to explain the origin of their tunability, and identify several promising vanadate photoanode compounds,” says Neaton.

Added Gregoire, “The key advance made by the team was to combine the best capabilities enabled by theory and supercomputers with novel high throughput experiments to generate scientific knowledge at an unprecedented rate.”

18 pages of supplemental information

Significance

Combining high-throughput computation and experiment accelerates the discovery of photoelectrocatalysts for water oxidation and explains the origin of their functionality, establishing ternary metal vanadates as a prolific class of photoanode materials for generation of chemical fuels from sunlight.

Abstract

The limited number of known low-band-gap photoelectrocatalytic materials poses a significant challenge for the generation of chemical fuels from sunlight. Using high-throughput ab initio theory with experiments in an integrated workflow, we find eight ternary vanadate oxide photoanodes in the target band-gap range (1.2–2.8 eV). Detailed analysis of these vanadate compounds reveals the key role of VO4 structural motifs and electronic band-edge character in efficient photoanodes, initiating a genome for such materials and paving the way for a broadly applicable high-throughput-discovery and materials-by-design feedback loop. Considerably expanding the number of known photoelectrocatalysts for water oxidation, our study establishes ternary metal vanadates as a prolific class of photoanode materials for generation of chemical fuels from sunlight and demonstrates our high-throughput theory–experiment pipeline as a prolific approach to materials discovery.

SOURCES- PNAS, Lawrence Berkeley Labs

About The Author

Add comment

E-mail is already registered on the site. Please use the Login form or enter another.

You entered an incorrect username or password

Sorry, you must be logged in to post a comment.