Green Car Congress  
Home Topics Archives About Contact  RSS Headlines

« UCLA, ARB, WVU measure on-road particle numbers for heavy-duty diesel and CNG trucks in California | Main | IBM Research Alliance builds new transistor for 5nm technology »

Print this post

BNL, VT team creates Ru,Rh supramolecular photocatalysts for enhanced hydrogen production via artificial photosynthesis

4 June 2017

Scientists have been trying to artificially replicate photosynthesis to convert solar energy to stored chemical energy, with the objective of producing environmentally friendly and sustainable fuels, such as hydrogen and methanol. However, mimicking key functions of the photosynthetic center, where specialized biomolecules carry out photosynthesis, has proven challenging. Artificial photosynthesis requires a molecular system that can absorb light; transport and separate electrical charge; and catalyze fuel-producing reactions. These complicated processes must operate synchronously to achieve high energy-conversion efficiency.

Now, chemists from the US Department of Energy’s (DOE) Brookhaven National Laboratory (BNL) and Virginia Tech have designed two supramolecular photocatalysts that incorporate individual components specialized for light absorption, charge separation, or catalysis. In both molecular systems, multiple light-harvesting centers made of ruthenium (Ru) metal ions are connected to a single catalytic center made of rhodium (Rh) metal ions through a bridging molecule that promotes electron transfer from the Ru centers to the Rh catalyst, where hydrogen is produced. A paper on the work is published in the Journal of the American Chemical Society.

This first example of a heptametallic Ru,Rh photocatalyst produces over 300 turnovers of H2 upon photolysis of a solution of acetonitrile, water, triflic acid, and N,N-dimethylaniline as an electron donor. In contrast, the tetrametallic Ru3Rh produces only 40 turnovers of H2 due to differences in the excited state properties and nature of the catalysts upon reduction as ascertained from electrochemical data, transient absorption spectroscopy, and flash-quench experiments.

—Manbeck et al.

In the study, they compared the hydrogen-production performance and analyzed the physical properties of the supramolecules to understand why the photocatalyst with six as opposed to three Ru light absorbers produces more hydrogen and remains stable for a longer period of time.

Developing efficient molecular systems for hydrogen production is difficult because processes are occurring at different rates. Completing the catalytic turnover of hydrogen before the separated charges—the negatively charged light-excited electron and positive “hole” left behind after the excited molecule absorbs light energy—have a chance to recombine and wastefully produce heat is one of the major challenges.

—lead author Gerald Manbeck

Another complication is that two electrons are needed to produce each hydrogen molecule. For catalysis to happen, the system must be able to hold the first electron long enough for the second to show up.

Using supramolecules with multiple light absorbers that may work independently increases the probability of using each electron productively and improving the molecules’ ability to function under low light conditions, said Manbeck.

Manbeck began making the supramolecules at Virginia Tech in 2012 with the late Karen Brewer, coauthor and his postdoctoral advisor. He discovered that the four-metal (tetrametallic) system with three Ru light-absorbing centers and one Rh catalytic center yielded only 40 molecules of hydrogen for every catalyst molecule and ceased functioning after about four hours.

In comparison, the seven-metal (heptametallic) system with six Ru centers and one Rh center was more than seven times more efficient, cycling 300 times to produce hydrogen for 10 hours. This great disparity in efficiency and stability was puzzling because the supramolecules contain very similar components.

This depiction of the heptametallic system upon exposure to light shows light harvesting by the six Ru centers (red) and electron transfer to the Rh catalyst (black), where hydrogen is produced. Efficient electron transfer to Rh is essential for realizing high catalytic performance. Source: BNL.

Manbeck joined Brookhaven in 2013 and has since carried out a series of experiments with coauthor Etsuko Fujita, leader of the artificial photosynthesis group, to understand the fundamental causes for the difference in performance.

Through cyclic voltammetry—an electrochemical technique that shows the energy levels within a molecule—the scientists found that the Rh catalyst of the heptametallic system is slightly more electron-poor and thus more receptive to receiving electrons than its counterpart in the tetrametallic system. This result suggested that the charge transfer was favorable in the heptametallic but not the tetrametallic system.

They verified their hypothesis with a time-resolved technique called nanosecond transient absorption spectroscopy, in which a molecule is promoted to an excited state by an intense laser pulse and the decay of the excited state is measured over time. The resulting spectra revealed the presence of a Ru-to-Rh charge transfer in the heptametallic system only.

The data not only confirmed our hypothesis but also revealed that the excited-state charge separation occurs much more rapidly than we had imagined. In fact, the charge migration happens faster than the time resolution of our instrument, and probably involves short-lived, high-energy excited states.

—Gerald Manbeck

The researchers plan to seek a collaborator with faster instrumentation who can measure the exact rate of charge separation to help clarify the mechanism.

In a follow-up experiment, the scientists performed the transient absorption measurement under photocatalytic operating conditions, with a reagent used as the ultimate source of electrons to produce hydrogen (a scalable artificial photosynthesis of hydrogen fuel from water would require replacing the reagent with electrons released during water oxidation). The excited state generated by the laser pulse rapidly accepted an electron from the reagent. They discovered that the added electron resides on Rh in the heptametallic system only, further supporting the charge migration to Rh predicted by cyclic voltammetry.

The high photocatalytic turnover of the heptametallic system and the principles governing charge separation that were uncovered in this work encourage further studies using multiple light-harvesting units linked to single catalytic sites.

—Gerald Manbeck

This research is supported by DOE’s Office of Science.


  • Gerald F. Manbeck, Etsuko Fujita, and Karen J. Brewer (2017) “Tetra- and Heptametallic Ru(II),Rh(III) Supramolecular Hydrogen Production Photocatalysts” Journal of the American Chemical Society doi: 10.1021/jacs.7b02142

June 4, 2017 in Catalysts, Fuels, Hydrogen, Hydrogen Production, Solar fuels | Permalink | Comments (2)


When can it be mass produced. This seems like the real answer to clean sustainable energy.

Millions and millions of customers complaint about the high prices of gasoline-diesel, yep nobody is commenting this article.

I said till 6 months to start commercialising a small gasoline serial hybrid car where exhaust pressure and heat is converted to live electricity and feed the primary fuel source by this hydrogen at 1$ per kilo. Sell this car each and everywhere to lower his production cost to 6 000$ and sell it at 9 000$ brand new with 5 years garentee.

Verify your Comment

Previewing your Comment

This is only a preview. Your comment has not yet been posted.

Your comment could not be posted. Error type:
Your comment has been posted. Post another comment

The letters and numbers you entered did not match the image. Please try again.

As a final step before posting your comment, enter the letters and numbers you see in the image below. This prevents automated programs from posting comments.

Having trouble reading this image? View an alternate.


Post a comment

Green Car Congress © 2017 BioAge Group, LLC. All Rights Reserved. | Home | BioAge Group