New research possibilities at NanoMAX

X-rays can penetrate materials and are therefore useful for studying chemical processes as they occur inside reactors, cells, and batteries. A common ingredient in such chemical systems is metal nanoparticles, which are often used as catalysts for important reactions. As the NanoMAX beamline provides a very small X-ray focal spot, single nanoparticles can in principle be studied as they perform their catalytic functions.

In this paper, we show that gold nanoparticles sitting inside an electrochemical cell can be imaged at NanoMAX. These preliminary results come from nanoparticles around 60 nm (60 millionths of a millimetre) in size, and we show that even smaller particles could be studied. If successful, future experiments will allow “filming” nanoparticles as they catalyze reactions in real-time, and give new understanding of how catalysis works. That could in turn help design new materials for energy conversion, chemical production, and water purification.

>Read more on the MAX IV Laboratory
Image (extract, full image here): Coherent Bragg imaging of 60 nm Au nanoparticles under electrochemical control at the NanoMAX beamline

Using reed waste for sustainable batteries

With the changing climate, researchers are focusing on finding sustainable alternatives to conventional fuel cells and battery designs. Traditional catalysts used in vehicles contribute to increasing carbon dioxide emissions and mining for materials used in their design has a negative impact on the environment. Prof. Shuhui Sun, a researcher from the Institut National de la Recherche Scientifique (INRS) in Montreal, and his team used the Canadian Light Source (CLS) at the University of Saskatchewan to investigate an Iron-Nitrogen-Carbon catalyst using reed waste.

They hope to use the bio-based materials to create high-performance fuel cells and metal-air batteries, which could be used in electric cars. “An efficient oxygen electrocatalyst is extremely important for the development of high-performance electrochemical energy conversion and storage devices. Currently, the rare and expensive Pt-based catalysts are commonly used in these devices. Therefore, developing highly efficient and low-cost non-precious metal (e.g., Fe-based) catalysts to facilitate a sluggish cathodic oxygen reduction reaction (ORR) is a key issue for metal air batteries and fuel cells,” said Qilang Wei, the first author of the paper.

>Read more on the Canadian Light Source website

A step closer to smart catalysts for fuel generation

Researchers at the Universidade Federal do Rio Grande do Sul in Brazil in collaboration with the ALBA Synchrotron have performed the first detailed measurement of the strong metal-support interaction (SMSI) effect in Cu-Ni nanoparticles supported on cerium oxide.

A better understanding of this effect is essential for developing smart catalysts that are more selective, stable and sustainable. The quest for the best catalysts in industry has been a long one, but a new study by Universidade Federal do Rio Grande do Sul in Brazil, in collaboration with the ALBA Synchrotron, has come a step closer. For the first time, researchers have found evidence of what could be the origin of the SMSI effect in catalysts supported on cerium oxide.

Catalysts are used to increase the reaction rate of a given chemical reaction, and have applications in a wide variety of fields. In heterogeneous catalysis, the catalyst is usually composed of metal nanoparticles supported on metal oxides. Among them, CeO2-based catalysts have unique structural and atomic properties that make them suitable in the cutting-edge environmental industry of fuel cells and hydrogen. In this field, they are being explored as high-end photocatalytic reactors for the thermal splitting of water and carbon dioxide. However, what has been termed as the SMSI effect can undermine their desired properties.

>Read more on the ALBA website

Image: (extract, full picture here) Near Ambient Pressure – X-ray Photoemission Spectroscopy allowed the identification of the chemical components of the nanoparticles in situ.

Catalyst improves cycling life of magnesium/sulfur batteries

Comprising earth-abundant elements, cathodes made of magnesium/sulfur compounds could represent the next step in battery technology. However, despite being dendrite free and having a high theoretical energy density compared with lithium batteries, magnesium/sulfur batteries have suffered from high polarization and extremely limited recharging capabilities. To gain electrochemical insights into magnesium/sulfur batteries during charge–discharge cycles, researchers used the Advanced Light Source (ALS) to investigate and optimize battery chemistry.

The in situ x-ray absorption spectroscopy (XAS) capabilities at ALS Beamlines 5.3.1 and 10.3.2 provided information on the oxidation state of sulfur under real operating conditions. The group found that the conversion of sulfur in the first discharging process was divided into three stages: formation of MgSand MgSat a fast reaction rate, reduction of MgSto Mg3S8, and a sluggish further reduction of Mg3Sto MgS. The in situ XAS analysis revealed that Mg3Sand MgS are more electrochemically inert and cannot revert to the active forms of sulfur, thereby dramatically reducing the battery’s cycling life.

>Read more on the ALS website

Image: Efforts to develop magnesium/sulfur batteries have been stymied by a loss of capacity after the first discharging process. In situ XAS revealed the accumulation of Mg3S8 and MgS during the discharging process, which are inert forms of the magnesium/sulfur compounds. Introducing a titanium-sulfide catalyst activated the compounds, reversing the chemical mechanism so that the battery could be recharged multiple times.

 

Publication of the first scientific paper

June 1, 2019 marks a historically important accomplishment for SESAME, where the very first scientific paper presenting results using data obtained at SESAME’s X-ray absorption fine structure/X-ray fluorescence (XAFS/XRF) spectroscopy beamline was published in Applied Catalysis B: Environmental.

S: Bac et al. Applied Catalysis B: Environmental, 259, 2019, 117808 https://www.sciencedirect.com/science/article/pii/S0926337319305545

Synchrotron measurements performed at SESAME were carried out by the research group of Associate Professor Emrah Ozensoy (Bilkent University Chemistry Department and UNAM-National Nanotechnology Center Ankara, Turkey), in collaboration with the research group of Professor Ahmet Kerim Avcı (Boğaziçi University, Chemical Engineering Department, Istanbul, Turkey) and Dr Messaoud Harfouche (XAFS/XRF beamline scientist, SESAME, Allan, Jordan).
The paper entitled Exceptionally active and stable catalysts for CO2 reforming of glycerol to syngas is the outcome of a measurement campaign at SESAME in July 2018 and focuses on the catalytic valorization of a biomass waste material (i.e. glycerol) to obtain synthesis gas (or syngas, CO + H2). Glycerol is an important renewable feedstock for the large-scale catalytic production of synthetic liquid fuels through a process called Fischer-Tropsch synthesis. In the words of Emrah Ozensoy “XAFS/XRF experiments performed at SESAME were instrumental for us to understand the electronic structure of the Co/CoOx and Ni/NiOx nanoparticles serving as the catalytic active sites. Particularly, complementing the experimental data acquired in our labs with the results obtained at SESAME allowed us to examine the nature of the fresh catalysts and compare them with that of the spent catalysts obtained after the catalytic reaction, revealing crucial molecular-level insights regarding the catalytic aging and poisoning mechanisms.”

>Read more on the SESAME website

Image: Kerem Emre Ercan Some of the researchers who contributed to the publication and data acquisition (from left to right, Yusuf Koçak, Kerem E. Ercan, and M. Fatih Genişel)

New materials for the reduction of vehicle pollution

Research develops nanostructured material with high oxygen storage and release capacity for the improvement of catalytic converters

Complete combustion of both fossil and biofuels generates carbon dioxide (CO2) and water as final products. However, incomplete combustion of these substances can occur in automobile engines, generating important pollutants such as carbon monoxide (CO), hydrocarbons, and nitrogen oxides (such as NO and NO2).
To reduce the emission of these toxic substances, an equipment called a catalytic converter is used in the exhaust of vehicles. Materials called catalysts promote and accelerate chemical reactions without being consumed during the process. They retain on their surface the reactant molecules, weakening the bonds between the atoms and causing the pollutants to be converted into less harmful gases.
The action of the catalytic converter happens in three stages. The first stage converts the nitrogen oxides into nitrogen (N2) and oxygen (O2) gases. The second stage breaks down bonds of unburnt hydrocarbons and carbon monoxide, turning them into CO2. Finally, the third stage has an oxygen sensor to regulate the intake of air and fuel to the engine, so that the amount of oxygen is always close to the most efficient for the different reactions.

>Read more on the Brazilian Light Laboratory (LNLS) website

Catalyst renders nerve agents harmless

Scientists used a multimodal approach to understand how a catalyst decomposes nerve agents in real-life environments

A team of scientists including researchers at the U.S. Department of Energy’s (DOE) Brookhaven National Laboratory has studied a catalyst that decomposes nerve agents, eliminating their harmful and lethal effects. The research was published Friday, April 19, in the Journal of Physical Chemistry Letters.

“Our work is part of an ongoing, multiagency effort to protect soldiers and civilians from chemical warfare agents (CWAs),” said Anatoly Frenkel, a physicist with a joint appointment at Brookhaven Lab and Stony Brook University and the lead author on the paper. “The research requires us to understand molecular interactions on a very small scale, and to develop special characterization methods that are capable of observing those interactions. It is a very complex set of problems that also has a very immediate societal impact.”

>Read more on the National Synchrotron Light Source-II website

Image: Lead author Anatoly Frenkel is shown at NSLS-II’s X-ray Powder Diffraction beamline, where part of the research was conducted.

Urea susbstitutes noble metal catalysts

… for the photodegradation of organic polluants.

A new laser-based technique developed by the Institute of Materials Science (ICMAB-CSIC) uses urea, a common substance in the chemical industry and a low-cost alternative to noble metal co-catalyst, to enable a more efficient, one-step production of hybrid graphene-based organic-inorganic composite layers for environmental remediation, photodegradation of antibiotic contaminants from wastewater. The composition and chemical bonds of the urea-enriched thin layers were studied in detail using synchrotron light at the ALBA Synchrotron.
Human activity is increasing the amount of pollutants in water and air, as well as in all sorts of materials at home and work place. The existence of antibiotic contamination is undeniably one of the most threatening challenges to date, at a time when antibiotic-resistant bacteria has already been flagged as the next world-wide pandemic crisis.
Semiconductor photocatalysts have long been investigated for environmental remediation because they can degrade or mineralize a wide range of organic contaminants as well as pathogens. Research focuses on addressing some drawbacks that prevent their use on a large scale. On the one hand, many photocatalysts are activated only by UV radiation which represents solely a small fraction of the total available solar emission. On the other hand, the recombination of the photogenerated  electron-hole pairs that enable the decomposition of the pollutant is usually faster than the oxidation reactions that cause the degradation of organic molecules. As a consequence, noble metal co-catalysts acting as electron scavengers, such as gold or platinum, are needed in the process.

Image: Researchers Ángel Pérez  del Pino and Enikö György from the ICMAB-CSIC together with Ibraheem Yousef, scientists responsible of MIRAS beamline at ALBA.

Watching molecules in a light-triggered catalyst ring ‘like an ensemble of bells’

A better understanding of these systems will aid in developing next-generation energy technologies.

Photocatalysts ­– materials that trigger chemical reactions when hit by light – are important in a number of natural and industrial processes, from producing hydrogen for fuel to enabling photosynthesis.
Now an international team has used an X-ray laser at the Department of Energy’s SLAC National Accelerator Laboratory to get an incredibly detailed look at what happens to the structure of a model photocatalyst when it absorbs light.
The researchers used extremely fast laser pulses to watch the structure change and see the molecules vibrating, ringing “like an ensemble of bells,” says lead author Kristoffer Haldrup, a senior scientist at Technical University of Denmark (DTU). This study paves the way for deeper investigation into these processes, which could help in the design of better catalysts for splitting water into hydrogen and oxygen for next-generation energy technologies.
“If we can understand such processes, then we can apply that understanding to developing molecular systems that do tricks like that with very high efficiency,” Haldrup says.

>Read more on the Linac Coherent Light Source at SLAC website

Image: When photocatalyst molecules absorb light, they start vibrating in a coordinated way, like an ensemble of bells. Capturing this response is a critical step towards understanding how to design molecules for the efficient transformation of light energy to high-value chemicals.
Credit: Gregory Stewart/SLAC National Accelerator Laboratory

Platinum forms nano-bubbles

Technologically important noble metal oxidises more readily than expected.

Platinum, a noble metal, is oxidised more quickly than expected under conditions that are technologically relevant. This has emerged from a study jointly conducted by the DESY NanoLab and the Vienna University of Technology. Devices that contain platinum, such as the catalytic converters used to reduce exhaust emissions in cars, can suffer a loss in efficacy as a result of this reaction. The team around principal author Thomas Keller, from DESY and the University of Hamburg, is presenting its findings in the journal Solid State Ionics. The result is also a topic at the users’ meeting of DESY’s X-ray light sources with more than 1000 participants currently taking place in Hamburg.
“Platinum is an extremely important material in technological terms,” says Keller. “The conditions under which platinum undergoes oxidation have not yet been fully established. Examining those conditions is important for a large number of applications.”
The scientists studied a thin layer of platinum which had been applied to an yttria-stabilised zirconia crystal (YSZ crystal), the same combination that is used in the lambda sensor of automotive exhaust emission systems. The YSZ crystal is a so-called ion conductor, meaning that it conducts electrically charged atoms (ions), in this case oxygen ions. The vapour-deposited layer of platinum serves as an electrode. The lambda sensor measures the oxygen content of the exhaust fumes in the car and converts this into an electrical signal which in turn controls the combustion process electronically to minimize toxic exhausts.

>Read more on the DESY (PETRA III) website

Image: Electron microscope view into the interior of a platinum bubble. The cross-section was exposed with a focused ion beam. Below the hollow Pt bubble the angular YSZ crystal can be seen.
Credit: DESY, Satishkumar Kulkarni

Single atoms can make more efficient catalysts

Detailed observations of iridium atoms at work could help make catalysts that drive chemical reactions smaller, cheaper and more efficient.

Catalysts are chemical matchmakers: They bring other chemicals close together, increasing the chance that they’ll react with each other and produce something people want, like fuel or fertilizer.

Since some of the best catalyst materials are also quite expensive, like the platinum in a car’s catalytic converter, scientists have been looking for ways to shrink the amount they have to use.

Now scientists have their first direct, detailed look at how a single atom catalyzes a chemical reaction. The reaction is the same one that strips poisonous carbon monoxide out of car exhaust, and individual atoms of iridium did the job up to 25 times more efficiently than the iridium nanoparticles containing 50 to 100 atoms that are used today.

>Read more on the SSRL at SLAC website

Image: Scientists used a combination of four techniques, represented here by four incoming beams, to reveal in unprecedented detail how a single atom of iridium catalyzes a chemical reaction.
Credit: Greg Stewart/SLAC National Accelerator Laboratory

Illuminating nanoparticle growth with X-rays

Ultrabright x-rays at NSLS-II reveal key details of catalyst growth for more efficient hydrogen fuel cells

Hydrogen fuel cells are a promising technology for producing clean and renewable energy, but the cost and activity of their cathode materials is a major challenge for commercialization. Many fuel cells require expensive platinum-based catalysts—substances that initiate and speed up chemical reactions—to help convert renewable fuels into electrical energy. To make hydrogen fuel cells commercially viable, scientists are searching for more affordable catalysts that provide the same efficiency as pure platinum.

“Like a battery, hydrogen fuel cells convert stored chemical energy into electricity. The difference is that you’re using a replenishable fuel so, in principle, that ‘battery’ would last forever,” said Adrian Hunt, a scientist at the National Synchrotron Light Source II (NSLS-II), a U.S. Department of Energy (DOE) Office of Science User Facility at DOE’s Brookhaven National Laboratory. “Finding a cheap and effective catalyst for hydrogen fuel cells is basically the holy grail for making this technology more feasible.”

>Read more on the NSLS-II website

Image: Brookhaven Lab scientists Mingyuan Ge, Iradwikanari Waluyo, and Adrian Hunt are pictured left to right at the IOS beamline, where they studied the growth pathway of an efficient catalyst for hydrogen fuel cells.

Light-activated, single- ion catalyst breaks down carbon dioxide

X-ray studies reveal structural details that may point the way to designing better catalysts for converting pollutant gas into useful products

A team of scientists has discovered a single-site, visible-light-activated catalyst that converts carbon dioxide (CO2) into “building block” molecules that could be used for creating useful chemicals. The discovery opens the possibility of using sunlight to turn a greenhouse gas into hydrocarbon fuels.

The scientists used the National Synchrotron Light Source II, a U.S. Department of Energy (DOE) Office of Science user facility at Brookhaven National Laboratory, to uncover details of the efficient reaction, which used a single ion of cobalt to help lower the energy barrier for breaking down CO2. The team describes this single-site catalyst in a paper just published in the Journal of the American Chemical Society.

Converting CO2 into simpler parts—carbon monoxide (CO) and oxygen—has valuable real-world applications. “By breaking CO2, we can kill two birds with one stone—remove CO2 from the atmosphere and make building blocks for making fuel,” said Anatoly Frenkel, a chemist with a joint appointment at Brookhaven Lab and Stony Brook University. Frenkel led the effort to understand the activity of the catalyst, which was made by Gonghu Li, a physical chemist at the University of New Hampshire.

>Read more on the NSLS-II at Brookhaven National Laboratory website

Image: National Synchrotron Light Source II (NSLS-II) QAS beamline scientist Steven Ehrlich, Stony Brook University (SBU) graduate student Jiahao Huang, and Brookhaven Lab-SBU joint appointee Anatoly Frenkel at the QAS beamline at NSLS-II.

Transition metal complexes: mixed works better

A team at BESSY II has investigated how various iron-complex compounds process energy from incident light. They were able to show why certain compounds have the potential to convert light into electrical energy. 

The results are important for the development of organic solar cells. The study has now been published in the journal PCCP, and its illustration selected for the cover.
Transition-metal complexes – that is a cumbersome word for a class of molecules with important properties: An element from the group of transition metals sits in the centre. The outer electrons of the transition-metal atom are located in cloverleaf-like extended d-orbitals that can be easily influenced by external excitation. Some transition-metal complexes act as catalysts to accelerate certain chemical reactions, and others can even convert sunlight into electricity. The well-known dye solar cell developed by Michael Graetzel (EPFL) in the 1990s is based on a ruthenium complex.

Why not Iron?
However, it has not yet been possible to replace the rare and expensive transition metal ruthenium with a less expensive element, such as iron. This is astonishing, because the same number of electrons is found on extended outer d-orbitals of iron. However, excitation with light from the visible region does not release long-lived charge carriers in most of the iron complex compounds investigated so far.

>Read more on the Bessy II at HZB website

Image: The illustration shows a molecule with an iron atom at its centre, bound to 4 CN groups and a bipyridine molecule. The highest occupied iron orbital is shown as a green-red cloud. As soon as a cyan group is present, the outer iron orbitals are observed to delocalize so that electrons are also densely present around the nitrogen atoms.
Credit: T. Splettstoesser/HZB

The search for clean hydrogen fuel

The world is transitioning away from fossil fuels and hydrogen is poised to be the replacement.

Two things are needed if we are to make the transition to a low carbon, “hydrogen economy” they are clean and high yielding sources of hydrogen, as well as efficient means of producing and storing energy using hydrogen.

Hydrogen powered cars are the perfect case study for how a hydrogen-fuelled future would look. While they work and show a great deal of promise, the best examples of hydrogen being used in fuel require very clean sources of hydrogen. If the source of hydrogen is mixed with contaminants like carbon monoxide, the efficiency of the fuel goes down and causes downstream problems in the fuel cell.

A team from KTH led by Jonas Weissenrieder is visiting MAX IV this week to try and solve this exact problem, how can we generate clean hydrogen for fuel cells? The team is working on a process to catalyse the oxidation of carbon monoxide, which adversely affects fuel cell performance, to harmless carbon dioxide. The catalysis reaction must be selective, and not affect the hydrogen gas that could be oxidised to water which is not great for running car engines.

>Read more on the MAX IV Laboratory website

Single atoms break carbon’s strongest bond

Scientists discovered that single atoms of platinum can break the bond between carbon and fluorine, one of the strongest known chemical bonds.

An international team of scientists including researchers at Yale University and the U.S. Department of Energy’s (DOE) Brookhaven National Laboratory have developed a new catalyst for breaking carbon-fluorine bonds, one of the strongest chemical bonds known. The discovery, published on Sept. 10 in ACS Catalysis, is a breakthrough for efforts in environmental remediation and chemical synthesis.

“We aimed to develop a technology that could degrade polyfluoroalkyl substances (PFAS), one of the most challenging pollutant remediation problems of the present day,” said Jaehong Kim, a professor in the department of chemical and environmental engineering at Yale University. “PFAS are widely detected all over the world, from Arctic biota to the human body, and concentrations in contaminated groundwater significantly exceed the regulatory limit in many areas. Currently, there are no energy-efficient methods to destroy these contaminants. Our collaboration with Brookhaven Lab aims to solve this problem by taking advantage of the unique properties of single atom catalysts.”

>Read more on the NSLS-II at Brookhaven National Laboratory website

Image: Brookhaven scientist Eli Stavitski is shown at NSLS-II’s Inner Shell Spectroscopy beamline, where researchers imaged the physical and chemical complexity of a single-atom catalyst that breaks carbon-fluorine bonds.