Researchers have made real-time movies of copper nanoparticles as they evolve to convert carbon dioxide and water into renewable fuels and chemicals. Their new insights could help advance the next generation of solar fuels.
From: DOE/Lawrence Berkeley National Laboratory
February 16, 2023 -- Since
the 1970s, scientists have known that copper has a special ability to transform
carbon dioxide into valuable chemicals and fuels. But for many years,
scientists have struggled to understand how this common metal works as an
electrocatalyst, a mechanism that uses energy from electrons to chemically
transform molecules into different products.
Now, a research team
led by Lawrence Berkeley National Laboratory (Berkeley Lab) has gained new
insight by capturing real-time movies of copper nanoparticles (copper particles
engineered at the scale of a billionth of a meter) as they convert CO2 and
water into renewable fuels and chemicals: ethylene, ethanol, and propanol,
among others. The work was reported in the journal Nature last
week.
"This is very
exciting. After decades of work, we're finally able to show -- with undeniable
proof -- how copper electrocatalysts excel in CO2 reduction,"
said Peidong Yang, a senior faculty scientist in Berkeley Lab's Materials
Sciences and Chemical Sciences Divisions who led the study. Yang is also a
professor of chemistry and materials science and engineering at UC Berkeley.
"Knowing how copper is such an excellent electrocatalyst brings us steps
closer to turning CO2 into new, renewable solar fuels through
artificial photosynthesis."
The work was made
possible by combining a new imaging technique called operando 4D
electrochemical liquid-cell STEM (scanning transmission electron microscopy)
with a soft X-ray probe to investigate the same sample environment: copper
nanoparticles in liquid. First author Yao Yang, a UC Berkeley Miller
postdoctoral fellow, conceived the groundbreaking approach under the guidance
of Peidong Yang while working toward his Ph.D. in chemistry at Cornell
University.
Scientists who study
artificial photosynthesis materials and reactions have wanted to combine the
power of an electron probe with X-rays, but the two techniques typically can't
be performed by the same instrument.
Electron microscopes
(such as STEM or TEM) use beams of electrons and excel at characterizing the
atomic structure in parts of a material. In recent years, 4D STEM (or "2D
raster of 2D diffraction patterns using scanning transmission electron
microscopy") instruments, such as those at Berkeley Lab's Molecular
Foundry, have pushed the boundaries of electron microscopy even further,
enabling scientists to map out atomic or molecular regions in a variety of
materials, from hard metallic glass to soft, flexible films.
On the other hand, soft
(or lower-energy) X-rays are useful for identifying and tracking chemical
reactions in real time in an operando, or real-world,
environment.
But now, scientists can
have the best of both worlds. At the heart of the new technique is an
electrochemical "liquid cell" sample holder with remarkable
versatility. A thousand times thinner than a human hair, the device is
compatible with both STEM and X-ray instruments.
The electrochemical
liquid cell's ultrathin design allows reliable imaging of delicate samples
while protecting them from electron beam damage. A special electrode
custom-designed by co-author Cheng Wang, a staff scientist at Berkeley Lab's
Advanced Light Source, enabled the team to conduct X-ray experiments with the
electrochemical liquid cell. Combining the two allows researchers to
comprehensively characterize electrochemical reactions in real time and at the
nanoscale.
Getting granular
During 4D-STEM
experiments, Yao Yang and team used the new electrochemical liquid cell to
observe copper nanoparticles (ranging in size from 7 nanometers to 18
nanometers) evolve into active nanograins during CO2 electrolysis
-- a process that uses electricity to drive a reaction on the surface of an
electrocatalyst.
The experiments
revealed a surprise: copper nanoparticles combined into larger metallic copper
"nanograins" within seconds of the electrochemical reaction.
To learn more, the team
turned to Wang, who pioneered a technique known as "resonant soft X-ray
scattering (RSoXS) for soft materials," at the Advanced Light Source more
than 10 years ago.
With help from Wang,
the research team used the same electrochemical liquid cell, but this time
during RSoXS experiments, to determine whether copper nanograins facilitate CO2 reduction.
Soft X-rays are ideal for studying how copper electrocatalysts evolve during CO2 reduction,
Wang explained. By using RSoXS, researchers can monitor multiple reactions
between thousands of nanoparticles in real time, and accurately identify chemical
reactants and products.
The RSoXS experiments
at the Advanced Light Source -- along with additional evidence gathered at
Cornell High Energy Synchrotron Source (CHESS) -- proved that metallic copper
nanograins serve as active sites for CO2 reduction. (Metallic
copper, also known as copper(0), is a form of the element copper.)
During CO2 electrolysis,
the copper nanoparticles change their structure during a process called
"electrochemical scrambling." The copper nanoparticles' surface layer
of oxide degrades, creating open sites on the copper surface for CO2 molecules
to attach, explained Peidong Yang. And as CO2 "docks"
or binds to the copper nanograin surface, electrons are then transferred to CO2,
causing a reaction that simultaneously produces ethylene, ethanol, and propanol
along with other multicarbon products.
"The copper
nanograins essentially turn into little chemical manufacturing factories,"
Yao Yang said.
Further experiments at
the Molecular Foundry, the Advanced Light Source, and CHESS revealed that size
matters. All of the 7-nanometer copper nanoparticles participated in CO2 reduction,
whereas the larger nanoparticles did not. In addition, the team learned that
only metallic copper can efficiently reduce CO2 into
multicarbon products. The findings have implications for "rationally
designing efficient CO2 electrocatalysts," Peidong Yang
said.
The new study also
validated Peidong Yang's findings from 2017: That the 7-nanometer-sized copper
nanoparticles require low inputs of energy to start CO2 reduction.
As an electrocatalyst, the 7-nanometer copper nanoparticles required a
record-low driving force that is about 300 millivolts less than typical bulk
copper electrocatalysts. The best-performing catalysts that produce multicarbon
products from CO2 typically operate at high driving force of 1
volt.
The copper nanograins
could potentially boost the energy efficiency and productivity of some
catalysts designed for artificial photosynthesis, a field of research that aims
to produce solar fuels from sunlight, water, and CO2. Currently,
researchers within the Department of Energy-funded Liquid Sunlight Alliance
(LiSA) plan to use the copper nanograin catalysts in the design of future solar
fuel devices.
"The technique's
ability to record real-time movies of a chemical process opens up exciting
opportunities to study many other electrochemical energy conversion processes.
It's a huge breakthrough, and it would not have been possible without Yao and
his pioneering work," Peidong Yang said.
Researchers from
Berkeley Lab, UC Berkeley, and Cornell University contributed to the work.
Other authors on the paper include co-first authors Sheena Louisa and Sunmoon
Yu, former UC Berkeley Ph.D. students in Peidong Yang's group, along with
Jianbo Jin, Inwhan Roh, Chubai Chen, Maria V. Fonseca Guzman, Julian Feijóo,
Peng-Cheng Chen, Hongsen Wang, Christopher Pollock, Xin Huang, Yu-Tsuan Shao,
Cheng Wang, David A. Muller, and Héctor D. Abruña.
Parts of the
experiments were performed by Yao Yang at Cornell under the supervision of
Héctor Abruña, professor of chemistry and chemical biology, and David A.
Muller, professor of engineering.
This work was supported
by the DOE Office of Science.
The Molecular Foundry
and Advanced Light Source are user facilities at Berkeley Lab.
How a
record-breaking copper catalyst converts CO2 into liquid fuels -- ScienceDaily
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