Two-dimensional, "sheet-like" nanostructures are commonly employed in biological systems such as cell membranes, and their unique properties have inspired interest in materials such as graphene. Now, Berkeley Lab scientists have made the largest two-dimensional polymer crystal self-assembled in water to date. This entirely new material mirrors the structural complexity of biological systems with the durable architecture needed for membranes or integration into functional devices.
These self-assembling sheets are made of peptoids, engineered polymers that can flex and fold like proteins while maintaining the robustness of manmade materials. Each sheet is just two molecules thick yet hundreds of square micrometers in area—akin to 'molecular paper' large enough to be visible to the naked eye.
 Caption: Ron Zuckermann (left) and Ki Tae Nam with Berkeley Lab's Molecular Foundry, have developed a "molecular paper" material whose properties can be precisely tailored to control the flow of molecules, or serve as a platform for chemical and biological detection. Credit: Photo by Roy Kaltschmidt, Berkeley Lab Public Affairs. Usage Restrictions: None. | What's more, unlike a typical polymer, each building block in a peptoid nanosheet is encoded with structural 'marching orders'—suggesting its properties can be precisely tailored to an application. For example, these nanosheets could be used to control the flow of molecules, or serve as a platform for chemical and biological detection. "Our findings bridge the gap between natural biopolymers and their synthetic counterparts, which is a fundamental problem in nanoscience," said Ronald Zuckermann, Director of the Biological Nanostructures Facility at the Molecular Foundry. "We can now translate fundamental sequence information from proteins to a non-natural polymer, which results in a robust synthetic nanomaterial with an atomically-defined structure." |
Zuckermann and coauthor Christian Kisielowski reached another first by using the TEAM 0.5 microscope at the National Center for Electron Microscopy (NCEM) to observe individual polymer chains within the peptoid material, confirming the precise ordering of these chains into sheets and their unprecedented stability while being bombarded with electrons during imaging.
"The design of nature-inspired, functional polymers that can be assembled into membranes of large lateral dimensions marks a new chapter for materials synthesis with direct impact on Berkeley Lab's strategically relevant initiatives such as the Helios project or Carbon Cycle 2.0," said NCEM's Kisielowski. "The scientific possibilities that come with this achievement challenge our imagination, and will also help move electron microscopy toward direct imaging of soft materials."
"This new material is a remarkable example of molecular biomimicry on many levels, and will no doubt lead to many applications in device fabrication, nanoscale synthesis and imaging," Zuckermann added. ###
This research is reported in a paper titled, "Free floating ultra-thin two-dimensional crystals from sequence-specific peptoid polymers," appearing in the journal Nature Materials and available in Nature Materials online. Co-authoring the paper with Zuckermann and Kisielowski were Ki Tae Nam, Sarah Shelby, Phillip Choi, Amanda Marciel, Ritchie Chen, Li Tan, Tammy Chu, Ryan Mesch, Byoung-Chul Lee and Michael Connolly.
This work at the Molecular Foundry was supported by DOE's Office of Science and the Defense Threat Reduction Agency.
The Molecular Foundry is one of the five DOE Nanoscale Science Research Centers (NSRCs), premier national user facilities for interdisciplinary research at the nanoscale. Together the NSRCs comprise a suite of complementary facilities that provide researchers with state-of-the-art capabilities to fabricate, process, characterize and model nanoscale materials, and constitute the largest infrastructure investment of the National Nanotechnology Initiative. The NSRCs are located at DOE's Argonne, Brookhaven, Lawrence Berkeley, Oak Ridge and Sandia and Los Alamos National Laboratories. For more information about the DOE NSRCs, please visit nano.energy.gov.
Berkeley Lab is a U.S. Department of Energy national laboratory located in Berkeley, California. It conducts unclassified scientific research and is managed by the University of California. Visit our website at www.lbl.gov.
Contact: Aditi Risbud asrisbud@lbl.gov 510-486-4861 DOE/Lawrence Berkeley National Laboratory
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Nanoscale molecular research holds the key to research progress by data density, which depends on the atomic topological function used. Recent advancements in quantum science have produced the picoyoctometric, 3D, interactive video atomic model imaging function, in terms of chronons and spacons for exact, quantized, relativistic animation. This format returns clear numerical data for a full spectrum of variables. The atom's RQT (relative quantum topological) data point imaging function is built by combination of the relativistic Einstein-Lorenz transform functions for time, mass, and energy with the workon quantized electromagnetic wave equations for frequency and wavelength.
The atom labeled psi (Z) pulsates at the frequency {Nhu=e/h} by cycles of {e=m(c^2)} transformation of nuclear surface mass to forcons with joule values, followed by nuclear force absorption. This radiation process is limited only by spacetime boundaries of {Gravity-Time}, where gravity is the force binding space to psi, forming the GT integral atomic wavefunction. The expression is defined as the series expansion differential of nuclear output rates with quantum symmetry numbers assigned along the progression to give topology to the solutions.
Next, the correlation function for the manifold of internal heat capacity energy particle 3D functions is extracted by rearranging the total internal momentum function to the photon gain rule and integrating it for GT limits. This produces a series of 26 topological waveparticle functions of the five classes; {+Positron, Workon, Thermon, -Electromagneton, Magnemedon}, each the 3D data image of a type of energy intermedon of the 5/2 kT J internal energy cloud, accounting for all of them.
Those 26 energy data values intersect the sizes of the fundamental physical constants: h, h-bar, delta, nuclear magneton, beta magneton, k (series). They quantize atomic dynamics by acting as fulcrum particles. The result is the exact picoyoctometric, 3D, interactive video atomic model data point imaging function, responsive to software application keyboard input of virtual photon gain events by relativistic, quantized shifts of electron, force, and energy field states and positions. This system also gives a new equation for the magnetic flux variable B, which appears as a waveparticle of changeable frequency. Molecular modeling and chip design engineering application software developer features for programming flow are built-in.
Images of the h-bar magnetic energy waveparticle of ~175 picoyoctometers are available online at http://www.symmecon.com with the complete RQT atomic modeling manual titled The Crystalon Door, copyright TXu1-266-788. TCD conforms to the unopposed motion of disclosure in U.S. District (NM) Court of 04/02/2001 titled The Solution to the Equation of Schrodinger.
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