Lifeboat Foundation

According to scientists at the U.S. Department of Energy’s National Renewable Energy Laboratory (NREL), a bifacial perovskite solar cell holds the potential to produce higher energy yields at lower overall costs.

The bifacial solar cell captures direct sunlight on the front and reflected sunlight on the back. As a result, this type of device can outperform its monofacial counterparts, according to the new study.

“This perovskite cell can operate very effectively from either side,” said Kai Zhu, a senior scientist in the Chemistry and Nanoscience Center at NREL and lead author of a new paper.

A team of researchers from the Instituto de Carboquímica of the Spanish National Research Council (CSIC) has made a remarkable step forward in the development of efficient and sustainable electronic devices. They have found a special combination of two extraordinary nanomaterials that successfully results in a new hybrid product capable of turning light into electricity, and vice-versa, faster than conventional materials.

The research is published in the journal Chemistry of Materials.

This new material consists of a one-dimensional conductive polymer called polythiophene, ingeniously integrated with a two-dimensional derivative of graphene known as graphene oxide. The unique features exhibited by this hybrid material hold incredible promise for improving the efficiency of optoelectronic devices, such as smart devices screens, and solar panels, among others.

Scientists have witnessed something extraordinary. According to new reports and research, scientists watched healing metal, where cracked metal fused back together without any kind of human intervention. The discovery is one that could completely change how machines work, because machines are often victims of what we call fatigue damage.

Fatigue damage is essentially one of the main ways that machines wear out, causing them to break over time. This is a natural condition that happens as machines go through repeated stress and motion, which causes microscopic cracks to form in the metal. Over time those cracks grow more, eventually spreading until the entire device breaks or fails.

Continue reading “Scientists watched cracked metal heal itself in an ‘absolutely stunning’ discovery” »

A combination of gentle stimulated emission depletion microscopy imaging and deep-learning-based improvements in signal-to-noise ratio enables high-resolution reconstruction of neuronal architecture in living tissue.

A team of scientists from Sandia National Laboratories and Texas A&M University has recently witnessed for the first time a stunning phenomenon: pieces of metal cracking, then fusing back together without any human intervention.

If this amazing phenomenon can be harnessed, it could give rise to an engineering revolution in which self-healing bridges, engines, or airplanes could reverse damage caused by wear and tear and thus become safer and longer-lasting.

“This was absolutely stunning to watch first-hand,” said Brad Boyce, a materials scientist at Sandia. “What we have confirmed is that metals have their own intrinsic, natural ability to heal themselves, at least in the case of fatigue damage at the nanoscale.”

Over the past decade, teams of engineers, chemists and biologists have analyzed the physical and chemical properties of cicada wings, hoping to unlock the secret of their ability to kill microbes on contact. If this function of nature can be replicated by science, it may lead to development of new products with inherently antibacterial surfaces that are more effective than current chemical treatments.

When researchers at Stony Brook University’s Department of Materials Science and Chemical Engineering developed a simple technique to duplicate the cicada wing’s nanostructure, they were still missing a key piece of information: How do the nanopillars on its surface actually eliminate bacteria? Thankfully, they knew exactly who could help them find the answer: Jan-Michael Carrillo, a researcher with the Center for Nanophase Materials Sciences at the Department of Energy’s Oak Ridge National Laboratory.

For nanoscience researchers who seek computational comparisons and insights for their experiments, Carrillo provides a singular service: large-scale, high-resolution molecular dynamics (MD) simulations on the Summit supercomputer at the Oak Ridge Leadership Computing Facility at ORNL.

Waveguiding scheme enables highly confined subnanometer optical fields.

Researchers have pioneered a novel method for confining light to subnanometer scales. This development offers promising potential for advancements in areas such as light-matter interactions and super-resolution nanoscopy.

Advancements in Light Confinement Technology.

DNA-programmed self-assembly leverages the chemical specificity of DNA hybridization to stabilize user-prescribed crystal structures^1,2. Pioneering studies have demonstrated that DNA hybridization can guide the self-assembly of a wide variety of nanoparticle crystal lattices, which can grow to micrometer dimensions and contain millions of particles^{3,4,5,6,7,8,9}. Attention has now turned toward the goal of assembling photonic crystals from optical-scale particles (i.e., roughly 100‑1000 nm in diameter)^10,11,12 using DNA-programmed interactions. To this end, progress over the past decade has established that DNA can indeed program the self-assembly of bespoke crystalline structures from micrometer-sized colloidal particles^{13,14,15,16,17,18,19}. However, growing single-domain crystals comprising millions of DNA-functionalized, micrometer-sized colloidal particles remains an unresolved barrier to the development of practical technologies based on DNA-programmed assembly. Prior efforts have yielded either single-domain crystals no more than a few dozen micrometers in size^13,14,15,16 or larger polycrystalline materials with heterogeneous domain sizes^12,15,17,20. These features—small crystal domains, polycrystallinity, and size dispersity—have therefore precluded the use of DNA-coated colloidal crystals in photonic metamaterial applications.

Assembling macroscopic materials from DNA-functionalized, micrometer-sized colloids is challenging due to the vastly different length scales between the DNA molecules and the colloidal particles (Fig. 1a). This combination leads to crystallization kinetics that are extremely sensitive to temperature and prone to kinetic trapping^1,21,22,23. The resulting challenges are both practical and fundamental in nature. For example, recent work has shown that crystal nucleation rates can vary by orders of magnitude over a temperature range of only 0.25 °C¹⁹. Extremely precise temperature control would therefore be required to self-assemble single-domain crystals from a bulk solution (Fig. 1b). At the same time, annealing polycrystalline materials is difficult due to the combination of the short-range attraction and the friction arising from the DNA-mediated colloidal interactions, which slows the rolling and sliding of colloidal particles at crystalline interfaces^15,19,24,25.

For many, the word “crystals” conjures images of shimmering suncatchers that create a prism of rainbow colors or semi-transparent stones thought to possess healing abilities. But in the realm of science and engineering, crystals take on a more technical definition. They’re perceived as materials whose components – be it atoms, molecules, or nanoparticles –are arranged regularly in space. In other words, crystals are defined by the regular arrangement of their constituents. Familiar examples include diamonds, table salt, and sugar cubes.