Mostrando entradas con la etiqueta Fotoelectricidad. Mostrar todas las entradas
Mostrando entradas con la etiqueta Fotoelectricidad. Mostrar todas las entradas

martes, 28 de enero de 2014

How to Tap the Sun’s Energy Through Heat as Well as Light

New approach developed at MIT could generate power from sunlight efficiently and on demand.

A new approach to harvesting solar energy, developed by MIT researchers, could improve efficiency by using sunlight to heat a high-temperature material whose infrared radiation would then be collected by a conventional photovoltaic cell. This technique could also make it easier to store the energy for later use, the researchers say.
Photo courtesy John Freidah. A nanophotonic solar thermophotovoltaic device composed of
  • an array of multi‑walled carbon nanotubes as the absorber
  • a one‑dimensional silicon/silicon dioxide photonic crystal as the emitter, and 
  • a 0.55 eV photovoltaic cell
In this case, adding the extra step improves performance, because it makes it possible to take advantage of wavelengths of light that ordinarily go to waste. The process is described in a paper published this week in the journal Nature Nanotechnology, written by graduate student Andrej Lenert, associate professor of mechanical engineering Evelyn Wang, physics professor Marin Soljačić, principal research scientist Ivan Celanović, and three others.

A conventional silicon-based solar cell “doesn’t take advantage of all the photons,” Wang explains. That’s because converting the energy of a photon into electricity requires that the photon’s energy level match that of a characteristic of the photovoltaic (PV) material called a bandgap. Silicon’s bandgap responds to many wavelengths of light, but misses many others.

To address that limitation, the team inserted a two-layer absorber-emitter device — made of novel materials including carbon nanotubes and photonic crystals — between the sunlight and the PV cell. This intermediate material collects energy from a broad spectrum of sunlight, heating up in the process. When it heats up, as with a piece of iron that glows red hot, it emits light of a particular wavelength, which in this case is tuned to match the bandgap of the PV cell mounted nearby.


This basic concept has been explored for several years, since in theory such solar thermophotovoltaic (STPV) systems could provide a way to circumvent a theoretical limit on the energy-conversion efficiency of semiconductor-based photovoltaic devices. That limit, called the Shockley-Queisser limit, imposes a cap of 33.7 percent on such efficiency, but Wang says that with TPV systems, “the efficiency would be significantly higher — it could ideally be over 80 percent.

There have been many practical obstacles to realizing that potential; previous experiments have been unable to produce a STPV device with efficiency of greater than 1 percent. But Lenert, Wang, and their team have already produced an initial test device with a measured efficiency of 3.2 percent, and they say with further work they expect to be able to reach 20 percent efficiencyenough, they say, for a commercially viable product.

The design of the two-layer absorber-emitter material is key to this improvement. Its outer layer, facing the sunlight, is an array of multiwalled carbon nanotubes, which very efficiently absorbs the light’s energy and turns it to heat. This layer is bonded tightly to a layer of a photonic crystal, which is precisely engineered so that when it is heated by the attached layer of nanotubes, it “glows” with light whose peak intensity is mostly above the bandgap of the adjacent PV, ensuring that most of the energy collected by the absorber is then turned into electricity.

In their experiments, the researchers used simulated sunlight, and found that its peak efficiency came when its intensity was equivalent to a focusing system that concentrates sunlight by a factor of 750. This light heated the absorber-emitter to a temperature of 962 degrees Celsius.

This level of concentration is already much lower than in previous attempts at STPV systems, which concentrated sunlight by a factor of several thousand. But the MIT researchers say that after further optimization, it should be possible to get the same kind of enhancement at even lower sunlight concentrations, making the systems easier to operate.

Such a system, the team says, combines the advantages of solar photovoltaic systems, which turn sunlight directly into electricity, and solar thermal systems, which can have an advantage for delayed use because heat can be more easily stored than electricity. The new solar thermophotovoltaic systems, they say, could provide

  • efficiency because of their broadband absorption of sunlight
  • scalability and compactness, because they are based on existing chip-manufacturing technology; and 
  • ease of energy storage, because of their reliance on heat.
Some of the ways to further improve the system are quite straightforward. Since the intermediate stage of the system, the absorber-emitter, relies on high temperatures, its size is crucial: The larger an object, the less surface area it has in relation to its volume, so heat losses decline rapidly with increasing size. The initial tests were done on a 1-centimeter chip, but follow-up tests will be done with a 10-centimeter chip, they say.

Zhuomin Zhang, a professor of mechanical engineering at the Georgia Institute of Technology who was not involved in this research, says, “This work is a breakthrough in solar thermophotovoltaics, which in principle may achieve higher efficiency than conventional solar cells because STPV can take advantage of the whole solar spectrum. … This achievement paves the way for rapidly boosting the STPV efficiency.

The research team also included MIT graduate students David Bierman and Walker Chan, former postdoc Youngsuk Nam, and research scientist Ivan Celanović. The work was funded by the U.S. Department of Energy through MIT’s Solid-State Solar Thermal Energy Conversion (S3TEC) Center, as well as the Martin Family Society, the MIT Energy Initiative, and the National Science Foundation.



ORIGINAL: Tech Review
By David L. Chandler
January 23, 2014

jueves, 31 de enero de 2013

It’s (Almost) Alive! Scientists Create a Near-Living Crystal

ORIGINAL: Wired
01.31.13


Three billion years after inanimate chemistry first became animate life, a newly synthesized laboratory compound is behaving in uncannily lifelike ways.

The particles aren’t truly alive — but they’re not far off, either. Exposed to light and fed by chemicals, they form crystals that move, break apart and form again.

There is a blurry frontier between active and alive,” said biophysicist Jérémie Palacci of New York University. “That is exactly the kind of question that such works raise.”

Palacci and fellow NYU physicist Paul Chaikin led a group of researchers in developing the particles, which are described Jan. 31 in Science as forming “living crystals” in the right chemical conditions.

Their experiments are rooted in the researchers’ interest in self-organizing collective behaviors, which are easier to study in controlled particle form than in schooling fish or flocking birds.

Each particle is made from a microscopic cube of hematite, a compound consisting of iron and oxygen, sheathed in a spherical polymer coat. One corner is left exposed.

Under certain wavelengths of blue light, hematite conducts electricity. When the particles are placed in a hydrogen peroxide bath under blue light, chemical reactions catalyze around the exposed tips.

'There is a blurry frontier between active and alive.'As the hydrogen peroxide breaks down, concentration gradients form. The particles travel down these, aggregating into crystals that also follow the gradients.

Random forces pull the crystals apart, but eventually they merge again. The process repeats again and again, stopping only when the lights go out.

The ultimate goal of the work is to study how complicated collective behaviors arise from simple individual properties, perhaps informing molecular self-assembly projects, but it’s hard not to think about the origin-of-life implications.

Here we show that with a simple, synthetic active system, we can reproduce some features of living systems,” Palacci said. “I do not think this makes our systems alive, but it stresses the fact that the limit between the two is somewhat arbitrary.”

Chaikin notes that life is difficult to define, but can be said to possess metabolism, mobility, and the ability to self-replicate. His crystals have the first two, but not the last.

Some scientists think that life’s building blocks once existed in such a form, bouncing back and forth for millions of years until coalescing in configurations that possessed the ability to copy themselves.

Add slight imperfections in the copies — mutations, in other words — and the necessary conditions for natural selection and evolution would be fulfilled.

Inasmuch as it’s possible to say what might have happened billions of years ago, the rest was evolutionary history.

As for what’s happening now in Palacci and Chaikin’s lab, a particle currently under development isn’t mobile, but it has a metabolism and is self-replicating.

We’re working on it,” Chaikin said.

Citation: “Living Crystals of Light-Activated Colloidal Surfers.” By Jeremie Palacci, Stefano Sacanna, Asher Preska Steinberg, David J. Pine, Paul M. Chaikin. Science, Vol. 339 No. 6119, 1 February 2013.