Solar nanowire array may increase percentage of sun’s frequencies available for energy conversion

Sandia nanowire template permits flexible energy absorption

Publication Date:

Sandia news media contact

Neal Singer
nsinger@sandia.gov
505-845-7078

Media Downloads

Caption

Cross-sectional images of the indium gallium nitride nanowire solar cell.

Credits

Image courtesy of Sandia National Laboratories

ALBUQUERQUE, N.M. — Researchers creating electricity through photovoltaics want to convert as many of the sun’s wavelengths as possible to achieve maximum efficiency. Otherwise, they’re eating only a small part of a shot duck: wasting time and money by using only a tiny bit of the sun’s incoming energies.

For this reason, they see indium gallium nitride as a valuable future material for photovoltaic systems. Changing the concentration of indium allows researchers to tune the material’s response so it collects solar energy from a variety of wavelengths. The more variations designed into the system, the more of the solar spectrum can be absorbed, leading to increased solar cell efficiencies. Silicon, today’s photovoltaic industry standard, is limited in the wavelength range it can ‘see’ and absorb.

But there is a problem: Indium gallium nitride, part of a family of materials called III-nitrides, is typically grown on thin films of gallium nitride. Because gallium nitride atomic layers have different crystal lattice spacings from indium gallium nitride atomic layers, the mismatch leads to structural strain that limits both the layer thickness and percentage of indium that can be added. Thus, increasing the percentage of indium added broadens the solar spectrum that can be collected, but reduces the material’s ability to tolerate the strain.

Image of Nanowire solar cell.

Sandia National Laboratories scientists Jonathan Wierer Jr. and George Wang reported in the journal Nanotechnology that if the indium mixture is grown on a phalanx of nanowires rather than on a flat surface, the small surface areas of the nanowires allow the indium shell layer to partially “relax” along each wire, easing strain. This relaxation allowed the team to create a nanowire solar cell with indium percentages of roughly 33 percent, higher than any other reported attempt at creating III-nitride solar cells.

This initial attempt also lowered the absorption base energy from 2.4eV to 2.1 eV, the lowest of any III-nitride solar cell to date, and made a wider range of wavelengths available for power conversion. Power conversion efficiencies were low — only 0.3 percent compared to a standard commercial cell that hums along at about 15 percent — but the demonstration took place on imperfect nanowire-array templates. Refinements should lead to higher efficiencies and even lower energies.

Several unique techniques were used to create the III-nitride nanowire array solar cell. A top-down fabrication process was used to create the nanowire array by masking a gallium nitride (GaN) layer with a colloidal silica mask, followed by dry and wet etching. The resulting array consisted of nanowires with vertical sidewalls and of uniform height.

Next, shell layers containing the higher indium percentage of indium gallium nitride (InGaN) were formed on the GaN nanowire template via metal organic chemical vapor deposition. Lastly, In0.02Ga0.98N was grown, in such a way that caused the nanowires to coalescence. This process produced a canopy layer at the top, facilitating simple planar processing and making the technology manufacturable.

The results, says Wierer, although modest, represent a promising path forward for III-nitride solar cell research. The nano-architecture not only enables higher indium proportion in the InGaN layers but also increased absorption via light scattering in the faceted InGaN canopy layer, as well as air voids that guide light within the nanowire array.

The research was funded by DOE’s Office of Science through the Solid State Lighting Science Energy Frontier Research Center, and Sandia’s Laboratory Directed Research and Development program.