• Energy Research

The integration of nanophotonic and plasmonic structures with solar cells offers the ability to control and confine light in nanoscale dimensions. These nanostructures can be used to couple incident sunlight into both localized and guided modes, enhancing absorption while reducing the quantity of material. Here we use electromagnetic modeling to study the resonances in a solar cell containing both plasmonic metal back contacts and nanostructured semiconductor top contacts, identify the local and guided modes contributing to enhanced absorption, and optimize the design. We then study the role of the different interfaces and show that Al is a viable plasmonic back contact material.

Low-intensity high-temperature solar cells that operate effectively in the atmosphere of Venus at various altitudes and also survive on the 465 °C surface of Venus are being developed. Thermal stability, high-temperature current–voltage ( I–V ), and external quantum efficiency measurements on GaInP/GaAs double-junction solar cells are presented. Solar-cell modeling under the atmospheric conditions of Venus is used to design the optimum solar-cell structure.

The optical transparency and high electron mobility of graphene make it an attractive material for photovoltaics. We present a field-effect solar cell using graphene to form a tunable junction barrier with an Earth-abundant and low cost zinc phosphide (Zn3P2) thin-film light absorber. Adding a semitransparent top electrostatic gate allows for tuning of the graphene Fermi level and hence the energy barrier at the graphene-Zn3P2 junction, going from an ohmic contact at negative gate voltages to a rectifying barrier at positive gate voltages. We perform current and capacitance measurements at different gate voltages in order to demonstrate the control of the energy barrier and depletion width in the zinc phosphide. Our photovoltaic measurements show that the efficiency conversion is increased 2-fold when we increase the gate voltage and the junction barrier to maximize the photovoltaic response. At an optimal gate voltage of +2 V, we obtain an open-circuit voltage of V oc = 0.53 V and an efficiency of 1.9% under AM 1.5 1-sun solar illumination. This work demonstrates that the field effect can be used to modulate and optimize the response of photovoltaic devices incorporating graphene.

In this paper we investigate the use of holographic filters in solar spectrum splitting applications. Photovoltaic (PV) systems utilizing spectrum splitting have higher theoretical conversion efficiency than single bandgap cell modules. Dichroic band-rejection filters have been used for spectrum splitting applications with some success however these filters are limited to spectral control at fixed reflection angles. Reflection holographic filters are fabricated by recording interference pattern of two coherent beams at arbitrary construction angles. This feature can be used to control the angles over which spectral selectivity is obtained. In addition focusing wavefronts can also be used to increase functionality in the filter. Holograms fabricated in dichromated gelatin (DCG) have the benefit of light weight, low scattering and absorption losses. In addition, reflection holograms recorded in the Lippmann configuration have been shown to produce strong chirping as a result of wet processing. Chirping broadens the filter rejection bandwidth both spectrally and angularly. It can be tuned to achieve spectral bandwidth suitable for spectrum splitting applications. We explore different DCG film fabrication and processing parameters to improve the optical performance of the filter. The diffraction efficiency bandwidth and scattering losses are optimized by changing the exposure energy, isopropanol dehydration bath temperature and hardening bath duration. A holographic spectrum-splitting PV module is proposed with Gallium Arsenide (GaAs) and silicon (Si) PV cells with efficiency of 25.1% and 19.7% respectively. The calculated conversion efficiency with a prototype hologram is 27.94% which is 93.94% compared to the ideal spectrum-splitting efficiency of 29.74%.

Continuum modeling elucidates non-equilibrium behavior in bipolar membranes (BPMs) used for carbon capture. The model resolves contributions to applied voltage, identifying CO2bubble removal and water dissociation catalysis as the dominant energy losses.

Silicon microwire arrays have recently demonstrated their potential for low-cost, high-efficiency photovoltaics and photoelectrochemical fuel generation. A remaining challenge to making this technology commercially viable is scaling up of microwire-array growth. We discuss here a technique for vapor–liquid–solid growth of microwire arrays on the scale of six-inch wafers using a cold-wall radio-frequency heated chemical vapor deposition furnace, enabling fairly uniform growth over large areas with rapid cycle time and improved run-to-run reproducibility. We have also developed a technique to embed these large-area wire arrays in polymer and to peel them intact from the growth substrate, which could enable lightweight, flexible solar cells with efficiencies as high as multicrystalline Si solar cells. We characterize these large-area microwire arrays using scanning electron microscopy and confocal microscopy to assess their structure and fidelity, and we test their energy-conversion properties using a methyl viologen (MV $^{2+/+}$ ) liquid junction contact in a photoelectrochemical cell. Initial photoelectrochemical conversion efficiencies suggest that the material quality of these microwire arrays is similar to smaller (∼1 cm $^2$ ) wire arrays that we have grown in the past, indicating that this technique is a viable way to scale up microwire-array devices.

AbstractResonant dielectric structures are a promising platform for addressing the key challenge of light trapping in thin‐film solar cells. We experimentally and theoretically demonstrate efficiency enhancements in solar cells from dielectric nanosphere arrays. Two distinct amorphous silicon photovoltaic architectures were improved using this versatile light‐trapping platform. In one structure, the colloidal monolayer couples light into the absorber in the near‐field acting as a photonic crystal light‐trapping element. In the other, it acts in the far‐field as a graded index antireflection coating to further improve a cell which already included a state‐of‐the‐art random light‐trapping texture to achieve a conversion efficiency over 11%. For the near‐field flat cell architecture, we directly fabricated the colloidal monolayer on the device through Langmuir–Blodgett deposition in a scalable process that does not degrade the active material. In addition, we present a novel transfer printing method, which utilizes chemical crosslinking of an optically thin adhesion layer to tether sphere arrays to the device surface. The minimally invasive processing conditions of this transfer method enable the application to a wide range of solar cells and other optoelectronic devices. magnified image False‐color SEM image of an amorphous silicon solar cell with resonant spheres on top.

AbstractSpectrum‐splitting photovoltaics incorporate optical elements to separate sunlight into frequency bands, which can be targeted at solar cells with bandgaps optimized for each sub‐band. Here, we present the design of a holographic diffraction grating‐based spectrum‐splitting photovoltaic module integrating eight III‐V compound semiconductor cells as four dual‐junction tandems. Four stacks of simple sinusoidal volume phase holographic diffraction gratings each simultaneously split and concentrate sunlight onto cells with bandgaps spanning the solar spectrum. The high‐efficiency cells get an additional performance boost from concentration incorporated using a single or a compound trough concentrator, providing up to 380X total concentration. Cell bandgap optimization incorporated an experimentally derived bandgap‐dependent external radiative efficiency function. Simulations show 33.2% module conversion efficiency is achievable. One grating stack is experimentally fabricated and characterized.