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Dive into the research topics where Michael D. McGehee is active.

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Featured researches published by Michael D. McGehee.


Nature Materials | 2014

Perovskite solar cells: Continuing to soar

Michael D. McGehee

The dream of printing highly efficient solar cells is closer than ever to being realized. Solvent engineering has enabled the deposition of uniform perovskite semiconductor films that yield greater than 15% power-conversion efficiency.


Advanced Materials | 2017

Progress in Understanding Degradation Mechanisms and Improving Stability in Organic Photovoltaics.

William R. Mateker; Michael D. McGehee

Understanding the degradation mechanisms of organic photovoltaics is particularly important, as they tend to degrade faster than their inorganic counterparts, such as silicon and cadmium telluride. An overview is provided here of the main degradation mechanisms that researchers have identified so far that cause extrinsic degradation from oxygen and water, intrinsic degradation in the dark, and photo-induced burn-in. In addition, it provides methods for researchers to identify these mechanisms in new materials and device structures to screen them more quickly for promising long-term performance. These general strategies will likely be helpful in other photovoltaic technologies that suffer from insufficient stability, such as perovskite solar cells. Finally, the most promising lifetime results are highlighted and recommendations to improve long-term performance are made. To prevent degradation from oxygen and water for sufficiently long time periods, OPVs will likely need to be encapsulated by barrier materials with lower permeation rates of oxygen and water than typical flexible substrate materials. To improve stability at operating temperatures, materials will likely require glass transition temperatures above 100 °C. Methods to prevent photo-induced burn-in are least understood, but recent research indicates that using pure materials with dense and ordered film morphologies can reduce the burn-in effect.


Nano Letters | 2009

Optical Absorption Enhancement in Amorphous Silicon Nanowire and Nanocone Arrays

Jia Zhu; Z. Yu; George F. Burkhard; Ching-Mei Hsu; Stephen T. Connor; Yueqin Xu; Qi Wang; Michael D. McGehee; Shanhui Fan; Yi Cui

Hydrogenated amorphous Si (a-Si:H) is an important solar cell material. Here we demonstrate the fabrication of a-Si:H nanowires (NWs) and nanocones (NCs), using an easily scalable and IC-compatible process. We also investigate the optical properties of these nanostructures. These a-Si:H nanostructures display greatly enhanced absorption over a large range of wavelengths and angles of incidence, due to suppressed reflection. The enhancement effect is particularly strong for a-Si:H NC arrays, which provide nearly perfect impedance matching between a-Si:H and air through a gradual reduction of the effective refractive index. More than 90% of light is absorbed at angles of incidence up to 60 degrees for a-Si:H NC arrays, which is significantly better than NW arrays (70%) and thin films (45%). In addition, the absorption of NC arrays is 88% at the band gap edge of a-Si:H, which is much higher than NW arrays (70%) and thin films (53%). Our experimental data agree very well with simulation. The a-Si:H nanocones function as both absorber and antireflection layers, which offer a promising approach to enhance the solar cell energy conversion efficiency.


Applied Physics Letters | 2006

Organic solar cells with carbon nanotube network electrodes

Michael W. Rowell; Mark A. Topinka; Michael D. McGehee; Hans-Jürgen Prall; Gilles Dennler; Niyazi Serdar Sariciftci; Liangbing Hu; G. Grüner

We fabricated flexible transparent conducting electrodes by printing films of single-walled carbon nanotube (SWNT) networks on plastic and have demonstrated their use as transparent electrodes for efficient, flexible polymer-fullerene bulk-heterojunction solar cells. The printing method produces relatively smooth, homogeneous films with a transmittance of 85% at 550nm and a sheet resistance (Rs) of 200Ω∕◻. Cells were fabricated on the SWNT/plastic anodes identically to a process optimized for ITO/glass. Efficiencies, 2.5% (AM1.5G), are close to ITO/glass and are affected primarily by Rs. Bending test comparisons with ITO/plastic show the SWNT/plastic electrodes to be far more flexible.


Energy and Environmental Science | 2014

Hysteresis and transient behavior in current–voltage measurements of hybrid-perovskite absorber solar cells

Eva L. Unger; Eric T. Hoke; Colin D. Bailie; William H. Nguyen; Andrea R. Bowring; Thomas Heumüller; Mark G. Christoforo; Michael D. McGehee

Hybrid organo-metal halide perovskites are an exciting new class of solar absorber materials and have exhibited a rapid increase in solar cell efficiencies throughout the past two years to over 17% in both meso-structured and thin-film device architectures. We observe slow transient effects causing hysteresis in the current–voltage characterization of these devices that can lead to an over- or underestimation of the solar cell device efficiency. We find that the current–voltage (IV) measurement scan direction, measurement delay time, and light and voltage bias conditions prior to measurement can all have a significant impact upon the shape of the measured IV light curves and the apparent device efficiency. We observe that hysteresis-free light IV curves can be obtained at both extremely fast and slow voltage scan rates but only in the latter case are quasi-steady-state conditions achieved for a valid power conversion efficiency measurement. Hysteretic effects are also observed in devices utilizing alternative selective contacts but differ in magnitude and time scale, suggesting that the contact interfaces have a big effect on transients in perovskite-absorber devices. The transient processes giving rise to hysteresis are consistent with a polarization response of the perovskite absorber that results in changes in the photocurrent extraction efficiency of the device. The strong dependence of the hysteresis on light and voltage biasing conditions in thin film devices for a period of time prior to the measurement suggests that photo-induced ion migration may additionally play an important role in device hysteresis. Based on these observations, we provide recommendations for correct measurement and reporting of IV curves for perovskite solar cell devices.


Advanced Materials | 2000

Semiconducting (Conjugated) Polymers as Materials for Solid‐State Lasers

Michael D. McGehee; Alan J. Heeger

Light-emissive polymers are outstanding laser materials because they are intrinsically “4-level” systems, they have luminescence efficiencies higher than 60 % even in undiluted films, they emit at colors that span the visible spectrum, and they can be processed into optical quality films by spin casting. The important materials issues are reviewed and the prospects for making polymer diode lasers are discussed.


Materials Today | 2007

Polymer-based solar cells

Alex C. Mayer; Shawn R. Scully; Brian E. Hardin; Michael W. Rowell; Michael D. McGehee

A significant fraction of the cost of solar panels comes from the photoactive materials and sophisticated, energy-intensive processing technologies. Recently, it has been shown that the inorganic components can be replaced by semiconducting polymers capable of achieving reasonably high power conversion efficiencies. These polymers are inexpensive to synthesize and can be solution-processed in a roll-to-roll fashion with high throughput. Inherently poor polymer properties, such as low exciton diffusion lengths and low mobilities, can be overcome by nanoscale morphology. We discuss polymer-based solar cells, paying particular attention to device design and potential improvements.


Nano Letters | 2010

Electrospun Metal Nanofiber Webs as High-Performance Transparent Electrode

Hui Wu; Liangbing Hu; Michael W. Rowell; Desheng Kong; Judy J. Cha; James R. McDonough; Jia Zhu; Yuan Yang; Michael D. McGehee; Yi Cui

Transparent electrodes, indespensible in displays and solar cells, are currently dominated by indium tin oxide (ITO) films although the high price of indium, brittleness of films, and high vacuum deposition are limiting their applications. Recently, solution-processed networks of nanostructures such as carbon nanotubes (CNTs), graphene, and silver nanowires have attracted great attention as replacements. A low junction resistance between nanostructures is important for decreasing the sheet resistance. However, the junction resistances between CNTs and boundry resistances between graphene nanostructures are too high. The aspect ratios of silver nanowires are limited to ∼100, and silver is relatively expensive. Here, we show high-performance transparent electrodes with copper nanofiber networks by a low-cost and scalable electrospinning process. Copper nanofibers have ultrahigh aspect ratios of up to 100000 and fused crossing points with ultralow junction resistances, which result in high transmitance at low sheet resistance, e.g., 90% at 50 Ω/sq. The copper nanofiber networks also show great flexibility and stretchabilty. Organic solar cells using copper nanowire networks as transparent electrodes have a power efficiency of 3.0%, comparable to devices made with ITO electrodes.


Angewandte Chemie | 2014

A Layered Hybrid Perovskite Solar‐Cell Absorber with Enhanced Moisture Stability

Ian C. Smith; Eric T. Hoke; Diego Solis-Ibarra; Michael D. McGehee; Hemamala I. Karunadasa

Two-dimensional hybrid perovskites are used as absorbers in solar cells. Our first-generation devices containing (PEA)2(MA)2[Pb3I10] (1; PEA=C6H5(CH2)2NH3(+), MA=CH3NH3(+)) show an open-circuit voltage of 1.18 V and a power conversion efficiency of 4.73%. The layered structure allows for high-quality films to be deposited through spin coating and high-temperature annealing is not required for device fabrication. The 3D perovskite (MA)[PbI3] (2) has recently been identified as a promising absorber for solar cells. However, its instability to moisture requires anhydrous processing and operating conditions. Films of 1 are more moisture resistant than films of 2 and devices containing 1 can be fabricated under ambient humidity levels. The larger bandgap of the 2D structure is also suitable as the higher bandgap absorber in a dual-absorber tandem device. Compared to 2, the layered perovskite structure may offer greater tunability at the molecular level for material optimization.


Advanced Materials | 2011

Smooth Nanowire/Polymer Composite Transparent Electrodes

Whitney Gaynor; George F. Burkhard; Michael D. McGehee; Peter Peumans

IO N Transparent electrodes are critical components of thin-fi lm optoelectronic devices such as displays and thin-fi lm solar cells. Most high-performance transparent conducting fi lms in use today are composed of sputtered metal oxides. [ 1 , 2 ] These fi lms can have sheet resistances under 20 Ω − 1 with 90% transmission when deposited at a high temperature onto glass and resistances increasing to 40–200 Ω − 1 with the same transmission when deposited at lower temperatures onto plastic substrates. [ 2 , 3 ] Recent research has focused on replacing conductive metal oxides with alternative materials that can be deposited from solution and can reproduce the performance of metal oxides on glass on various substrates, including plastics. In addition, metal oxides are brittle, [ 4 , 5 ] and thus alternative transparent conductor technologies are also focusing on fl exibility and robustness to enable lightweight, fl exible solar cells and other thin fi lm devices. Strategies for non-vacuum deposition of transparent electrodes make use of materials other than metal oxides [ 6 ]

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Michael F. Toney

SLAC National Accelerator Laboratory

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Michael Grätzel

École Polytechnique Fédérale de Lausanne

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