We specialize in the synthesis, understanding, and deployment of nanoscale materials to enable new electronic, photonic, and energy technologies. 

Image from: I. R. Musin, D. S. Boyuk, M. A. Filler, Surface Chemistry Controlled Diameter-Modulated Semiconductor Nanowire Superstructures, J. Vac. Sci. Technol. B. 31 020603 (2013). 

 

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Explore our publications appearing in scientific journals including the Journal of the American Chemical Society, Angewandte Chemie, Nano Letters, ACS Nano, and many more.

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Prof. Filler

Dr. Michael A. Filler is an Associate Professor and the Traylor Faculty Fellow in the School of Chemical & Biomolecular Engineering at the Georgia Institute of Technology. 

Our research aims to overcome the challenges that stand in the way of using nanoscale materials. 

 

Challenge #1: A LACK OF ATOMIC-lEVEL design rules

 The synthesis of functional nanoscale objects remains a largely trial-and-error endeavor. We do not have the fundamental chemical knowledge needed to a priori control structure and properties. 

Challenge #2: Scale-up is harD 

Future technologies will require large quantities -- tons rather than grams -- of nanoscale objects from which to build new materials and devices. Attempts to scale production usually sacrifice structural fidelity and destroy function. 

Challenge #3: AssemblY is very hard

The production of macroscopic materials and devices via the assembly of nanoscopic building blocks, each with tailored properties, has been a long-standing goal. Processes to do this with the necessary speed, precision, and error-tolerance do not exist.   

 
 

Understanding semiconductor nanowire growth

Semiconductor nanowires are quintessential nanoscale building blocks and the vapor-liquid-solid technique – where a liquid “catalyst” droplet collects atoms from the vapor and directs crystallization of individual solid layers – is a workhorse method for their synthesis. The encoding of different functionalities (e.g., heterostructures, pn junctions, etc.) along the length of individual nanowires makes these materials interesting for a range of electronic, photonic, and energy applications. 

 
Vapor-liquid-solid (VLS) nanowire synthesis and the functional encoding (left, doping; right, heterostructuring) possible by tuning gas phase composition. 


Vapor-liquid-solid (VLS) nanowire synthesis and the functional encoding (left, doping; right, heterostructuring) possible by tuning gas phase composition. 

 

The inability to synthesize many desired, and even simple, nanowire structures demonstrates that the mechanistic understanding of growth is far from complete. We combine in situ infrared spectroscopy with electron microscopy to connect the specific, short-lived chemical bonds present during growth with nanowire crystal structure and physical properties. Our studies are providing an atomic-level chemical framework with which to understand nanowire growth and rationally tune the relative rates of important, structure-directing surface reactions. 

 
Transient sidewall chemistry controls Ge nanowire growth stability (From: Sivaram et al, J. Am. Chem. Soc. 2015)


Transient sidewall chemistry controls Ge nanowire growth stability (From: Sivaram et al, J. Am. Chem. Soc. 2015)

 

Engineering nanowire structure

We are leveraging our understanding of nanowire growth to design chemistries that endow nanowires with a structural precision and functional diversity superior to the state-of-the-art. Independent control of the chemical bonding at each of the heterointerfaces involved in vapor-liquid-solid growth is essential, but not possible with conventional 2-D thin film precursors (e.g., hydrides). Our approach utilizes multiple distinct precursors, each designed to direct a specific heterointerfacial process, to choreograph synthesis. This precursor "toolkit" allows us to engineer nanowire crystal orientation, bilayer stacking sequence, diameter, dopant profile, and more.  

 
Kinking superstructures via precursor design (From: Musin et al, Nano Lett. 2012)


Kinking superstructures via precursor design (From: Musin et al, Nano Lett. 2012)

Surface passivation blocks sidewall deposition and permits programming of nanowire diameter (From: Musin et al, J. Vac. Sci. Technol. B 2013)


Surface passivation blocks sidewall deposition and permits programming of nanowire diameter (From: Musin et al, J. Vac. Sci. Technol. B 2013)

 

Semiconductor nanowire plasmonics

Surface plasmons enable the confinement and transport of light in deep-subwavelength volumes. Noble metals offer this extraordinary capability in the visible/near-infrared, yielding extreme chemical sensitivity (e.g., surface enhanced Raman scattering), high resolution near-field imaging, compact waveguides, and more. However, conventional metals cannot support truly localized surface plasmon resonances (LSPRs) at mid-/far-infrared wavelengths since they become nearly perfect conductors. 

Nanoscale semiconductors are emerging as alternative, more flexible materials for manipulating light-matter interactions in the infrared. The tunability of semiconductor permittivity via chemical doping and/or electrostatic gating is central to their promise. Vapor-liquid-solid growth of semiconductor nanowires, which offers nanoscale control of dopant profile, provides an intriguing route to engineer both near- and far-field optical response. We are synthesizing and characterizing a range of plasmonic semiconductor nanowires with the goal of enabling narrowband infrared light sources, compact thermal waveguides, and ultrasensitive chemical sensors.

 
Using coupled localized surface plasmon resonances (LSPRs) in semiconductor nanowires to focus infrared light (From: Boyuk et al, ACS Photon. 2016)


Using coupled localized surface plasmon resonances (LSPRs) in semiconductor nanowires to focus infrared light (From: Boyuk et al, ACS Photon. 2016)

 

Plasmon-enhanced catalysis

Surface plasmons, specifically their decay via local heating, energy transfer, or hot electron-hole pair generation, can influence heterogeneous chemical reactions. The inherent catalytic behavior, earth-abundance, and stability of many metal oxides, coupled with an ability to tune their plasmonic properties, makes these materials intriguing plasmonic catalysts. We are studying how surface plasmons supported by these materials can modify both reaction rate and product distribution.  

 

We are grateful for the financial support of the following agencies and organizations:

National Science Foundation

U.S. Department of Energy

Air Force Office of Scientific Research

The Camille & Henry Dreyfus Foundation

Chih Foundation

Georgia Institute of Technology