NSF Workshop: Emerging Opportunities of Nanoscience to Energy Conversion and Storage

 

 

Section 6: BioNano Techniques for Energy Applications

 

T.H. LaBean, D. Feldheim, H. Yan, T. Lin, N. Seeman

 

 

The State of Energy Usage.

            The following energy facts were taken from [Maugeri, Science, 2004, 304, 1114.].

The current global rate of energy consumption is 400,000 PetaJoules per year, equal to 4 million nuclear bombs. Twenty-five percent of that is consumed by the US, and eighty-five percent is generated from fossil fuels. This leads to a total carbon output per year of 7 GigaTons (109 Tons), which is enough CO2 to fill Lake Michigan every year. Global energy demand by the year 2050 will exceed 1 Million PetaJoules (1021 J), and the amount of CO2 in the atmosphere will double, causing a global temperature rise of up to 4 ¼C. Further calculations by major sources claim that current world oil reserves equal 1 trillion barrels, and since the current global consumption rate is 28 billion barrels per year, we have a maximum of 35 years of oil remaining.

 

Alternative Sources of Energy.

Examination of the usual list of alternative energy resources shows that we could potentially produce approximately 150,000 PJ from biomass, 40,000 PJ from wind, 20,000 PJ from hydroelectric. So allowing for growth in consumption, we would need something like 250,000 PJ from nuclear, which could only be provided if one new power plant is opened every 2 days until 2050. Instead, we must turn to alternative methods for exploiting solar power. In fact, more energy is available from the sun in one hour than we use in one year. Harvesting solar energy is a $7 Billion Industry that is growing at a rate of 32% per year. Besides active (photovoltaic) solar energy harvesting and passive solar designs for lighting and heating, we can finally follow the lead of visionary Jules Verne, who in 1874 commented, ÒWater will be the coal of the future.Ó

 

Photocatalytic Water Splitting (Energy Storage)

Hydrogen Oxidation (Energy Release)

Without catalysts these reactions are useless!

 

New catalysts are needed to produce and utilize alternative fuels. Catalyst design is exceedingly difficult; catalyst discovery relies largely on serendipity.  We now know that RNA can evolve in response to selection pressures (magnetism) to catalyze the formation of materials with a desired property. Can biomolecule evolution be used to discover new catalysts for alternative energy and CO2 sequestration?

 

 

BioNano Assembly and Selection Approaches.

Bionanomaterials can help on at least two different fronts:

1). Nanofabrication of photovoltaic, thermoelectric, and nanoelectronic materials by biomolecule-guided self-assembly

2). Biomolecule-driven evolution of inorganic catalysts for energy applications.

 

 

 

            Bionanoassembly makes use of biological inspiration and biomacromolecules for fabrication of specific nanostructures via molecular recognition reactions.  Assembly of a variety of nanoscale materials into complex structures have been accomplished by programmable assembly using DNA and viral particles.  Using DNA tile building blocks, objects have been created with sizes between microns and millimeters and having feature resolution less than 5-10 nanometers.  We hope to apply these achievements to solve problems in photovoltaics, thermoelectrics, nanophotonics, battery, fuel cell, and fuel conversion areas which would benefit from the ability to organize nanomaterials into designed structures with low nanometer resolution.

 

            Directed evolution of biomolecules capable of templating the deposition of diverse inorganic materials into specific nanocrystalline forms holds great promise for finding useful catalysts for a wide range of chemical reactions critical to energy applications.

 

 

Current Nanopatterning Methods. 

            Conventional techniques for fabrication of nanostructures include electron-beam lithography (EBL), dip-pen lithography (DPL), nanostamping, molecular beam epitaxy (MBE) and vapor-liquid-solid (VLS) growth. These methods offer several positive aspects for high-efficiency thermoelectric and nanoelectronic materials fabrication.

EBL and DPL are extremely useful for fabrication of complex two-dimensional nanoelectronic patterns, however they are quite slow and limited to writing single copies or at best a fairly small number of simultaneous copies. Through the ability to deposit single atomic layers with high crystal quality, MBE and VLS are able to generate quantum-confined nanostructures with high mobility, leading to high Seebeck coefficient and high electrical conductivity (both of which are required for high thermoelectric efficiency). Recent work in MBE quantum well superlattices and self-organized MBE quantum dot superlattices (QDS) in the Stranski-Krastanov growth mode have led to some of the best thermoelectric materials to date [1,2], while VLS-grown nanowires show great promise for high thermoelectric efficiency [3].

            A main course for future improvement in these methods will be to study the mechanisms that lead to high thermoelectric figures-of-merit. As of now, a self-consistent picture of electrical and thermal transport in quantum-confined nanostructures (especially QDS nanocomposites) remains elusive. Current techniques for creating QDS materials lead to arrays with random spacing and much variation in dot size, making study of thermoelectric effects difficult. Pursuing these mechanisms to further increase efficiency will likely require the fabrication of regular, periodic arrays of quantum dots with consistent sizes and shapes using techniques such as direct matrix seeding [4]. In this way, mechanisms such as phonon band gaps [1], miniband formation [5], and acoustic phonon scattering off of inclusions [6] can be precisely understood.

 

 

 

References

 

 

Maugeri, Science, 2004, 304, 1114.

 

 

S.-H. Park, C. Pistol, S.- J. Ahn, J. H. Reif, A. Lebeck, C. Dwyer, and T.H. LaBean (2005)  Finite-size, Fully-Addressable DNA Tile Lattices Formed by Hierarchical Assembly Procedures. (accepted for publication, Angew. Chem. Int. Ed).

Kurt V. Gothelf and Thomas H. LaBean (2005) DNA-programmed assembly of nanostructures. Organic & Biomolec. Chem. 3, 4023.

S-H. Park, P. Yin, Y. Liu, J.H. Reif, T.H. LaBean, and Hao Yan (2005) Programmable DNA Self-assemblies for Nanoscale Organization of Ligands and Proteins. Nano Letters 5, 729-733.

S-H. Park, R. Barish, H. Li, J.H. Reif , G. Finkelstein , H. Yan, and T.H. LaBean (2005) Three-Helix Bundle DNA Tiles Self-assemble into 2D Lattice or 1D Templates for Silver Nanowires. Nano Letters 5, 693-696.

Sung Ha Park, Hao Yan, John H. Reif, Thomas H. LaBean and Gleb Finkelstein (2004) Electronic nanostructures templated on self-assembled DNA scaffolds.  Nanotechnology 15, S525-S527.

D. Liu, S- H. Park, J. H. Reif, and T.H. LaBean (2004) DNA nanotubes self-assembled from TX tiles as templates for conductive nanowires. Proc. Nat. Acad. Sci., USA 101, 717-722.

H. Li, S- H. Park, J. H. Reif, T. H. LaBean, and Hao Yan, (2004) DNA Templated Self-Assembly of Protein and Nanoparticle Linear Arrays, J. Am. Chem. Soc. 126, 418-419.

H. Yan, S.H. Park, G. Finkelstein, J.H. Reif, and T.H. LaBean (2003) DNA-Templated Self-Assembly of Protein Arrays and Highly Conductive Nanowires. Science 301, 1882-1884.

 

 

 

 

1R. Venkatasubramanian, E. Siivola, T. Colpitts, and B. O'Quinn, "Thin-Film Thermoelectric Devices with High Room-Temperature Figures of Merit", Nature 413, 597 (2001).

2T.C. Harman, P.J. Taylor, M.P. Walsh, and B.E. LaForge, "Quantum Dot Superlattice Thermoelectric Materials and Devices", Science 297, 2229 (2002).

3Y.M. Lin and M.S. Dresselhaus, "Thermoelectric Properties of Superlattice Nanowires", Physical Review B 68, 075304 (2003) and references therein.

4X. Weng, W. Ye, S.J. Clarke, R.S. Goldman, V. Rotberg, A. Daniel, and R. Clarke, "Matrix-Seeded Growth of Nitride Semiconductor Nanostructures Using Ion Beams", Journal of Applied Physics 97, 064301 (2005).

5A.A. Balandin and O.L. Lazarenkova, "Mechanism for Thermoelectric Figure-of-Merit Enhancement in Regimented Quantum Dot Superlattices", Appl. Phys. Lett. 82, 415 (2003).

6J.M. Zide, D.O. Klenov, S. Stemmer, A.C. Gossard, G. Zeng, J.E. Bowers, D. Vashaee, and A. Shakouri, "Thermoelectric Power Factor in Semiconductors with Buried Epitaxial Semimetallic Nanoparticles", Applied Physics Letters 87, (2005).