@article {1593,
	title = { Electrically Controlled Plasmonic Behavior of Gold Nanocube@ Polyaniline Nanostructures: Transparent Plasmonic Aggregates},
	journal = {Chem. Mater.},
	year = {2016},
	author = {Jeon, J.-W. and Ledin, P. A. and Geldmeier, J. A. and Ponder, J. F. and Mahmoud, M A and El-Sayed, M. and Reynolds, J. R. and Tsukruk, V. V.}
}
@article {1622,
	title = {Optimizing the antitumor efficacy of AuNR-assisted plasmonic photothermal therapy and its molecular impact},
	journal = {Cancer Research},
	year = {2016},
	author = {Rahman, MA and et al.}
}
@article {1582,
	title = {Cytotoxic effects of cytoplasmic-targeted and nuclear-targeted gold and silver nanoparticles in HSC-3 cells{\textendash}A mechanistic study},
	journal = {Toxicology in Vitro},
	volume = {29},
	year = {2015},
	pages = {694{\textendash}705},
	author = {Lauren A. Austin and Ahmad, Samera and Kang, Bin and Rommel, Kathryn R and Mahmoud, Mahmoud and Peek, Mary E and El-Sayed, Mostafa A.}
}
@article {1575,
	title = {Light-responsive plasmonic arrays consisting of silver nanocubes and a photoisomerizable matrix.},
	journal = {ACS Appl Mater Interfaces},
	volume = {7},
	year = {2015},
	month = {2015 Mar 4},
	pages = {4902-12},
	abstract = {We report on the synthesis of novel branched organic-inorganic azo-polyhedral oligomeric silsesquioxane (POSS) conjugates (Azo-POSS) and their use as a stable active medium to induce reversible plasmonic modulations of embedded metal nanostructures. A dense monolayer of silver nanocubes was deposited on a quartz substrate using the Langmuir-Blodgett technique and subsequently coated with an ultrathin Azo-POSS layer. The reversible light-induced photoisomerization between the trans and cis states of the azobenzene-terminated branched POSS material results in significant changes in the refractive index (up to 0.17) at a wavelength of 380 nm. We observed that the pronounced and reversible change in the surrounding refractive index results in a corresponding hypsochromic plasmonic shift of 6 nm in the plasmonic band of the embedded silver nanocubes. The reversible tuning of the plasmonic modes of noble-metal nanostructures using a variable-refractive-index medium opens up the possibility of fabricating photoactive, hybrid, ultrathin coatings with robust, real-time, photoinitiated responses for prospective applications in photoactive materials that can be reversibly tuned by light illumination.},
	issn = {1944-8252},
	doi = {10.1021/am508993z},
	author = {Ledin, Petr A and Russell, Michael and Geldmeier, Jeffrey A and Tkachenko, Ihor M and Mahmoud, Mahmoud A. and Shevchenko, Valery and El-Sayed, Mostafa A. and Tsukruk, Vladimir V.}
}
@article {1576,
	title = {Silver nanocube aggregation gradient materials in search for total internal reflection with high phase sensitivity},
	journal = {Nanoscale},
	volume = {7},
	year = {2015},
	pages = {5230-5239},
	abstract = {We fabricated monolayer coatings of a silver nanocube aggregation to create a step-wise optical strip by applying different surface pressures during slow Langmuir-Blodgett deposition. The varying amount of randomly distributed nanocube aggregates with different surface coverages in gradient manner due to changes in surface pressure allows for continuous control of the polarization sensitive absorption of the incoming light over a broad optical spectrum. Optical characterization under total internal reflection conditions combined with electromagnetic simulations reveal that the broadband light absorption depends on the relative orientation of the nanoparticles to the polarization of the incoming light. By using computer simulations, we found that the electric field vector of the s-polarized light interacts with the different types of silver nanocube aggregations to excite different plasmonic resonances. The s-polarization shows dramatic changes of the plasmonic resonances at different angles of incidence (shift of 64 nm per 10[degree] angle of incidence). With a low surface nanocube coverage (from 5\% to 20\%), we observed a polarization-selective high absorption of 80\% (with an average 75\%) of the incoming light over a broad optical range in the visible region from 400 nm to 700 nm. This large-area gradient material with location-dependent optical properties can be of particular interest for broadband light absorption, phase-sensitive sensors, and imaging.},
	doi = {10.1039/C4NR06430E},
	url = {http://dx.doi.org/10.1039/C4NR06430E},
	author = {Konig, Tobias A. F. and Ledin, Petr A and Russell, Michael and Geldmeier, Jeffrey A and Mahmoud, Mahmoud. A. and El-Sayed, Mostafa A. and Tsukruk, Vladimir V.}
}
@article {1363,
	title = {Electrically Tunable Plasmonic Behavior of Nanocube-Polymer Nanomaterials Induced by a Redox Active Electrochromic Polymer},
	journal = {ACS nano},
	year = {2014},
	isbn = {1936-0851},
	author = {K{\"o}nig, Tobias AF and Ledin, Petr A and Kerszulis, Justin and Mahmoud, Mahmoud A. and El-Sayed, Mostafa A. and Reynolds, John R and Tsukruk, Vladimir V.}
}
@article {1368,
	title = {P-Glycoprotein-Dependent Trafficking of Nanoparticle-Drug Conjugates},
	journal = {Small},
	volume = {10},
	number = {9},
	year = {2014},
	pages = {1719-1723},
	isbn = {1613-6829},
	author = {Dreaden, Erik C. and Raji, Idris O and Austin, Lauren and Fathi, Shaghayegh and Mwakwari, Sandra C and Humphries, William H and Kang, Bin and Oyelere, Adegboyega K and El-Sayed, Mostafa A}
}
@article {1331,
	title = {Aggregation and Interaction of Cationic Nanoparticles on Bacterial Surfaces},
	journal = {Journal of the American Chemical Society},
	volume = {134},
	number = {16},
	year = {2012},
	note = {Times Cited: 1Hayden, Steven C. Zhao, Gengxiang Saha, Krishnendu Phillips, Ronnie L. Li, Xiaoning Miranda, Oscar R. Rotello, Vincent M. El-Sayed, Mostafa A. Schmidt-Krey, Ingeborg Bunz, Uwe H. F.},
	month = {Apr},
	pages = {6920-6923},
	abstract = {Cationic monolayer-protected gold nanoparticles (AuNPs) with sizes of 6 or 2 nm interact with the cell membranes of Escherichia coli (Gram-) and Bacillus subtilis (Gram+), resulting in the formation of strikingly distinct AuNP surface aggregation patterns or lysis depending upon the size of the AuNPs. The aggregation phenomena were investigated by transmission electron microscopy and UV-vis spectroscopy. Upon proteolytic treatment of the bacteria, the distinct aggregation patterns disappeared.},
	isbn = {0002-7863},
	doi = {10.1021/ja301167y},
	author = {Hayden, S. C. and Zhao, G. X. and Saha, K. and Phillips, R. L. and Li, X. N. and Miranda, O. R. and Rotello, V. M. and El-Sayed, M. A. and Schmidt-Krey, I. and Bunz, U. H. F.}
}
@article {1180,
	title = {Eu3+ binding to europium-regenerated bacteriorhodopsin upon delipidation and monomerization},
	journal = {Febs Letters},
	volume = {562},
	number = {1-3},
	year = {2004},
	note = {Heyes, CD Reynolds, KB El-Sayed, MA},
	month = {Mar},
	pages = {207-210},
	abstract = {We have studied the effect of monomerization of the purple membrane lattice, as well as removal of 75\% of the lipids, on the binding properties of Eu3+ ions. We found that delipidation and monomerization do not cause the cations to lose their binding ability to the protein. This suggests that the three most strongly bound Eu3+ cations do not bind to the lipids, but directly bind to the protein. Furthermore, we found that delipidation actually causes a slight increase in the binding affinity. This is likely a result of reduced aggregation of europium-regenerated bacteriorhodopsin (bR) upon lipid removal causing more exposure of the binding sites to the Eu3+ cations. These results, taken with those from our previous publication [Heyes and El-Sayed, Biophys. J. 85 (2003) 426-434], might suggest that the cations remain bound upon delipidation of bR, but have no effect on the function. This is discussed with respect to the role of cations in the function of native bR. (C) 2004 Published by Elsevier B.V. on behalf of the Federation of European Biochemical Societies.},
	isbn = {0014-5793},
	doi = {10.1016/s0014-5793(04)00182-6},
	author = {Heyes, C D and Reynolds, K. B. and El-Sayed, Mostafa A}
}
@article {1247,
	title = {The effect of low and high temperature anneals on the hydrogen content and passivation of Si surface coated with SiO2 and SiN films},
	journal = {Journal of the Electrochemical Society},
	volume = {146},
	number = {5},
	year = {1999},
	note = {Ebong, A Doshi, P Narasimha, S Rohatgi, A Wang, J El-Sayed, MA},
	month = {May},
	pages = {1921-1924},
	abstract = {A detailed comparison of the passivation quality and its dependence on the low and high temperature anneals is presented for various promising Si surface passivation schemes. The passivation schemes investigated in this study include: conventional furnace oxide (CFO), rapid thermal oxide (RTO), belt line oxide (BLO), plasma deposited oxide (PDO), SiN deposited by plasma enhanced chemical vapor deposition (PECVD), CFO/SiN, RTO/SiN, BLO/SiN, PDO/SiN, and RTO/PDO. Passivated low resistivity (1 Ohm cm) p-type silicon samples were subjected to three annealing treatments: (a) 400 degrees C in forming gas (FGA), (b) 730 degrees C in air, and (c) 850 degrees C in air, to simulate heat-treatments, which are typically used for contact anneal, front ohmic contacts, and back surface field formation, respectively, for screen printed silicon solar cells. It is found that the passivation quality of PDO, SiN, RTO, and CFO single layers improves significantly after the 400 degrees C FGA and 730 degrees C thermal cycles with RTO resulting in the lowest surface recombination velocities (S-eff) of 154 and 405 cm/s, respectively. Silicon wafers coated with belt oxide (BLO and BLO/SiN) did not show any improvement in S-eff, which remained at 5000 cm/s due to the inferior quality of BLO formed in compressed air. The oxide/ nitride stack passivation is found to be far superior to single-layer passivation resulting in S-eff Of 70 cm/s for the RTO/SiN scheme after the two high temperature anneals (850 and 730 degrees C). The hydrogen concentration measurements by Fourier transform infrared spectroscopy show a greater decrease in the hydrogen content in the annealed RTO/SiN stack compared to the as-deposited SiN single layer after the 730 and 850 degrees C anneals. A combination of reduced hydrogen content and very low S-eff in the RTO/SiN stack suggests that the release of hydrogen from SiN during the anneal further passivates the RTO/Si interface underneath. (C) 1999 The Electrochemical Society. S0013-4651(98)08-117-8. All rights reserved.},
	isbn = {0013-4651},
	doi = {10.1149/1.1391866},
	author = {Ebong, A. and Doshi, P. and Narasimha, S. and Rohatgi, A. and Wang, Jianping and El-Sayed, Mostafa A}
}
@article {866,
	title = {Detection of a Yb3+ binding site in regenerated bacteriorhodopsin that is coordinated with the protein and phospholipid head groups.},
	journal = {Proceedings of the National Academy of Sciences of the United States of America},
	volume = {93},
	year = {1996},
	month = {1996 Dec 10},
	pages = {14333-7},
	abstract = {Near infrared Yb3+ vibronic sideband spectroscopy was used to characterize specific lanthanide binding sites in bacteriorhodopsin (bR) and retinal free bacteriorhodopsin (bO). The VSB spectra for deionized bO regenerated with a ratio of 1:1 and 2:1 ion to bO are identical. Application of a two-dimensional anti-correlation technique suggests that only a single Yb3+ site is observed. The Yb3+ binding site in bO is observed to consist of PO2- groups and carboxylic acid groups, both of which are bound in a bidentate manner. An additional contribution most likely arising from a phenolic group is also observed. This implies that the ligands for the observed single binding site are the lipid head groups and amino acid residues. The vibronic sidebands of Yb3+ in deionized bR regenerated at a ratio of 2:1 ion to bR are essentially identical to those in bO. The other high-affinity binding site is thus either not evident or its fluorescence is quenched. A discussion is given on the difference in binding of Ca2+ (or Mg2+) and lanthanides in phospholipid membrane proteins.},
	keywords = {Bacteriorhodopsins, Binding Sites, Metals, Rare Earth, Phospholipids, Retinaldehyde, Spectroscopy, Near-Infrared},
	issn = {0027-8424},
	author = {Roselli, Cecile and Boussac, A and Mattioli, T A and Griffiths, Jennifer A. and El-Sayed, Mostafa A}
}
@article {1265,
	title = {Effects of rapid thermal anneal on refractive index and hydrogen content of plasma-enhanced chemical vapor deposited silicon nitride films},
	journal = {J. Appl. Phys.Journal of Applied Physics},
	volume = {80},
	year = {1996},
	month = {1996},
	pages = {5384},
	publisher = {AIP},
	abstract = {The objective of this paper is to understand and quantify the effects of rapid thermal anneal (RTA) on refractive index, thickness, and hydrogen content of plasma-enhanced, chemical vapor-deposited (PECVD) silicon nitride films. It is shown that RTA is more effective than identical furnace anneal. A threshold in as-deposited refractive index value is found, above which the index of a silicon nitride film increases, while the thickness and bonded hydrogen content decreases as result of the RTA. In addition, the magnitude of increase in the index is proportional to the as-deposited index value. The threshold index value increases with the increase in silicon nitride deposition temperature. A direct correlation is found between the annealing-induced increase in refractive index and the corresponding decrease in total bonded hydrogen concentration in the PECVD silicon nitride films. Finally, it is shown that the release of bonded hydrogen from the film can passivate defects in the underlying silicon substrate and increase the performance of silicon devices such as solar cells. },
	keywords = {ANNEALING, CRYSTAL DEFECTS, CVD, DESORPTION, HYDROGEN, IMPURITIES, REFRACTIVE INDEX, SILICON NITRIDES, THICKNESS, THIN FILMS},
	doi = {10.1063/1.363480},
	url = {http://dx.doi.org/10.1063/1.363480},
	author = {Cai, L.},
	editor = {Rohatgi, A. and Yang, Difei and El-Sayed, Mostafa A}
}
@article {1271,
	title = {Monodentate vs Bidentate Binding of Lanthanide Cations to PO2- in Bacteriorhodopsin},
	journal = {The Journal of Physical Chemistry},
	volume = {100},
	year = {1996},
	note = {doi: 10.1021/jp9533279},
	month = {1996},
	pages = {6863 - 6866},
	publisher = {American Chemical Society},
	abstract = {The frequency difference between the symmetric and antisymmetric stretching vibration of PO2- in phosphatidylglycerol phospate (PGP) is used to differentiate between monodentate and bidentate binding of these groups to metal cations in the membrane of bacteriorhodopsin (bR) and phosphatidylglycerol phospate. The binding of Ca2+ to PGP is found to have a frequency difference corresponding to monodentate binding. The symmetric and antisymmetric PO2- bands in bR show similar frequency shifts upon Ca2+ binding, which is independent of pH. This suggests that Ca2+ has a monodentate type binding with the PO2- in bR. In contrast, the PO2- symmetric and antisymmetric frequencies of PGP complexes with trivalent lanthanide cations with higher charge density (Ho3+ and Dy3+) are observed to have smaller separations and to increase their separation with increasing pH toward the value observed for Ca2+ binding. Lanthanide cations (Ho3+, Dy3+, Eu3+, Nd3+, and La3+) binding in bR at pH 4 show small frequency separations that are observed to have similar frequency shifts with pH, the magnitude of which is dependent on the cation. It is proposed that at low pH the lanthanide cations with higher charge density have bidentate binding to bR, while at high pH, complexation with the OH- competes with one of the oxygens of the PO2- for the binding of the lanthanide ion thus changing the bidentate to monodentate type binding.The frequency difference between the symmetric and antisymmetric stretching vibration of PO2- in phosphatidylglycerol phospate (PGP) is used to differentiate between monodentate and bidentate binding of these groups to metal cations in the membrane of bacteriorhodopsin (bR) and phosphatidylglycerol phospate. The binding of Ca2+ to PGP is found to have a frequency difference corresponding to monodentate binding. The symmetric and antisymmetric PO2- bands in bR show similar frequency shifts upon Ca2+ binding, which is independent of pH. This suggests that Ca2+ has a monodentate type binding with the PO2- in bR. In contrast, the PO2- symmetric and antisymmetric frequencies of PGP complexes with trivalent lanthanide cations with higher charge density (Ho3+ and Dy3+) are observed to have smaller separations and to increase their separation with increasing pH toward the value observed for Ca2+ binding. Lanthanide cations (Ho3+, Dy3+, Eu3+, Nd3+, and La3+) binding in bR at pH 4 show small frequency separations that are observed to have similar frequency shifts with pH, the magnitude of which is dependent on the cation. It is proposed that at low pH the lanthanide cations with higher charge density have bidentate binding to bR, while at high pH, complexation with the OH- competes with one of the oxygens of the PO2- for the binding of the lanthanide ion thus changing the bidentate to monodentate type binding.},
	isbn = {0022-3654},
	doi = {doi: 10.1021/jp9533279},
	url = {http://dx.doi.org/10.1021/jp9533279},
	author = {Griffiths, Jennifer A. and Masciangioli, Tina M. and Roselli, Cecile and El-Sayed, Mostafa A}
}
@article {1286,
	title = {Enhancement of Metallic Silver Monomer Evaporation by the Adhesion of Polar Molecules to Silver Nanocluster Ions},
	journal = {The Journal of Physical Chemistry},
	volume = {99},
	year = {1995},
	note = {doi: 10.1021/j100019a061},
	month = {1995},
	pages = {7723 - 7730},
	publisher = {American Chemical Society},
	abstract = {View http://dx.doi.org/10.1021/j100019a061 for article{\textquoteright}s front page in lieu of an abstract},
	isbn = {0022-3654},
	doi = {doi: 10.1021/j100019a061},
	url = {http://dx.doi.org/10.1021/j100019a061},
	author = {Fagerquist, Clifton K. and Sensharma, Dilip K. and El-Sayed, Mostafa A and Rubio, Angel and Cohen, Marvin L.}
}
