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4th EucheMs chemistry congress

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wednesday, 29-Aug 2012<br />

s843<br />

chem. Listy 106, s587–s1425 (2012)<br />

solid state Chemistry Materials <strong>chemistry</strong>/New materials<br />

Nanoporous Materials – iii<br />

o - 4 1 0<br />

MetAL orGAniC frAMeworKS for CLeAn<br />

enerGy APPLiCAtionS<br />

G. ShiMizu 1 , r. vAidhyAnAthAn 1 , S. ireMonGer 1 ,<br />

J. tAyLor 1<br />

1 University of Calgary SA 109, Department of Chemistry,<br />

Calgary Alberta, Canada<br />

Until affordable green options are available, fossil fuels will<br />

remain a primary source of energy. Carbon capture represents a<br />

means of mitigating the greenhouse effects of fossil fuel<br />

combustion. This approach also presently carries significant costs<br />

making widespread adoption challenging. Part of this presentation<br />

will focus on the opportunities and challenges to make fossil fuel<br />

energy production greener including the idea of solid sorbents,<br />

such as metal organic frameworks (MOFs), for gases.<br />

MOFs represent tunable molecular scaffolding that can be<br />

adjusted for a breadth of applications. This presentation will<br />

concern our efforts towards tailoring the properties of MOFs<br />

towards energy challenges. [1] The first concerns our efforts to<br />

make MOFs with amine lined pores for CO capture. In contrast<br />

2<br />

to liquid amines which chemisorb CO and have high energy costs<br />

2<br />

for regeneration, the MOF approach gives physisorbed gases and<br />

hence more facile release. Despite the weaker binding mode, we<br />

will show that high selectivities are possible owing to heats of<br />

adsorption over 40 kJ/mol. [2] A key challenge for this field is to<br />

make MOFs that are more hydrolytically stable. Some of our<br />

recent results concern efforts to make more water stable MOFs<br />

using phosphonates and related linkers. [3]<br />

references:<br />

1. a) J. Long, O. Yaghi,Chem. Soc. Rev., 2009, 38, 1213.<br />

b) G. Férey et al., Chem. Soc. Rev. 2011, 40, 550.<br />

c) K. Sumida et al., Chem. Rev., 2012, 112, 724.<br />

d) J. Li et al. Chem. Rev., 2012, 112, 869.<br />

e) S. Keskin et al. ChemSusChem, 2010, 3, 879.<br />

2. a) R. Vaidhyanathan et al. Science, 2010, 330, 650-653.<br />

b) R. Vaidhyanathan et al. Angew. Chem, 2012, 51, 1826.<br />

3. Iremonger, S. S. et al., J. Am. Chem. Soc. 2011, 133, 20048.<br />

Keywords: MOFs; CO capture; Porous solids;<br />

2<br />

Nanoporous Materials – iii<br />

4 th <strong>EucheMs</strong> <strong>chemistry</strong> <strong>congress</strong><br />

o - 4 1 1<br />

LuMineSCent MoLeCuLeS Confined<br />

in PorouS And LAyered MAteriALS:<br />

enhAnCed PhotoeMiSSion ProPertieS<br />

And oPtoeLeCtroniC APPLiCAtionS<br />

L. MArCheSe 1 , CArniAto f. 1 , CuCinottA f. 1 ,<br />

C. BiSio1 1 Dipartimento di Scienze e Innovazione Tecnologica and<br />

Nano-SiSTeMI Interdisciplinary Centre, Universitá del<br />

Piemonte Orientale A. Avogadro, Viale T. Michel 11, I-15121<br />

Alessandria, Italy<br />

The confinement of luminescent dyes and polymers into the<br />

nanospaces of porous or layered materials may prevent molecules<br />

aggregation and improve their thermal and photochemical<br />

stability along with their photoemission properties. These<br />

requirements are key points for the development of efficient<br />

hybrid optoelectronic devices (HLED). In this field, our research<br />

group recently developed novel hybrid luminescent solids based<br />

on nano-sized MCM-41 and platelet SBA-15 silica containing<br />

inside the pores fluorescein and electroluminescent<br />

polyphenylenevinylene (PPV) co-polymer (super yellow),<br />

respectively. [1] Higher quantum efficiency, mainly related to a<br />

reduction of aggregates of the pure dyes, and improved<br />

photostability were observed in both host-guest systems.<br />

Moreover, hybrid photonic antenna based on SBA-15 solid, where<br />

an encapsulated donor (PPV co-polymer) transfers the<br />

photoexcitation energy directly to an acceptor (cyanine dye)<br />

covalently linked on the external surface was also developed as<br />

promising candidate for use in optoelectronic devices.<br />

Recently, luminescent organo-modified layered materials<br />

were syntesized and tested as light-emitting film in HLED<br />

devices. The structural properties along with their tunable<br />

hydrophilicity/hydrophobicity render these solids suitable to host<br />

and stabilize different luminescent entities. In this respect, two<br />

systemes will be described: i) a synthetic saponite intercalated<br />

with a luminescent polyhedral oligomeric silsesquioxane (POSS)<br />

bearing in the structure a cyanine molecule and ii) a hydrotalcite<br />

decorated on the surface with electroluminescent semiconductor<br />

quantum dot crystals. [2] Both systemes were used as emitting films<br />

in LED devices, because of their enhanced quantum yield<br />

efficiency and improved photostability.<br />

references:<br />

1. F Cucinotta, F. Carniato, C. Bisio, L. Marchese et al.,<br />

Chem. Mater., 2011, 23, 2803; F. Carniato, C. Bisio, L.<br />

Marchese et al., J. Mater. Chem., 2010, 20(26), 5504.<br />

2. J.S. Bendall, L. Marchese et al., Adv. Funct. Mater., 2010,<br />

20, 3298.<br />

AUGUst 26–30, 2012, PrAGUE, cZEcH rEPUbLIc

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