Chemical versus physical grafting of photoluminescent amino-functional carbon dots onto transparent nematic nanocellulose gels and aerogels
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In: Cellulose, Vol. 26.2019, No. 30 September, 30.09.2019, p. 7781-7796.
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TY - JOUR
T1 - Chemical versus physical grafting of photoluminescent amino-functional carbon dots onto transparent nematic nanocellulose gels and aerogels
AU - Quraishi, Sakeena
AU - Plappert, Sven F.
AU - Grießer, Thomas
AU - Gindl-Altmutter, Wolfgang
AU - Liebner, Falk W.
PY - 2019/9/30
Y1 - 2019/9/30
N2 - Transparent matrices of low refractive index are promising carriers for photoluminescent nanoparticles targeting true volumetric 3D display applications. Complementation of transparency with a highly open-porous nanomorphology renders respective hybrid gels and aerogels additionally attractive for liquid and gas detection devices. Herein, we present virtually fully bio-based hybrids obtained by decorating highly transparent, nematically ordered gels and aerogels (15–20 mg cm−3) from carboxylated and individualized cellulose nanofibers (i-CNF) with amino-functional photoluminescent carbon dots (CD). The latter were obtained by microwave-assisted hydrothermolysis of lemon juice. As the way of anchoring the CDs onto the large internal surface of the porous i-CNF scaffolds (320 m2 g−1) has a great impact on the final properties of the hybrid materials including leaching of CDs and reusability of the hybrid, this study assessed the respective pros and cons of a physical and chemical bonding approach. The results confirmed the superiority of covalent grafting. Aqueous carbodiimide coupling of amino-functionalized CDs afforded higher yields of CDs in the final hybrid aerogels, distinctly higher specific surface values (491 m2 g−1) and slightly enhanced mechanical properties while the high light transmittance and nanomorphology of the i-CNF precursor alcogels is virtually not compromised. Therefore, we conclude that the luminescent i-CNF/CD-chem hybrid materials of this study are promising candidates for environmentally friendly chemical sensing and volumetric display applications.
AB - Transparent matrices of low refractive index are promising carriers for photoluminescent nanoparticles targeting true volumetric 3D display applications. Complementation of transparency with a highly open-porous nanomorphology renders respective hybrid gels and aerogels additionally attractive for liquid and gas detection devices. Herein, we present virtually fully bio-based hybrids obtained by decorating highly transparent, nematically ordered gels and aerogels (15–20 mg cm−3) from carboxylated and individualized cellulose nanofibers (i-CNF) with amino-functional photoluminescent carbon dots (CD). The latter were obtained by microwave-assisted hydrothermolysis of lemon juice. As the way of anchoring the CDs onto the large internal surface of the porous i-CNF scaffolds (320 m2 g−1) has a great impact on the final properties of the hybrid materials including leaching of CDs and reusability of the hybrid, this study assessed the respective pros and cons of a physical and chemical bonding approach. The results confirmed the superiority of covalent grafting. Aqueous carbodiimide coupling of amino-functionalized CDs afforded higher yields of CDs in the final hybrid aerogels, distinctly higher specific surface values (491 m2 g−1) and slightly enhanced mechanical properties while the high light transmittance and nanomorphology of the i-CNF precursor alcogels is virtually not compromised. Therefore, we conclude that the luminescent i-CNF/CD-chem hybrid materials of this study are promising candidates for environmentally friendly chemical sensing and volumetric display applications.
KW - Aerogels
KW - Carbon dots
KW - Cellulose nanofibers
KW - Hybrid
KW - Nanocellulose
KW - Photoluminescence
UR - http://www.scopus.com/inward/record.url?scp=85069453665&partnerID=8YFLogxK
U2 - 10.1007/s10570-019-02619-2
DO - 10.1007/s10570-019-02619-2
M3 - Article
AN - SCOPUS:85069453665
VL - 26.2019
SP - 7781
EP - 7796
JO - Cellulose
JF - Cellulose
SN - 0969-0239
IS - 30 September
ER -