Please use this identifier to cite or link to this item: https://hdl.handle.net/10356/97380
Title: CuOx nanotubes via an unusual complexation induced block copolymer-like self-assembly of poly(acrylic acid)
Authors: Liang, Yen Nan
Hu, Jinhua
Tam, Michael Kam Chiu
Hu, Xiao
Issue Date: 2012
Source: Liang, Y. N., Hu, J., Tam, M. K. C., & Hu, X. (2012). CuOx nanotubes via an unusual complexation induced block copolymer-like self-assembly of poly(acrylic acid). RSC Advances, 2(25), 9531-9537.
Series/Report no.: RSC advances
Abstract: Polyelectrolyte (PEL) mediated synthesis of functional inorganic nano-materials is attractive due to its versatility and compatibility inside aqueous media. Block copolymers are often employed to facilitate the formation of novel nanostructures. In this work, we report the synthesis of copper oxide (CuOx) crystals with an unexpected hollow nano-tubular morphology using only poly(acrylic acid) (PAA), i.e., a homopolymer. The quantification of the pH dependent binding limit of Cu2+ to PAA, which has often been given little emphasis previously, is found to be critical in understanding the formation mechanism of such nanotubes. Further quantification of the interdependent relationship of pH, α, and [Cu2+] : [COOH]0 using the pKa-α curves provided important insight. The formation of the CuOx nanotubes is believed to be due to an unusual copolymer-like self-assembly of PAA as a homopolymer in aqueous solution; caused by interactions between Cu2+ and charged PAA chains. Such a unique copolymer-like self-assembly behaviour of the PAA–Cu2+ complex manifests within a specific window of [Cu2+] : [COOH]0 ratio around the binding limit. Discussion is also carried out on the possibilities and potential limitations of applying this new concept to other PELs and metal ions.
URI: https://hdl.handle.net/10356/97380
http://hdl.handle.net/10220/10585
ISSN: 2046-2069
DOI: 10.1039/c2ra20951a
Rights: © 2012 The Royal Society of Chemistry.
Fulltext Permission: none
Fulltext Availability: No Fulltext
Appears in Collections:MSE Journal Articles

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