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dc.contributor.authorLi, Cheng-Peng
dc.contributor.authorZhou, Hang
dc.contributor.authorWang, Jia-Jun
dc.contributor.authorLiu, Bo-Lan
dc.contributor.authorWang, Si
dc.contributor.authorYang, Xi
dc.contributor.authorWang, Zhong-Liang
dc.contributor.authorLiu, Chun-Sen
dc.contributor.authorDu, Miao
dc.contributor.authorZhou, Wuzong
dc.date.accessioned2020-10-23T23:38:56Z
dc.date.available2020-10-23T23:38:56Z
dc.date.issued2019-11-13
dc.identifier.citationLi , C-P , Zhou , H , Wang , J-J , Liu , B-L , Wang , S , Yang , X , Wang , Z-L , Liu , C-S , Du , M & Zhou , W 2019 , ' Mechanism–property correlation in coordination polymer crystals toward design of a superior sorbent ' , ACS Applied Materials & Interfaces , vol. 11 , no. 45 , pp. 42375-42384 . https://doi.org/10.1021/acsami.9b16386en
dc.identifier.issn1944-8244
dc.identifier.otherPURE: 263759041
dc.identifier.otherPURE UUID: 0a1aa88f-63fe-4c60-9974-b8c1504ce96c
dc.identifier.otherRIS: urn:00069A217E182A16BC12A10907671DD8
dc.identifier.otherScopus: 85074919271
dc.identifier.otherORCID: /0000-0001-9752-7076/work/65345213
dc.identifier.otherWOS: 000497263600058
dc.identifier.urihttp://hdl.handle.net/10023/20816
dc.descriptionThis work was financially supported by the National Natural Science Foundation of China (21571158 and 21771139), Tianjin Natural Science Foundation (17JCYBJC22800), and the Program for Innovative Research Team in University of Tianjin (TD13-5074).en
dc.description.abstractA methodology was developed to design superior sorbents of oxoanions. To integrate the high efficiency of chemisorption, selectivity, and recyclability into one sorbent, understanding the nature of oxoanions–sorbent interactions and the structural evolution of the sorbents is essential. Three cationic Ag(I) coordination polymers (CPs) are synthesized for dichromate (Cr2O72–) removal, and three distinct oxoanion-exchange mechanisms are identified, namely, the replacement, breath, and reconstruction processes, depending on the degree of framework distortion induced by the dichromate–CP interactions. The single crystal to single crystal transformation during the oxoanion exchange has been investigated by using single-crystal X-ray diffraction and energy-dispersive X-ray microanalysis. The replacement process, due to a weak chemisorption, shows excellent recyclability at the cost of reduction of efficiency and selectivity of adsorption. The reconstruction process may achieve a high efficiency and selectivity, but it loses recyclability. Due to the formation of a Ag–O(dichromate) bond and the breathing effect of the framework, the sorbent with the breath mechanism shows both superior efficiency and high recyclability in dichromate removal. The study of perrhenate (ReO4–) removal using the same CPs demonstrates that one CP performing the reconstruction process during dichromate removal turns to the breath process in removal of perrhenate anions. These results of mechanism–property correlation provide an insight into improvement of the methodology to fabricate a superior CP sorbent for oxoanion removal.
dc.format.extent10
dc.language.isoeng
dc.relation.ispartofACS Applied Materials & Interfacesen
dc.rightsCopyright © 2019 American Chemical Society. This work has been made available online in accordance with publisher policies or with permission. Permission for further reuse of this content should be sought from the publisher or the rights holder. This is the author created accepted manuscript following peer review and may differ slightly from the final published version. The final published version of this work is available at https://doi.org/10.1021/acsami.9b16386en
dc.subjectCoordination polymeren
dc.subjectAnion exchangeen
dc.subjectDichromateen
dc.subjectPerrhenateen
dc.subjectSuperior sorbenten
dc.subjectMechanism-property correlationen
dc.subjectQD Chemistryen
dc.subjectDASen
dc.subject.lccQDen
dc.titleMechanism–property correlation in coordination polymer crystals toward design of a superior sorbenten
dc.typeJournal articleen
dc.description.versionPostprinten
dc.contributor.institutionUniversity of St Andrews.School of Chemistryen
dc.contributor.institutionUniversity of St Andrews.EaSTCHEMen
dc.identifier.doihttps://doi.org/10.1021/acsami.9b16386
dc.description.statusPeer revieweden
dc.date.embargoedUntil2020-10-24


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