Facet-Dependent Atomic Distances Shape Vanadate Adsorption Complexes on Hematite Nanocrystals

The environmental fate of vanadate (V(V)) is significantly influenced by iron oxide nanocrystals through adsorption. Nevertheless, the underlying driving force controlling V(V) adsorption on hematite (Fe2O3) facets is poorly understood. Herein, V(V) adsorption on the {001}, {110}, and {214} Fe2O3 fa...

Ausführliche Beschreibung

Bibliographische Detailangaben
Veröffentlicht in:Langmuir : the ACS journal of surfaces and colloids. - 1992. - (2023) vom: 06. Jan.
1. Verfasser: Zheng, Chao (VerfasserIn)
Weitere Verfasser: Zhong, Wen, Yan, Li, Jing, Chuanyong
Format: Online-Aufsatz
Sprache:English
Veröffentlicht: 2023
Zugriff auf das übergeordnete Werk:Langmuir : the ACS journal of surfaces and colloids
Schlagworte:Journal Article
LEADER 01000caa a22002652 4500
001 NLM35119018X
003 DE-627
005 20240216232359.0
007 cr uuu---uuuuu
008 231226s2023 xx |||||o 00| ||eng c
024 7 |a 10.1021/acs.langmuir.2c02192  |2 doi 
028 5 2 |a pubmed24n1295.xml 
035 |a (DE-627)NLM35119018X 
035 |a (NLM)36607912 
040 |a DE-627  |b ger  |c DE-627  |e rakwb 
041 |a eng 
100 1 |a Zheng, Chao  |e verfasserin  |4 aut 
245 1 0 |a Facet-Dependent Atomic Distances Shape Vanadate Adsorption Complexes on Hematite Nanocrystals 
264 1 |c 2023 
336 |a Text  |b txt  |2 rdacontent 
337 |a ƒaComputermedien  |b c  |2 rdamedia 
338 |a ƒa Online-Ressource  |b cr  |2 rdacarrier 
500 |a Date Revised 16.02.2024 
500 |a published: Print-Electronic 
500 |a Citation Status Publisher 
520 |a The environmental fate of vanadate (V(V)) is significantly influenced by iron oxide nanocrystals through adsorption. Nevertheless, the underlying driving force controlling V(V) adsorption on hematite (Fe2O3) facets is poorly understood. Herein, V(V) adsorption on the {001}, {110}, and {214} Fe2O3 facets was explored using batch adsorption experiments, spectroscopic studies, and density functional theory (DFT) calculations. Adsorption experiments suggested that the order of V(V) adsorption capacity followed {001} > {110} > {214}. However, the affinity of V(V) to the {001} facet was the weakest, as evidenced by its least resistance to phosphate and sulfate competition. Our extended X-ray absorption fine structure (EXAFS) study indicated the formation of the inner-sphere monodentate mononuclear (1V) complex on the {001} facet and bidentate corner-sharing (2C) complexes on the {110} and {214} facets. Density functional theory (DFT) calculations showed the 1V complex is preferable when the adjacent Fe-Fe atomic distance is significantly larger than the O-O atomic distance of V(V). Otherwise, the 2C complex is formed if the distance is comparable. This determining factor in surface complex formation can be safely extended to other oxyanions that the compatibility in the atomic distance of Fe-Fe on Fe2O3 facets and O-O in oxyanions shapes the surface complex. The molecular-level understanding of the facet-dependent adsorption mechanism provides the basis for the design and application of oxyanion adsorbents 
650 4 |a Journal Article 
700 1 |a Zhong, Wen  |e verfasserin  |4 aut 
700 1 |a Yan, Li  |e verfasserin  |4 aut 
700 1 |a Jing, Chuanyong  |e verfasserin  |4 aut 
773 0 8 |i Enthalten in  |t Langmuir : the ACS journal of surfaces and colloids  |d 1992  |g (2023) vom: 06. Jan.  |w (DE-627)NLM098181009  |x 1520-5827  |7 nnns 
773 1 8 |g year:2023  |g day:06  |g month:01 
856 4 0 |u http://dx.doi.org/10.1021/acs.langmuir.2c02192  |3 Volltext 
912 |a GBV_USEFLAG_A 
912 |a SYSFLAG_A 
912 |a GBV_NLM 
912 |a GBV_ILN_22 
912 |a GBV_ILN_350 
912 |a GBV_ILN_721 
951 |a AR 
952 |j 2023  |b 06  |c 01