2020
DOI: 10.1039/c9cp06478h
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Investigation of copper oxidation states in plasmonic nanomaterials by XAS and Raman spectroscopy

Abstract: A shell-isolated nanoparticle enhanced surface Raman technique and XANES for detection of copper(ii) or copper(i) plasmonic-nanocatalysts.

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Cited by 8 publications
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“…It is generally accepted that the N atom of the BTH thiazole ring can coordinate with Cu­(II). , The in situ confocal Raman spectrum of Cu­(II)/PDS/BTH (Figure c) shows emerging bands at 293, 447, and 463 cm –1 , which can be attributed to the stretching vibrations of Cu­(I)–N and Cu­(II)–N (both symmetric and asymmetric). , The weak vibrations at 273 and 499 cm –1 originate from Cu­(II)–S stretching and ring deformation of the BTH molecules. , The Raman characterization further exhibits the Cu­(II)-BTH coordination and the subsequent interaction of the coordinated Cu­(II) with PDS. To further verify whether S of the thiazole ring contributes to BTH degradation by PDS/Cu­(II), two BTH analogues [i.e., benzothiophene (BTP) and benzoxazole (BXZ)] were treated.…”
Section: Resultsmentioning
confidence: 97%
“…It is generally accepted that the N atom of the BTH thiazole ring can coordinate with Cu­(II). , The in situ confocal Raman spectrum of Cu­(II)/PDS/BTH (Figure c) shows emerging bands at 293, 447, and 463 cm –1 , which can be attributed to the stretching vibrations of Cu­(I)–N and Cu­(II)–N (both symmetric and asymmetric). , The weak vibrations at 273 and 499 cm –1 originate from Cu­(II)–S stretching and ring deformation of the BTH molecules. , The Raman characterization further exhibits the Cu­(II)-BTH coordination and the subsequent interaction of the coordinated Cu­(II) with PDS. To further verify whether S of the thiazole ring contributes to BTH degradation by PDS/Cu­(II), two BTH analogues [i.e., benzothiophene (BTP) and benzoxazole (BXZ)] were treated.…”
Section: Resultsmentioning
confidence: 97%