2021
DOI: 10.1021/jacs.1c08877
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Identifying Highly Photoelectrochemical Active Sites of Two Au21 Nanocluster Isomers toward Bright Near-Infrared Electrochemiluminescence

Abstract: Thus far, no correlation between nanocluster structures and their electrochemiluminescence (ECL) has been identified. Herein, we report how face-centered-cubic and hexagonal close-packed structures of two Au21(SR)15 nanocluster isomers determine their chemical reactivity. The relationships were explored by means of ECL and photoluminescence spectroscopy. Both isomers reveal unprecedented ECL efficiencies in the near-infrared region, which are >10- and 270-fold higher than that of standard Ru­(bpy)3 2+, respect… Show more

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Cited by 58 publications
(55 citation statements)
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“…The 45 nm difference between the onset peak wavelength and the maximum intensity wavelength is probably due to the formation of different excited states of Cu NCs in the process of potential negative scanning as the valence state of the obtained Cu NCs is between 0 and +1 as demonstrated from XPS. Although it is hard to decide the exact content of Cu(0) and Cu­(I) in the obtained Cu NCs, a series of similar valence-state-dependent ECL emission wavelength investigations on gold nanoclusters have been concluded by the Ding group. , Upon sweeping the potential further negative and backwards, the ECL intensity decreased owing to the depletion of the Cu NCs –• and SO 4 –• species and led to the ECL devolution (Figure C).…”
Section: Experimental Sectionmentioning
confidence: 72%
“…The 45 nm difference between the onset peak wavelength and the maximum intensity wavelength is probably due to the formation of different excited states of Cu NCs in the process of potential negative scanning as the valence state of the obtained Cu NCs is between 0 and +1 as demonstrated from XPS. Although it is hard to decide the exact content of Cu(0) and Cu­(I) in the obtained Cu NCs, a series of similar valence-state-dependent ECL emission wavelength investigations on gold nanoclusters have been concluded by the Ding group. , Upon sweeping the potential further negative and backwards, the ECL intensity decreased owing to the depletion of the Cu NCs –• and SO 4 –• species and led to the ECL devolution (Figure C).…”
Section: Experimental Sectionmentioning
confidence: 72%
“…In recent years, electrochemiluminescence (ECL) as another optical analysis tool has attracted great interests, especially in bioanalysis. For ECL to occur, photons-releasing excited states are produced in the vicinity of the electrode through electron transfer reactions of electrogenerated radical species. There are two general routes giving ECL. The first is the annihilation pathway, where the radical cation and radical anion generated by reduction and oxidation of electrochemiluminophore (ECLphore) at the electrode, respectively, are annihilated to produce excited states, giving off light .…”
Section: Introductionmentioning
confidence: 99%
“…As a kind of promising ECL luminophore, Au nanoclusters (AuNCs) have attracted extensive attention for their ultra-small size, unique optical properties, excellent stability, and high biocompatibility. A series of AuNCs have been developed, most of them are modified or synthesized with proteins or amino acids as capping agents, such as bovine serum albumin, , methionine, and glutathione, or nonlinear sulfhydryl chains containing more functional groups, such as captopril, N-acetyl- l -cysteine, , and lipoic acid . Due to the interaction of various functional groups and/or branched chains of capping agents at the surface of these AuNCs, it is still difficult to discriminate the function of the carbon skeleton on the ECL of AuNCs.…”
mentioning
confidence: 99%