2021
DOI: 10.1039/d1nr04400a
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Coupling plasmonic catalysis and nanocrystal growth through cyclic regeneration of NADH

Abstract: In a typical colloidal synthesis, the molecules of the reducing agent are irreversibly oxidized during nanocrystal growth. Such a scenario is of questionable sustainability when confronted with naturally occurring processes...

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Cited by 2 publications
(2 citation statements)
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“…In the depicted mechanism (Figure a), moderate concentration (1 mM) of NAD + attributes to a higher possibility of adsorption of both the substrates on adjacent locations so that it can produce reduced NADH and oxidized TEOA* via a direct electron transfer. The standard redox potentials of NAD + and TEOA are −0.32 and +1.07 V, respectively, creating a possibility of a spontaneous NADH regeneration, responsible for the direct electron transfer from TEOA to NAD + in dark conditions. , A higher concentration of NAD + can inhibit the redox process by occupying both the adsorption sites of NAD + and TEOA. The obtained results can be validated by the bimolecular Langmuir–Hinshelwood (L-H) model, where adsorption interaction (or sites) is the same for both the reactants (competitive adsorption). , The obtained trend can be interpreted with the following eq , where [A] and [B] are the concentration of the substrates (NAD + and TEOA, respectively), K eff is the catalytic rate constant, and a is the equilibrium constant for substrate adsorption. …”
Section: Resultsmentioning
confidence: 99%
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“…In the depicted mechanism (Figure a), moderate concentration (1 mM) of NAD + attributes to a higher possibility of adsorption of both the substrates on adjacent locations so that it can produce reduced NADH and oxidized TEOA* via a direct electron transfer. The standard redox potentials of NAD + and TEOA are −0.32 and +1.07 V, respectively, creating a possibility of a spontaneous NADH regeneration, responsible for the direct electron transfer from TEOA to NAD + in dark conditions. , A higher concentration of NAD + can inhibit the redox process by occupying both the adsorption sites of NAD + and TEOA. The obtained results can be validated by the bimolecular Langmuir–Hinshelwood (L-H) model, where adsorption interaction (or sites) is the same for both the reactants (competitive adsorption). , The obtained trend can be interpreted with the following eq , where [A] and [B] are the concentration of the substrates (NAD + and TEOA, respectively), K eff is the catalytic rate constant, and a is the equilibrium constant for substrate adsorption. …”
Section: Resultsmentioning
confidence: 99%
“…To increase the domain of these bimetallic composites in photocatalysis, we have explored Au–Pd core–shell nanoparticles (Au–Pd CS NPs) to regenerate NADH from its oxidized form β-NAD + in a colloidal solution of this bimetallic composite. Previously, few reports have successfully demonstrated NADH regeneration using immobilized Au–Pd nanorods over cellulose fibers and agarose matrix. , NADH is a coenzyme (cofactor) molecule used as a hydride source by almost 80% of existing oxidoreductase enzymes. These enzymes have many applications, including enzyme catalysis to synthesize chemicals and pharmaceuticals, biodegradation, and detoxification. , Despite being a mainstream coenzyme, NADH has relatively less utilization in industries due to its high cost.…”
Section: Introductionmentioning
confidence: 99%