Photocatalytic Mechanism Control and Study of Carrier Dynamics in CdS@C3N5 Core–Shell Nanowires

We present a potential solution to the problem of extraction of photogenerated holes from CdS nanocrystals and nanowires. The nanosheet form of C3N5 is a low-band-gap (E g = 2.03 eV), azo-linked graphenic carbon nitride framework formed by the polymerization of melem hydrazine (MHP). C3N5 nanosheets...

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Published in:ACS applied materials & interfaces Vol. 13; no. 40; pp. 47418 - 47439
Main Authors: Alam, Kazi M, Jensen, Charles E, Kumar, Pawan, Hooper, Riley W, Bernard, Guy M, Patidar, Aakash, Manuel, Ajay P, Amer, Naaman, Palmgren, Anders, Purschke, David N, Chaulagain, Narendra, Garcia, John, Kirwin, Phillip S, Shoute, Lian C.T, Cui, Kai, Gusarov, Sergey, Kobryn, Alexander E, Michaelis, Vladimir K, Hegmann, Frank A, Shankar, Karthik
Format: Journal Article
Language:English
Published: American Chemical Society 13-10-2021
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Summary:We present a potential solution to the problem of extraction of photogenerated holes from CdS nanocrystals and nanowires. The nanosheet form of C3N5 is a low-band-gap (E g = 2.03 eV), azo-linked graphenic carbon nitride framework formed by the polymerization of melem hydrazine (MHP). C3N5 nanosheets were either wrapped around CdS nanorods (NRs) following the synthesis of pristine chalcogenide or intercalated among them by an in situ synthesis protocol to form two kinds of heterostructures, CdS-MHP and CdS-MHPINS, respectively. CdS-MHP improved the photocatalytic degradation rate of 4-nitrophenol by nearly an order of magnitude in comparison to bare CdS NRs. CdS-MHP also enhanced the sunlight-driven photocatalytic activity of bare CdS NWs for the decolorization of rhodamine B (RhB) by a remarkable 300% through the improved extraction and utilization of photogenerated holes due to surface passivation. More interestingly, CdS-MHP provided reaction pathway control over RhB degradation. In the absence of scavengers, CdS-MHP degraded RhB through the N-deethylation pathway. When either hole scavenger or electron scavenger was added to the RhB solution, the photocatalytic activity of CdS-MHP remained mostly unchanged, while the degradation mechanism shifted to the chromophore cleavage (cycloreversion) pathway. We investigated the optoelectronic properties of CdS-C3N5 heterojunctions using density functional theory (DFT) simulations, finite difference time domain (FDTD) simulations, time-resolved terahertz spectroscopy (TRTS), and photoconductivity measurements. TRTS indicated high carrier mobilities >450 cm2 V–1 s–1 and carrier relaxation times >60 ps for CdS-MHP, while CdS-MHPINS exhibited much lower mobilities <150 cm2 V–1 s–1 and short carrier relaxation times <20 ps. Hysteresis in the photoconductive J–V characteristics of CdS NWs disappeared in CdS-MHP, confirming surface passivation. Dispersion-corrected DFT simulations indicated a delocalized HOMO and a LUMO localized on C3N5 in CdS-MHP. C3N5, with its extended π-conjugation and low band gap, can function as a shuttle to extract carriers and excitons in nanostructured heterojunctions, and enhance performance in optoelectronic devices. Our results demonstrate how carrier dynamics in core–shell heterostructures can be manipulated to achieve control over the reaction mechanism in photocatalysis.
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ISSN:1944-8244
1944-8252
DOI:10.1021/acsami.1c08550