Theoretical study on the carbon nanomaterial-supported Pt complex electrocatalysts for efficient and selective chlorine evolution reaction

© 2024 Wiley Periodicals LLC.

Bibliographische Detailangaben
Veröffentlicht in:Journal of computational chemistry. - 1984. - 45(2024), 31 vom: 05. Dez., Seite 2602-2611
1. Verfasser: Hossen, Jewel (VerfasserIn)
Weitere Verfasser: Nakatani, Naoki
Format: Online-Aufsatz
Sprache:English
Veröffentlicht: 2024
Zugriff auf das übergeordnete Werk:Journal of computational chemistry
Schlagworte:Journal Article carbon nanomaterials chlorine evolution reaction density functional theory electrocatalyst platinum complex
LEADER 01000caa a22002652c 4500
001 NLM37504096X
003 DE-627
005 20250306102206.0
007 cr uuu---uuuuu
008 240717s2024 xx |||||o 00| ||eng c
024 7 |a 10.1002/jcc.27466  |2 doi 
028 5 2 |a pubmed25n1249.xml 
035 |a (DE-627)NLM37504096X 
035 |a (NLM)39016463 
040 |a DE-627  |b ger  |c DE-627  |e rakwb 
041 |a eng 
100 1 |a Hossen, Jewel  |e verfasserin  |4 aut 
245 1 0 |a Theoretical study on the carbon nanomaterial-supported Pt complex electrocatalysts for efficient and selective chlorine evolution reaction 
264 1 |c 2024 
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 10.10.2024 
500 |a published: Print-Electronic 
500 |a Citation Status PubMed-not-MEDLINE 
520 |a © 2024 Wiley Periodicals LLC. 
520 |a Chlorine is an important chemical which has long been produced in chlor-alkali process using dimensionally stable anodes (DSA). However, some serious drawbacks of DSA inspire the development of alternative anodes for chlorine evolution reaction (CER). In this study, we focused on the graphene- and carbon nanotube-supported platinum tetra-phenyl porphyrins as electrocatalysts for CER, which have been theoretically investigated based on density functional theory. Our results reveal that the supported substrates possess potential CER electrocatalytic activity with very low thermodynamic overpotentials (0.012-0.028 V) via Cl* pathway instead of ClO*. The electronic structures analyses showed that electron transfer from the support to the adsorbed chlorine via the Pt center leads to strong Pt-Cl interactions. Furthermore, the supported electrocatalysts exhibited excellent selectivity toward CER because of high overpotentials and reaction barriers of oxygen evolution process. Therefore, our results may pave the way for designing CER electrocatalyst utilizing emerging carbon nanomaterials 
650 4 |a Journal Article 
650 4 |a carbon nanomaterials 
650 4 |a chlorine evolution reaction 
650 4 |a density functional theory 
650 4 |a electrocatalyst 
650 4 |a platinum complex 
700 1 |a Nakatani, Naoki  |e verfasserin  |4 aut 
773 0 8 |i Enthalten in  |t Journal of computational chemistry  |d 1984  |g 45(2024), 31 vom: 05. Dez., Seite 2602-2611  |w (DE-627)NLM098138448  |x 1096-987X  |7 nnas 
773 1 8 |g volume:45  |g year:2024  |g number:31  |g day:05  |g month:12  |g pages:2602-2611 
856 4 0 |u http://dx.doi.org/10.1002/jcc.27466  |3 Volltext 
912 |a GBV_USEFLAG_A 
912 |a SYSFLAG_A 
912 |a GBV_NLM 
912 |a GBV_ILN_350 
951 |a AR 
952 |d 45  |j 2024  |e 31  |b 05  |c 12  |h 2602-2611