| نویسندگان | غزاله جعفری,عادل رئیسی |
| نشریه | Journal of Power Sources |
| شماره صفحات | 238579 |
| شماره مجلد | 660 |
| ضریب تاثیر (IF) | 8.4 |
| نوع مقاله | Full Paper |
| تاریخ انتشار | 2025-10-08 |
| رتبه نشریه | علمی - پژوهشی |
| نوع نشریه | الکترونیکی |
| کشور محل چاپ | ایران |
| نمایه نشریه | JCR ,SCOPUS |
| کلید واژه ها | single, atom Hydrogen evolution reaction (HER) Oxygen evolution reaction (OER) 8, 16, 4 graphyne (GY) Density functional theory (DFT, D2) |
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چکیده مقاله
The advancement of clean energy technologies depends on the rational design of cost-effective single-atom
catalysts capable of efficiently driving the hydrogen evolution reaction (HER) and oxygen evolution reaction
(OER). Here, we report for the first time sulfur (S) or phosphorus (P) doping of 8-16-4 graphyne (GY) decorated
with single Fe or Co atoms to enhance electronic properties and catalytic activity for overall water splitting.
Using density functional theory (DFT), we evaluate the stability, electronic structure, and HER/OER performance
of TM-S1-GY, TM-S2-GY, TM-P1-GY, and TM-P2-GY (TM =Fe, Co). Doping modifies charge distribution, weakens
OER intermediate adsorption, and improves HER by increasing active sites. Fe-S1-GY, Fe-P1-GY, and Co-P1-GY
show superior bifunctional activity compared to undoped Fe-GY and Co-GY. Linear scaling relationships between
ΔGHOO* and ΔGHO*, and between ΔGO* and ΔGHO*, confirm that OER activity can be predicted through these
correlations. Exchange current density (i0) versus ΔGH* analysis indicates optimal HER activity for Fe-P1-GY (P),
Fe-P1-GY (C1), and Co-P1-GY (C1). Volcano plot analysis further demonstrates that Co-S1-GY, Co-P1-GY, Co-S2-
GY, and Fe-S1-GY exhibit outstanding OER efficiency. The work provides critical insights for rational design of
bifunctional electrocatalysts, offering new opportunities in water-splitting applications.