TY - JOUR
T1 - Unraveling the Enhanced N2 Activity on CuNi Alloy Catalysts for Ammonia Production
T2 - Experiments, DFT, and Statistical Analysis
AU - Agharezaei, Parastoo
AU - Tomohiro, Noguchi Goroh
AU - Kobayashi, Hirokazu
AU - Schlenz, Hartmut
AU - Yamauchi, Miho
AU - Ghuman, Kulbir Kaur
N1 - Publisher Copyright:
© 2024 American Chemical Society
PY - 2024/3/7
Y1 - 2024/3/7
N2 - One of the main challenges in designing catalysts for ammonia synthesis is to create active sites on the surface of the catalyst that prefers to reduce the strong N2 molecule despite its highly stable structure. Binary alloys have been demonstrated as potential ammonia synthesis catalysts in the literature. However, for binary alloys to be commercially viable, one needs to improve their catalytic activity for N2 reduction by strategically manipulating the several unique active sites present on their surface. Herein, by using computational tools, we created five different compositions of CuxNi1-x (0.5 ≤ x ≤ 0.9) alloys via special quasi-random structure (SQS) and genetic algorithm (GA). The alloy with about 50% of Cu and 50% of Ni is predicted to have the highest catalytic activity based on the shift of the d-band center toward the Fermi level. We then synthesized MgO-supported Cu0.5Ni0.5 nanoparticles and compared their activity for ammonia synthesis with that of Ni/MgO and Cu/MgO. It was found that the MgO-supported Cu0.5Ni0.5 alloy possesses 21 times higher activity than Cu/MgO and 3 times higher than Ni/MgO for ammonia synthesis, confirming the computational results. To demonstrate the impact of alloying on the catalytic activity, we further investigated all the possible unique sites on the surface of the Cu0.5Ni0.5 alloy for nitrogen reduction reaction (NRR) via density functional theory (DFT). The investigation of the 96 unique active sites on the Cu0.5Ni0.5 surface demonstrated that the position and concentration of Ni atoms near each investigated adsorption site have a linear correlation with the adsorption energy of the N2. Along with the structural and electronic properties of the active sites modified by Ni, orientation of the N2 molecule also plays an important role in determining the activity of the CuNi catalyst. These findings not only explained the notable increase in the activity of CuNi catalysts compared to the pure metals for NH3 synthesis but also offered critical insights required to tailor the specific surface environment of CuNi catalysts for NRR. This knowledge can serve as a foundation for further developments in designing binary alloy catalysts for sustainable ammonia synthesis.
AB - One of the main challenges in designing catalysts for ammonia synthesis is to create active sites on the surface of the catalyst that prefers to reduce the strong N2 molecule despite its highly stable structure. Binary alloys have been demonstrated as potential ammonia synthesis catalysts in the literature. However, for binary alloys to be commercially viable, one needs to improve their catalytic activity for N2 reduction by strategically manipulating the several unique active sites present on their surface. Herein, by using computational tools, we created five different compositions of CuxNi1-x (0.5 ≤ x ≤ 0.9) alloys via special quasi-random structure (SQS) and genetic algorithm (GA). The alloy with about 50% of Cu and 50% of Ni is predicted to have the highest catalytic activity based on the shift of the d-band center toward the Fermi level. We then synthesized MgO-supported Cu0.5Ni0.5 nanoparticles and compared their activity for ammonia synthesis with that of Ni/MgO and Cu/MgO. It was found that the MgO-supported Cu0.5Ni0.5 alloy possesses 21 times higher activity than Cu/MgO and 3 times higher than Ni/MgO for ammonia synthesis, confirming the computational results. To demonstrate the impact of alloying on the catalytic activity, we further investigated all the possible unique sites on the surface of the Cu0.5Ni0.5 alloy for nitrogen reduction reaction (NRR) via density functional theory (DFT). The investigation of the 96 unique active sites on the Cu0.5Ni0.5 surface demonstrated that the position and concentration of Ni atoms near each investigated adsorption site have a linear correlation with the adsorption energy of the N2. Along with the structural and electronic properties of the active sites modified by Ni, orientation of the N2 molecule also plays an important role in determining the activity of the CuNi catalyst. These findings not only explained the notable increase in the activity of CuNi catalysts compared to the pure metals for NH3 synthesis but also offered critical insights required to tailor the specific surface environment of CuNi catalysts for NRR. This knowledge can serve as a foundation for further developments in designing binary alloy catalysts for sustainable ammonia synthesis.
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U2 - 10.1021/acs.jpcc.3c06417
DO - 10.1021/acs.jpcc.3c06417
M3 - Article
AN - SCOPUS:85186086122
SN - 1932-7447
VL - 128
SP - 3703
EP - 3717
JO - Journal of Physical Chemistry C
JF - Journal of Physical Chemistry C
IS - 9
ER -