Chakraborty, Soumita ; Kalita, Daizy ; Agarwal, Sakshi ; Vashishth, Surishi ; Mathew, Nijita ; Maity, Sisir ; Goud, Devender ; Rao, Ankit ; Peter, Sebastian C. ; Singh, Abhishek K. ; Eswaramoorthy, Muthusamy (2024) Tuning the electrocatalytic activity of pd nanocatalyst toward hydrogen evolution and carbon dioxide reduction reactions by nickel incorporation Chemistry of Materials, 36 (13). pp. 6547-6557. ISSN 0897-4756
Full text not available from this repository.
Official URL: https://doi.org/10.1021/acs.chemmater.4c00809
Related URL: http://dx.doi.org/10.1021/acs.chemmater.4c00809
Abstract
Electrochemical H2generation and CO2reduction address the energy and environmental crisis plaguing the world. An efficient electrocatalyst would require the lowest overpotential for these reactions. Given its position on the volcano plot near platinum, palladium presents itself as a viable alternative for the hydrogen evolution reaction (HER). However, the activity is limited by a high overpotential. It is also a good electrocatalyst for the CO2reduction reaction (CO2RR) due to the favorable position of the d-band center. Nevertheless, the CO poisoning of the active site results in low electrocatalytic stability. Herein, we report a Ni-incorporated palladium catalyst, NiPd, which reduces water to H2at a very low overpotential of 25 mV η10). Furthermore, it reduces CO2to formate with a very high faradaic efficiency of 97% at a potential of -0.25 V (vs RHE). DFT studies show that Ni inclusion leads to the facile activation of CO2due to a bent adsorption configuration at the catalyst surface. The NiPd catalyst exhibits a strong and stable performance for HER (400 h) as well as for CO2RR (9 h) with high structural integrity as proven by postreaction characterization studies.
Item Type: | Article |
---|---|
Source: | Copyright of this article belongs to American Chemical Society. |
ID Code: | 139194 |
Deposited On: | 21 Aug 2025 06:29 |
Last Modified: | 21 Aug 2025 06:29 |
Repository Staff Only: item control page