TY - JOUR
T1 - Engineering MoS2/SiC interfaces for superior electrocatalytic oxygen and hydrogen evolution reactions
AU - Alsaiari, Norah Salem
AU - Manzoor, Iram
AU - Siddique, Zobia
AU - fareed, Zubaida
AU - Ouladsmane, Mohamed
AU - Naz, Maryum
AU - Rehman, Shafiq Ur
AU - Rashid, Abdul Rasheed
AU - Benettayeb, Asmaa
AU - Sillanpaa, Mika
N1 - Publisher Copyright:
© The Korean Ceramic Society 2025.
PY - 2025
Y1 - 2025
N2 - Electrochemical water splitting is a green, eco-friendly, and efficient hydrogen synthesis process that consists of two half-reactions: the oxygen evolution reaction (OER) and the hydrogen evolution reaction. Because of the sluggish reaction kinetics of the OER and HER, electrochemical water splitting frequently requires an elevated voltage than theoretical, resulting in significant energy loss. Herein, we report MoS2/SiC/GC by the integration of MoS2 with SiC by a straightforward hydrothermal method. X-rays diffraction (XRD) indicates that MoS2/SiC has a crystallite structure, which improves catalytic performance for OER and HER with the best electrocatalytic activity by showing overpotentials of 230 mV for OER and 317 mV for HER in 1 M KOH at 10 mAcm−2 with Tafel slope of 65 mVdec−1 and 91 mVdec−1. Furthermore, with a non-faradic CV region, the MoS2/SiC/GC composite exhibited high capacitance and high electrochemical active surface area (528 cm2). The chronoamperometric test confirmed the long-term endurance of OER/HER for 35/64 h without compromising current density. Hence, overall, this work provides a notable composite approach using Si and Mo based elements, bringing in a new era of good design and the development of noble material alternatives in the commercial electrolysis sector.
AB - Electrochemical water splitting is a green, eco-friendly, and efficient hydrogen synthesis process that consists of two half-reactions: the oxygen evolution reaction (OER) and the hydrogen evolution reaction. Because of the sluggish reaction kinetics of the OER and HER, electrochemical water splitting frequently requires an elevated voltage than theoretical, resulting in significant energy loss. Herein, we report MoS2/SiC/GC by the integration of MoS2 with SiC by a straightforward hydrothermal method. X-rays diffraction (XRD) indicates that MoS2/SiC has a crystallite structure, which improves catalytic performance for OER and HER with the best electrocatalytic activity by showing overpotentials of 230 mV for OER and 317 mV for HER in 1 M KOH at 10 mAcm−2 with Tafel slope of 65 mVdec−1 and 91 mVdec−1. Furthermore, with a non-faradic CV region, the MoS2/SiC/GC composite exhibited high capacitance and high electrochemical active surface area (528 cm2). The chronoamperometric test confirmed the long-term endurance of OER/HER for 35/64 h without compromising current density. Hence, overall, this work provides a notable composite approach using Si and Mo based elements, bringing in a new era of good design and the development of noble material alternatives in the commercial electrolysis sector.
KW - Green energy
KW - HER
KW - Hydrothermal method
KW - MoS/SiC
KW - Nanocomposite
KW - OER
UR - https://www.scopus.com/pages/publications/105013816142
U2 - 10.1007/s43207-025-00532-y
DO - 10.1007/s43207-025-00532-y
M3 - Article
AN - SCOPUS:105013816142
SN - 1229-7801
JO - Journal of the Korean Ceramic Society
JF - Journal of the Korean Ceramic Society
ER -