TY - JOUR
T1 - Interfacial engineering of ZnS–ZnO decorated MoS2 supported on 2D Ti3C2Tx MXene sheets for enhanced hydrogen evolution reaction
AU - Rasool, Faisal
AU - Pirzada, Bilal Masood
AU - Misbah Uddin, Mohammed
AU - Mohideen, M. Infas H.
AU - Yildiz, Ibrahim
AU - Elkadi, Mirella
AU - Qurashi, Ahsanulhaq
N1 - Publisher Copyright:
© 2024
PY - 2024/3/15
Y1 - 2024/3/15
N2 - Molybdenum disulfide (MoS2) contains inactive basal and edge planes, which hinders its effectiveness in facilitating environmentally clean Hydrogen Evolution Reaction (HER) in electrocatalytic water splitting. Herein, we report a single-step synthesis strategy for developing ZnS–ZnO–MoS2/Ti3C2Tx MXene (ZZM/MX) nanostructures through a hydrothermal approach. The SEM micrographs clearly demonstrate edge plane modification in MoS2, making them sharper and more exposed outward. XRD analysis exhibited the formation of ZnS and ZnO phases over MoS2 surface which was further supported by XPS analysis. The molar percentage of Zn precursor was increased from 1 % to 6 % and the resultant samples were designated as ZZM/MX-1, ZZM/MX-2, ZZM/MX-4, and ZZM/MX-6, respectively. Among the prepared samples, ZZM/MX-4 electrocatalyst exhibited the least overpotential of 327.6 mV @ 10 mA cm−2; and a low Tafel slope of 79.5 mVdec−1 in 0.5 M H2SO4 electrolyte for HER. Also, it demonstrated excellent stability, withstanding 50 h of operation under acidic conditions. The higher electrocatalytic performance in this material can be attributed to the robust interaction between hetero-phase interfaces along ZnS–ZnO–MoS2 and MXene (Ti3C2Tx) support, which activates MoS2 basal planes and enhances the charge transfer properties. Further, the activation of MoS2 edges by introduction of ZnS/ZnO phases led to enhanced number of active sites for HER electrocatalysis. This work showcases an opportunity to apply dual modification of edge and basal planes in various other chalcogenide materials to enhance environmentally friendly clean HER performance and stability.
AB - Molybdenum disulfide (MoS2) contains inactive basal and edge planes, which hinders its effectiveness in facilitating environmentally clean Hydrogen Evolution Reaction (HER) in electrocatalytic water splitting. Herein, we report a single-step synthesis strategy for developing ZnS–ZnO–MoS2/Ti3C2Tx MXene (ZZM/MX) nanostructures through a hydrothermal approach. The SEM micrographs clearly demonstrate edge plane modification in MoS2, making them sharper and more exposed outward. XRD analysis exhibited the formation of ZnS and ZnO phases over MoS2 surface which was further supported by XPS analysis. The molar percentage of Zn precursor was increased from 1 % to 6 % and the resultant samples were designated as ZZM/MX-1, ZZM/MX-2, ZZM/MX-4, and ZZM/MX-6, respectively. Among the prepared samples, ZZM/MX-4 electrocatalyst exhibited the least overpotential of 327.6 mV @ 10 mA cm−2; and a low Tafel slope of 79.5 mVdec−1 in 0.5 M H2SO4 electrolyte for HER. Also, it demonstrated excellent stability, withstanding 50 h of operation under acidic conditions. The higher electrocatalytic performance in this material can be attributed to the robust interaction between hetero-phase interfaces along ZnS–ZnO–MoS2 and MXene (Ti3C2Tx) support, which activates MoS2 basal planes and enhances the charge transfer properties. Further, the activation of MoS2 edges by introduction of ZnS/ZnO phases led to enhanced number of active sites for HER electrocatalysis. This work showcases an opportunity to apply dual modification of edge and basal planes in various other chalcogenide materials to enhance environmentally friendly clean HER performance and stability.
KW - 2D-2D heterostructure
KW - Dual activation
KW - Edges and basal planes
KW - Hydrogen evolution reaction
KW - MXene
KW - ZnS–ZnO–MoS
UR - http://www.scopus.com/inward/record.url?scp=85183970349&partnerID=8YFLogxK
U2 - 10.1016/j.ijhydene.2024.01.152
DO - 10.1016/j.ijhydene.2024.01.152
M3 - Article
AN - SCOPUS:85183970349
SN - 0360-3199
VL - 59
SP - 63
EP - 73
JO - International Journal of Hydrogen Energy
JF - International Journal of Hydrogen Energy
ER -