Unveiling the Electrocatalytic Performances of the Pd-MoS<sub>2</sub> Catalyst for Methanol-Mediated Overall Water Splitting

Herein, this work elucidates the synthesis of the Pd-MoS<sub>2</sub> catalyst for application in methanol-mediated overall water splitting. The scanning electron microscope (SEM) and transmission electron microscope (TEM) pictures offer an exciting nanostructured shape of the Pd-MoS<s...

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Main Authors: Aviraj M. Teli, Sagar M. Mane, Rajneesh Kumar Mishra, Wookhee Jeon, Jae Cheol Shin
Format: Article
Language:English
Published: MDPI AG 2025-01-01
Series:Inorganics
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Online Access:https://www.mdpi.com/2304-6740/13/1/21
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author Aviraj M. Teli
Sagar M. Mane
Rajneesh Kumar Mishra
Wookhee Jeon
Jae Cheol Shin
author_facet Aviraj M. Teli
Sagar M. Mane
Rajneesh Kumar Mishra
Wookhee Jeon
Jae Cheol Shin
author_sort Aviraj M. Teli
collection DOAJ
description Herein, this work elucidates the synthesis of the Pd-MoS<sub>2</sub> catalyst for application in methanol-mediated overall water splitting. The scanning electron microscope (SEM) and transmission electron microscope (TEM) pictures offer an exciting nanostructured shape of the Pd-MoS<sub>2</sub>, depicting a high surface area. Further, high-resolution TEM (HRTEM) pictures confirm the lattice plane (100), lattice spacing (0.26 nm), and hexagonal crystal structure of the Pd-MoS<sub>2</sub>. Moreover, high-angle annular dark-field (HAADF) images and related color maps disclose the Mo, S, and Pd elements of the Pd-MoS<sub>2</sub>. The Pd-MoS<sub>2</sub> catalyst exhibits lower overpotentials of 224.6 mV [methanol-mediated hydrogen evolution reaction (MM-HER)] at −10 mA cm<sup>−2</sup> and 133 mV [methanol-mediated oxygen evolution reaction (MM-OER)] at 10 mA cm<sup>−2</sup>. Further, the Pd-MoS<sub>2</sub> illustrates noteworthy stability for 15.5 h for MM-HER and 18 h for MM-OER by chronopotentiometry test. Excitingly, the Pd-MoS<sub>2</sub>∥Pd-MoS<sub>2</sub> cell reveals a small potential of 1.581 V compared to the MoS<sub>2</sub>∥MoS<sub>2</sub> cell (1.648 V) in methanol-mediated overall water splitting. In addition, the Pd-MoS<sub>2</sub>∥Pd-MoS<sub>2</sub> combination reveals brilliant durability over 18 h at 10 mA cm<sup>−2</sup>.
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spelling doaj-art-b7be7e8dc8e94caeb99eddf4942da4b32025-01-24T13:35:30ZengMDPI AGInorganics2304-67402025-01-011312110.3390/inorganics13010021Unveiling the Electrocatalytic Performances of the Pd-MoS<sub>2</sub> Catalyst for Methanol-Mediated Overall Water SplittingAviraj M. Teli0Sagar M. Mane1Rajneesh Kumar Mishra2Wookhee Jeon3Jae Cheol Shin4Division of Electronics and Electrical Engineering, Dongguk University-Seoul, Seoul 04620, Republic of KoreaDepartment of Fiber System Engineering, Yeungnam University, 280 Dehak-Ro, Gyeongsan 38541, Gyeongbuk, Republic of KoreaDepartment of Physics, Yeungnam University, Gyeongsan 38541, Gyeongbuk, Republic of KoreaDepartment of Semiconductor, Convergence Engineering, Sungkyunkwan University, Suwon 16419, Gyeonggi, Republic of KoreaDivision of Electronics and Electrical Engineering, Dongguk University-Seoul, Seoul 04620, Republic of KoreaHerein, this work elucidates the synthesis of the Pd-MoS<sub>2</sub> catalyst for application in methanol-mediated overall water splitting. The scanning electron microscope (SEM) and transmission electron microscope (TEM) pictures offer an exciting nanostructured shape of the Pd-MoS<sub>2</sub>, depicting a high surface area. Further, high-resolution TEM (HRTEM) pictures confirm the lattice plane (100), lattice spacing (0.26 nm), and hexagonal crystal structure of the Pd-MoS<sub>2</sub>. Moreover, high-angle annular dark-field (HAADF) images and related color maps disclose the Mo, S, and Pd elements of the Pd-MoS<sub>2</sub>. The Pd-MoS<sub>2</sub> catalyst exhibits lower overpotentials of 224.6 mV [methanol-mediated hydrogen evolution reaction (MM-HER)] at −10 mA cm<sup>−2</sup> and 133 mV [methanol-mediated oxygen evolution reaction (MM-OER)] at 10 mA cm<sup>−2</sup>. Further, the Pd-MoS<sub>2</sub> illustrates noteworthy stability for 15.5 h for MM-HER and 18 h for MM-OER by chronopotentiometry test. Excitingly, the Pd-MoS<sub>2</sub>∥Pd-MoS<sub>2</sub> cell reveals a small potential of 1.581 V compared to the MoS<sub>2</sub>∥MoS<sub>2</sub> cell (1.648 V) in methanol-mediated overall water splitting. In addition, the Pd-MoS<sub>2</sub>∥Pd-MoS<sub>2</sub> combination reveals brilliant durability over 18 h at 10 mA cm<sup>−2</sup>.https://www.mdpi.com/2304-6740/13/1/21Pd-MoS<sub>2</sub>methanol-mediated hydrogen evolution reactionmethanol-mediated oxygen evolution reaction (MM-OER)methanol-mediated overall water splittingoutstanding stability
spellingShingle Aviraj M. Teli
Sagar M. Mane
Rajneesh Kumar Mishra
Wookhee Jeon
Jae Cheol Shin
Unveiling the Electrocatalytic Performances of the Pd-MoS<sub>2</sub> Catalyst for Methanol-Mediated Overall Water Splitting
Inorganics
Pd-MoS<sub>2</sub>
methanol-mediated hydrogen evolution reaction
methanol-mediated oxygen evolution reaction (MM-OER)
methanol-mediated overall water splitting
outstanding stability
title Unveiling the Electrocatalytic Performances of the Pd-MoS<sub>2</sub> Catalyst for Methanol-Mediated Overall Water Splitting
title_full Unveiling the Electrocatalytic Performances of the Pd-MoS<sub>2</sub> Catalyst for Methanol-Mediated Overall Water Splitting
title_fullStr Unveiling the Electrocatalytic Performances of the Pd-MoS<sub>2</sub> Catalyst for Methanol-Mediated Overall Water Splitting
title_full_unstemmed Unveiling the Electrocatalytic Performances of the Pd-MoS<sub>2</sub> Catalyst for Methanol-Mediated Overall Water Splitting
title_short Unveiling the Electrocatalytic Performances of the Pd-MoS<sub>2</sub> Catalyst for Methanol-Mediated Overall Water Splitting
title_sort unveiling the electrocatalytic performances of the pd mos sub 2 sub catalyst for methanol mediated overall water splitting
topic Pd-MoS<sub>2</sub>
methanol-mediated hydrogen evolution reaction
methanol-mediated oxygen evolution reaction (MM-OER)
methanol-mediated overall water splitting
outstanding stability
url https://www.mdpi.com/2304-6740/13/1/21
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