Ru/Mo2C@NC Schottky junction-loaded hollow nanospheres as an efficient hydrogen evolution electrocatalyst

The development and design of low-cost, high-performance catalysts with small overpotentials for hydrogen evolution in the universal-pH range still represent defiance for replacing the high-cost Pt metal catalysts and future energy technology. Herein, we designed a new electrocatalyst, N-doped carbo...

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Veröffentlicht in:Journal of materials chemistry. A, Materials for energy and sustainability Materials for energy and sustainability, 2021-09, Vol.9 (36), p.20518-20529
Hauptverfasser: Salah, Abdulwahab, Hong-Da Ren, Al-Ansi, Nabilah, Fei-Yang, Yu, Zhong-Ling, Lang, Tan, Huaqiao, Yang-Guang, Li
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container_end_page 20529
container_issue 36
container_start_page 20518
container_title Journal of materials chemistry. A, Materials for energy and sustainability
container_volume 9
creator Salah, Abdulwahab
Hong-Da Ren
Al-Ansi, Nabilah
Fei-Yang, Yu
Zhong-Ling, Lang
Tan, Huaqiao
Yang-Guang, Li
description The development and design of low-cost, high-performance catalysts with small overpotentials for hydrogen evolution in the universal-pH range still represent defiance for replacing the high-cost Pt metal catalysts and future energy technology. Herein, we designed a new electrocatalyst, N-doped carbon hollow nanospheres loaded with Ru/Mo2C Schottky junctions (denoted as Ru/Mo2C@NC), through a one-step approach by polymerization-induced self-assembly of a Mo–polydopamine hollow framework modified with ruthenium (Ru) in alkaline solution followed by in situ carbonization at high temperature. In 1 M KOH, the Ru/Mo2C@NC (Ru wt% = 3.93%) catalyst exhibits superb HER activity with a small overpotential at 10 mA cm−2 (η10 = 13 mV), a low Tafel slope of 33.24 mV dec−1, and long-term temporal stability for 72 h. Besides, the fabricated catalyst also displays low overpotentials of 21 and 41 mV to realize 10 mA cm−2 in both 0.5 M H2SO4 and 1 M PBS media, respectively, which are smaller and better than those of 20% Pt/C (26 and 59 mV). According to density functional theory (DFT) calculations, the introduction of metallic Ru into Mo2C has succeeded in constructing new active sites for H with optimal adsorption/desorption ability (ΔGH* = −0.09 eV) and maintaining relatively low water dissociation (ΔGb = 0.35 eV) in alkaline medium, endowing the composite with superb HER activity in the universal-pH range. Additionally, the outstanding catalytic HER performance is also fundamentally related to the effective influence of separating and transferring electrons from Mo2C to Ru via the Schottky junction.
doi_str_mv 10.1039/d1ta05876b
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Herein, we designed a new electrocatalyst, N-doped carbon hollow nanospheres loaded with Ru/Mo2C Schottky junctions (denoted as Ru/Mo2C@NC), through a one-step approach by polymerization-induced self-assembly of a Mo–polydopamine hollow framework modified with ruthenium (Ru) in alkaline solution followed by in situ carbonization at high temperature. In 1 M KOH, the Ru/Mo2C@NC (Ru wt% = 3.93%) catalyst exhibits superb HER activity with a small overpotential at 10 mA cm−2 (η10 = 13 mV), a low Tafel slope of 33.24 mV dec−1, and long-term temporal stability for 72 h. Besides, the fabricated catalyst also displays low overpotentials of 21 and 41 mV to realize 10 mA cm−2 in both 0.5 M H2SO4 and 1 M PBS media, respectively, which are smaller and better than those of 20% Pt/C (26 and 59 mV). According to density functional theory (DFT) calculations, the introduction of metallic Ru into Mo2C has succeeded in constructing new active sites for H with optimal adsorption/desorption ability (ΔGH* = −0.09 eV) and maintaining relatively low water dissociation (ΔGb = 0.35 eV) in alkaline medium, endowing the composite with superb HER activity in the universal-pH range. 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A, Materials for energy and sustainability</jtitle><date>2021-09-28</date><risdate>2021</risdate><volume>9</volume><issue>36</issue><spage>20518</spage><epage>20529</epage><pages>20518-20529</pages><issn>2050-7488</issn><eissn>2050-7496</eissn><abstract>The development and design of low-cost, high-performance catalysts with small overpotentials for hydrogen evolution in the universal-pH range still represent defiance for replacing the high-cost Pt metal catalysts and future energy technology. Herein, we designed a new electrocatalyst, N-doped carbon hollow nanospheres loaded with Ru/Mo2C Schottky junctions (denoted as Ru/Mo2C@NC), through a one-step approach by polymerization-induced self-assembly of a Mo–polydopamine hollow framework modified with ruthenium (Ru) in alkaline solution followed by in situ carbonization at high temperature. In 1 M KOH, the Ru/Mo2C@NC (Ru wt% = 3.93%) catalyst exhibits superb HER activity with a small overpotential at 10 mA cm−2 (η10 = 13 mV), a low Tafel slope of 33.24 mV dec−1, and long-term temporal stability for 72 h. Besides, the fabricated catalyst also displays low overpotentials of 21 and 41 mV to realize 10 mA cm−2 in both 0.5 M H2SO4 and 1 M PBS media, respectively, which are smaller and better than those of 20% Pt/C (26 and 59 mV). According to density functional theory (DFT) calculations, the introduction of metallic Ru into Mo2C has succeeded in constructing new active sites for H with optimal adsorption/desorption ability (ΔGH* = −0.09 eV) and maintaining relatively low water dissociation (ΔGb = 0.35 eV) in alkaline medium, endowing the composite with superb HER activity in the universal-pH range. 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source Royal Society Of Chemistry Journals 2008-
subjects Catalysts
Density functional theory
Electrocatalysts
Energy technology
High temperature
Hydrogen evolution
Nanospheres
pH effects
Ruthenium
Self-assembly
Sulfuric acid
title Ru/Mo2C@NC Schottky junction-loaded hollow nanospheres as an efficient hydrogen evolution electrocatalyst
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