Constructing Heterogeneous Interface by Growth of Carbon Nanotubes on the Surface of MoB2 for Boosting Hydrogen Evolution Reaction in a Wide pH Range
Transition metal diborides represented by MoB2 have attracted widespread attention for their excellent acidic hydrogen evolution reaction (HER). Nevertheless, their electrocatalytic performance is generally unsatisfactory in high‐pH electrolytes. Heterogeneous interface engineering is one of the mos...
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Published in | Small (Weinheim an der Bergstrasse, Germany) Vol. 20; no. 10; pp. e2304573 - n/a |
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Main Authors | , , , , , , |
Format | Journal Article |
Language | English |
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01.03.2024
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ISSN | 1613-6810 1613-6829 1613-6829 |
DOI | 10.1002/smll.202304573 |
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Abstract | Transition metal diborides represented by MoB2 have attracted widespread attention for their excellent acidic hydrogen evolution reaction (HER). Nevertheless, their electrocatalytic performance is generally unsatisfactory in high‐pH electrolytes. Heterogeneous interface engineering is one of the most promising methods for optimizing the composition and structure of electrocatalysts, thereby greatly affecting their electrochemical performance. Herein, a heterostructure, composed of MoB2 and carbon nanotubes (CNTs), is rationally constructed by boronizing precursors including (NH4)4[NiH6Mo6O24]·5H2O (NiMo6) and Co complexes on the carbon cloth (Co,Ni–MoB2@CNT/CC). In this method, NiMo6 is boronized to form MoB2 by a modified molten‐salt‐assisted borothermal reduction. Meanwhile, Co catalyzes extra carbon sources to grow CNTs on the surface of MoB2. Thanks to the successful production of the heterostructure, Co,Ni–MoB2@CNT/CC exhibits remarkable HER performance with a low overpotential of 98.6, 113.0, and 73.9 mV at 10 mA cm−2 in acidic, neutral, and alkaline electrolytes, respectively. Notably, even at 500 mA cm−2, the electrochemical activity of Co,Ni–MoB2@CNT/CC exceeds that of Pt/C/CC in an alkaline solution and maintains over 50 h. Theoretical calculations reveal that the construction of the heterostructure is beneficial to both water dissociation and reactive intermediate adsorption, resulting in superior alkaline HER performance.
A carbon nanotubes‐modified MoB2 on a carbon cloth integrated electrode is prepared by an operable heterogeneous interface engineering strategy. The reasonably constructed heterogeneous interface provides abundant active sites and optimizes intermediate adsorption barriers, thus improving its electrocatalytic HER performance in a wide pH range. Especially at high current density, its activity is comparable to Pt. |
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AbstractList | Transition metal diborides represented by MoB2 have attracted widespread attention for their excellent acidic hydrogen evolution reaction (HER). Nevertheless, their electrocatalytic performance is generally unsatisfactory in high‐pH electrolytes. Heterogeneous interface engineering is one of the most promising methods for optimizing the composition and structure of electrocatalysts, thereby greatly affecting their electrochemical performance. Herein, a heterostructure, composed of MoB2 and carbon nanotubes (CNTs), is rationally constructed by boronizing precursors including (NH4)4[NiH6Mo6O24]·5H2O (NiMo6) and Co complexes on the carbon cloth (Co,Ni–MoB2@CNT/CC). In this method, NiMo6 is boronized to form MoB2 by a modified molten‐salt‐assisted borothermal reduction. Meanwhile, Co catalyzes extra carbon sources to grow CNTs on the surface of MoB2. Thanks to the successful production of the heterostructure, Co,Ni–MoB2@CNT/CC exhibits remarkable HER performance with a low overpotential of 98.6, 113.0, and 73.9 mV at 10 mA cm−2 in acidic, neutral, and alkaline electrolytes, respectively. Notably, even at 500 mA cm−2, the electrochemical activity of Co,Ni–MoB2@CNT/CC exceeds that of Pt/C/CC in an alkaline solution and maintains over 50 h. Theoretical calculations reveal that the construction of the heterostructure is beneficial to both water dissociation and reactive intermediate adsorption, resulting in superior alkaline HER performance.
A carbon nanotubes‐modified MoB2 on a carbon cloth integrated electrode is prepared by an operable heterogeneous interface engineering strategy. The reasonably constructed heterogeneous interface provides abundant active sites and optimizes intermediate adsorption barriers, thus improving its electrocatalytic HER performance in a wide pH range. Especially at high current density, its activity is comparable to Pt. Transition metal diborides represented by MoB2 have attracted widespread attention for their excellent acidic hydrogen evolution reaction (HER). Nevertheless, their electrocatalytic performance is generally unsatisfactory in high-pH electrolytes. Heterogeneous interface engineering is one of the most promising methods for optimizing the composition and structure of electrocatalysts, thereby greatly affecting their electrochemical performance. Herein, a heterostructure, composed of MoB2 and carbon nanotubes (CNTs), is rationally constructed by boronizing precursors including (NH4 )4 [NiH6 Mo6 O24 ]·5H2 O (NiMo6 ) and Co complexes on the carbon cloth (Co,Ni-MoB2 @CNT/CC). In this method, NiMo6 is boronized to form MoB2 by a modified molten-salt-assisted borothermal reduction. Meanwhile, Co catalyzes extra carbon sources to grow CNTs on the surface of MoB2 . Thanks to the successful production of the heterostructure, Co,Ni-MoB2 @CNT/CC exhibits remarkable HER performance with a low overpotential of 98.6, 113.0, and 73.9 mV at 10 mA cm-2 in acidic, neutral, and alkaline electrolytes, respectively. Notably, even at 500 mA cm-2 , the electrochemical activity of Co,Ni-MoB2 @CNT/CC exceeds that of Pt/C/CC in an alkaline solution and maintains over 50 h. Theoretical calculations reveal that the construction of the heterostructure is beneficial to both water dissociation and reactive intermediate adsorption, resulting in superior alkaline HER performance.Transition metal diborides represented by MoB2 have attracted widespread attention for their excellent acidic hydrogen evolution reaction (HER). Nevertheless, their electrocatalytic performance is generally unsatisfactory in high-pH electrolytes. Heterogeneous interface engineering is one of the most promising methods for optimizing the composition and structure of electrocatalysts, thereby greatly affecting their electrochemical performance. Herein, a heterostructure, composed of MoB2 and carbon nanotubes (CNTs), is rationally constructed by boronizing precursors including (NH4 )4 [NiH6 Mo6 O24 ]·5H2 O (NiMo6 ) and Co complexes on the carbon cloth (Co,Ni-MoB2 @CNT/CC). In this method, NiMo6 is boronized to form MoB2 by a modified molten-salt-assisted borothermal reduction. Meanwhile, Co catalyzes extra carbon sources to grow CNTs on the surface of MoB2 . Thanks to the successful production of the heterostructure, Co,Ni-MoB2 @CNT/CC exhibits remarkable HER performance with a low overpotential of 98.6, 113.0, and 73.9 mV at 10 mA cm-2 in acidic, neutral, and alkaline electrolytes, respectively. Notably, even at 500 mA cm-2 , the electrochemical activity of Co,Ni-MoB2 @CNT/CC exceeds that of Pt/C/CC in an alkaline solution and maintains over 50 h. Theoretical calculations reveal that the construction of the heterostructure is beneficial to both water dissociation and reactive intermediate adsorption, resulting in superior alkaline HER performance. Transition metal diborides represented by MoB2 have attracted widespread attention for their excellent acidic hydrogen evolution reaction (HER). Nevertheless, their electrocatalytic performance is generally unsatisfactory in high‐pH electrolytes. Heterogeneous interface engineering is one of the most promising methods for optimizing the composition and structure of electrocatalysts, thereby greatly affecting their electrochemical performance. Herein, a heterostructure, composed of MoB2 and carbon nanotubes (CNTs), is rationally constructed by boronizing precursors including (NH4)4[NiH6Mo6O24]·5H2O (NiMo6) and Co complexes on the carbon cloth (Co,Ni–MoB2@CNT/CC). In this method, NiMo6 is boronized to form MoB2 by a modified molten‐salt‐assisted borothermal reduction. Meanwhile, Co catalyzes extra carbon sources to grow CNTs on the surface of MoB2. Thanks to the successful production of the heterostructure, Co,Ni–MoB2@CNT/CC exhibits remarkable HER performance with a low overpotential of 98.6, 113.0, and 73.9 mV at 10 mA cm−2 in acidic, neutral, and alkaline electrolytes, respectively. Notably, even at 500 mA cm−2, the electrochemical activity of Co,Ni–MoB2@CNT/CC exceeds that of Pt/C/CC in an alkaline solution and maintains over 50 h. Theoretical calculations reveal that the construction of the heterostructure is beneficial to both water dissociation and reactive intermediate adsorption, resulting in superior alkaline HER performance. |
Author | Yang, Jin Tian, Yuyang Sun, Jianhang Guo, Feifan Zou, Xiaoxin Ai, Xuan Zhu, Guangshan |
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Snippet | Transition metal diborides represented by MoB2 have attracted widespread attention for their excellent acidic hydrogen evolution reaction (HER). Nevertheless,... |
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SubjectTerms | Carbon Carbon nanotubes Electrocatalysts Electrochemical analysis Electrolytes heterogeneous interface engineering Heterostructures hydrogen evolution reaction Hydrogen evolution reactions metal boride Transition metals wide pH range |
Title | Constructing Heterogeneous Interface by Growth of Carbon Nanotubes on the Surface of MoB2 for Boosting Hydrogen Evolution Reaction in a Wide pH Range |
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