4.6 Article

Boron-Doped Edges as Active Sites for Water Adsorption in Activated Carbons

Journal

LANGMUIR
Volume 37, Issue 45, Pages 13179-13186

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.langmuir.1c00871

Keywords

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Funding

  1. National Research Foundation of Korea (NRF) - Korean government (MSIP) [2021R1I1A305628711]

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In this study, the effect of boron (B) doping on the surface properties of activated carbon materials was explored based on water adsorption behavior and oxygen reduction reaction. It was found that B-doped AC materials at 1400 degrees Celsius have an open pore structure with B-O bonds, while at 1600 degrees Celsius a nonporous structure with a large amount of B-C bonds prevails. The B-O species act as active sites for water adsorption on the carbon surface, while B-C bonds decrease electrocatalytic activity due to their stable structure.
Investigating the surface properties of heteroatom-doped carbon materials is essential because these versatile materials have found use in a variety of energy and environmental applications; an understanding of these properties would also lead to an improved appreciation of the direct interaction between the reactant and the functionalized surface. Herein, we explore the effect of boron (B) doping on the surface properties of activated carbon (AC) materials based on their water adsorption behavior and oxygen reduction reaction. In the high-temperature B doping process, B-doped AC materials at 1400 degrees C exhibit an open pore structure with B-O bonds, whereas at a temperature of 1600 degrees C, a nonporous structure containing a large amount of B-C bonds prevails. The B-O species act as active sites for water adsorption on the carbon surface. On the basis of the isothermal adsorption heat, we suggest that B atoms are present at the pore openings and on the surfaces. The B-O moieties at the open edges improve the electrocatalytic activity, whereas the B-C bonds at the closed edges decrease the electrocatalytic activity because of the stable structure of these bonds. Our findings provide new evidence for the electrocatalytic properties associated with the structure of B-doped edges.

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