TY - JOUR
T1 - Efficient Electrochemical Ozone and Hydrogen Peroxide Production by Synergistic Effect of Atomically Dispersed Pt, Boron and Nitrogen Doped 2D Diamonds
AU - Lu, Mengmeng
AU - Liu, Xu
AU - Jing, Changfei
AU - Wang, Xiaosa
AU - Ding, Lei
AU - Gao, Fengying
AU - Ren, Linhan
AU - Dai, Sheng
AU - Zhong, Xing
AU - Wang, Jianguo
N1 - Publisher Copyright:
© 2024 Wiley-VCH GmbH.
PY - 2024
Y1 - 2024
N2 - The electrochemical co-synthesis of H₂O₂ and O₃ holds substantial potential for environmental sustainability and energy conservation. However, synthesizing electrocatalysts with appropriate adsorption energies for intermediates in the electrochemical pairwise electrosynthesis of H₂O₂ and O₃ remains a major challenge. In this study, boron and nitrogen-doped 2D diamonds (BND) and atomically dispersed Pt₁/BND electrocatalysts are systematically designed and synthesized to facilitate the two-electron oxygen reduction reaction (2e⁻ ORR) and electrochemical ozone production (EOP), respectively. The BND and Pt₁/BND electrocatalysts exhibit remarkable electrochemical activity, with BND achieving 90.7% selectivity for H₂O₂ and Pt₁/BND attaining a Faradaic efficiency (FE) of 12.54% for EOP. The Pt monatomic species, with a loading of 0.13%, are predominantly distributed along the edges of the Pt₁/BND. Theoretical calculations reveal that their superior properties primarily stem from the phase transition to graphene fractions at the edges, which facilitate moderate adsorption of oxygen intermediates and modulate the electronic structure through synergistic interactions between the dopant elements. Additionally, the 2D diamonds exhibit favorable mass transfer properties. The integration of H₂O₂ and O₃ for the synergistic degradation of organic contaminants and sterilization further showcase the practical utility of BND and Pt₁/BND electrocatalysts.
AB - The electrochemical co-synthesis of H₂O₂ and O₃ holds substantial potential for environmental sustainability and energy conservation. However, synthesizing electrocatalysts with appropriate adsorption energies for intermediates in the electrochemical pairwise electrosynthesis of H₂O₂ and O₃ remains a major challenge. In this study, boron and nitrogen-doped 2D diamonds (BND) and atomically dispersed Pt₁/BND electrocatalysts are systematically designed and synthesized to facilitate the two-electron oxygen reduction reaction (2e⁻ ORR) and electrochemical ozone production (EOP), respectively. The BND and Pt₁/BND electrocatalysts exhibit remarkable electrochemical activity, with BND achieving 90.7% selectivity for H₂O₂ and Pt₁/BND attaining a Faradaic efficiency (FE) of 12.54% for EOP. The Pt monatomic species, with a loading of 0.13%, are predominantly distributed along the edges of the Pt₁/BND. Theoretical calculations reveal that their superior properties primarily stem from the phase transition to graphene fractions at the edges, which facilitate moderate adsorption of oxygen intermediates and modulate the electronic structure through synergistic interactions between the dopant elements. Additionally, the 2D diamonds exhibit favorable mass transfer properties. The integration of H₂O₂ and O₃ for the synergistic degradation of organic contaminants and sterilization further showcase the practical utility of BND and Pt₁/BND electrocatalysts.
KW - 2D diamonds
KW - electrochemical ozone production
KW - electrodegradation
KW - hydrogen peroxide
KW - sterilization
UR - http://www.scopus.com/inward/record.url?scp=85202632765&partnerID=8YFLogxK
U2 - 10.1002/adfm.202412170
DO - 10.1002/adfm.202412170
M3 - Article
AN - SCOPUS:85202632765
SN - 1616-301X
JO - Advanced Functional Materials
JF - Advanced Functional Materials
ER -