NBOH Site‐Activated Graphene Quantum Dots for Boosting Electrochemical Hydrogen Peroxide Production

• Published in: Advanced materials (Weinheim) Vol. 35; no. 17; pp. e2209086 - n/a
• Main Authors: Fan, Mengmeng, Wang, Zeming, Sun, Kang, Wang, Ao, Zhao, Yuying, Yuan, Qixin, Wang, Ruibin, Raj, Jithu, Wu, Jingjie, Jiang, Jianchun, Wang, Liang
• Format: Journal Article
• Language: English
• Published: Germany Wiley Subscription Services, Inc 01.04.2023
• Subjects: 2 e − electrocatalysis; Activated carbon; Carbon; Chemical reduction; Chemical synthesis; Density functional theory; Dopants; Electrocatalysts; Electrodes; Flow stability; Graphene; graphene quantum dots; Hydrogen peroxide; hydrogen peroxide synthesis; Hydrothermal reactions; Materials science; N‐B‐OH sites; oxygen reduction reaction; Oxygen reduction reactions; Quantum dots; Rotating disks; Stability tests; Substrates; hydrogen peroxide synthesis; oxygen reduction reaction; graphene quantum dots; 2 e − electrocatalysis; N-B-OH sites
• ISSN: 0935-9648; 1521-4095
• DOI: 10.1002/adma.202209086

Carbon materials are considered promising 2/4 e− oxygen reduction reaction (ORR) electrocatalysts for synthesizing H2O2/H2O via regulating heteroatom dopants and functionalization. Here, various doped and functionalized graphene quantum dots (GQDs) are designed to reveal the crucial active sites of carbon materials for ORR to produce H2O2. Density functional theory (DFT) calculations predict that the edge structure involving edge N, B dopant pairs and further OH functionalization to the B (NBOH) is an active center for 2e− ORR. To verify the above predication, GQDs with an enriched density of NBOH (NBO‐GQDs) are designed and synthesized by the hydrothermal reaction of NH2 edge‐functionalized GQDs with H3BO3 forming six‐member heterocycle containing the NBOH structure. When dispersed on conductive carbon substrates, the NBO‐GQDs show H2O2 selectivity of over 90% at 0.7 –0.8 V versus reversible hydrogen electrode in the alkaline solution in a rotating ring‐disk electrode setup. The selectivity retains 90% of the initial value after 12 h stability test. In a flow cell setup, the H2O2 production rate is up to 709 mmol gcatalyst−1 h−1, superior to most reported carbon‐ and metal‐based electrocatalysts. This work provides molecular insight into the design and formulation of highly efficient carbon‐based catalysts for sustainable H2O2 production. Density functional theory calculations predict that the edge structure involving edge N, B dopant pairs and further OH functionalization to the B is an active center for 2 e− ORR. GQDs with an enriched density of NBOH show high H2O2 selectivity (over 90%), stability and H2O2 production rate (709 mmol gcatalyst−1 h−1), superior to most reported carbon‐ and metal‐based electrocatalysts.