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NBOH 位敏化石墨烯量子点用于提升电化学过氧化氢的生成。

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

机构信息

Jiangsu Co-Innovation Center of Efficient Processing and Utilization of Forest Resources, International Innovation Center for Forest Chemicals and Materials, College of Chemical Engineering, Nanjing Forestry University, Nanjing, 210037, China.

Key Lab of Biomass Energy and Material, Jiangsu Province, Jiangsu Co-Innovation Center of Efficient Processing and Utilization of Forest Resources, Institute of Chemical Industry of Forest Products, Chinese Academy of Forestry, Nanjing, 210042, China.

出版信息

Adv Mater. 2023 Apr;35(17):e2209086. doi: 10.1002/adma.202209086. Epub 2023 Mar 19.

Abstract

Carbon materials are considered promising 2/4 e oxygen reduction reaction (ORR) electrocatalysts for synthesizing H O /H O 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 H O . 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 NH edge-functionalized GQDs with H BO forming six-member heterocycle containing the NBOH structure. When dispersed on conductive carbon substrates, the NBO-GQDs show H O 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 H O production rate is up to 709 mmol g  h , 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 H O production.

摘要

碳材料被认为是很有前途的 2/4 电子氧还原反应(ORR)电催化剂,可通过调节杂原子掺杂和功能化来合成 H2O/H2O。在这里,设计了各种掺杂和功能化的石墨烯量子点(GQDs),以揭示碳材料对于产生 H2O 的 ORR 的关键活性位点。密度泛函理论(DFT)计算预测,涉及边缘 N、B 掺杂对和进一步对 B(NBOH)的 OH 功能化的边缘结构是 2e ORR 的活性中心。为了验证上述预测,通过 NH 边缘功能化的 GQDs 与 H3BO3 在水热反应中设计并合成了富含 NBOH(NBO-GQDs)的 GQDs,形成了含有 NBOH 结构的六元杂环。当分散在导电碳基底上时,在碱性溶液中,NBO-GQDs 在旋转环盘电极装置中,在 0.7-0.8 V 相对于可逆氢电极处表现出超过 90%的 H2O 选择性。在 12 h 的稳定性测试后,选择性保留了初始值的 90%。在流动池装置中,H2O 的生成速率高达 709 mmol g-1 h-1,优于大多数报道的碳基和金属基电催化剂。这项工作为设计和制备高效可持续的 H2O 生产的碳基催化剂提供了分子见解。

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