Suppr超能文献

通过原位制备的少层硼纳米片实现工业级电流密度下的电化学合成过氧化氢。

Electrochemically synthesized HO at industrial-level current densities enabled by in situ fabricated few-layer boron nanosheets.

作者信息

Wu Yuhan, Zhao Yuying, Yuan Qixin, Sun Hao, Wang Ao, Sun Kang, Waterhouse Geoffrey I N, Wang Ziyun, Wu Jingjie, Jiang Jianchun, Fan Mengmeng

机构信息

Jiangsu Co-Innovation Center of Efficient Processing and Utilization of Forest Resources, 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

Nat Commun. 2024 Dec 30;15(1):10843. doi: 10.1038/s41467-024-55071-7.

Abstract

Carbon nanomaterials show outstanding promise as electrocatalysts for hydrogen peroxide (HO) synthesis via the two-electron oxygen reduction reaction. However, carbon-based electrocatalysts that are capable of generating HO at industrial-level current densities (>300 mA cm) with high selectivity and long-term stability remain to be discovered. Herein, few-layer boron nanosheets are in-situ introduced into a porous carbon matrix, creating a metal-free electrocatalyst (B-C) with HO production rates of industrial relevance in neutral or alkaline media. B-C maintained > 95% Faradaic efficiency during a 140-hour test at 300 mA cm and 0.1 V vs. RHE, and delivered a mass activity of 25.1 mol g h in 1.0 M NaSO using a flow cell. Theoretical simulations and experimental studies demonstrate that the superior catalytic performance originates from B atoms with adsorbed O atoms in the boron nanosheets. B-C outperforms all metal-based and metal-free carbon catalysts reported to date for HO synthesis at industrial-level current densities.

摘要

碳纳米材料作为通过两电子氧还原反应合成过氧化氢(HO)的电催化剂显示出巨大的潜力。然而,能够在工业级电流密度(>300 mA cm)下以高选择性和长期稳定性生成HO的碳基电催化剂仍有待发现。在此,将少层硼纳米片原位引入多孔碳基质中,制备出一种无金属电催化剂(B-C),其在中性或碱性介质中具有与工业相关的HO生成速率。在相对于可逆氢电极(RHE)为300 mA cm和0.1 V的条件下进行140小时测试期间,B-C保持>95%的法拉第效率,并使用流通池在1.0 M NaSO中实现了25.1 mol g h的质量活性。理论模拟和实验研究表明,优异的催化性能源于硼纳米片中吸附有O原子的B原子。在工业级电流密度下,B-C在HO合成方面优于迄今为止报道的所有金属基和无金属碳催化剂。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/880a/11685507/7e3ffb377e90/41467_2024_55071_Fig1_HTML.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验