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源自N,O共掺杂碳阴极材料中协同吡咯氮和邻苯二酚构型的有氧自氧化自充电概念

Aerobically Autoxidized Self-Charge Concept Derived from Synergistic Pyrrolic Nitrogen and Catechol Configurations in N, O Co-Doped Carbon Cathode Material.

作者信息

Wang Junyan, Zhang Bosen, Zhang Jiamin, Xing Hanyu, Shi Yuning, Tian Kesong, Guo Wanchun, Xu Junjie, Liu Shuhu, Li Xueai, Xie Haijiao, Wang Haiyan

机构信息

State Key Laboratory of Metastable Materials Science and Technology, Hebei Key Laboratory of Heavy Metal Deep-Remediation in Water and Resource Reuse, School of Environmental and Chemical Engineering, Yanshan University, Qinhuangdao, 066004, P. R. China.

Xi'an Rare Metal Materials Institute Co., Ltd, Xi'an, 710016, P. R. China.

出版信息

Small. 2024 Jul;20(27):e2310928. doi: 10.1002/smll.202310928. Epub 2024 Feb 2.

Abstract

Aerobically autoxidized self-charging concept has drawn significant attraction due to its promising chemical charge features without external power supply. Particularly, heteroatom-doped carbon materials with abundant oxidizable sites and good conductivity are expected to be ideal cathode materials. However, there is no well-defined aerobically autoxidized self-charging concept based on heteroatom-doped carbon materials, significantly hindering the design of related carbon cathodes. An aerobically autoxidized self-chargeable concept derived from synergistic effect of pyrrolic nitrogen and catechol configuration in carbon cathode using model single pyrrolic nitrogen and oxygen (N-5, O) co-doped carbon and O-enriched carbon is proposed. First, self-charging of N-5, O co-doped carbon cathode can be achieved by aerobic oxidation of pyrrolic nitrogen and catechol to oxidized pyrrolic nitrogen and ortho-quinone configurations, respectively. Second, introducing a single pyrrolic nitrogen configuration enhanced acidic wettability of N-5, O co-doped carbon facilitating air self-charge/galvanic discharge involving proton removal/introduction. Third, synergistic effect of pyrrolic nitrogen and hydroxyl species with the strong electron-donating ability to conjugated carbon-based backbone endows N-5, O co-doped carbon with a higher highest occupied molecular orbital (HOMO) energy level more susceptible to oxidation charging. The assembled Cu/Carbon batteries can drive a timer after every air-charging run. This promising aerobically autoxidized self-charging concept can inspire exploring high-efficiency self-charging devices.

摘要

由于其在无外部电源情况下具有有前景的化学充电特性,有氧自氧化自充电概念已引起了极大的关注。特别是,具有丰富可氧化位点和良好导电性的杂原子掺杂碳材料有望成为理想的阴极材料。然而,基于杂原子掺杂碳材料的明确的有氧自氧化自充电概念尚不存在,这严重阻碍了相关碳阴极的设计。本文提出了一种基于碳阴极中吡咯氮和儿茶酚结构协同效应的有氧自氧化自充电概念,使用模型单吡咯氮和氧(N-5,O)共掺杂碳和富氧碳。首先,N-5,O共掺杂碳阴极的自充电可通过吡咯氮和儿茶酚分别有氧氧化为氧化吡咯氮和邻醌结构来实现。其次,引入单一吡咯氮结构增强了N-5,O共掺杂碳的酸性润湿性,促进了涉及质子去除/引入的空气自充电/原电池放电。第三,吡咯氮和具有强给电子能力的羟基物种与共轭碳基主链的协同效应赋予N-5,O共掺杂碳更高的最高占据分子轨道(HOMO)能级,使其更易发生氧化充电。组装好的铜/碳电池在每次空气充电运行后都能驱动一个定时器。这种有前景的有氧自氧化自充电概念能够激发对高效自充电装置的探索。

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