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由配位聚合物衍生的氮掺杂碳纳米立方体封装的核壳CoS/FeS异质结用于电催化碱性水/海水分解

Core-Shell CoS/FeS Heterojunction Encapsulated in N-Doped Carbon Nanocubes Derived from Coordination Polymers for Electrocatalytic Alkaline Water/Seawater Splitting.

作者信息

Zhang Xiaoyin, Liu Yan, Zeng Zihan, Zou Yan, Wang Wanzhen, Zhang Jing, Wang Jing, Kong Xiangfeng, Meng Xiangmin

机构信息

Institute of Oceanographic Instrumentation, Qilu University of Technology (Shandong Academy of Sciences), Qingdao 266061, China.

College of Marine Science and Biological Engineering, Qingdao University of Science and Technology, Qingdao 266042, China.

出版信息

Polymers (Basel). 2025 Jun 19;17(12):1701. doi: 10.3390/polym17121701.

DOI:10.3390/polym17121701
PMID:40574229
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12196570/
Abstract

Utilizing renewable energy for green hydrogen production via electrolyzed seawater is a promising technology for the future. However, undesired chlorine evolution and the corrosive nature of seawater are crucial challenges for direct seawater splitting technology. In this work, heterojunctions of CoS/FeS encapsulated in N-doped carbon nanocubes (denoted as CoS/FeS@NC) were designed by proposing the synchronous pyrolysis and vulcanization of polydopamine-coated coordination polymers. Such a synthetic strategy was demonstrated to be effective in increasing the favorable exposure of active sites, moderately regulating electronic structure, and remarkably facilitating charge transfer due to the controllable generation of unique core-shell structures with suitable carbon shells, leading to the excellent bifunctional electrocatalytic performance and enhanced stability of electrocatalysts. As a result, CoS/FeS@NC can be revealed as a superior water splitting catalyst, possessing a small voltage of 1.75 V and requiring 100.0 mA cm in 1 M KOH alkaline solution and 1.80 V for alkaline seawater media, with satisfactory long-term stability. This work presents fresh strategies for designing core-shell heterostructures and developing green technology for hydrogen production.

摘要

通过电解海水利用可再生能源生产绿色氢气是一项具有未来前景的技术。然而,不期望的析氯反应以及海水的腐蚀性是直接海水分解技术面临的关键挑战。在这项工作中,通过提出对聚多巴胺包覆的配位聚合物进行同步热解和硫化,设计了封装在氮掺杂碳纳米立方体中的CoS/FeS异质结(表示为CoS/FeS@NC)。这种合成策略被证明在增加活性位点的有利暴露、适度调节电子结构以及由于可控生成具有合适碳壳的独特核壳结构而显著促进电荷转移方面是有效的,从而导致优异的双功能电催化性能和增强的电催化剂稳定性。结果,CoS/FeS@NC可被揭示为一种优异的水分解催化剂,在1 M KOH碱性溶液中具有1.75 V的小电压且需要100.0 mA cm,在碱性海水介质中为1.80 V,具有令人满意的长期稳定性。这项工作为设计核壳异质结构和开发绿色制氢技术提出了新策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d4d6/12196570/eb0c42b14431/polymers-17-01701-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d4d6/12196570/87ba34a7a9a1/polymers-17-01701-sch001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d4d6/12196570/3c84eb3cc444/polymers-17-01701-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d4d6/12196570/e9747d3a28b4/polymers-17-01701-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d4d6/12196570/4b90cb495678/polymers-17-01701-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d4d6/12196570/2ee56108c128/polymers-17-01701-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d4d6/12196570/fa53e752c54d/polymers-17-01701-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d4d6/12196570/eb0c42b14431/polymers-17-01701-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d4d6/12196570/87ba34a7a9a1/polymers-17-01701-sch001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d4d6/12196570/3c84eb3cc444/polymers-17-01701-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d4d6/12196570/e9747d3a28b4/polymers-17-01701-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d4d6/12196570/4b90cb495678/polymers-17-01701-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d4d6/12196570/2ee56108c128/polymers-17-01701-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d4d6/12196570/fa53e752c54d/polymers-17-01701-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d4d6/12196570/eb0c42b14431/polymers-17-01701-g006.jpg

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