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用于在弱碱性溶液中实现超稳定海水分解的非贵金属电催化剂的多尺度工程

Multiscale Engineering of Nonprecious Metal Electrocatalyst for Realizing Ultrastable Seawater Splitting in Weakly Alkaline Solution.

作者信息

Li Jiankun, Yu Tingting, Wang Keyu, Li Zhiheng, He Juan, Wang Yixing, Lei Linfeng, Zhuang Linzhou, Zhu Minghui, Lian Cheng, Shao Zongping, Xu Zhi

机构信息

State Key Laboratory of Chemical Engineering, School of Chemical Engineering, East China University of Science and Technology, Shanghai, 200237, China.

School of Chemical Engineering, China University of Petroleum, Qingdao, 266580, China.

出版信息

Adv Sci (Weinh). 2022 Sep;9(25):e2202387. doi: 10.1002/advs.202202387. Epub 2022 Jul 7.

DOI:10.1002/advs.202202387
PMID:35798320
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9443442/
Abstract

Seawater electrolysis is an attractive technique for mass production of high-purity hydrogen considering the abundance of seawater. Nevertheless, due to the complexity of seawater environment, efficient anode catalyst, that should be, cost effective, highly active for oxygen evolution reaction (OER) but negligible for Cl /ClO formation, and robust toward chlorine corrosion, is urgently demanded for large-scale application. Although catalysis typically appears at surface, while the bulk properties and morphology structure also have a significant impact on the performance, thus requiring a systematic optimization. Herein, a multiscale engineering approach toward the development of cost-effective and robust OER electrocatalyst for operation in seawater is reported. Specifically, the engineering of hollow-sphere structure can facilitate the removal of gas product, while atom-level synergy between Co and Fe can promote Co sites transforming to active phase, and in situ transformation of sulfate ions layer protects catalysts from corrosion. As a result, the as-developed hollow-sphere structured CoFeS electrocatalyst can stably operate at a high current density of 100 mA cm in the alkaline simulated seawater (pH = 13) for 700 h and in a neutral seawater for 20 h without attenuation. It provides a new strategy for the development of electrocatalysts with a broader application potential.

摘要

考虑到海水的丰富性,海水电解是一种极具吸引力的大规模生产高纯度氢气的技术。然而,由于海水环境的复杂性,迫切需要一种高效的阳极催化剂,这种催化剂应具有成本效益,对析氧反应(OER)具有高活性,但对Cl⁻/ClO⁻的形成可忽略不计,并且对氯腐蚀具有耐受性,以实现大规模应用。虽然催化作用通常出现在表面,但体相性质和形态结构对性能也有显著影响,因此需要进行系统优化。在此,报道了一种用于开发在海水中运行的具有成本效益且耐用的OER电催化剂的多尺度工程方法。具体而言,空心球结构的工程设计可以促进气体产物的去除,而Co和Fe之间的原子级协同作用可以促进Co位点转变为活性相,并且硫酸根离子层的原位转变可以保护催化剂免受腐蚀。结果,所开发的空心球结构的CoFeS电催化剂能够在碱性模拟海水(pH = 13)中100 mA cm⁻²的高电流密度下稳定运行700小时,在中性海水中稳定运行20小时而不衰减。它为开发具有更广泛应用潜力的电催化剂提供了一种新策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9ca1/9443442/ff451a1bffd0/ADVS-9-2202387-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9ca1/9443442/33ca176e5499/ADVS-9-2202387-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9ca1/9443442/c27bebad974f/ADVS-9-2202387-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9ca1/9443442/d33f62de0e25/ADVS-9-2202387-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9ca1/9443442/ff451a1bffd0/ADVS-9-2202387-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9ca1/9443442/33ca176e5499/ADVS-9-2202387-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9ca1/9443442/c27bebad974f/ADVS-9-2202387-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9ca1/9443442/d33f62de0e25/ADVS-9-2202387-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9ca1/9443442/ff451a1bffd0/ADVS-9-2202387-g005.jpg

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