4.6 Article

Hydrogen bond-mediated pH-universal electrocatalytic hydrogen production by conjugated porous poly-indigo

期刊

JOURNAL OF MATERIALS CHEMISTRY A
卷 11, 期 20, 页码 10699-10709

出版社

ROYAL SOC CHEMISTRY
DOI: 10.1039/d2ta08365e

关键词

-

向作者/读者索取更多资源

High-performing metal-free pH-universal HER catalysts are smarter options for producing carbon-free green fuels via water electrolysis. In this study, an indigo-based organic conjugated porous polymer with surface-decorated hydrogen bonding sites was developed, which exhibited promising electrochemical HER activity in acidic, alkaline, and neutral media. The material showed comparable performance to contemporary metal-free carbonaceous electrocatalysts and state-of-the-art metal-based catalytic systems, with an overpotential of only 28 mV at 10 mA cm(-2) current density under appropriate conditions.
High-performing catalysts for the hydrogen evolution reaction (HER) via water electrolysis are of great importance for producing carbon-free green fuels. Compared to the routinely used metal-based systems under acidic conditions, metal-free pH-universal HER catalysts are smarter options taking into account the practical usability, sustainability, biocompatibility, and nominal cytotoxicity. Herein, we present an indigo-based organic conjugated porous polymer featuring a pronounced 2D few-layered morphology with surface-decorated hydrogen bonding sites for a deep catalyst-water contact and promising electrochemical HER activity. Indigo, being a vat dye, reduces in situ to its anionic leuco analogue and further promotes catalytic activity. The material manifested equipotent activity in acidic, alkaline, and neutral media superior to the contemporary metal-free carbonaceous electrocatalysts and comparable to the state-of-the-art metal-based catalytic systems. Under appropriate conditions, the material showed an overpotential of only 28 mV at 10 mA cm(-2) current density.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.6
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据