4.7 Article

Phytic acid-assisted fabrication of porous leaf-like hollow structured Co2P @ C for efficient hydrogen evolution

期刊

JOURNAL OF ALLOYS AND COMPOUNDS
卷 934, 期 -, 页码 -

出版社

ELSEVIER SCIENCE SA
DOI: 10.1016/j.jallcom.2022.167924

关键词

Transition metal phosphides; Hydrogen evolution reaction; Hollow structure; Phytic acid; Zeolitic-imidazolate frameworks

向作者/读者索取更多资源

Here, an eco-friendly phytic acid (PA)-assisted phosphidation strategy was developed to synthesize a novel porous leaf-like hollow structured Co2P @ C catalyst (Co2P @ C ML) for the hydrogen evolution reaction (HER). The Co2P @ C ML catalyst exhibited excellent HER catalytic performances in 0.5 M H2SO4 and 1 M KOH. The presented PA-assisted phosphidation synthetic strategy can be extended to the design and synthesis of other well-defined hollow structured TMPs@C materials.
Transition metal phosphides (TMPs) are considered promising electrocatalysts for the hydrogen evolution reaction (HER). Although wet-chemistry and gas-solid reaction methods are widely used for TMPs synth-esis, it remains challenging to synthesize porous hollow structured TMPs via a facile, green and sustainable pathway. We report here an eco-friendly phytic acid (PA)-assisted phosphidation strategy to synthesize a novel porous leaf-like hollow structured Co2P @ C catalyst (Co2P @ C ML). Its synthesis involves pre-cipitation of leaf-like microstructured Co-based zeolitic-imidazolate frameworks (Co-ZIF ML), chemical etching of Co-ZIF ML to form PA cross-linked Co complexes and a final pyrolysis step to get Co2P @ C ML with abundant Co2P nanoparticles loaded on P-doped carbon matrix. The Co2P @ C ML catalyst demon-strates excellent HER catalytic performances with low overpotentials at 10 mA cm-2, small Tafel slopes and high catalytic durability in 0.5 M H2SO4 and 1 M KOH. The presented PA-assisted phosphidation synthetic strategy can be readily extended to the design and synthesis of other well-defined hollow structured TMPs@C materials for various applications.(c) 2022 Elsevier B.V. All rights reserved.

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

4.7
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