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层状氢氧化钴纳米带的层间扩展可极大提高析氧电催化性能。

Interlayer Expansion of Layered Cobalt Hydroxide Nanobelts to Highly Improve Oxygen Evolution Electrocatalysis.

机构信息

Chemical Synthesis and Pollution Control Key Laboratory of Sichuan Province, College of Chemistry and Chemical Engineering, China West Normal University , Shida Road 1#, Nanchong 637002, P. R. China.

出版信息

ACS Appl Mater Interfaces. 2017 Mar 1;9(8):7059-7067. doi: 10.1021/acsami.6b14479. Epub 2017 Feb 13.

DOI:10.1021/acsami.6b14479
PMID:28117968
Abstract

The water oxidation reaction is known to be energy-inefficient and generally considered as a major bottleneck for water splitting. Exploring electrocatalysts with high-efficiency and at low cost is vital to widespread utilization of this technology, but is still a big challenge. Here we report an effective strategy based on an expanding interlayer of layered structures to realize a great enhancement of the catalytic performance of the oxygen evolution reaction from water splitting. Well-defined nanobelts of layer-structured cobalt benzoate hydroxide (Co(OH)(CHCOO)·HO) are successfully prepared in terms of a simple hydrothermal process. Intercalation with benzoate ions induces the interlayer expansion of the cobalt hydroxide, which is useful for the accommodation of more electrolyte ions and favorable for their diffusion and transport. The as-prepared Co(OH)(CHCOO)·HO nanobelts need significantly smaller overpotential (∼0.36 V) to reach 10 mA·cm of current density compared with their Co(OH) (∼0.44 V) and CoO (∼0.387 V) counterparts, and even favorably compare with most of the layered hydroxide-based electrocatalysts. Moreover, the Co(OH)(CHCOO)·HO nanobelts retain a much higher stability than the RuO reference in alkaline solution. This approach would be utilized to design and develop high-performance layered hydroxide-based electrocatalysts.

摘要

水氧化反应的能量效率低,通常被认为是水分解的主要瓶颈。探索高效、低成本的电催化剂对于这项技术的广泛应用至关重要,但这仍然是一个巨大的挑战。在这里,我们报告了一种基于层状结构的层间扩展的有效策略,以实现水分解析氧反应催化性能的显著提高。通过简单的水热法成功制备了具有明确结构的层状结构的苯甲酸钴氢氧化物(Co(OH)(CHCOO)·HO)纳米带。苯甲酸盐离子的插层诱导了氢氧化钴的层间扩展,这有利于容纳更多的电解质离子,有利于它们的扩散和传输。与 Co(OH)(∼0.44 V)和 CoO(∼0.387 V)相比,所制备的 Co(OH)(CHCOO)·HO 纳米带达到 10 mA·cm 的电流密度所需的过电位(∼0.36 V)明显更小,甚至优于大多数基于层状氢氧化物的电催化剂。此外,在碱性溶液中,Co(OH)(CHCOO)·HO 纳米带的稳定性比 RuO 参比电极高得多。这种方法将用于设计和开发高性能的基于层状氢氧化物的电催化剂。

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Recent Progress on Layered Double Hydroxides and Their Derivatives for Electrocatalytic Water Splitting.
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