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退火温度对铜钴氧化物纳米片析氧反应活性的影响

Effects of Annealing Temperature on the Oxygen Evolution Reaction Activity of Copper-Cobalt Oxide Nanosheets.

作者信息

Kim Geul Han, Park Yoo Sei, Yang Juchan, Jang Myeong Je, Jeong Jaehoon, Lee Ji-Hoon, Park Han-Saem, Park Yong Ho, Choi Sung Mook, Lee Jooyoung

机构信息

Department of Energy & Electronic Materials, Surface Materials Division, Korea Institute of Materials Science, Changwon 642831, Korea.

Department of Materials Science and Engineering, Pusan National University, Busan 46241, Korea.

出版信息

Nanomaterials (Basel). 2021 Mar 8;11(3):657. doi: 10.3390/nano11030657.

DOI:10.3390/nano11030657
PMID:33800286
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7998886/
Abstract

Developing high performance, highly stable, and low-cost electrodes for the oxygen evolution reaction (OER) is challenging in water electrolysis technology. However, Ir- and Ru-based OER catalysts with high OER efficiency are difficult to commercialize as precious metal-based catalysts. Therefore, the study of OER catalysts, which are replaced by non-precious metals and have high activity and stability, are necessary. In this study, a copper-cobalt oxide nanosheet (CCO) electrode was synthesized by the electrodeposition of copper-cobalt hydroxide (CCOH) on Ni foam followed by annealing. The CCOH was annealed at various temperatures, and the structure changed to that of CCO at temperatures above 250 °C. In addition, it was observed that the nanosheets agglomerated when annealed at 300 °C. The CCO electrode annealed at 250 °C had a high surface area and efficient electron conduction pathways as a result of the direct growth on the Ni foam. Thus, the prepared CCO electrode exhibited enhanced OER activity (1.6 V at 261 mA/cm) compared to those of CCOH (1.6 V at 144 mA/cm), CoO (1.6 V at 39 mA/cm), and commercial IrO (1.6 V at 14 mA/cm) electrodes. The optimized catalyst also showed high activity and stability under high pH conditions, demonstrating its potential as a low cost, highly efficient OER electrode material.

摘要

在水电解技术中,开发用于析氧反应(OER)的高性能、高稳定性和低成本电极具有挑战性。然而,具有高OER效率的基于铱和钌的OER催化剂作为贵金属基催化剂难以商业化。因此,有必要研究用非贵金属替代且具有高活性和稳定性的OER催化剂。在本研究中,通过在泡沫镍上电沉积氢氧化铜钴(CCOH)然后退火,合成了一种铜钴氧化物纳米片(CCO)电极。CCOH在不同温度下退火,在250℃以上的温度下结构转变为CCO。此外,观察到在300℃退火时纳米片会团聚。由于在泡沫镍上直接生长,在250℃退火的CCO电极具有高表面积和有效的电子传导途径。因此,制备的CCO电极与CCOH(144 mA/cm下1.6 V)、CoO(39 mA/cm下1.6 V)和商用IrO(14 mA/cm下1.6 V)电极相比,表现出增强的OER活性(261 mA/cm下1.6 V)。优化后的催化剂在高pH条件下也显示出高活性和稳定性,证明了其作为低成本、高效OER电极材料的潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/801e/7998886/a7d32d95299c/nanomaterials-11-00657-g008.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/801e/7998886/a7d32d95299c/nanomaterials-11-00657-g008.jpg
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