Ranjith Bose, Surya Prakash Gajagouni, Imad Barsoum, Sung Oh Cho and Akram Alfantazi
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引用次数: 0
Abstract
Stainless steel (SS)-based electrocatalysts have attracted considerable attention in renewable energy research, emerging as viable replacements for precious noble metal-based catalysts owing to their cost-effectiveness and widespread availability. Further, SS's ability to function as an electrode material in alkaline water electrolyzers and its inherent corrosion resistance make it a key component of sustainable energy solutions. This study focuses on the fabrication of a self-ordered nanoporous oxide layer on SS through an anodization method, followed by an investigation into the electrocatalytic activity of the resulting films for hydrogen evolution reaction (HER) and corrosion properties. Anodization creates a highly organized nano-porous metal oxide structure featuring extensive surface areas that offer abundant active sites for electrochemical reactions via the oxide formation-dissolution mechanism. The nano-porous oxide film produced demonstrates exceptional HER activity, reaching a cathodic current density of 10 mA cm−2 with a minimal overpotential of 343 mV (versus the reversible hydrogen electrode (RHE)) in a strong alkaline medium. Moreover, the stability of the derived nano-porous oxide film remains unaffected during 50 hours of uninterrupted electrolysis, demonstrating remarkable operational resilience. Conversely, potentiodynamic polarization measurements reveal that the resulting films exhibit superior corrosion resistance in both NaCl and KOH electrolytes compared to bare SS. This enhanced resistance is attributed to the self-ordered nano-porous structure, which fosters the construction of a more uniform film with a more robust passive layer. The straightforwardness of the procedure and the widespread availability of the initial material make this an unexpectedly effective endeavour. The research demonstrated that anodized SS can achieve both corrosion resistance and catalytic activity for the HER, making this material system a viable candidate for alkaline water electrolyzer systems.
以不锈钢(SS)为基础的电催化剂因其成本效益高、供应广泛而成为贵金属催化剂的可行替代品,在可再生能源研究领域引起了广泛关注。此外,SS 还能在碱性水电解槽中用作电极材料,其固有的耐腐蚀性使其成为可持续能源解决方案的关键组成部分。本研究的重点是通过阳极氧化法在 SS 上制备自有序纳米多孔氧化物层,然后对所制备薄膜的氢进化反应(HER)电催化活性和腐蚀特性进行研究。阳极氧化法形成了高度有序的纳米多孔金属氧化物结构,具有广泛的表面积,通过氧化物形成-溶解机制为电化学反应提供了丰富的活性位点。由此产生的纳米多孔氧化物薄膜具有出色的 HER 活性,在强碱性介质中,以 343 mV 的最小过电位(相对于可逆氢电极 (RHE))达到 10 mA cm-2 的阴极电流密度。此外,在 50 小时不间断电解过程中,衍生纳米多孔氧化物薄膜的稳定性仍未受到影响,显示出显著的操作弹性。相反,电位动力极化测量结果表明,与裸 SS 相比,所得薄膜在 NaCl 和 KOH 电解液中均表现出卓越的耐腐蚀性。这种增强的耐腐蚀性归功于自有序纳米多孔结构,这种结构有助于形成更均匀的薄膜和更坚固的被动层。这种方法简单明了,初始材料也很容易获得,因此取得了意想不到的效果。研究证明了在阳极氧化 SS 中实现耐腐蚀性和对 HER 的催化活性的可行性,使这种材料系统成为碱性水电解槽系统的可行候选材料。
期刊介绍:
The Journal of Materials Chemistry A, B & C covers a wide range of high-quality studies in the field of materials chemistry, with each section focusing on specific applications of the materials studied. Journal of Materials Chemistry A emphasizes applications in energy and sustainability, including topics such as artificial photosynthesis, batteries, and fuel cells. Journal of Materials Chemistry B focuses on applications in biology and medicine, while Journal of Materials Chemistry C covers applications in optical, magnetic, and electronic devices. Example topic areas within the scope of Journal of Materials Chemistry A include catalysis, green/sustainable materials, sensors, and water treatment, among others.