Ullah Sana, Hussain Asif, Farid Muhammad Asim, Anjum Faiza, Amin Roohul, Du Shangfeng, Zou Ji-Jun, Huang Zhen-Feng, Tahir Muhammad
School of Chemical Engineering and Technology, Tianjin University, Tianjin, China.
Department of Physics, University of Lahore, 53700 Lahore, Pakistan.
Heliyon. 2024 Jun 13;10(12):e32989. doi: 10.1016/j.heliyon.2024.e32989. eCollection 2024 Jun 30.
The advancement in electrocatalysis, particularly in the development of efficient catalysts for hydrogen and oxygen evolution reactions (HER and OER), is crucial for sustainable energy generation through processes like overall water splitting. A notable bifunctional electrocatalyst, CoFeO/CoFe, has been engineered to facilitate both OER and HER concurrently, aiming to reduce overpotentials. In the pursuit of further enhancing catalytic efficiency, a morphological transformation has been achieved by introducing a sulphur source and multi-walled carbon nanotubes (MWCNTs) into the catalyst system, resulting in S-CoFeO/CoFe/MWCNTs. This modification has significantly improved the activity for both OER and HER. An onset overpotential of 250 mV@10 mAcm for the OER and 270 mV@50 mAcm for the HER, indicating efficient catalytic activity at relatively low overpotentials. S-CoFeO/CoFe/MWCNTs display an outstanding long-term stability in alkaline electrolytes, with minimal Tafel slopes of 77 mV/dec for the OER and 70 mV/dec for the HER, suggesting sustained catalytic performance over extended periods. Furthermore, when employed as both the cathode and anode in the context of complete water splitting, S-CoFeO/CoFe/MWCNTs demonstrate an impressive cell voltage of 1.52 V at a current density of 10 mA cm in a 1 M KOH solution, showcasing its viability for practical applications. Given its cost-effectiveness and superior activity, S-CoFeO/CoFe/MWCNTs hold significant promise for widespread applications in overall water splitting electrocatalysis, contributing to the advancement of cleaner and sustainable fuel generation technologies.
电催化领域的进展,特别是在用于析氢反应(HER)和析氧反应(OER)的高效催化剂开发方面,对于通过全水解等过程实现可持续能源生产至关重要。一种著名的双功能电催化剂CoFeO/CoFe已被设计出来,可同时促进OER和HER,旨在降低过电位。为了进一步提高催化效率,通过将硫源和多壁碳纳米管(MWCNTs)引入催化剂体系实现了形态转变,得到了S-CoFeO/CoFe/MWCNTs。这种改性显著提高了OER和HER的活性。OER的起始过电位为250 mV@10 mAcm,HER的起始过电位为270 mV@50 mAcm,表明在相对较低的过电位下具有高效的催化活性。S-CoFeO/CoFe/MWCNTs在碱性电解质中表现出出色的长期稳定性,OER的塔菲尔斜率最小为77 mV/dec,HER的塔菲尔斜率最小为70 mV/dec,表明在较长时间内具有持续的催化性能。此外,当在全水解的情况下用作阴极和阳极时,S-CoFeO/CoFe/MWCNTs在1 M KOH溶液中,在电流密度为10 mA cm时,表现出令人印象深刻的电池电压1.52 V,展示了其在实际应用中的可行性。鉴于其成本效益和卓越的活性,S-CoFeO/CoFe/MWCNTs在全水解电催化中具有广泛应用的巨大潜力,有助于推动更清洁、可持续的燃料生产技术的进步。