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用于高活性水氧化的钴胶体衍生高效耐用纳米级电催化薄膜

Cobalt Colloid-derived Efficient and Durable Nanoscale Electrocatalytic Films for High-Activity Water Oxidation.

作者信息

Babar Noor-Ul-Ain, Joya Khurram Saleem

机构信息

Department of Chemistry, University of Engineering and Technology (UET), G.T Road, 54890 Lahore, Pakistan.

出版信息

ACS Omega. 2020 May 7;5(19):10651-10662. doi: 10.1021/acsomega.9b03576. eCollection 2020 May 19.

Abstract

Oxygen evolution reaction is of immense importance and is vitally necessary for devices such as electrolyzers, fuel cells, and other solar and chemical energy conversion devices. The major challenges that remain in this quest are due to the lack of effective catalytic assemblages operating with optimum efficiency and obtainable following much simpler setups and easily accessible methods. Here, we demonstrate that the robust electrocatalytic activity toward water oxidation can be achieved employing straightforwardly obtainable nanoscale electrocatalysts derived from easily made colloidal-cobalt nanoparticles (Co-CNPs) prepared in clean carbonate systems. Thin-film non-noble metal nanoscale electrocatalysts such as simple Co-CNPs/FTO and annealed Co-CNPs/FTO and Co-CNPs/FTO obtained by depositing Co-CNPs on the FTO substrate are shown to initiate water oxidation at much lower overpotentials such as just 240 mV for Co-CNPs/FTO under mildly alkaline conditions while demonstrating an impressive Tafel slope of just 40 mV dec. Furthermore, the robust catalyst demonstrated a high electrochemical surface area of 91 cm and high turnover frequency and mass activity of 0.26 s and 18.84 mA mg, respectively, just at 0.35 V, and superior durability during long-term electrolysis. These outstanding catalytic outcomes using easily prepared Co-CNPs/FTO-type catalytic systems are comparable and even better than other noble and non-noble metal-based nanoscale catalytic assemblages obtained by much difficult methods. Most advantageously, the colloidal route also offers the easiest approach of incorporating carbon contents in the catalytic layer, which can ultimately increase mechanical stability and mass transfer capability of the system.

摘要

析氧反应极为重要,对于诸如电解槽、燃料电池以及其他太阳能和化学能转换装置等设备来说至关重要。在这一探索过程中仍然存在的主要挑战是,缺乏能够以最佳效率运行且可通过更简单的设置和易于获取的方法获得的有效催化组件。在此,我们证明,使用直接从在清洁碳酸盐体系中制备的易于制备的胶体钴纳米颗粒(Co-CNP)衍生而来的纳米级电催化剂,可以实现对水氧化的强大电催化活性。诸如简单的Co-CNP/FTO、退火的Co-CNP/FTO以及通过将Co-CNP沉积在FTO基板上获得的Co-CNP/FTO等薄膜非贵金属纳米级电催化剂,在温和碱性条件下,显示出在低得多的过电位下引发水氧化,例如Co-CNP/FTO仅为240 mV,同时表现出仅40 mV dec的令人印象深刻的塔菲尔斜率。此外,这种强大的催化剂在0.35 V时分别显示出91 cm²的高电化学表面积、0.26 s⁻¹的高周转频率和18.84 mA mg⁻¹的高质量活性,以及在长期电解过程中的优异耐久性。使用易于制备的Co-CNP/FTO型催化系统所取得的这些出色催化成果与通过困难得多的方法获得的其他基于贵金属和非贵金属的纳米级催化组件相当,甚至更好。最有利的是,胶体路线还提供了在催化层中掺入碳含量的最简单方法,这最终可以提高系统的机械稳定性和传质能力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e416/7240820/327d0840bc11/ao9b03576_0010.jpg

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