Cheng Po-Yin, Ting Yu-Chieh, Cheng Chih-Chieh, Senthil Raja Duraisamy, Lin Shin-Hong, Yeh Yong-Xian, Su Jing-Ting, Lu Shih-Yuan
Department of Chemical Engineering, National Tsing Hua University, Hsinchu 30013, Taiwan.
Department of Chemical Engineering, National Tsing Hua University, Hsinchu 30013, Taiwan.
J Colloid Interface Sci. 2022 Oct;623:327-336. doi: 10.1016/j.jcis.2022.05.036. Epub 2022 May 10.
Developments of non-precious metal based active and stable catalysts are of great importance and challenge to green hydrogen production from acidic electrocatalytic water splitting. Design of composite catalysts with synergy between active and stable components proves to be a promising approach. Herein, N-doped carbon armored CoO hollow nanocubes electrochemically anchored on fluorine-doped tin oxide (FTO) substrates are developed as efficient and stable catalysts for acidic oxygen evolution reactions. CoO acts as the active component with N-doped carbon coating layer serving as the stable protection component, shielding CoO from direct attack of anodic dissolution. Electrochemical fixation offers firm holding of the composite catalyst onto acid-tolerant FTO substrates and hollow nanocubes serve as nano-reactors for confined fast reactions. Under optimal conditions, the composite catalyst achieves an overpotential of 465 mV at 10 mA cm in 0.5 M HSO, and stays stable for 12 hr with a 10% increment in applied potentials.
开发基于非贵金属的活性和稳定催化剂对于酸性电催化水分解制绿氢具有重要意义且极具挑战性。设计具有活性和稳定组分协同作用的复合催化剂被证明是一种很有前景的方法。在此,电化学锚定在氟掺杂氧化锡(FTO)基底上的氮掺杂碳包覆CoO空心纳米立方体被开发为用于酸性析氧反应的高效稳定催化剂。CoO作为活性组分,氮掺杂碳涂层作为稳定保护组分,保护CoO免受阳极溶解的直接攻击。电化学固定使复合催化剂牢固地附着在耐酸FTO基底上,空心纳米立方体作为受限快速反应的纳米反应器。在最佳条件下,该复合催化剂在0.5 M H₂SO₄中10 mA cm⁻²时的过电位为465 mV,并在施加电位增加10%的情况下保持稳定12小时。