Liu Liyuan, Zhang Zhen, Gu Shiyu, Liu Yanan, Deng Ying, Li Yuqing, Xiao Zhenyu, Liu Kang, Wu Zexing, Wang Lei
Key Laboratory of Eco-chemical Engineering, Ministry of Education, International Science and Technology Cooperation Base of Eco-chemical Engineering and Green Manufacturing, College of Chemistry and Molecular Engineering, Qingdao University of Science and Technology, Qingdao 266042, P. R. China.
Key Laboratory of Eco-chemical Engineering, Ministry of Education, International Science and Technology Cooperation Base of Eco-chemical Engineering and Green Manufacturing, College of Chemistry and Molecular Engineering, Qingdao University of Science and Technology, Qingdao 266042, P. R. China; Shandong Engineering Research Center for Marine Environment Corrosion and Safety Protection, College of Environment and Safety Engineering, Qingdao University of Science and Technology, Qingdao 266042, P. R. China.
J Colloid Interface Sci. 2024 Dec 15;676:52-60. doi: 10.1016/j.jcis.2024.07.098. Epub 2024 Jul 14.
The seawater electrolysis technology powered by renewable energy is recognized as the promising "green hydrogen" production method to solve serious energy and environmental problems. The lack of low-cost and ampere-level current OER (oxygen evolution reaction) and HER (hydrogen evolution reaction) catalysis limits their industrial application. In this work, a unique tri-metal (Co/Fe/Ni) layered double hydroxide hollow array anode catalyst (CFN-LDH/NF) and the CoP/FeNiP heterojunction hollow array cathode are successfully prepared via one in-situ growth of Co-MOF on nickel foam (Co-MOF/NF) precursor, which exhibits excellent catalytic performance. The η values of 352 and 392 mV are achieved for CFN-LDH/NF (OER catalyst) in 1.0 M KOH and alkaline seawater solution, respectively. The CFNP/NF with a low overpotential of 281 mV is required to reach 1000 mA cm current density for HER in 1.0 M KOH solution, while the η in alkaline seawater solution is 312 mV. The CFN-LDH/NF||CFNP/NF electrolyzer exhibits excellent long-term durability over 100 h, achieving current density of 500 mA cm at 1.825 V in 1.0 M KOH solution. The construction of hollow tri-metal LDH and phosphides heterostructures may open a new and relatively unexplored path for fabricating high performance seawater splitting catalysis.
由可再生能源驱动的海水电解技术被认为是解决严重能源和环境问题的有前景的“绿色制氢”方法。缺乏低成本且能达到安培级电流的析氧反应(OER)和析氢反应(HER)催化剂限制了它们的工业应用。在这项工作中,通过在泡沫镍(Co-MOF/NF)前驱体上原位生长Co-MOF,成功制备了一种独特的三金属(Co/Fe/Ni)层状双氢氧化物空心阵列阳极催化剂(CFN-LDH/NF)和CoP/FeNiP异质结空心阵列阴极,其表现出优异的催化性能。CFN-LDH/NF(OER催化剂)在1.0 M KOH溶液和碱性海水溶液中的η值分别为352和392 mV。在1.0 M KOH溶液中,HER达到1000 mA cm电流密度所需的CFNP/NF的低过电位为281 mV,而在碱性海水溶液中的η为312 mV。CFN-LDH/NF||CFNP/NF电解槽在100 h以上表现出优异的长期耐久性,在1.0 M KOH溶液中于1.825 V时实现了500 mA cm的电流密度。空心三金属层状双氢氧化物和磷化物异质结构的构建可能为制备高性能海水分解催化剂开辟一条新的且相对未被探索的途径。