Song Zhongxin, Wang Kaixi Cathy, Sun Qian, Zhang Lei, Li Junjie, Li Dingjiu, Sze Pok-Wai, Liang Yue, Sun Xueliang, Fu Xian-Zhu, Luo Jing-Li
Shenzhen Key Laboratory of Polymer Science and Technology Guangdong Research Center for Interfacial Engineering of Functional Materials College of Materials Science and Engineering Shenzhen University Shenzhen 518060 China.
Department of Mechanical and Materials Engineering University of Western Ontario London ON N6A 5B9 Canada.
Adv Sci (Weinh). 2021 May 16;8(14):2100498. doi: 10.1002/advs.202100498. eCollection 2021 Jul.
The development of highly efficient electrocatalysts toward the oxygen evolution reaction is imperative for advancing water splitting technology to generate clean hydrogen energy. Herein, a two dimensional (2D) nanosheet ammonium cobalt phosphate hydrate (NHCoPO·HO) catalyst based on the earth-abundant non-noble metal is reported. When used for the challenging alkaline saline water electrolysis, the NHCoPO·HO catalyst with the optimal thickness of 30 nm achieves current densities of 10 and 100 mA cm at the record low overpotentials of 252 and 268 mV, respectively, while maintaining remarkable stability during the alkaline saline water oxidation at room temperature. X-ray absorption fine spectra reveal that the activation of Co (II) ions (in NHCoPO·HO) to Co (III) species constructs the electrocatalytic active sites. The 2D nanosheet morphology of NHCoPO·HO provides a larger active surface area and more surface-exposed active sites, which enable the nanosheet catalyst to facilitate the alkaline freshwater and simulated seawater oxidation with excellent activity. The facile and environmentally-benign HO-mediated synthesis route under mild condition makes NHCoPO·HO catalyst highly feasible for practical manufacturing. In comparison with noble metals, this novel electrocatalyst offers a cost-effective alternative for economic saline water oxidation to advance water electrolysis technology.
开发高效的析氧反应电催化剂对于推动水分解技术以产生清洁氢能至关重要。在此,报道了一种基于储量丰富的非贵金属的二维(2D)纳米片水合磷酸钴铵(NHCoPO·HO)催化剂。当用于具有挑战性的碱性盐水电解时,最佳厚度为30nm的NHCoPO·HO催化剂在创纪录的低过电位252和268mV下分别实现了10和100mA cm的电流密度,同时在室温下碱性盐水氧化过程中保持了显著的稳定性。X射线吸收精细光谱表明,Co(II)离子(在NHCoPO·HO中)向Co(III)物种的活化构建了电催化活性位点。NHCoPO·HO的二维纳米片形态提供了更大的活性表面积和更多表面暴露的活性位点,这使得纳米片催化剂能够以优异的活性促进碱性淡水和模拟海水氧化。在温和条件下通过简便且环境友好的HO介导的合成路线使得NHCoPO·HO催化剂在实际制造中具有高度可行性。与贵金属相比,这种新型电催化剂为经济的盐水氧化提供了一种经济高效的替代方案,以推动水电解技术的发展。