Nagita Kenji, Yuhara Yoshiki, Fujii Kenta, Katayama Yu, Nakayama Masaharu
Department of Applied Chemistry, Graduate School of Sciences and Technology for Innovation, Yamaguchi University, 2-16-1 Tokiwadai, Ube 755-8611, Japan.
Blue Energy Center for SGE Technology (BEST), Ube 755-8611, Japan.
ACS Appl Mater Interfaces. 2021 Jun 23;13(24):28098-28107. doi: 10.1021/acsami.1c04422. Epub 2021 May 27.
We fabricated a thin film of layered MnO whose interlayer space was occupied by hydrated Ni and Cu ions. The process consisted of electrodeposition of layered MnO intercalated with tetrabutylammonium cations (TBA) by anodic oxidation of aqueous Mn ions in the presence of TBA, followed by ion exchange of the initially incorporated bulkier TBA with the denser transition metals in solution. The resulting layered MnO co-intercalated with Ni and Cu ions (NiCu/MnO) catalyzed the ammonia oxidation reaction (AOR) in an alkaline electrolyte with a much lower overpotential than its Ni- and Cu-intercalated single-cation counterparts. Surprisingly, the NiCu/MnO electrode achieved a faradic efficiency as high as nearly 100% (97.4%) for nitrogen evolution at a constant potential of +0.6 V vs Hg/HgO. This can be ascribed to the occurrence of the AOR in the potential region where water is stable and dimerization of the partially dehydrogenated ammonia species is preferred, thereby forming an N-N bond, rather than to be further oxidized into NO species.
我们制备了一种层状MnO薄膜,其层间空间被水合镍离子和铜离子占据。该过程包括在四丁基铵阳离子(TBA)存在下,通过对水相锰离子进行阳极氧化来电沉积插层有TBA的层状MnO,随后将最初引入的体积较大的TBA与溶液中密度更大的过渡金属进行离子交换。所得的共插层有镍离子和铜离子的层状MnO(NiCu/MnO)在碱性电解质中催化氨氧化反应(AOR),其过电位远低于插层有镍离子和铜离子的单阳离子对应物。令人惊讶的是,在相对于Hg/HgO为 +0.6 V的恒定电位下,NiCu/MnO电极在析氮方面实现了高达近100%(97.4%)的法拉第效率。这可归因于AOR发生在水稳定且部分脱氢氨物种优先二聚从而形成N - N键的电位区域,而不是进一步氧化成NO物种。