Menezes Prashanth W, Yao Shenglai, Beltrán-Suito Rodrigo, Hausmann J Niklas, Menezes Pramod V, Driess Matthias
Department of Chemistry: Metalorganics and Inorganic Materials, Technische Universität Berlin, Strasse des 17 Juni 135, Sekr. C2, 10623, Berlin, Germany.
Institut für Elektrochemie, Universität Ulm, Albert-Einstein-Allee 47, 89081, Ulm, Germany.
Angew Chem Int Ed Engl. 2021 Feb 23;60(9):4640-4647. doi: 10.1002/anie.202014331. Epub 2021 Feb 2.
Identifying novel classes of precatalysts for the oxygen evolution reaction (OER by water oxidation) with enhanced catalytic activity and stability is a key strategy to enable chemical energy conversion. The vast chemical space of intermetallic phases offers plenty of opportunities to discover OER electrocatalysts with improved performance. Herein we report intermetallic nickel germanide (NiGe) acting as a superior activity and durable Ni-based electro(pre)catalyst for OER. It is produced from a molecular bis(germylene)-Ni precursor. The ultra-small NiGe nanocrystals deposited on both nickel foam and fluorinated tin oxide (FTO) electrodes showed lower overpotentials and a durability of over three weeks (505 h) in comparison to the state-of-the-art Ni-, Co-, Fe-, and benchmark NiFe-based electrocatalysts under identical alkaline OER conditions. In contrast to other Ni-based intermetallic precatalysts under alkaline OER conditions, an unexpected electroconversion of NiGe into γ-Ni OOH with intercalated OH /CO transpired that served as a highly active structure as shown by various ex situ methods and quasi in situ Raman spectroscopy.
识别具有增强催化活性和稳定性的析氧反应(通过水氧化进行析氧反应,即OER)的新型预催化剂类别是实现化学能转换的关键策略。金属间相广阔的化学空间为发现性能更优的OER电催化剂提供了大量机会。在此,我们报道金属间化合物锗化镍(NiGe)作为一种用于OER的具有卓越活性和耐久性的镍基电(预)催化剂。它由分子双(锗烯)-镍前驱体制备而成。与在相同碱性OER条件下的现有镍基、钴基、铁基及基准镍铁基电催化剂相比,沉积在泡沫镍和氟化锡氧化物(FTO)电极上的超小NiGe纳米晶体表现出更低的过电位以及超过三周(505小时)的耐久性。与碱性OER条件下的其他镍基金属间预催化剂不同,NiGe意外地电转化为插层有OH⁻/CO₃²⁻的γ-NiOOH,各种非原位方法和准原位拉曼光谱表明其为一种高活性结构。