ACS Appl Mater Interfaces. 2018 Sep 12;10(36):30400-30408. doi: 10.1021/acsami.8b09854. Epub 2018 Aug 30.
Non-noble-metal electrocatalysts for water splitting hold great promises for developing sustainable and clean energy sources. Herein, a highly efficient bifunctional electrode consisting of Ni-doped molybdenum nitride nanorods on Ni foam is prepared through topotactic transformation of NiMoO nanorods that are in situ hydrothermally grown on Ni foam. The electrode not only contains rich, accessible, electrochemically active sites but also possesses extraordinary chemical stability. It exhibits excellent hydrogen evolution reaction and oxygen evolution reaction performance in 1.0 M KOH with low overpotentials of 15 and 218 mV, respectively, at a current density of 10 mA cm, superior to the commercial benchmark materials Pt/C and RuO under the same condition. A simple water electrolyzer using the obtained electrode as both the anode and cathode needs a very low cell potential of 1.49 V to reach a current density of 10 mA cm and maintains stability for 110 h without degradation. The excellent performance of the electrode could be attributed to the formation of highly conductive, corrosion- and oxidation-resistant metal nitrides and the synergetic effect between intimately interconnected, electrochemically active nickel molybdenum nitride and Ni or NiO nanoparticles. This study shows that the use of transition metal nitrides in combination of nanostructured heterojunctions of multiple active components enables one to develop highly stable and efficient water electrolyzers without precious metals. The preparative strategy used in this work could be applied to devise new electrocatalysts.
非贵金属电催化剂在开发可持续清洁能源方面具有广阔的前景。在此,通过原位水热生长在泡沫镍上的 NiMoO 纳米棒的拓扑转变,制备了一种由泡沫镍上生长的 Ni 掺杂氮化钼纳米棒组成的高效双功能电极。该电极不仅含有丰富、可及的、电化学活性位点,而且具有非凡的化学稳定性。在 1.0 M KOH 中,它表现出优异的析氢反应和析氧反应性能,在 10 mA cm 的电流密度下,其过电位分别低至 15 和 218 mV,优于相同条件下的商业基准材料 Pt/C 和 RuO。使用所制备的电极作为阳极和阴极的简单水电解槽仅需 1.49 V 的电池电势即可达到 10 mA cm 的电流密度,并且在 110 h 内保持稳定而没有降解。电极的优异性能可归因于高导电性、耐腐蚀和抗氧化金属氮化物的形成以及相互连接的电化学活性镍钼氮化物与 Ni 或 NiO 纳米颗粒之间的协同效应。本研究表明,在多相活性组分的纳米结构异质结中使用过渡金属氮化物,可以开发出高效稳定且无需贵金属的水电解槽。本工作中使用的制备策略可用于设计新型电催化剂。