Bahuguna Gaurav, Cohen Adam, Harpak Nimrod, Filanovsky Boris, Patolsky Fernando
School of Chemistry, Faculty of Exact Sciences, Tel Aviv University, Tel Aviv, 69978, Israel.
Department of Materials Science and Engineering, the Iby and Aladar Fleischman Faculty of Engineering, Tel Aviv University, Tel Aviv, 69978, Israel.
Small Methods. 2022 Jun;6(6):e2200181. doi: 10.1002/smtd.202200181. Epub 2022 May 1.
Hydrogen, undoubtedly the next-generation fuel for supplying the world's energy demands, needs economically scalable bifunctional electrocatalysts for its sustainable production. Non-noble transition metal-based electrocatalysts are considered an economic solution for water splitting applications. A single-step solid-state approach for the economically scalable transformation of Ni-based substrates into single-crystalline nickel sulfide nanoplate arrays is developed. X-ray diffraction and transmission electron microscopy measurements reveal the influence of the transformation temperature on the crystal growth direction, which in turn can manipulate the chemical state at the catalyst surface. Ni-based sulfide formed at 450 °C exhibits an enhanced concentration of electrocatalytically-active Ni at their surface and a reduced electron density around sulfur atoms, optimal for efficient H production. The Ni-based sulfide electrocatalysts display exceptional electrocatalytic performance for both oxygen and hydrogen evolution, with overpotentials of 170 and 90 mV respectively. Remarkably, the two-electrode cell for overall electrolysis of alkaline water demonstrates an ultra-low cell potential of 1.46 V at 10 mA cm and 1.69 V at 100 mA cm . In addition to the exceptionally low water-splitting cell voltage, this self-standing electrocatalyst is of binderfree nature, with the electrode preparation being a low-cost and single-step process, easily scalable to industrial scales.
氢气无疑是满足全球能源需求的下一代燃料,其可持续生产需要经济上可扩展的双功能电催化剂。基于非贵金属过渡金属的电催化剂被认为是用于水分解应用的经济解决方案。开发了一种将镍基衬底经济上可扩展地转变为单晶硫化镍纳米板阵列的单步固态方法。X射线衍射和透射电子显微镜测量揭示了转变温度对晶体生长方向的影响,这反过来又可以控制催化剂表面的化学状态。在450°C下形成的镍基硫化物在其表面表现出增强的电催化活性镍浓度,并且硫原子周围的电子密度降低,这对于高效制氢是最佳的。镍基硫化物电催化剂对析氧和析氢均表现出优异的电催化性能,过电位分别为170和90 mV。值得注意的是,用于碱性水电解的两电极电池在10 mA cm时表现出1.46 V的超低电池电位,在100 mA cm时表现出1.69 V的超低电池电位。除了极低的水分解电池电压外,这种自立式电催化剂具有无粘结剂的性质,电极制备是低成本的单步过程,易于扩展到工业规模。