Wang Yueqing, Zhang Baohua, Pan Wei, Ma Houyi, Zhang Jintao
Key Laboratory for Colloid and Interface Chemistry of State Education Ministry, School of Chemistry and Chemical Engineering, Shandong University, Jinan, 250100, P. R. China.
College of Chemistry, Chemical Engineering and Materials Science, Shandong Normal University, Jinan, 250014, P. R. China.
ChemSusChem. 2017 Nov 9;10(21):4170-4177. doi: 10.1002/cssc.201701456. Epub 2017 Oct 12.
Exploring highly efficient and durable bifunctional electrocatalysts from earth-abundant low-cost transition metals is central to obtaining clean hydrogen energy through large-scale electrolytic water splitting. Porous nickel-cobalt nitride nanosheets on macroporous Ni foam (NF) are synthesized through facile electrodeposition followed by a one-step annealing process in a NH atmosphere. The transformation from a metal hydroxide into a metal nitride could efficiently enhance the electrocatalytic performance for both the oxygen evolution reaction (OER) and hydrogen evolution reaction (HER). Interestingly, the incorporation of nickel further boosts the catalytic activity of cobalt nitride. When used as bifunctional electrocatalysts, the obtained nickel-cobalt nitride electrocatalyst shows good stability and superior catalytic performance toward both HER and OER with low overpotentials of 0.29 and 0.18 V, respectively, to achieve a current density of 10 mA cm . The good electrocatalytic performance was also evidenced by the fabrication of an electrolyzer for overall water splitting, which exhibits a high gas generation rate for hydrogen and oxygen with excellent stability during prolonged alkaline water electrolysis. The present work provides an efficient approach to prepare a 3 D interconnected porous nickel-cobalt nitride network with exposed inner active sites for overall water splitting.
从储量丰富的低成本过渡金属中探索高效耐用的双功能电催化剂是通过大规模电解水制氢获得清洁氢能的关键。通过简便的电沉积法在大孔泡沫镍(NF)上合成多孔氮化镍钴纳米片,随后在NH气氛中进行一步退火处理。从金属氢氧化物到金属氮化物的转变可以有效提高析氧反应(OER)和析氢反应(HER)的电催化性能。有趣的是,镍的掺入进一步提高了氮化钴的催化活性。当用作双功能电催化剂时,所制备的氮化镍钴电催化剂表现出良好的稳定性,对HER和OER均具有优异的催化性能,在电流密度为10 mA cm时,过电位分别低至0.29 V和0.18 V。用于全水解的电解槽的制备也证明了其良好的电催化性能,该电解槽在长时间碱性水电解过程中表现出高的氢气和氧气产生速率以及出色的稳定性。本工作提供了一种有效的方法来制备具有暴露内部活性位点的三维互连多孔氮化镍钴网络用于全水解。