Ghosh Sourav, Jana Rajkumar, Ganguli Sagar, Inta Harish Reddy, Tudu Gouri, Koppisetti Heramba V S R M, Datta Ayan, Mahalingam Venkataramanan
Department of Chemical Sciences, Indian Institute of Science Education and Research (IISER) Kolkata Mohanpur West Bengal 741246 India
Technical Research Centre, S. N. Bose National Centre for Basic Sciences Block-JD, Sector-III, Salt Lake Kolkata-700106 India.
Nanoscale Adv. 2021 Apr 27;3(13):3770-3779. doi: 10.1039/d1na00034a. eCollection 2021 Jun 30.
The quest for developing next-generation non-precious electrocatalysts has risen in recent times. Herein, we have designed and developed a low cost electrocatalyst by a ligand-assisted synthetic strategy in an aqueous medium. An oxalate ligand-assisted non-oxide electrocatalyst was developed by a simple wet-chemical technique for alkaline water oxidation application. The synthetic parameters for the preparation of nickel-cobalt oxalate (NiCoCO) were optimized, such as the metal precursor (Ni/Co) ratio, oxalic acid amount, reaction temperature, and time. Microstructural analysis revealed a mesoporous block-like architecture for nickel-cobalt oxalate (NiCoCO). The required overpotential of NiCoCO for the alkaline oxygen evolution reaction (OER) was found to be 330 mV for achieving 10 mA cm , which is superior to that of NiCO, CoCO, NiCoO and the state-of-the-art RuO. The splendid performance of NiCoCO was further verified by its low charge transfer resistance, impressive stability performance, and 87% faradaic efficiency in alkaline medium (pH = 14). The improved electrochemical activity was further attributed to double layer capacitance ( ), which indefinitely divulged the inferiority of NiCoO compared to NiCoCO for the alkaline oxygen evolution reaction (OER). The obtained proton reaction order ( ) was about 0.80, thus indicating the proton decoupled electron transfer (PDET) mechanism for OER in alkaline medium. Post-catalytic investigation revealed the formation of a flake-like porous nanostructure, indicating distinct transformation in morphology during the alkaline OER process. Further, XPS analysis demonstrated complete oxidation of Ni and Co centres into Ni and Co, respectively under high oxidation potential, thereby indicating active site formation throughout the microstructural network. Additionally, from BET-normalised LSV investigation, the intrinsic activity of NiCoCO was also found to be higher than that of NiCoO. Finally, NiCoCO delivered a TOF value of around 3.28 × 10 s, which is 5.56 fold that of NiCoO for the alkaline OER process. This report highlights the unique benefit of NiCoCO over NiCoO for the alkaline OER. The structure-catalytic property relationship was further elucidated using density functional theory (DFT) study. To the best of our knowledge, nickel-cobalt oxalate (NiCoCO) was introduced for the first time as a non-precious non-oxide electrocatalyst for alkaline OER application.
近年来,开发下一代非贵金属电催化剂的需求日益增加。在此,我们通过配体辅助合成策略在水介质中设计并开发了一种低成本电催化剂。采用简单的湿化学技术制备了一种用于碱性水氧化的草酸盐配体辅助非氧化物电催化剂。优化了草酸镍钴(NiCoCO)制备的合成参数,如金属前驱体(Ni/Co)比例、草酸用量、反应温度和时间。微观结构分析揭示了草酸镍钴(NiCoCO)具有介孔块状结构。发现NiCoCO在碱性析氧反应(OER)中达到10 mA cm 所需的过电位为330 mV,优于NiCO、CoCO、NiCoO和最先进的RuO。NiCoCO的出色性能还通过其低电荷转移电阻、令人印象深刻的稳定性以及在碱性介质(pH = 14)中87%的法拉第效率得到进一步验证。电化学活性的提高进一步归因于双层电容( ),这明确揭示了在碱性析氧反应(OER)中NiCoO相比NiCoCO的劣势。获得的质子反应级数( )约为0.80,表明碱性介质中OER的质子解耦电子转移(PDET)机制。催化后研究揭示了片状多孔纳米结构的形成,表明碱性OER过程中形态发生了明显转变。此外,XPS分析表明在高氧化电位下,Ni和Co中心分别完全氧化为Ni 和Co,从而表明在整个微观结构网络中形成了活性位点。此外,通过BET归一化的LSV研究发现,NiCoCO的本征活性也高于NiCoO。最后,NiCoCO在碱性OER过程中的TOF值约为3.28 × 10 s,是NiCoO的5.56倍。本报告突出了NiCoCO相比NiCoO在碱性OER方面的独特优势。利用密度泛函理论(DFT)研究进一步阐明了结构 - 催化性能关系。据我们所知,草酸镍钴(NiCoCO)首次作为用于碱性OER的非贵金属非氧化物电催化剂被引入。