Nguyen Tuyen, Carmezim M João, Montemor M Fátima
CQE - Centro de Química Estrutural, Insituto Superior Técnico, Universidade de Lisboa, Lisboa 1049-001, Portugal.
Phys Chem Chem Phys. 2016 Apr 28;18(17):12368-74. doi: 10.1039/c6cp00709k.
Current transient evolution and in situ electrochemical AFM were used to study the initial stages of growth of electrochemically deposited nickel cobalt hydroxide films for energy storage applications. Current transients were taken at constant potentials, from -700 mV to -1000 mV, with a step of 50 mV. The current transients were fitted with three different nucleation models: Scharifker-Hill, Scharifker-Mostany and Mirkin-Nilov-Heerman-Tarallo and the results revealed that film growth was governed by a 3D instantaneous nucleation mechanism. In situ electrochemical AFM studies confirmed the instantaneous nucleation mechanism and revealed the early stage formation of nanosheets. The in situ AFM results were supported by the ex situ FEG-SEM results, showing the formation of nanoneedles at the first stages of nucleation and the growth into nanosheets with the increasing deposition time.
利用电流瞬态演化和原位电化学原子力显微镜研究了用于储能应用的电化学沉积氢氧化镍钴薄膜生长的初始阶段。在-700 mV至-1000 mV的恒定电位下,以50 mV的步长采集电流瞬态。电流瞬态采用三种不同的成核模型进行拟合:Scharifker-Hill模型、Scharifker-Mostany模型和Mirkin-Nilov-Heerman-Tarallo模型,结果表明薄膜生长受三维瞬时成核机制控制。原位电化学原子力显微镜研究证实了瞬时成核机制,并揭示了纳米片的早期形成。原位原子力显微镜结果得到了非原位场发射枪扫描电子显微镜结果的支持,显示在成核的第一阶段形成纳米针,并随着沉积时间的增加生长成纳米片。