Abstract

Atomic layer deposition (ALD) provides a promising route for depositing uniform thin-film electrodes for Li-ion batteries. In this work, bis(methylcyclopentadienyl) nickel(II) (Ni(MeCp)2) and bis(cyclopentadienyl) nickel(II) (NiCp2) were used as precursors for NiO ALD. Oxygen plasma was used as a counter-reactant. The films were studied by spectroscopic ellipsometry, scanning electron microscopy, atomic force microscopy, X-ray diffraction, X-ray reflectometry, and X-ray photoelectron spectroscopy. The results show that the optimal temperature for the deposition for NiCp2 was 200–300 °C, but the optimal Ni(MeCp)2 growth per ALD cycle was 0.011–0.012 nm for both precursors at 250–300 °C. The films deposited using NiCp2 and oxygen plasma at 300 °C using optimal ALD condition consisted mainly of stoichiometric polycrystalline NiO with high density (6.6 g/cm3) and low roughness (0.34 nm). However, the films contain carbon impurities. The NiO films (thickness 28–30 nm) deposited on stainless steel showed a specific capacity above 1300 mAh/g, which is significantly more than the theoretical capacity of bulk NiO (718 mAh/g) because it includes the capacity of the NiO film and the pseudo-capacity of the gel-like solid electrolyte interface film. The presence of pseudo-capacity and its increase during cycling is discussed based on a detailed analysis of cyclic voltammograms and charge–discharge curves (U(C)).

Highlights

  • In recent years, a large number of studies have been actively conducted to study the possibility of using nickel oxide (NiO) nanofilms as electrocatalysts for water decomposition [1], chemical sensors [2], active components of solar cells [3], and antiferromagnetic layers [4]

  • The necessary condition for correct Atomic layer deposition (ALD) is the use of an excess of reagent vapors to saturate the surface during chemical reactions

  • This excess can be achieved by increasing the vapor pressure by heating the evaporator or/and by increasing the pulse time

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Summary

Introduction

A large number of studies have been actively conducted to study the possibility of using nickel oxide (NiO) nanofilms as electrocatalysts for water decomposition [1], chemical sensors [2], active components of solar cells [3], and antiferromagnetic layers [4]. The value of the theoretical electrochemical capacity for NiO (718 mAh/g [6]) is close to the values for several other promising anode materials, such as SnO2 (790 mAh/g) [7], CoO (715 mAh/g) [8], and MnO (650 mAh/g) [8]. The capacity of these oxide materials is more than twice the capacity of graphite (372 mAh/g) used in the industry of lithium-ion batteries [9]. The stability of NiO nanofilms during charge/discharge cycling at high current densities [10] allows us to consider NiO as promising material for creating negative electrodes of portable energy sources of biosensors, microchips, pacemakers, and other devices. [11].

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