Tunable Electrical and Optical Properties of Nickel Oxide (NiOx) Thin

Oct 15, 2018 - Isabel Pintor-Monroy , Diego Barrera , Bayron Murillo-Borjas , Francisco Ochoa-Estrella , Julia W.P. Hsu , and Manuel A. Quevedo-López...
0 downloads 0 Views 1MB Size
Subscriber access provided by Kaohsiung Medical University

Functional Inorganic Materials and Devices

Tunable Electrical and Optical Properties of Nickel Oxide (NiOx) Thin Films for Fully Transparent NiOx-Ga2O3 p-n Junction Diodes Isabel Pintor-Monroy, Diego Barrera, Bayron Murillo-Borjas, Francisco Ochoa-Estrella, Julia W.P. Hsu, and Manuel A. Quevedo-López ACS Appl. Mater. Interfaces, Just Accepted Manuscript • DOI: 10.1021/acsami.8b08095 • Publication Date (Web): 15 Oct 2018 Downloaded from http://pubs.acs.org on October 15, 2018

Just Accepted “Just Accepted” manuscripts have been peer-reviewed and accepted for publication. They are posted online prior to technical editing, formatting for publication and author proofing. The American Chemical Society provides “Just Accepted” as a service to the research community to expedite the dissemination of scientific material as soon as possible after acceptance. “Just Accepted” manuscripts appear in full in PDF format accompanied by an HTML abstract. “Just Accepted” manuscripts have been fully peer reviewed, but should not be considered the official version of record. They are citable by the Digital Object Identifier (DOI®). “Just Accepted” is an optional service offered to authors. Therefore, the “Just Accepted” Web site may not include all articles that will be published in the journal. After a manuscript is technically edited and formatted, it will be removed from the “Just Accepted” Web site and published as an ASAP article. Note that technical editing may introduce minor changes to the manuscript text and/or graphics which could affect content, and all legal disclaimers and ethical guidelines that apply to the journal pertain. ACS cannot be held responsible for errors or consequences arising from the use of information contained in these “Just Accepted” manuscripts.

is published by the American Chemical Society. 1155 Sixteenth Street N.W., Washington, DC 20036 Published by American Chemical Society. Copyright © American Chemical Society. However, no copyright claim is made to original U.S. Government works, or works produced by employees of any Commonwealth realm Crown government in the course of their duties.

Page 1 of 22 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 37 38 39 40 41 42 43 44 45 46 47 48 49 50 51 52 53 54 55 56 57 58 59 60

ACS Applied Materials & Interfaces

Tunable Electrical and Optical Properties of Nickel Oxide (NiOx) Thin Films for Fully Transparent NiOx-Ga2O3 p-n Junction Diodes Maria Isabel Pintor-Monroy†, Diego Barrera†, Bayron L. Murillo-Borjas†, Francisco Javier Ochoa-Estrella+, Julia W.P. Hsu† and Manuel A. Quevedo-Lopez†* †

Department of Materials Science and Engineering, The University of Texas at Dallas

800 W. Campbell Road, Richardson, Texas, 75080, USA +

Departamento de Investigación en Física, Universidad de Sonora.

Rosales y Luis Encinas, Hermosillo, Sonora, 83000, México Keywords: oxide semiconductors, pn junction, pulsed laser deposition, nickel oxide, gallium oxide

Abstract: One of the major limitations of oxide semiconductors technology is the lack of proper p-type materials to enable devices such as pn junctions, light-emitting diodes, and photodetectors. This limitation has resulted in an increased research focused on these materials. In this work, p-type NiOx thin films with tunable optical and electrical properties as well as its dependence with oxygen pressure during pulsed laser deposition (PLD) are demonstrated. The

ACS Paragon Plus Environment

1

ACS Applied Materials & Interfaces 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 37 38 39 40 41 42 43 44 45 46 47 48 49 50 51 52 53 54 55 56 57 58 59 60

Page 2 of 22

control of NiOx films resistivity ranged from ~109 Ω-cm to ~102 Ω-cm, showing p-type behavior with Eg tuning from 3.4 eV to 3.9 eV. Chemical composition and the resulting band diagrams are also discussed. The all-oxide NiOx-Ga2O3 pn junction showed very low leakage current, ideality factor of ~2, 105 on/off ratio and 0.6 V built-in potential. Its J-V temperature-dependence is also analyzed. C-V measurements demonstrate diodes with carrier concentration of 1015 cm-3 for the Ga2O3 layer, which is fully depleted. These results show stable, promising diode, attractive for future photoelectronic devices.

1. Introduction

Although n-type TCO have been extensively studied and improved in recent years, high performance p-type oxides are still a challenge, even when using high-temperature processes.

1

Nickel oxide (NiO) is a 3d-transition-metal-oxide part of the MO family, where M = Co, Ni, Fe, and Cu.2 NiO is a transparent conductive oxide (TCO), with a cubic, rock salt structure, wide band gap (Eg) (3.15-4.3 eV) and p-type conductivity.1, 3-7 As semiconductor, NiO is an attractive material with an extensive range of applications, for example, it has been used in antiferromagnetic devices, electrochemical electrodes, active optical fibers, fuel cells electrodes, hole transport layer (HTL) in solar cells and organic light emitting devices (OLEDs), chemical sensors, battery systems, CO oxidation catalyst,1,

2, 5, 8

and as active channel in thin film

transistors.9 NiO is especially important for p-type conducting films in optical windows for devices where hole injection/transport is required while being transparent in the ultraviolet, visible and near infrared range is desired.3 An additional advantage of NiO is that it is abundant and stable, which makes it ideal for commercial applications.10

ACS Paragon Plus Environment

2

Page 3 of 22 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 37 38 39 40 41 42 43 44 45 46 47 48 49 50 51 52 53 54 55 56 57 58 59 60

ACS Applied Materials & Interfaces

Thin films of NiO have been deposited by several techniques including sol-gel, spin coating, radio frequency sputtering, pulsed laser deposition (PLD), thermal evaporation, electrochemical evaporation, spray pyrolysis, chemical deposition and metalorganic chemical vapor deposition (MOCVD).2,

5, 11-16

Among these deposition methods, PLD offers the advantages of excellent

thickness control, low porosity, less defects, smooth surfaces and, in general, more homogeneity throughout the film. In addition, PLD deposition can be carried out at low temperatures, ideal for their implementation in organic photovoltaic devices (OPVs).12 Some of the parameters that affect PLD deposition include laser wavelength, laser energy and energy density, atmosphere, pressure, temperature, distance substrate-target and repetition rate. Although PLD deposition of NiO has been previously studied,4-6, 12 in this paper we demonstrate the tuning of the electrical and optical properties of NiOx films deposited at room temperature, without any further heat treatment, by controlling the oxygen pressure, and study its transport behavior. Finally, the films are used to demonstrate working devices including a semi-transparent NiOx/Ga2O3 pn junction which proves to being stable even at higher temperatures. Although thin-film oxide pn junctions deposited by PLD have been demonstrated before, at least one of its contacts is not transparent. In addition, previous reports use ZnO as the n-type layer, and leakage current is higher than the reported here (10-8 A/mm2).

17-19

We present a novel NiOx/amorphous-Ga2O3 pn junction

deposited at room temperature, which has not been reported before. The only report found in literature is for a Ga2O3 single-crystal with Li-NiO deposited by sol-gel spin coating on top by Kokubun et al. and using metals as contacts.20 Films are also used to fabricate conventional poly(3-hexylthiophene):phenyl-C60-butyric acid methyl ester (P3HT:PCBM) and poly(5-bromo4-(2-octyldodecyl)selenophen-2-yl)-5,6-difluorobenzothiadiazole-5,5’-bis(trimethylstannyl)2,2’-bithiophene:phenyl-C71-butyric acid methyl ester (PFBT2Se2Th:PC71BM) OPVs. In

ACS Paragon Plus Environment

3

ACS Applied Materials & Interfaces 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 37 38 39 40 41 42 43 44 45 46 47 48 49 50 51 52 53 54 55 56 57 58 59 60

Page 4 of 22

addition of being p-type, highly transparent and having high work function (Φ), an HTL material must be highly conductive.21-22 Albeit these challenges, OPVs using NiOx as HTL have been demonstrated before.4, 23-25 Herein we correlate the resistivity of the as-deposited NiOx films with OPV devices performance, optimize the NiO electrical properties, and demonstrate the application of these NiOx films deposited by PLD as HTL in OPV devices with two different active layer systems (Supporting information).

2. Electrical properties of NiOx films

NiOx thin films were deposited by PLD at room temperature, without any further heat treatment, on glass substrates to study their electrical and morphological properties as well as their composition. Figure 1a shows the dependence of the resistivity for as-deposited 30 nm-thick films as function of oxygen pressure as measured by circular transmission line method (CTLM).26 The resistivity shows a minimum at ~ 10mTorr likely due to more nickel vacancies and higher carrier concentration. Higher resistivity for P10mTorr is due to a different Ni:O ratio, of 2:3, or Ni2O3. Ni2O3 has a wider Eg and, in general, is less stable.27-29 Resistivity of the films for different oxygen partial pressures agrees with values for films deposited by other methods discussed in literature,5, 7, 11, 13, 30-32 ranging from insulating (stoichiometric NiO at low oxygen pressures) to conductive films (at 10 mTorr oxygen pressure).33

The conductivity of NiOx films is determined by cation vacancies, compensated by electronic holes with low formation energies;34 therefore, deviation from stoichiometry is directly related

ACS Paragon Plus Environment

4

Page 5 of 22 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 37 38 39 40 41 42 43 44 45 46 47 48 49 50 51 52 53 54 55 56 57 58 59 60

ACS Applied Materials & Interfaces

with the electrical conductivity of the films. It has been previously demonstrated by Molaei et al. that the concentration of charge carriers depends on the temperature and the oxygen pressure during deposition for p-type NiO samples deposited by PLD.35 To maintain neutrality in the crystal, Ni2+ cations are converted to Ni3+ cations, trapping positive holes. At high enough oxygen pressures, the number of Ni3+ cations and oxygen excess leads to the formation of Ni2O3 instead of increasing the number of carriers.

Due to the high resistivity for films deposited at low and high pressures, Hall measurements could not be performed. However, Hall measurements for 10 mTorr samples showed carrier concentration (p-type) in the order of ~1017cm-3, carrier mobility around 0.52 cm2/Vs and resistivity of 127 (~102) Ω-cm. These values agree with values reported by Chen et al. for films deposited by sputtering at room temperature and 200 W.14 Hall measurements as function of temperature (150 K – 300 K) for 10 mTorr samples were also carried out to study its transport properties. Resistivity, mobility and carrier concentration values for the different temperatures are shown in Figure 1b; resistivity increases as the temperature decreases, as expected for a semiconducting material, from 105 Ω-cm at 150 K to 102 Ω-cm at room temperature. This behavior is due to carrier excitation/generation as the temperature increases. The carrier concentration increases from ~1013 cm-3 at 150 K to ~1017 cm-3 at room temperature. Mobility, on the other hand, decreases as temperature increases, from 1.78 (150 K) to 0.52 cm2 /Vs (300 K). The temperature effect on mobility is lower compared with the effect on carrier concentration. The resistivity behavior at low temperatures resembles the values measured by Morin for an oxygen-rich NiO sample obtained at 1473 K by decomposition of Ni(NO3)2, with a resistivity of 107 Ω-cm at 150 K and 2×102 Ω-cm at 300 K.36 The mobility values have a linear

ACS Paragon Plus Environment

5

ACS Applied Materials & Interfaces 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 37 38 39 40 41 42 43 44 45 46 47 48 49 50 51 52 53 54 55 56 57 58 59 60

Page 6 of 22

dependence on T-3/2, which is related to lattice scattering, rather than to impurity scattering, which dominates at lower temperatures (10 mTorr) the valence and the conduction band vary due to an increase in the Eg and an increase in the IE of the films. This is explained as the increase in oxygen leads to more

and Ni3+ to maintain the

neutrality of the films which, at higher oxygen pressures, results in the formation of more Ni2O3.

3. Oxygen pressure effects

Figure 2a shows the transmittance spectra and Eg of the films in the inset. Eg was calculated from a standard plot of (αhν)2 versus hν using the absorbance spectra obtained from UV-Vis measurements. Samples deposited at lower oxygen pressures show a fairly constant Eg value of ~3.42 eV, however Eg tends to increase as the oxygen pressure is increased during the deposition (>10 mTorr). This is likely due to increased nickel vacancies as well as more Ni2O3. The presence of Ni2O3 is further demonstrated by the XRD analysis discussed below.

ACS Paragon Plus Environment

7

ACS Applied Materials & Interfaces 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 37 38 39 40 41 42 43 44 45 46 47 48 49 50 51 52 53 54 55 56 57 58 59 60

Page 8 of 22

The grazing incidence X-ray diffraction (GIXRD) patterns for films deposited at different oxygen pressures at room temperature are shown in Figure 2b. Films deposited at oxygen pressure