Saeid
Masudy-Panah
,
Roozbeh Siavash
Moakhar
,
Chin Sheng
Chua
,
Ajay
Kushwaha
,
Ten It
Wong
and
Goutam Kumar
Dalapati
*
Institute of Materials Research and Engineering, A*STAR (Agency for Science Technology and Research), 2 Fusionopolis Way, #08-03, Innovis, Singapore 138634, Singapore. E-mail: dalapatig@imre.a-star.edu.sg
First published on 16th March 2016
We designed a stable and efficient CuO based photocathode by tuning the crystallinity and surface morphology of films by rapid thermal treatment. The role of the annealing temperature on film crystallinity, optical absorption and grain size is studied. The impact of these parameters upon the photocatalytic water splitting performance of CuO films is investigated. We observed that a higher annealing temperature improves the film crystallinity and increases the grain size of CuO film, which significantly enhance the photocurrent generation capability. Rapid thermal annealing at 550 °C is found the best temperature to achieve the highest PEC performance. The thickness of the CuO photocathodes is also optimized and we observed that 550 nm thick films results in the highest photocurrent of 1.68 mA cm−2. Our optimized CuO photocathode has shown better stability against photo-corrosion and a 30% decrease in the initial value of photocurrent is measured after 15 min, while a 60% decrease in the photocurrent is noticed in case of the as-deposited film.
Copper oxide is most promising candidate for fabricating photocathode due to its abundance in earth crust, non-toxicity, simple growth process and high optical absorption in visible range.6,7 The two most common forms of copper oxide are known as cuprous oxide (Cu2O) and cupric oxide (CuO). Cu2O is a direct band-gap semiconductor with the band gap energy of 2.1–2.6 eV and is predicted to produce a maximum theoretical photocurrent of 14.7 mA cm−2 under AM 1.5G illumination.6,8 On the other hand, CuO, an indirect band gap material, has a lower band gap energy of 1.2–1.6 eV, which makes it more ideal for visible light harvesting and renewable energy applications. CuO is theoretically capable of generating a much higher photocurrent of 35 mA cm−2.9 Its conduction band edge is also appropriate to do hydrogen evolution.8,10 Despite these promising properties of CuO, there are scant reports available on using CuO as the active light-harvesting material for PEC water splitting application.8,11–18 Most reports on CuO are merely interested in using it as a co-catalyst material for hydrogen evolution or solar cell application.19–29
Various methods are available for the deposition of CuO thin film including electrochemical deposition, evaporation, sputtering, thermal oxidation and sputter deposition.30–35 Sputtering method has attracted special interest due to its simplicity and reproducibility of the film properties. The sputtering process also allows precise tuning of the film's microstructure and its thickness by adjusting of the sputtering conditions.36–41 The performance of the PEC water splitting can be limited by the light absorption capabilities of the photoelectrodes and recombination of the photogenerated electrons and holes. These parameters are strongly affected by the thickness, grain size and crystallinity of the deposited film. Thus, a systematic investigation is required to address these issues to design a stable and efficient photoelectrode to demonstrate its potential for real PEC water splitting application. In similar context, a series of CuO thin films with different thicknesses ranging from 200 to 700 nm is sputter-deposited on the FTO substrate. After that rapid thermal treatment is performed to tune the crystalline property and surface morphology of CuO film. Heat treatment significantly improve the crystallinity of the film and grain size become larger which is very beneficial to enhance the PEC water splitting performance. The separation and transportation of photo-generated charge carrier is become prominent in rapid thermal annealed films and also reduce the charge recombination leading to an increase in photocurrent value and stability of the photocathode. Our investigation suggest that careful selection of film growth parameters and post growth modification can make CuO an attractive candidate for efficient water splitting application, which is not considered in previous studies.
Structural quality and crystallinity of the sputter-deposited CuO films were studied by Bruker D-8 general area detector XRD system (GADDS) in θ–2θ scan using a CuKα (λ = 0.15418 nm) radiation, high-resolution transmission electron microscopy (HRTEM) analysis and Raman spectroscopy measurements (Witec Alpha 300R confocal Raman microscope equipped with a 532 nm Nd:YAG laser). Surface morphology of the films was investigated by atomic force microscopy (AFM) and scanning electron microscope (SEM). Chemical composition of the CuO thin films were examined by using VG ESCALAB 220i-XL XPS system.
The photoelectrochemical properties of as-sputtered and rapid thermal annealed CuO films were evaluated in 0.1 M Na2SO4 aqueous electrolyte solution with a pH of 5.84 at room temperature by linear sweep voltammetry (LSV) and chronoamperometry (CA). LSV curves were measured at the scan rate of 50 mV s−1. CA plots were obtained at the potential of 0.2 V vs. RHE. Electrochemical impedance spectroscopy (EIS) was performed at open circuit potential and 10 mV amplitude over the frequency range of 105 to 10−2 Hz. All electrochemical measurements were carried out by Autolab 302N potentiostat/galvanostat equipped with FRA32M using a 3-electrode configuration consisting of a Pt counter electrode, an Ag/AgCl reference electrode and sputter-deposited CuO on FTO coated glass as the working electrode. An active area of 1 cm2 was defined by partially covering the film with black tape. Electrode edges have been fully covered by epoxy resin. The electrodes were then immersed in a 0.1 M Na2SO4 aqueous electrolyte solution with a pH of 5.84. The desired potential of the electrodes was supplied by A Metrohm Autolab PGSTAT101 potentiostat. NOVA 1.10 software was interfaced with the potentiostat to record the data and to be used for EIS fitting. Oriel solar simulator equipped with an air mass 1.5 global (AM 1.5G) filter and a 150 W xenon arc lamp were used to measure the current under light and dark condition. The light intensity was calibrated with a Si photo-diode and maintained at 100 mW cm−2.
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Fig. 1 (a) XRD spectra of sputtered CuO films annealed at different temperature (300, 550 and 700 °C), (b) corresponding FWHM and (c) crystal size of the main XRD peaks of CuO (002) and CuO (111). |
Raman analysis is an effective method of evaluating the effects of annealing temperature on the structural disorder, defects in the host lattice and crystallinity of the film. The Raman spectra of AsD CuO film and films annealed at various temperatures such as 300, 550 and 700 °C are shown in Fig. 2a. The distinct peaks, observed at ∼287, 339 and 623 cm−1 are associated with CuO thin film.43,44 CuO tenorite has monoclinic symmetry with space group of C62h with two molecules per primitive cell. Zone center modes of CuO is Ag + 2Bg + 4Au + 5Bu. Only Ag + 2Bg modes are Raman active.45 The Raman peak at 287 cm−1 is assigned to the Ag modes and the Raman peaks at 339 and 623 cm−1 are assigned to the Bg mode. For the CuO nanocrystals the Raman intensity I(ω) is given by:46
![]() | (1) |
|C(k)|2 = exp(−k2d2/16π2) | (2) |
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Fig. 2 (a) Raman spectra CuO films annealed at different temperature (300, 550 and 700 °C) (b) FWHM plot calculated from Raman data of CuO films. |
The impact of the annealing temperature on the crystal quality of the CuO film is further observed from HR-TEM analysis. The HR-TEM image reveals clear and visible lattice fringes for CuO samples annealed at higher temperature (Fig. 3), indicating that the samples annealed at higher temperature have better atomic order and crystal quality. The crystal quality of the as-deposited film is affected by the mobility of ad-atoms along the grains. By increasing the annealing temperature, the ad-atoms become more mobile and migrates towards favorable sites in the crystal lattice, thus, resulting in an improvement in the crystallinity of the annealed samples at higher temperature.47 This improvement in crystal quality can result in the reduction of defect density and enhancement of carrier concentration of the CuO films annealed at higher temperatures.48 Based on the HR-TEM images shown in Fig. 3, the samples annealed at higher temperature of 500 and 700 °C are polycrystalline in nature with measured interplanar distances of ∼0.25 nm and 0.23 nm. This corresponds to the (002) and (111) planes of CuO, respectively.49,50
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Fig. 3 High resolution transmission electron microscopic images show lattice spacing of CuO films, (a) AsD film and (b–d) films annealed at 300, 550 and 700 °C. |
Distinct surface morphology is observed in scanning electron microscopic (SEM) images of AsD and rapid thermal annealed CuO films (Fig. 4). The AsD CuO films has very smooth surface formed with nano-sized crystallites which are not visible clearly. Annealing at 300 °C, induce some roughness on the film surface and beginning of the large crystallites are appeared in the SEM images, the dark part in the images seems as initial grain boundaries. Further increase in annealing temperature, increase the surface roughness and grain boundaries becomes clearly visible. The grain size is surprisingly increase and grain boundaries become very prominent when film is annealed at 700 °C (Fig. 4d). Thus, SEM analysis validates our XRD and Raman results and endorses that gain size increased and crystalline property improved after heat treatment. The effect of annealing temperature on surface morphology of the 200 nm CuO thin film is also characterized by tapping mode AFM, respective change in grain size and surface roughness is noticeably visible (Fig. 5). The surface roughness is measured to be 5 nm, 21 nm, 40 nm, and 55 nm for AsD, and annealed at 300, 550 and 700 °C films, respectively. It shows that higher annealing temperature renders more rough film. The high annealing temperature provides more energy, which facilitates the coalescence of the adjacent grains (or nuclei), resulting in the larger grain size and rougher surface.
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Fig. 5 Surface topography and roughness measurement using tapping mode AFM; (a) AsD CuO film and (b–d) CuO films rapid thermal treated at 300, 550 and 700 °C, respectively. |
Fig. 6 shows the PEC current–voltage characteristics of AsD and annealed (200 nm thick) CuO thin films, under the dark (“light off”) and under AM 1.5G illumination of 100 mW cm−2 (“light on”) condition. The following equation was then used to convert the measured potential to the reversible hydrogen electrode (RHE) scale:8
E(RHE) = E(Ag/AgCl) + 0.197 + 0.059pH | (3) |
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Fig. 6 Photoelectrochemical current–voltage measurements for AsD CuO photocathode (200 nm thick) and rapid thermal treated CuO photocathode (200 nm thick) at temperature 300, 550 and 700 °C. |
An amperometry analysis is performed at a fixed potential of 0 V vs. RHE as presented in Fig. 7. As shown at this figure increasing the annealing temperature up to 550 °C improves the photocurrent of the prepared samples, while further increase in the annealing temperature degrades the photocurrent of the prepared samples. The stability of the prepared sample also follows the same trend as that of photocurrent. The AsD sample could retain 40% of the initial photocurrent while the sample annealed at 550 °C could retain 65% of the initial current. By further increasing the annealing temperature to the 700 °C the stability of the sample degrades and it could retain only 45% of the initial photocurrent. The AsD film has minimum photocurrent and lowest stability due to poor crystalline quality. Separation of photo generated electron and its transportation from the CuO to the FTO as well as separation of photo generated holes towards electrolytes directly influence the photocurrent and its stability. Indeed, the improvement of crystallinity facilitates the generation and separation of large numbers of long-lived e−/h+ pairs in the CuO thin film that are then transported to their respective electrodes. This increases charge transfer significantly, which promotes the photocurrent and stability of PEC water splitting. Annealing increases the average grain size and hence the grains boundaries area over a given distance decreases. This results in a decrement of the trapped carriers in the grain boundary and reduction of grain boundary scattering which leads to a higher amount of free carriers and improved carrier diffusion length and ultimately results in the enhancement of carrier concentration and improvement of the photocurrent of the CuO film. Grain boundaries also act as photocorrosion centers51 and consequently influence the stability of the prepared samples. The enhanced photocurrent and improved stability in 550 °C treated films is mainly attributed to the reduction of e−/h+ pair recombination due to optimized crystallinity. By further increase in annealing temperature to 700 °C the reduction of photocurrent and its stability despite the enhancement of crystallinity and grain size of the prepared thin film, might be because of the degradation of conductivity of FTO coated substrate at very high annealing temperature of 700 °C.
The kinetics of interfacial charge transfer of the CuO electrodes are investigated using electrochemical impedance spectroscopy through Mott–Schottky (MS) plot. MS equation is described by:22
![]() | (4) |
The electrochemical impedance spectra (EIS) of AsD and annealed CuO thin films (300, 550 and 700 °C) under standard solar light illumination at a potential of 0 V vs. RHE were compared in Fig. 8b. The semicircle feature of Nyquist plot at high frequencies is attributed to the charge transfer process where the diameter of the semicircle is equal to the charge transfer resistance (Rct).22 It is clear from Nyquist plot that the Rct is significantly reduced with increasing annealing temperature. Rct of the prepared samples were tabulated in Table 1. The reduction of Rct is mainly attributed to the faster carrier transfer rate and better separation efficiency of photo induce charges, resulting from densification of the film due to increase in grain size of the samples annealed at higher temperatures. Since the densification of the samples reduces the recombination rate via efficient transport of charge carriers (e− and h+), it significantly enhances the migration of generated electrons and holes to the surface of the CuO and hence improves the Rct and promote the interfacial charge transport. These results indicate that the kinetics at the electrode–electrolyte interface is controlled by charge transfer resistance which is significantly influenced by crystal quality and grain size of the sputtered films.
AsD | 300 °C | 550 °C | 700 °C | |
---|---|---|---|---|
R ct (kΩ cm2) | 139.5 | 93.4 | 68.8 | 41.5 |
The enhancement of carrier concentration and reduction of Rct is mainly responsible for faster carrier transfer rate, due to improvement in crystallinity and densification of the film. Since the densification of the samples reduces the recombination rate via efficient transport of charge carriers (e− and h+), it significantly enhances the migration of generated electrons and holes to the surface of the CuO and hence improves the Rct. The enhancement of carrier concentration might also be ascribed to the fact that the trap probability of interstitial Cu is increased by increasing annealing temperature, resulting in efficient intrinsic doping.
Thickness of CuO layer significantly influences the light absorption and charge carrier transport properties. Therefore, it is also necessary to evaluate its influence on the performance of CuO based PEC water splitting. In Fig. 9 the PEC current–voltage and stability characteristics of the CuO thin film with thicknesses ranging from 200 to 700 nm were illustrated. When thickness of CuO is increased from 200 to 550 nm the value of photocurrent is also increased simultaneously. However, further increase in CuO thickness to 700 nm results in a degradation of the photocurrent. The initial enhancement of photocurrent is mainly attributed to improvement in light absorption capabilities of the thicker CuO film. However, carrier recombination also increases with the thickness of the film.52 Thus, the optimum thickness obtained is ∼550 nm which produces 1.68 mA cm−2 photocurrent at 0 V vs. RHE. The influence of CuO absorber layer on the stability of sputtered film is also demonstrated in Fig. 9b. Thicker CuO film results in a slightly more stable photocurrent. The 700 nm CuO film could retain 70% of its initial photocurrent which is slightly better than the 67% achieved by the 200 nm film.
Footnote |
† Electronic supplementary information (ESI) available. See DOI: 10.1039/c6ra03383k |
This journal is © The Royal Society of Chemistry 2016 |