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The Scientific World Journal
Volume 2013, Article ID 686497, 6 pages
http://dx.doi.org/10.1155/2013/686497
Research Article

LiNbO3 Coating on Concrete Surface: A New and Environmentally Friendly Route for Artificial Photosynthesis

1Sustainable Construction Materials and Building Systems (SUCOMBS) Research Group, Faculty of Engineering and Built Environment, Universiti Kebangsaan Malaysia, 43600 Bangi, Malaysia
2Department of Chemical & Process Engineering, Faculty of Engineering and Built Environment, Universiti Kebangsaan Malaysia, 43600 Bangi, Malaysia

Received 27 September 2013; Accepted 30 October 2013

Academic Editors: Y. Hara and Y. Kang

Copyright © 2013 Ranjit K. Nath et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Abstract

The addition of a photocatalyst to ordinary building materials such as concrete creates environmentally friendly materials by which air pollution or pollution of the surface can be diminished. The use of LiNbO3 photocatalyst in concrete material would be more beneficial since it can produce artificial photosynthesis in concrete. In these research photoassisted solid-gas phases reduction of carbon dioxide (artificial photosynthesis) was performed using a photocatalyst, LiNbO3, coated on concrete surface under illumination of UV-visible or sunlight and showed that LiNbO3 achieved high conversion of CO2 into products despite the low levels of band-gap light available. The high reaction efficiency of LiNbO3 is explained by its strong remnant polarization (70 µC/cm2), allowing a longer lifetime of photoinduced carriers as well as an alternative reaction pathway. Due to the ease of usage and good photocatalytic efficiency, the research work done showed its potential application in pollution prevention.

1. Introduction

In the last two centuries fossil fuels and the cheap energy have been provided for energy in the industrial development [1]. The excessive use of fossil fuels has produced CO2 in the earth’s atmosphere which is one of the responsible for greenhouse effect [2]. The effect of increasing atmospheric carbon dioxide is directly linked to global warming [3]. The reduction of CO2 by the process of artificial photosynthesis is believed to be one of the alternatives that emits oxygen using atmospheric CO2 and water in presence of photocatalyst [2].

Artificial photosynthesis was investigated by using a variety of approaches [4] like replication of the chemical reactions that take place in plants [5] and concerted efforts using ruthenium complexes and structures as an organic dye [6] to sensitize wide band-gap semiconductors in presence of visible light [7]. In this process a semiconductor is used as a photocatalyst that can absorb light and using this energy, it can chemically convert CO2 and water into formic acid and oxygen [8, 9]. In this work, we describe artificial photosynthesis taking place on photocatalyst LiNbO3 coated on concrete surface by producing formic acid and oxygen.

2. Approach to Artificial Photosynthesis

The goal of artificial photosynthesis is to mimic the green plants and other photosynthetic organisms that use sunlight to make valuable substances [10]. In natural photosynthesis, the first step is water splitting in which proton is generated and O2 is released using solar energy [11]. The second step is the Calvin cycle in which CO2 is reduced to hydrocarbons [4]. Schematic diagram is shown in Figure 1. This is a challenging goal because success requires integration of multiple chemical functions in stable chemical architecture.

686497.fig.001
Figure 1: Schematic diagram illustrating the photoelectrochemical reaction between CO2 and H2O to give HCOOH and O2 initiated by excitation and photoinjection in presence of photocatalyst.

2.1. Catalyst for CO2 Reduction

To perform artificial photosynthesis, the photocatalyst must be able to drive the reduction of CO2 and, ideally, the oxidation of water [12]. To achieve this, the reaction potentials must be inside the band edges of the photocatalyst [13]. Besides many tested semiconductors (ZnO, Fe2O3, CdS, ZnS, and TiO2), LiNbO3 can quickly reduce CO2 more than others [1416].

Figure 2 compares the potential of the valence and conduction bands of LiNbO3 and mostly used photocatalyst TiO2 in relation to the cell potential of the conversion of CO2 [17]. This figure shows that in TiO2 valence band holes can oxidize water and conduction band electrons cannot reduce CO2 to due to low energy than required Table 1. LiNbO3 drives the reaction of CO2 and water to formic acid, but the valence band holes do not oxidize water directly [8]. This is due to its valence band and conduction band energy level. The valence and conduction band energy of LiNbO3 are 0.48 v and −3.30 v. Conduction band electrons of LiNbO3 can reduce CO2 to due to high energy and valence band holes oxidize water by physisorbing due to its strong remnant polarization [8]. The reaction step of LiNbO3 allows a different reaction pathway because of its highly reducing conduction band electrons [7].

tab1
Table 1: Key reaction of artificial photosynthesis with redox potential [10].
686497.fig.002
Figure 2: Band positions of LiNbO3 and TiO2 versus SHE in relation to the redox reactions of artificial photosynthesis [7].
2.2. Water Oxidation Catalyst for Artificial Photosynthesis

Water oxidation is a more complex chemical reaction than proton reduction. In natural photosynthesis, the oxygen-evolving complex performs this reaction by accumulating reducing equivalents (electrons) in a manganese-calcium cluster within photosystem II (PS II) and then delivers them to water molecules [18], with the resulting production of molecular oxygen and protons:

Without a catalyst (natural or artificial), this reaction is very endothermic and it requires high temperatures (at least 2500 K) [19]. Many metal oxides have been found to have water oxidation catalytic activity [20, 21], especially those from relatively abundant transitional metals, but these metal oxides suffer from low turnover frequency and slow electron transfer properties, and their mechanism of action is hard to decipher and adjust [8].

Remnant polarization of LiNbO3 allows this process at different reaction pathway that leads to a charge occurring on the interface [22]. This charge interacts with species in contact with the surface, producing a tightly bound layer [2325] that changes the nature of bonding in physisorbed materials. In the case of water, LiNbO3 will physisorb a tight layer of molecules [26]. The valence band location of LiNbO3 (0.48 V versus SHE) is unable to oxidize water directly; the physisorbed water appears to prevent any further reactions on the surface of the catalyst [27]. In the gas-solid reaction, there is more CO2 available and bound on the surface of the LiNbO3 [8]. This bound CO2 reacts with photoexcited holes and electrons in the LiNbO3 and produces reactive species that react with H2O to form end products [10]. One such species is that reacts with water to produce formic acid and oxygen:

The physisorption of molecules on ferroelectric surfaces [27] affects the localization of electrons in the molecule and the bond angles. This condition allows for easier injection or removal of electrons than that in less chemically strained systems.

3. Materials and Methods

3.1. Materials

Ordinary portland cement, sand, and stone aggregate are used to prepare the concrete sample commercially available in Malaysia. In this research locally available coarse river sand and stone aggregate of 10 mm size were used. The specific gravity of sand and aggregate used in this research is 2.63 and 2.65, respectively. The LiNbO3 powder CAS 12031-63-9 and CO2 from Sigma-Aldrich were used as the photocatalyst in this study.

3.2. Sample Proportions

The concrete samples were fabricated in steel moulds with internal dimensions of . Cement, sand, and stone aggregate are mixed thoroughly with a mix ratio of 1 : 2 : 4 and water cement ratio of 0.5 and poured into the steel mould. Then the compaction was done by putting the steel moulds on a mechanical vibrating table. The surface of concrete was made smoothening with a glass plate. The concrete samples were removed from the moulds after 24 hours and putted into water for 28 days for proper curing. After curing, samples were allowed to dry in the air for a few hours. Dried sample was then coated with 0.75 mm LiNbO3 paste.

3.3. Equipment and Experimental Procedure

The central part of the experimental setup used is a reaction chamber allowing a sample of size to be fixed. All structural parts inside the box are to allow laminar flow of the gas along the sample surface and to make sure of the uniform distribution of CO2 gas. The reaction chamber was tested in experiments under reaction conditions before use and found to be air tight and nonreactive under prolonged UV irradiation. A fluorescent lamp of wavelengths 366 nm was used to supply photoirradiation to activate the photocatalyst. Two types of sensors were used to control the temperature and humidity. Figure 3 shows the illustration of the reaction chamber and the test setup for artificial photosynthesis. LiNbO3 coated concrete block is placed in the reaction chamber. A reservoir of 30 mL of distilled water was then added in a tray before filling it with CO2 gas to create a 30 : 70 mix with air. An irradiation was carried out using a UV lamp or by natural sunlight; after irradiation, the vessel was allowed to cool and samples were collected from the water reservoir for analysis.

686497.fig.003
Figure 3: LiNbO3 coated concrete slab in reaction chamber.

4. Results and Discussion

4.1. FT-IR Analyses

FT-IR analyses were carried out with Bio-Rad FTS-185 (Digilab) equipment using Attenuated Total Reflexion (ATR) unit. The spectra were usually recorded in the range of 4000–400 cm−1 with 2 cm−1 resolution, and 32 scans were collected each time.

Band assignments report available in literature are deducted from spectra performed in diffuse reflectance. In the present work, spectra acquisition is performed in ATR. A shift of about 3 wave number units is noted in spectra (Figure 4).

686497.fig.004
Figure 4: FT-IR spectra of water sample taken from reaction chamber after one day.

Nevertheless the band assignments are in close agreement with those previously reported [2830]. The FT-IR data for band assignments are presented in Table 2. The broad bands at 3401.2 cm−1, 3402.3 cm−1, and 3401.7 cm−1 are due to the stretching O–H bond from HCOOH. The asymmetric stretching bands at 1644.3 cm−1, 1645.2 cm−1, and 1644.8 cm−1 are due to C=O bond in HCOOH. The wide bands at 687.1 cm−1, 685.3 cm−1, and 680.7 cm−1 are due to C–O bond in HCOOH.

tab2
Table 2: FT-IR characterization of sample.
4.2. HPLC Analyses

The HPLC of sample was performed on ZORBAX ECLIPS C18, 150 mm 4.6 mm, 5 μ with a flow rate 0.6 mL/min keeping column temperature at 40°C.

The mobile phase consisted of 20 mM H2SO4 in acetonitrile and detection of formic acid was performed by injecting 20 μL of sample solution into a UV detector of wavelength 220 nm. The retention time () of main peak was 2.6 min under these conditions [31]. The main peak of standard formic acid solution appears at the retention time () 2.69 min. For comparison with the standard solution, spectrum of sample solution was taken at the same conditions. Each spectrum (Figure 5) gives the peak at the same retention time that indicates the presence of HCOOH.

686497.fig.005
Figure 5: HPLC of sample taken from reaction chamber.
4.3. SEM Observations

Figures 6(a) and 6(b) illustrated the scanning electron microscope (SEM) photomicrograph of the LiNbO3 before photocatalytic reaction on the specimen’s surface. The morphology of the particles is round and systematic structure particles. This is due to the carbonation of concrete that enhances the possibility of artificial photosynthesis. On the other hand microstructure of LiNbO3 particles is changed after the photocatalytic reaction. The SEM photomicrograph of the LiNbO3 after photocatalytic reaction on the specimen’s surface is shown in Figures 6(c) and 6(d). Larger and darker agglomerates were appeared the microstructure of LiNbO3. A net decrease in porosity is also observed: pores are progressively filled due to the carbonation of concrete material that increases the contact of CO2 with photocatalyst.

fig6
Figure 6: (a) SEM photomicrograph of the LiNbO3 before photocatalytic reaction on the specimen’s surface. (b) SEM photomicrograph of the LiNbO3 before photocatalytic reaction on the specimen’s surface. (c) SEM photomicrograph of the LiNbO3 after photocatalytic reaction on the specimen’s surface. (d) SEM photomicrograph of the LiNbO3 after photocatalytic reaction on the specimen’s surface.
4.4. EDX Analyses

Chemical composition change was expected from energy-dispersive X-ray (EDX) analysis. Figure 7 represents EDX analysis performed before and after photocatalytic reaction on specimens surface. Twenty punctual analyses are performed for each area. Expected change of chemical composition is observed. Figure shows that there is an increase in the amount of oxygen after photocatalytic reaction.

686497.fig.007
Figure 7: EDX analysis performed before and after photocatalytic reaction on specimens surface.

The amounts of O and NbL are 27.51 and 73.49% by weight before photocatalytic reaction and the amounts of O and NbL, are 32.55 and 73.24% by weight after photocatalytic reaction which indicates the occurrence of artificial photosynthesis on specimens’ surface.

5. Conclusions

This paper focuses on the application of LiNbO3 as photocatalytic material in concrete blocks. The addition of LiNbO3 in building materials adds an additional property to the concrete by creating artificial photosynthesis, which is the best way to convert CO2 into O2 and HCOOH and simultaneously reduce global CO2 level. This work demonstrates the impact of the photocatalytic reactions and shows LiNbO3 to be an exciting new material for use as a photocatalyst in construction.

Acknowledgments

The work is financed by Zamalah/Institutional Scholarship provided from the Universiti Kebangsaan Malaysia and the Ministry of Higher Education of Malaysia. The first author expresses honest appreciation to Chittagong University of Engineering & Technology (CUET), Chittagong, Bangladesh, for providing leave for this research.

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