Heterostructure Cu 2 O / ( 001 ) TiO 2 Effected on Photocatalytic Degradation of Ammonia of Livestock Houses

In this paper, a heterogeneous composite catalyst Cu2O/(001)TiO2 was prepared by the impregnation-reduction method. The crystal form, highly active facet content, morphology, optical properties, and the photogenerated electron-hole recombination rate of the as-prepared catalysts were investigated. The performance of Cu2O/(001)TiO2 was appraised by photocatalytic degradation of ammonia under sunlight and was compared with lone P25, Cu2O, and (001)TiO2 at the same reaction conditions. The results showed that 80% of the ammonia concentration (120 ± 3 ppm) was removed by Cu2O/(001)TiO2, which was a higher degradation rate than that of pure P25 (12%), Cu2O (12%), and (001)TiO2 (15%) during 120 min of reaction time. The reason may be due to the compound’s (Cu2O/(001)TiO2) highly active (001) facets content that increased by 8.2% and the band gap width decreasing by 1.02 eV. It was also found that the air flow impacts the photocatalytic degradation of ammonia. Therefore, learning how to maintain the degradation effect of Cu2O/(001)TiO2 with ammonia will be important in future practical applications.


Introduction
Ammonia is an important precursor of fine particulate matter PM2.5 in the atmosphere and promotes the formation of haze.China has been the one of largest ammonia emitters in the world [1].An investigation of the NH 3 emission sources and contribution rate in 2006 shows that the total ammonia emissions of China are 980 t/a, more than 96% and 45% of Europe and the USA, respectively, and contributes to global and Asian emissions by approximately 15% and 35%, respectively; of which, livestock manure accounts for approximately 54% of the total emissions [2].In terms of the global ammonia emissions, animal husbandry is clearly the major contributor for ammonia pollution, as it accounts for 70.9% of the total [3].The ammonia from animal husbandry may not only cause global climate change, but can also bring disease in animals and humans, such as paralysis centralis, endobronchitis, and others [4].Therefore, strengthening the control of ammonia pollution of animal husbandry has become an important task for agricultural, non-point source pollution treatment in China.
In the past, livestock farms adopted traditional physical methods of adsorption and ventilation to eliminate the ammonia generated in livestock and poultry houses [5].Although these methods can decrease the release concentration of ammonia over time, they cannot reduce the total amount of ammonia emissions and may aggravate the secondary ammonia pollution of the environment.With more exacting livestock air quality requirements from public authorities, some large-scale livestock farms have tried to erect biological exhaust air cleaning facilities to reduce ammonia, dust, and odor emissions, so that they can get a license to build livestock houses close to small towns or near farming households.Biological filters can clean NH 3 emissions effectively, but limitations still exist, such as unstable operation and high replacement costs [6]; the end result is that most livestock farm ammonia emissions are not eliminated at all.Therefore, it is very important to develop a stable and efficient degradation material to deal with the air pollution from livestock farms.
As an ideal semiconductor photocatalytic material, titanium dioxide was discovered to be able to photodissociate water under ultraviolet irradiation by Fujishima in 1972 [7].Since then, it has become a promising photocatalyst because of its good chemical stability, safety, non-toxicity, strong redox ability, and so on, and has been widely used in environmental control [8][9][10][11][12], exploitation of energy resources [13,14], bioengineering [15], self-cleaning material [16], anti-microbial [17], sensor [18], and other fields.In recent years, TiO 2 was used as pigment coating to reduce ammonia emissions under ultraviolet light [19,20], with a 90% conversion efficiency of 200 ppm NH 3 converted into N 2 at high temperature (673 K) [21].In the reaction process, the degradation product of NH 3 is mainly N 2 , with N 2 O, NO 2 − , and NO 3 − by-products [22,23].However, TiO 2 can only respond to high energy ultraviolet light due to its wide band gap (3.2 eV) [24], which makes the utilization ratio of TiO 2 very low under sunlight with low ultraviolet content in the solar spectrum [25].Meanwhile, the high photogenerated electron-hole recombination rate of TiO 2 leads to its catalytic activity [26].All of these considerations contribute to serious obstacles to TiO 2 application in practice.To overcome these shortcomings, much research has been attempted to improve the performance of TiO 2 by adjusting the exposure ratio of its highly active surface or combining the material with other semiconductors.Adjusting the (001) facets ratio of TiO 2 (anatase) has been reported to be a efficiency way to improve the photocatalytic efficiency (Keyue Wu, [27]), but most of the available anatase crystals are primary composed of thermodynamic stable (101) surfaces [28], whose surface energy (0.44 J/m 2 ) is much smaller than the (001) surface (0.90 J/m 2 ) [29].Another helpful way to facilitate charge separation and improve degradation performance is coupling with other semiconductors (C 3 N 4 [30], PbS [31], WO 3 [32], Cu 2 O [33], CdS [34], and others) with small band gaps; this can not only enhance the spectral response, but also transfer photogenerated electrons from one reporter to another.Among these semiconductors with small band gaps, the oxides of copper (Cu x O) are fascinating materials due to their remarkable optical, electrical, thermal, and magnetic properties [35], among the Cu x O, Cu 2 O has the advantages of simple preparation processes, low raw material price, environmental friendliness, and a good response in the visible range.Compared with other transition metal oxides, Cu 2 O is a promising green catalyst for environmental protection.As a p-type direct semiconductor [36], Cu 2 O can be coupled with n-type semiconductor TiO 2 into a heterostructure.This heterostructure displays much better performance than the single material and is widely used for decomposing water [37], solar cells [38], and degrading pollutants [39].At the same time, some interesting materials also need our attention.Syed et al. [40] synthesized α-Ga 2 O 3 by a sonication-assisted method, which has excellent photocatalytic activity is observed under solar light irradiation with an energy bandgap reduction, due to the presence of trap states, which are located at about 1.65 eV under the conduction band minimum.Datta et al. [41] synthesized 2D α-MoO 3−x nanosheets structural with defects and oxygen vacancies in the planar construction of molybdenum oxide nanosheets significantly increase the active sites of the catalyst, which act as key factors to promote the hydrogen evolution reaction (HER) performance.
In this paper, a heterogeneous composite catalyst Cu 2 O/(001)TiO 2 was prepared by the impregnation-reduction method and was used to degrade ammonia in a livestock house under sunlight for the first time, so as to realize the efficient utilization of solar energy and offer an efficient degradation material for the field of animal husbandry.

Morphology Analysis of Carrier (Polyester Fiber)
Figure 1 is a scanning electron microscope (SEM) view of the carrier (polyester fiber).It can be seen from the diagram that the carrier is folded by a lot of filaments into an interlaced three-dimensional structure, which can provide a large number of adhesion points to the catalysts.

Morphology Analysis of Carrier (Polyester Fiber)
Figure 1 is a scanning electron microscope (SEM) view of the carrier (polyester fiber).It can be seen from the diagram that the carrier is folded by a lot of filaments into an interlaced threedimensional structure, which can provide a large number of adhesion points to the catalysts.From Figure 2b, it can be seen that there was no S element in the Cu2O/(001)TiO2 composite, which indicated that the reaction was sufficient and CuSO4 was not contained in the product.In summary, the prepared composite catalyst Cu2O/(001)TiO2 contains CuO and may also contain Cu.

Crystal Facet Analysis of Catalysts
Figure 3a contains spacings of d = 0.352 nm and d = 0.235 nm, corresponding to the (101) and (001) facets of TiO2, respectively [44].This shows that the prepared TiO2 has the high activity (001) facets.The Figure 3b shows d = 0.235 nm and d = 0.245 nm spacings, corresponding to the (001) facets of TiO2 and the (111) surface of Cu2O, respectively [45], which shows that the prepared composite catalyst contains the high activity (001) facets.

Raman Analysis of Catalysts
It can be seen in Figure 4.The peak at 144 cm −1 was marked as Eg and 514 cm −1 was marked as A1g.The ratio of peak strength at A1g to peak strength at Eg is the (001) exposure ratio of crystal facets.The calculated (001) facet content of prepared TiO2 is I(101)/I(004) = 29% [46], which is significantly lower than that of the compounded, calculated to be I(101)/I(004) = 37%.The reasons for this may be as follows:   101) and (001) facets of TiO 2 , respectively [44].This shows that the prepared TiO 2 has the high activity (001) facets.The Figure 3b shows d = 0.235 nm and d = 0.245 nm spacings, corresponding to the (001) facets of TiO 2 and the (111) surface of Cu 2 O, respectively [45], which shows that the prepared composite catalyst contains the high activity (001) facets.

Crystal Facet Analysis of Catalysts
Figure 3a contains spacings of d = 0.352 nm and d = 0.235 nm, corresponding to the (101) and (001) facets of TiO2, respectively [44].This shows that the prepared TiO2 has the high activity (001) facets.The Figure 3b shows d = 0.235 nm and d = 0.245 nm spacings, corresponding to the (001) facets of TiO2 and the (111) surface of Cu2O, respectively [45], which shows that the prepared composite catalyst contains the high activity (001) facets.

Raman Analysis of Catalysts
It can be seen in Figure 4.The peak at 144 cm −1 was marked as Eg and 514 cm −1 was marked as A1g.The ratio of peak strength at A1g to peak strength at Eg is the (001) exposure ratio of crystal facets.The calculated (001) facet content of prepared TiO2 is I(101)/I(004) = 29% [46], which is significantly lower than that of the compounded, calculated to be I(101)/I(004) = 37%.The reasons for this may be as follows:

Raman Analysis of Catalysts
It can be seen in Figure 4.The peak at 144 cm −1 was marked as Eg and 514 cm −1 was marked as A1g.The ratio of peak strength at A1g to peak strength at Eg is the (001) exposure ratio of crystal facets.The calculated (001) facet content of prepared TiO 2 is I(101)/I(004) = 29% [46], which is significantly lower than that of the compounded, calculated to be I(101)/I(004) = 37%.The reasons for this may be as follows: In the experiment, the amounts of CuSO 4 and NaOH were 4.99 g and 4 g, respectively.Through the calculation of Reaction (1), it was found that the amount of NaOH is excessive.Assuming that all excessive sodium hydroxide existed in the whole system, the concentration range is about 0.197-0.317mol/L.In the process of adding glucose drop by drop, the concentration of NaOH was also decreasing gradually.It was found that NaOH and (001)TiO 2 not only increased the content of (001) facets, but also changed the morphology of the catalysts, which was consistent with the results of Hou et al. [47].
Catalysts 2019, 9, x FOR PEER REVIEW 5 of 18 CuSO + 2NaOH = Cu(OH) + Na SO ↓ (1) In the experiment, the amounts of CuSO4 and NaOH were 4.99 g and 4 g, respectively.Through the calculation of Reaction (1), it was found that the amount of NaOH is excessive.Assuming that all excessive sodium hydroxide existed in the whole system, the concentration range is about 0.197-0.317mol/L.In the process of adding glucose drop by drop, the concentration of NaOH was also decreasing gradually.It was found that NaOH and (001)TiO2 not only increased the content of (001) facets, but also changed the morphology of the catalysts, which was consistent with the results of Hou et al. [47].

Catalyst Morphology Analysis
Figure 5 shows the SEM morphology images of the catalysts.From Figure 5a, it can be seen that the prepared Cu2O crystals have no obvious agglomeration phenomenon and the size is basically uniform.Figure 5b reveals a smooth, spherical surface; Figure 5c displays a slight agglomeration of (001)TiO2, which forms an irregular spherical shape by extrusion.Figure 5d exhibits a flat sphere with concave and convex surfaces; Figure 5e,f shows that the prepared Cu2O/(001)TiO2 has uniform dispersion and different sizes; the composite (001)TiO2 was no longer a crushed sphere with a rough surface, but a crushed sphere.This is due to the influence of residual sodium hydroxide.Raman analysis in this experiment showed that excess sodium hydroxide was present, which indicates that the conjecture is correct.The composite Cu2O was no longer globular, but flaky.This may be due to the influence of (001)TiO2 on the Cu +1 crystal nucleus adhering to the (001)TiO2 surface during in situ growth, which cannot grow in the same way as before.This resulted in the growth of new pancakelike catalysts; the new morphology can provide a better place for the separation of photogenerated carriers.

Catalyst Morphology Analysis
Figure 5 shows the SEM morphology images of the catalysts.From Figure 5a, it can be seen that the prepared Cu 2 O crystals have no obvious agglomeration phenomenon and the size is basically uniform.Figure 5b reveals a smooth, spherical surface; Figure 5c displays a slight agglomeration of (001)TiO 2 , which forms an irregular spherical shape by extrusion.Figure 5d exhibits a flat sphere with concave and convex surfaces; Figure 5e,f shows that the prepared Cu 2 O/(001)TiO 2 has uniform dispersion and different sizes; the composite (001)TiO 2 was no longer a crushed sphere with a rough surface, but a crushed sphere.This is due to the influence of residual sodium hydroxide.Raman analysis in this experiment showed that excess sodium hydroxide was present, which indicates that the conjecture is correct.The composite Cu 2 O was no longer globular, but flaky.This may be due to the influence of (001)TiO 2 on the Cu +1 crystal nucleus adhering to the (001)TiO 2 surface during in situ growth, which cannot grow in the same way as before.This resulted in the growth of new pancake-like catalysts; the new morphology can provide a better place for the separation of photogenerated carriers.

Optical Characterization and Band Gap Energy
Figure 6a showed the UV-Vis absorption spectra of the catalysts.We found that the absorption of (001)TiO2 is slightly stronger than that of Cu2O/(001)TiO2 in the range of 200-328 nm, while in the range of 328-800 nm, the absorption enhancement of the composite catalyst Cu2O/(001)TiO2 is much stronger than that of the (001)TiO2, which indicated that Cu2O/(001)TiO2 has strong light absorption ability mainly in the visible range.The Diffuse Reflectance Spectra (DRS) of the catalysts were measured and shown in Figure 6b, which is useful to study the optical properties of the materials and the band gap.From the DRS spectra is possible the determination of Eg by applying the Kubelka-Munk method using the following equations (Equations ( 3) and ( 4)) [48]: where, F is the Kubelka-Munk function, R is the reflectance, hv is the photon energy, and Eg is the band gap.By plotting (hvF) 1/2 for indirect allowed transitions versus hv, the Eg of the semiconductor samples can be obtained.The energy bang gap of the different samples can be calculated by the linear fit of the curve reported in the Figure 6c and the Eg values are determined by the intercept in the xaxis.Reported in Table 1 are the band gap energy values of the different samples calculated with the Kubelka-Munk method.

Optical Characterization and Band Gap Energy
Figure 6a showed the UV-Vis absorption spectra of the catalysts.We found that the absorption of (001)TiO 2 is slightly stronger than that of Cu 2 O/(001)TiO 2 in the range of 200-328 nm, while in the range of 328-800 nm, the absorption enhancement of the composite catalyst Cu 2 O/(001)TiO 2 is much stronger than that of the (001)TiO 2 , which indicated that Cu 2 O/(001)TiO 2 has strong light absorption ability mainly in the visible range.The Diffuse Reflectance Spectra (DRS) of the catalysts were measured and shown in Figure 6b, which is useful to study the optical properties of the materials and the band gap.From the DRS spectra is possible the determination of Eg by applying the Kubelka-Munk method using the following equations (Equations ( 3) and ( 4)) [48]: where, F is the Kubelka-Munk function, R is the reflectance, hv is the photon energy, and Eg is the band gap.By plotting (hvF) 1/2 for indirect allowed transitions versus hv, the Eg of the semiconductor samples can be obtained.The energy bang gap of the different samples can be calculated by the linear fit of the curve reported in the Figure 6c and the Eg values are determined by the intercept in the x-axis.Reported in Table 1 are the band gap energy values of the different samples calculated with the Kubelka-Munk method.The band gaps of Cu2O, (001)TiO2, and Cu2O/(001)TiO2 are 2.12, 2.68, and 3.14 eV, respectively, which indicates that the composite Cu2O/(001)TiO2 is more easily excited than the single (001)TiO2, which enhanced its activity.

XPS Analysis of Catalyst
The elements and valence states of Cu 2 O/(001)TiO 2 were analyzed by XPS, as shown in Figure 7a.A survey spectra of Cu 2 O/(001) TiO 2 is seen, which contains information on C 1s, Ti 2p, O 1s, F 1s, and Cu 2p. Figure 7b showed that the binding energies for Ti 2p 3/2 and Ti 2p 1/2 are 458.90 and 464.59 eV, respectively, because Ti existed in the structure as Ti 4+ [49,50], which was favorable for charge transfer between TiO 2 and Cu 2 O. Figure 7c showed two characteristic peaks of O 1S in Cu 2 O/(001)TiO 2 , lattice oxygen of catalysts at 530.11 eV, and water molecules adsorbed on the catalyst surface at 532.64 eV [51,52].Figure 7d showed peaks near 932.90 and 952.77eV, which are characteristic of Cu +1 [53,54].

Fluorescent Analysis of Catalysts
Fluorescence spectra were used to characterize the photogenerated electron-hole combination of the photocatalysts.The higher the photogenerated electron-hole binding law, the stronger the fluorescence intensity [55].It can be seen from Figure 8 that the photogenerated electrons and photogenerated holes of (001)TiO2 were greatly reduced after the introduction of Cu2O composite, which significantly improved the degradation efficiency of the catalyst during the degradation process [56].

Fluorescent Analysis of Catalysts
Fluorescence spectra were used to characterize the photogenerated electron-hole combination of the photocatalysts.The higher the photogenerated electron-hole binding law, the stronger the fluorescence intensity [55].It can be seen from Figure 8 that the photogenerated electrons and photogenerated holes of (001)TiO 2 were greatly reduced after the introduction of Cu 2 O composite, which significantly improved the degradation efficiency of the catalyst during the degradation process [56].

Fluorescent Analysis of Catalysts
Fluorescence spectra were used to characterize the photogenerated electron-hole combination of the photocatalysts.The higher the photogenerated electron-hole binding law, the stronger the fluorescence intensity [55].It can be seen from Figure 8 that the photogenerated electrons and photogenerated holes of (001)TiO2 were greatly reduced after the introduction of Cu2O composite, which significantly improved the degradation efficiency of the catalyst during the degradation process [56].We will explore the reasons for the improvement of photocatalytic performance by discussing the compound material mechanism.The conduction band position of semiconductor can be calculated by empirical formula [57]: where, E CB is the conduction band energy of semiconductors, χ is the geometric average of the absolute electronegativity of atoms in semiconductors, Ec is a constant relative to the standard hydrogen electrode (4.5 eV), Eg is the band gap width of semiconductors, and E VB is the valence band energy of semiconductors.The values of (001)TiO 2 and Cu 2 O are about 5.86 and 5.33 eV, respectively.The Eg values of (001)TiO 2 and Cu 2 O were 3.14 and 2.12 eV, the E CB values of (001)TiO 2 and Cu 2 O were −0.21 and −0.23 eV, and the E VB values were 2.93 and 1 eV, respectively, as shown in Figure 9a.Therefore, the electron transfer took place from the p-type semiconductor Cu 2 O onto the surface of n-type semiconductor (001)TiO 2 , which is helpful for the separation of light carriers and the catalytic performance of the composite catalyst, since E F of Cu 2 O and (001)TiO 2 have differences in energy before and after catalyst contact.When p-type semiconductor contacts with n-type semiconductor, since the carriers type and concentration are different on both sides of the contact surface, the holes in the p-region are diffused toward the n-region, and the electrons in the n-region are also diffused into the p-region.This results in a decrease in the hole concentration on the side of the p-region near the interface, and a decrease in the electron concentration on the side of the n-region near the interface, so that there are almost no carriers that can move at the interface.Therefore, a positive space charge is generated in the n-region, and a negative space charge is generated in the p-region.These space charges form a self-built electric field near the interface, and the electric field direction points from the n-region to the p-region.Under the action of this electric field, under the action of this electric field, the carrier will drift and its direction is exactly opposite to the diffusion flow.The self-built electric field makes part of the holes entered the n-region return to the p-region, part of the electrons entered the p-region return to the n-region, and finally the diffusion flow and the drift flow reach an equilibrium state, and generally there is no macroscopic flow of carriers, as shown in Figure 9c.If there have no external electric field on either side of the p-n junction, then the entire system Fermi level should be the same.However, the existence of the space charge region will cause a self-built electric field in the vicinity of the interface, so that there is a potential difference near the p-n junction region, which eventually causes the energy band to bend, as shown in Figure 9b [58].

Compound Mechanism of Cu2O/(001)TiO2
We will explore the reasons for the improvement of photocatalytic performance by discussing the compound material mechanism.The conduction band position of semiconductor can be calculated by empirical formula [57]: where, ECB is the conduction band energy of semiconductors, χ is the geometric average of the absolute electronegativity of atoms in semiconductors, Ec is a constant relative to the standard hydrogen electrode (4.5 eV), Eg is the band gap width of semiconductors, and EVB is the valence band energy of semiconductors.The χ values of (001)TiO2 and Cu2O are about 5.86 and 5.33 eV, respectively.
The Eg values of (001)TiO2 and Cu2O were 3.14 and 2.12 eV, the ECB values of (001)TiO2 and Cu2O were −0.21 and −0.23 eV, and the EVB values were 2.93 and 1 eV, respectively, as shown in Figure 9a.Therefore, the electron transfer took place from the p-type semiconductor Cu2O onto the surface of n-type semiconductor (001)TiO2, which is helpful for the separation of light carriers and the catalytic performance of the composite catalyst, since EF of Cu2O and (001)TiO2 have differences in energy before and after catalyst contact.When p-type semiconductor contacts with n-type semiconductor, since the carriers type and concentration are different on both sides of the contact surface, the holes in the p-region are diffused toward the n-region, and the electrons in the n-region are also diffused into the p-region.This results in a decrease in the hole concentration on the side of the p-region near the interface, and a decrease in the electron concentration on the side of the n-region near the interface, so that there are almost no carriers that can move at the interface.Therefore, a positive space charge is generated in the n-region, and a negative space charge is generated in the p-region.These space charges form a self-built electric field near the interface, and the electric field direction points from the n-region to the p-region.Under the action of this electric field, under the action of this electric field, the carrier will drift and its direction is exactly opposite to the diffusion flow.The self-built electric field makes part of the holes entered the n-region return to the p-region, part of the electrons entered the p-region return to the n-region, and finally the diffusion flow and the drift flow reach an equilibrium state, and generally there is no macroscopic flow of carriers, as shown in Figure 9c.If there have no external electric field on either side of the p-n junction, then the entire system Fermi level should be the same.However, the existence of the space charge region will cause a self-built electric field in the vicinity of the interface, so that there is a potential difference near the p-n junction region, which eventually causes the energy band to bend, as shown in Figure 9b [58].

Controlled Test of Catalyst Carrier (Polyester Fiber Carrier)
The control experiment was conducted on the blank polyester fiber carrier (PET) that was not loaded with any photocatalyst; the absorptive photocatalytic efficiency of the blank PET on ammonia was measured in the presence or absence of light (Figure 10) within 120 min.Under the conditions of both dark and light, the degradation efficiency of the PET carrier on ammonia were 8% ± 1% respectively and the efficiency is not obviously improved, which means that the carrier of the PET itself hardly occurs photolysis.At the same time, the degradation rate of light is slightly lower than that of no light.It is possible that the temperature produced by light affects the stability of the gas.

Degradation of Ammonia by Different Catalysts
As can be seen from Figure 11, the degradation rates of ammonia by single p25, Cu2O, and (001)TiO2 continued to decline in the first 30 min until about 15% ± 2%.This may be due to the fact that the sunlight itself is not pure ultraviolet light, so that the number of active sites can be activated  The control experiment was conducted on the blank polyester fiber carrier (PET) that was not loaded with any photocatalyst; the absorptive photocatalytic efficiency of the blank PET on ammonia was measured in the presence or absence of light (Figure 10) within 120 min.Under the conditions of both dark and light, the degradation efficiency of the PET carrier on ammonia were 8% ± 1% respectively and the efficiency is not obviously improved, which means that the carrier of the PET itself hardly occurs photolysis.At the same time, the degradation rate of light is slightly lower than that of no light.It is possible that the temperature produced by light affects the stability of the gas.

Controlled Test of Catalyst Carrier (Polyester Fiber Carrier)
The control experiment was conducted on the blank polyester fiber carrier (PET) that was not loaded with any photocatalyst; the absorptive photocatalytic efficiency of the blank PET on ammonia was measured in the presence or absence of light (Figure 10) within 120 min.Under the conditions of both dark and light, the degradation efficiency of the PET carrier on ammonia were 8% ± 1% respectively and the efficiency is not obviously improved, which means that the carrier of the PET itself hardly occurs photolysis.At the same time, the degradation rate of light is slightly lower than that of no light.It is possible that the temperature produced by light affects the stability of the gas.

Degradation of Ammonia by Different Catalysts
As can be seen from Figure 11, the degradation rates of ammonia by single p25, Cu2O, and (001)TiO2 continued to decline in the first 30 min until about 15% ± 2%.This may be due to the fact that the sunlight itself is not pure ultraviolet light, so that the number of active sites can be activated

Degradation of Ammonia by Different Catalysts
As can be seen from Figure 11, the degradation rates of ammonia by single P25, Cu 2 O, and (001)TiO 2 continued to decline in the first 30 min until about 15% ± 2%.This may be due to the fact that the sunlight itself is not pure ultraviolet light, so that the number of active sites can be activated may be relatively less.This means that many ammonia molecules were brought to the tail gas treatment area without contact with the catalyst.The degradation rate of ammonia by the composite catalyst Cu 2 O/(001)TiO 2 maintained above 80% in the first 90 min, but decreased significantly in 90-120 min.This may be due to photocorrosion.Overall, the degradation effect of the composite catalyst was better than that of the single catalysts P25, Cu 2 O, and (001)TiO 2 .
Catalysts 2019, 9, x FOR PEER REVIEW 11 of 18 may be relatively less.This means that many ammonia molecules were brought to the tail gas treatment area without contact with the catalyst.The degradation rate of ammonia by the composite catalyst Cu2O/(001)TiO2 maintained above 80% in the first 90 min, but decreased significantly in 90-120 min.This may be due to photocorrosion.Overall, the degradation effect of the composite catalyst was better than that of the single catalysts P25, Cu2O, and (001)TiO2.

Degradation of Ammonia by Air Flow Rate
In the process of photocatalytic reaction of ammonia, the final reaction is carried out on the surface of photocatalyst, which generally undergoes the following continuous processes: ammonia diffuses to the surface of photocatalytic material; ammonia diffuses from the outer surface to the inner surface of the catalyst; ammonia molecules are adsorbed on the catalyst material; the adsorbed ammonia undergoes photocatalytic reaction; the products produced after photocatalytic reaction are desorbed from the surface of the catalyst; the products diffuse from the surface of the material to the outside surface; and the products desorb from the outside surface of the material to the air.
As can be seen from Figure 12, the air flow rate was varied between 0.5 min/L, 1 min/L, and 2 min/L.In this experiment, when other initial conditions were the same and the gas flow rate was gradually increased, the probability of ammonia adsorbed by the material decreases in unit time, the residence time on the catalyst surface was shortened, only NH3 adsorbed on the catalyst surface can be degraded, so the photocatalytic reaction was insufficient, and ultimately the degradation efficiency is reduced.Therefore, in the photocatalytic degradation of ammonia, it is very important to control the appropriate air flow rate.

Degradation of Ammonia by Air Flow Rate
In the process of photocatalytic reaction of ammonia, the final reaction is carried out on the surface of photocatalyst, which generally undergoes the following continuous processes: ammonia diffuses to the surface of photocatalytic material; ammonia diffuses from the outer surface to the inner surface of the catalyst; ammonia molecules are adsorbed on the catalyst material; the adsorbed ammonia undergoes photocatalytic reaction; the products produced after photocatalytic reaction are desorbed from the surface of the catalyst; the products diffuse from the surface of the material to the outside surface; and the products desorb from the outside surface of the material to the air.
As can be seen from Figure 12, the air flow rate was varied between 0.5 min/L, 1 min/L, and 2 min/L.In this experiment, when other initial conditions were the same and the gas flow rate was gradually increased, the probability of ammonia adsorbed by the material decreases in unit time, the residence time on the catalyst surface was shortened, only NH 3 adsorbed on the catalyst surface can be degraded, so the photocatalytic reaction was insufficient, and ultimately the degradation efficiency is reduced.Therefore, in the photocatalytic degradation of ammonia, it is very important to control the appropriate air flow rate.
Catalysts 2019, 9, x FOR PEER REVIEW 11 of 18 may be relatively less.This means that many ammonia molecules were brought to the tail gas treatment area without contact with the catalyst.The degradation rate of ammonia by the composite catalyst Cu2O/(001)TiO2 maintained above 80% in the first 90 min, but decreased significantly in 90-120 min.This may be due to photocorrosion.Overall, the degradation effect of the composite catalyst was better than that of the single catalysts P25, Cu2O, and (001)TiO2.

Degradation of Ammonia by Air Flow Rate
In the process of photocatalytic reaction of ammonia, the final reaction is carried out on the surface of photocatalyst, which generally undergoes the following continuous processes: ammonia diffuses to the surface of photocatalytic material; ammonia diffuses from the outer surface to the inner surface of the catalyst; ammonia molecules are adsorbed on the catalyst material; the adsorbed ammonia undergoes photocatalytic reaction; the products produced after photocatalytic reaction are desorbed from the surface of the catalyst; the products diffuse from the surface of the material to the outside surface; and the products desorb from the outside surface of the material to the air.
As can be seen from Figure 12, the air flow rate was varied between 0.5 min/L, 1 min/L, and 2 min/L.In this experiment, when other initial conditions were the same and the gas flow rate was gradually increased, the probability of ammonia adsorbed by the material decreases in unit time, the residence time on the catalyst surface was shortened, only NH3 adsorbed on the catalyst surface can be degraded, so the photocatalytic reaction was insufficient, and ultimately the degradation efficiency is reduced.Therefore, in the photocatalytic degradation of ammonia, it is very important to control the appropriate air flow rate.

Catalyst Reutilization Performance
As can be seen from Figure 13, the degradation rate of ammonia can be maintained at about 60% after three times of use, but the degradation effect will become worse as the number of times of use increases.This was because there was a loss of catalyst for each repeated use.As can be seen from Figure 13, the degradation rate of ammonia can be maintained at about 60% after three times of use, but the degradation effect will become worse as the number of times of use increases.This was because there was a loss of catalyst for each repeated use.

Preparation of (001)TiO2 Catalyst
Anhydrous ethanol (15.20 mL) was slowly added to 17.60 mL of butyl titanate and stirred until the solution was well distributed (designated solution A).Then, 15.20 mL of absolute ethanol was slowly added to 90 mL of ultra-pure water; 6 mL of hydrofluoric acid was then added to this solution (designated solution B).Next, the A solution was added to the B solution and was stirred under medium speed at room temperature for 2 h; the TiO2 gel was allowed to sit for 2 days and then moved to a stainless-steel reactor containing a PTFE inner container at 100 °C for 2 h.After cooling, the precipitates were separated and washed alternately with ultra-pure water and absolute ethanol for three times, drying in a 100 °C drying oven.After completion of a grinding process, the obtained powder was marked as (001)TiO2.

Preparation of Cu2O/(001)TiO2 Catalyst
CuSO4 (4.99 g) was weighed and dispersed in 100 mL distilled water.Then, 12.48 g (001)TiO2 was added to form a mixture.Ultrasound was used for 20 min.NaOH (4 g) was dissolved in 20 mL of distilled water; glucose (7.5 g) was dissolved in 75 mL of distilled water; then, the dissolved sodium hydroxide solution was added to the mixture of CuSO4 and (001)TiO2 dropwise, forming a blue precipitate.Then, the glucose solution was placed on a constant temperature magnetic stirrer and stirred continuously until the solution was heated to 34 °C.The heated glucose solution was added to the blue precipitation solution dropwise; then, the mixed solution was placed on a constant

Preparation of (001)TiO 2 Catalyst
Anhydrous ethanol (15.20 mL) was slowly added to 17.60 mL of butyl titanate and stirred until the solution was well distributed (designated solution A).Then, 15.20 mL of absolute ethanol was slowly added to 90 mL of ultra-pure water; 6 mL of hydrofluoric acid was then added to this solution (designated solution B).Next, the A solution was added to the B solution and was stirred under medium speed at room temperature for 2 h; the TiO 2 gel was allowed to sit for 2 days and then moved to a stainless-steel reactor containing a PTFE inner container at 100 • C for 2 h.After cooling, the precipitates were separated and washed alternately with ultra-pure water and absolute ethanol for three times, drying in a 100 • C drying oven.After completion of a grinding process, the obtained powder was marked as (001)TiO 2 .

Preparation of Cu 2 O/(001)TiO 2 Catalyst
CuSO 4 (4.99 g) was weighed and dispersed in 100 mL distilled water.Then, 12.48 g (001)TiO 2 was added to form a mixture.Ultrasound was used for 20 min.NaOH (4 g) was dissolved in 20 mL of distilled water; glucose (7.5 g) was dissolved in 75 mL of distilled water; then, the dissolved sodium hydroxide solution was added to the mixture of CuSO 4 and (001)TiO 2 dropwise, forming a blue precipitate.Then, the glucose solution was placed on a constant temperature magnetic stirrer and stirred continuously until the solution was heated to 34 • C. The heated glucose solution was added to the blue precipitation solution dropwise; then, the mixed solution was placed on a constant temperature magnetic stirrer and was stirred continuously, heated, and reacted until the solution reached 70 • C, and kept for 15 min at that temperature.During the whole process, the solution gradually changed from blue to dark green.Eventually, a brick-red precipitate appeared.The brick-red precipitate solution was centrifuged and then washed repeatedly with deionized water for three times.The brick-red substance was obtained by drying at 60 • C. Cu 2 O/(001)TiO 2 was obtained by grinding the brick-red substance into powder.

Catalyst Powder Loading
In order to prevent the powder catalyst from blowing away, polyester fiber cotton was used as a carrier; this material has good light transmittance, is light-weight, and is easy to operate.The cotton was treated with 5 mol/L NaOH for 2 h, was washed repeatedly with deionized water until its pH was neutral, and was dried in a blast drying oven at 60 • C.
Before the catalysts from Sections 2.2 and 2.3 were dried, the treated carriers were put into the washed catalysts solution, ran at a medium speed for 4 h in an oscillator, and were removed and dried in a blast drying chamber at 60 • C.

Catalyst Characterization
The crystal phase characteristics of the catalysts were measured by X-ray diffractometry (XRD, D8 Advance, Bruker, Rheinstetten, Germany) with Cu Kαradiation (λ = 0.154 nm) under 40 kV at a scan speed of 6 • /min.The optical properties of the catalysts were characterized with a UV-Vis spectrophotometer (UV-Vis, U-3010, Hitachi, Tokyo, Japan).The detailed lattice spacing of the as-synthesized samples was evaluated by a high-resolution transmission electron microscope (HRTEM, Tecnai G2 F20, FEI, Hillsboro, OR, USA).The crystal facet contents of the catalysts were analyzed by using Raman spectroscopy (Raman, LabRAM XploRA INV, Horiba, France).The morphology of the catalysts was observed by a field-emission scanning electron microscope (FE-SEM, Inspect F50, Thermo Fisher Scientific, Waltham, USA) with an accelerating voltage of 25 kV.The elemental composition and element valence state of samples were analyzed by X-ray photoelectron spectroscopy (XPS, EscaLab 250Xi, Thermo Fisher Scientific, Waltham, USA).The photoelectron hole recombination of samples was evaluated by Photoluminescence emission spectra (PL, F-2700, Hitachi, Tokyo, Japan).

Experimental Equipment of Photocatalytic Ammonia Gas
As shown in Figure 14.A small air pump with a measuring range of 0-3 L/min was used as the source of air.The air from the air pump became clean air after being treated with activated carbon and silica gel; this clean air sent ammonia vaporized from ammonia water to the photocatalytic reaction chamber.The sampling inlet and sampling outlet were set before and after the photocatalytic reaction chamber, respectively, which were connected to the inlet and outlet of an INNOVA continuous detector to reflect the changes of concentration in the whole photocatalytic process.In the photocatalytic reaction chamber, a 300 W xenon lamp was used to simulate sunlight and a condensing reflux tube was installed outside the light source to reduce the influence of a large amount of heat generated by the light source on the experimental results; the remaining tail gas passed through the tail gas treatment device.The photocatalytic reaction tube was made of a quartz tube with a length of 6 cm, an outer diameter of 3 cm, and an inner diameter of 2.7 cm.The average load of the catalysts was 0.18 g.The remaining tail gas was treated by the tail gas treatment device.
where, Cin is the ammonia concentration at the inlet and Cout is the concentration of ammonia after the photocatalytic reaction.The blank polyester fiber without any catalyst was placed in the sealed reactor.The temperature of the reactor was about 18 °C.The ammonia concentration was 120 ± 3 ppm, the air flow rate was 0.5 L/min, and the 300 W xenon lamp was used as the light source for the photocatalytic reaction.

Degradation of Ammonia by Different Catalysts
The polyester fibers loaded with P25, Cu2O, (001)TiO2, Cu2O/(001)TiO2 were placed in the sealed reactor.The temperature of the reactor was about 18 °C.The ammonia concentration was 120 ± 3 ppm, the air flow rate was 0.5 L/min, and the 300 W xenon lamp was used as the light source for the photocatalytic reaction.

Degradation of Ammonia by Air Flow Rate
The polyester fibers loaded with Cu2O/(001)TiO2 was placed in the sealed reactor.The temperature of the reactor was about 18 °C.The ammonia concentration was 120 ± 3 ppm, the air flow rate were 0.5, 1, 2 L/min, separately, and the 300 W xenon lamp was used as the light source for the photocatalytic reaction.

Catalyst Reutilization Performance
The polyester fibers loaded with Cu2O/(001)TiO2 was placed in the sealed reactor.The temperature of the reactor was about 18 °C.The ammonia concentration was 120 ± 3 ppm, the air flow rate was 0.5 L/min, and the 300 W xenon lamp was used as the light source for the photocatalytic reaction, after the reaction, the carrier was removed and baked at 70 °C for 30 min for the next reaction.

Conclusions
In this paper, the preparation of (001)TiO2 by the sol-gel method has been achieved and a heterogeneous structure of Cu2O/(001)TiO2 has been prepared by the impregnation-reduction There are two test ports before and after the reaction tube for ammonia degradation, namely, the sample intake and sample outtake, which are connected to INNOVA's intake and outtake, respectively.INNOVA is an instrument for continuously detecting ammonia concentration changes online.The degradation rate at this moment is as follows: The degradation rate (%) = where, C in is the ammonia concentration at the inlet and C out is the concentration of ammonia after the photocatalytic reaction.The blank polyester fiber without any catalyst was placed in the sealed reactor.The temperature of the reactor was about 18 • C. The ammonia concentration was 120 ± 3 ppm, the air flow rate was 0.5 L/min, and the 300 W xenon lamp was used as the light source for the photocatalytic reaction.

Degradation of Ammonia by Different Catalysts
The polyester fibers loaded with P25, Cu 2 O, (001)TiO 2 , Cu 2 O/(001)TiO 2 were placed in the sealed reactor.The temperature of the reactor was about 18 • C. The ammonia concentration was 120 ± 3 ppm, the air flow rate was 0.5 L/min, and the 300 W xenon lamp was used as the light source for the photocatalytic reaction.

Degradation of Ammonia by Air Flow Rate
The polyester fibers loaded with Cu 2 O/(001)TiO 2 was placed in the sealed reactor.The temperature of the reactor was about 18 • C. The ammonia concentration was 120 ± 3 ppm, the air flow rate were 0.5, 1, 2 L/min, separately, and the 300 W xenon lamp was used as the light source for the photocatalytic reaction.

Figure 1 .
Figure 1.SEM image of the carrier.

Figure 1 .
Figure 1.SEM image of the carrier.

Figure
Figure 3a contains spacings of d = 0.352 nm and d = 0.235 nm, corresponding to the (101) and (001) facets of TiO 2 , respectively[44].This shows that the prepared TiO 2 has the high activity (001) facets.The Figure3bshows d = 0.235 nm and d = 0.245 nm spacings, corresponding to the (001) facets of TiO 2 and the (111) surface of Cu 2 O, respectively[45], which shows that the prepared composite catalyst contains the high activity (001) facets.

Figure 4 .
Figure 4. Raman spectrum of the catalysts.

Figure 4 .
Figure 4. Raman spectrum of the catalysts.

Figure 6 .
Figure 6.(a) UV-vis Light Diffuse Reflectance spectra of the catalysts; (b) DRS spectra of the samples; (c) Band gap calculation from DRS spectra by Kubelka-Munk method of the materials.

Figure 6 .
Figure 6.(a) UV-vis Light Diffuse Reflectance spectra of the catalysts; (b) DRS spectra of the samples; (c) Band gap calculation from DRS spectra by Kubelka-Munk method of the materials.

Figure 9 .
Figure 9. Energy band diagrams for (a) Cu2O and TiO2 before contact; (b) Cu2O/TiO2 composite; (c) Charge variations before and after contact of different types of semiconductors.

Figure 10 .
Figure 10.Controlled test of catalyst carrier under light and dark conditions.

Figure
Figure Energy band diagrams for (a) Cu 2 O and TiO 2 before contact; (b) Cu 2 O/TiO 2 composite; (c) Charge variations before and after contact of different types of semiconductors.

Figure 10 .
Figure 10.Controlled test of catalyst carrier under light and dark conditions.

Figure 10 .
Figure 10.Controlled test of catalyst carrier under light and dark conditions.

Figure 11 .
Figure 11.Degradation of ammonia by different catalysts.

Figure 12 .
Figure 12.Effect of air velocity on ammonia degradation.

Figure 11 .
Figure 11.Degradation of ammonia by different catalysts.

Figure 11 .
Figure 11.Degradation of ammonia by different catalysts.

Figure 12 .
Figure 12.Effect of air velocity on ammonia degradation.

Figure 12 .
Figure 12.Effect of air velocity on ammonia degradation.

Table 1 .
The band gap energy values of the different samples.

Table 1 .
The band gap energy values of the different samples.