One-Pot Synthesis of Cu 2 O / Cu Self-Assembled Hollow Nanospheres with Enhanced Photocatalytic Performance

Cu 2 O/Cu hollow spheres are prepared using one-pot template-free solvent-thermal synthesis route with (CH 3 COO) 2 Cu⋅H 2 O as a precursor.With the reaction time increasing gradually from 2 h to 20 h, the morphology of the Cu 2 O/Cu evolves from nanoparticle to hollow nanosphere. The hollow structure is obtained when the cooling rate falls down to 0.7C/min. And the content of Cu in the hollow spheres also can be easily controlled by adjusting the solvent-thermal synthesis time. Using photocatalytic degradation of phenol as the probe molecules under visible-light illumination, we have investigated the influence of hollow structure on the photocatalytic activity of Cu 2 O/Cu. The prepared hollow sphere Cu 2 O/Cu particles exhibited a higher photodegradation capability than nanoparticles and solid spheres. When the content of Cu lies in the range of 11–86wt%, the samples exhibit higher photocatalytic performance, indicating that the Cu 2 O/Cu particles with hollow structure are promising candidates for the processing of pollutants.


Introduction
Semiconductor-based photocatalysts, activated by illumination at room temperature, are used for degradation of organic pollutants by redox reaction. The technique is environmentally clean and thus attracts more and more attention [1]. As is well known, the activity of a catalyst depends largely on geometry and morphology. Hollow/porous structures possess large area of surface and interface, which enhances not only the adsorption and desorption of products but also light harvesting, thereby improves the catalytic activity. Some existing works have demonstrated that morphology of materials can be well controlled in some important photocatalytic materials [2][3][4][5]. Various method have been developed to achieve these special structures, which involve hard templates or soft templates (PEG [6], CTAB [7]), as well as physical/chemical processes based on Kirkendall effect [8], Ostwald ripening [9], oriented attachment [10], and so forth. Although much progress has been made in the synthesis of hollow spheres, it remains a major challenge to develop a fast and facile solution route for the preparation of inorganic hollow nanostructures, especially one-pot synthesis nanocomposite with hollow structure.
As is well known, the maximum irradiation of sunlight lies in the visible range, and only photocatalysts with corresponding band gap could sufficiently use solar energy. The band gap of Cu 2 O is 2.0∼2.2 eV, and the component elements are inexpensive and abundantly available, making it a promising candidate for photocatalysts. Numerous reports have shown the superior performance of Cu 2 O on solar energy conversion [11], photocatalytic degradation of organic pollutants [12], and decomposition of water into H 2 and O 2 [13] A simple and green one-pot in situ synthetic route for nanosized Cu 2 O/Cu hollow nanospheres is introduced here. The synthesis of Cu 2 O/Cu is developed with a templatefree solvent-thermal route to control its morphology and phase composition. More importantly, the hollow structure of Cu 2 O/Cu can be obtained by adjusting the reaction conditions. A possible formation mechanism was proposed to account for the production of hollow structures. The effect of reaction time and cooling rate on its morphology was investigated. The adsorption and photocatalytic activity of samples were evaluated by the photocatalytic degradation of phenol under visible light illumination.

Preparation of Cu 2 O/Cu Hollow Spheres.
All the chemicals were analytical grade regents used without further purification. In a typical preparation, copper acetate ((CH 3 COO) 2 Cu⋅H 2 O, 0.02-0.05 M) was dissolved in a mixed organic solvent of N,N-dimethylformamide (DMF) and ethanol. After the solution was stirred for 30 min, 35 mL of this transparent blue solvent was sealed in a Teflon-lined stainless steel autoclave with a capacity of 50 mL and heated at 200 ∘ C for 2-20 h in electric oven. After reaction, the precipitation was separated from the solution by centrifugation, then washed with alcohol for several times, and finally dried at 70 ∘ C for 5 h in a vacuum oven. The denotations of samples prepared at different condition are shown in Table 1.

2.2.
Characterization. The samples were characterized by Xray powder diffraction (XRD) using a Rigaku 12 kW X-ray diffractometer with Cu K radiation ( = 0.15418 nm). Their morphology and size distribution were inspected with a JEM-S4800 field-emission scanning electron microscope (FESEM) operated at 15 Kv and a JEOL-2010 transmission electron microscope (TEM) working at 200 kV. N 2 adsorptiondesorption isotherms were obtained using a Quantachrome Autosorb-1 apparatus. Barret-Joyner-Halenda (BJH) method was employed to determine the pore diameter ( ) and pore volume ( ). The specific surface area ( BET ) was calculated using the Brunauer-Emmett-Teller (BET) method.

Measurement of Adsorption and Photocatalytic Activity.
The adsorption behavior and photocatalytic activity of the Cu 2 O/Cu were evaluated by the degradation of the solution of phenol at a concentration of 10 mg/L. 0.030 g Cu 2 O/Cu NCs powder was dispersed in a 50 mL probe molecular aqueous solution. Before illumination, the suspension was stirred in the dark for more than 120 min to achieve an adsorption/desorption equilibrium of organic molecules on the surface of Cu 2 O/Cu. The photocatalytic reaction was carried out at room temperature by using a 100 W tungsten lamp as a visible light source. At different time intervals during the experiment, 5 mL of solution was sampled each time for analysis. After centrifugation at 11000 rpm for 10 min, the absorbance of solution was measured using a UV-visible spectrophotometer (TU-1901).

Results and Discussions
3.1. Structure and Morphology. Sample S4 (precursor concentration is 0.02 M, reaction time is 14 h, and cooling rate is 0.7 ∘ C/min) possesses the typical morphology of all, whose TEM images are shown in Figure 1(a). Hollow spherical nanoparticles are observed, with the diameter of 140∼280 nm, whose shell is 30∼50 nm in thickness. It can be seen from  To study the formation process of the Cu 2 O hollow spheres, samples were collected at different reaction time and were characterized by the TEM analysis ( Figure 2). When the solution at 200 ∘ C for 2 h, the system appears brown precipitate; these are nanoparticles that can be seen  Figure 2(b) is a TEM image of the sample collected after 4 h, showing that Cu 2 O nanoparticles aggregated to form loose spheres, whose diameter are approximately 140-280 nm and part of them are hollow structure. When the reaction time increases to 10 h, the spherical selfassembled internal nanoparticles are significantly decreased; hollow structure can be seen from Figure 2(c), a thin-wall hollow spherical structure was formed, which diameter is approximately 180 nm and the wall thickness is about 30 nm. When the reaction time is 20 h, the color of the sample is completely changed to dark purple. The corresponding TEM photograph is shown in Figure 2(d), and the hollow structure obtained exhibits no change in morphology. This time-dependent self-assembly allows selective synthesis of hollow mesoporous spheres by changing reaction time, which is of great importance for designing catalysts with high activity.
In this experiment, the authors found that the cooling rate has great impact on the formation of hollow structure. Figure 3 shows the SEM of samples obtained at 200 ∘ C for 10 h with different cooling rate. Shown in the Figure 3(a) is the sample obtained when the stainless steel autoclave was quenched in ice water, the morphology of which is disorganized nanoparticles. Decreasing the cooling rate to 3 ∘ C/min (Figure 3(b)), the product exhibits spherical aggregated structure. When the cooling rate was decreased to 0.7 ∘ C/min, the hollow spheric structure with 140-280 nm diameter was formed, which could be indicated by the light and shade contrast as the arrow point inset Figure 3(c). Figure 4 illustrates the Schematic formation process of Cu 2 O/Cu hollow nanospheres. As indicated, the solid spheres are comprised of numerous smaller crystallites. Firstly, the nanocrystals formed and then driven by the minimization of the system energy; the small nanocrystals tend to aggregate together to form solid spherical groups. These aggregates exhibit various packing densities along the radial direction. With increasing reaction time, Ostwald ripening [9] then comes into effect; the particles with high surface energy move from the center to the surface. Voids in the cores of large aggregates gradually form and become bigger. The original driving force for this ripening is attributed to the existence of intrinsic density variations inside the starting solid aggregates. Figure 5 shows the XRD patterns of a series of samples prepared with different reaction time at 200 ∘ C. For the S1, all diffraction peaks can be indexed to be cubic phase of Journal of Nanomaterials  , where Cu 2 O(111) and Cu(111) are the height of the characteristic diffraction peaks of Cu 2 O (111) and Cu (111) planes, respectively. As calculated from XRD results (Figure 5), the corresponding content of Cu increases from 0 wt% to 86 wt% when the time increases from 4 h (S1) to 20 h (S5). Thus, the reaction time plays a crucial role in forming different ratios of Cu 2 O to Cu in the composite. Figure 6 shows the relationship between the morphology and the precursor concentration. Obviously, the concentration of precursor has a great effect on the morphology. At low precursor concentration of 0.02 M (S2, Figure 6(a)), hollow sphere is formed, whose diameter is approximately 140-280 nm. The contrast of light and shade can infer the possible hollow structure (the arrow inset Figure 6(b)). When the precursor concentration increases to 0.05 M, the diameter of microsphere increase to 2 m, and the spheres become merged together. Therefore, when the precursor concentration changed, the products changed not only in size but also in morphology of the grain. Figure 7 show the N 2 adsorption-desorption isotherm of S1 and S4 (S4 is representative for all the hollow spheric samples), and the two adsorption isotherms all exhibit type IV hysteresis, indicating S1 and S4 are porous structures. The corresponding parameters are listed in Table 1. The pore size of S1 (inset Figure 7(a)) ranges from 33 to 42 nm, which can be attributed to the aggregation of nanoparticles. But for S4 (inset Figure 7(b)), the pore size has shown the obvious bimodal pore size distribution, which is located in the microporous and mesoporous region, respectively, including the maximum probability diameter of 3.7-3.8 nm between the interior of the particle agglomeration hole and 17-40 nm agglomeration piled holes between particles.

Photocatalytic Activity.
Phenol is transparent to visible light and very hard to mineralize due to its resonance stability. The strong absorption peak at about 269 nm is selected to monitor the photocatalytic degradation process. With longer irradiation time, this characteristic peak becomes weaker and weaker, indicating the degradation of phenol. No new adsorption peaks appear and no obvious shift of the characteristic peak is observed, indicating the degradation of phenol.
In order to understand the hollow structure in enhancing the photocatalytic performance of Cu 2 O, pure Cu 2 O nanoparticles, nanospheres, and hollow nanospheres are prepared and the photocatalytic activity is studied. Shown in Figure 8 is the photocatalytic activity of Cu 2 O with different morphologies, which is characterized by the initial concentration ( 0 ) and the concentrations at different time interval (C). The sizes of Cu 2 O nanoparticle in the hollow spheres and nanospheres are approximately the same as the nanoparticles Cu 2 O. From Figure 8, we can see that without catalyst, phenol cannot be degraded under visible light irradiation, whereas it can be easily degraded with the presence of Cu 2 O photocatalysis. At an irradiation time of 120 min, 75% phenol is degraded with the presence of hollow spheric sample. On the contrary, the photocatalytic performance of nanoparticles and solid structure are relatively low; especially nanoparticles Cu 2 O, the degradation rate is only 23%. Compared to solid particles, hollow structures have large specific surface areas, the interior and exterior surfaces, which enhance not only the adsorption and desorption of products but also light harvesting, thereby improving the catalytic activity. Figure 9 shows the photocatalytic performance of Cu 2 O/ Cu hollow spheres, whose Cu contents are different. Among these samples, the performance of S1 is relatively low, while S3 exhibits the highest performance. As discussed above, S1 is the pure phase of Cu 2 O and the other samples (S2-5) are nanocomposites of Cu 2 O and Cu. The pure-phase semiconductor exhibits very low quantum efficiency due to the quick recombination of photoelectrons and holes [16]. According to the theory of metal/semiconductor heterostructure catalysis [17][18][19][20][21], the photocatalytic activity of semiconductor-based heterostructure depends greatly on the concentration of heterostructure interface and defect, which promotes interfacial charge-transfer kinetics between the metal and semiconductor and improves the separation of photogenerated electron-hole pairs, thus increasing photocatalytic activity [17]. In fact, a Schottky barrier was assumed to form at the Cu 2 O and Cu interface; Cu acts as an electron sink that reduces the recombination of photoinduced electrons and holes (2). However, Cu 2 O is known to absorb a relatively large amount of oxygen on the surface [22]. It has been proven that the electrons do accumulate on Cu particles, and the accumulation of electron on Cu will transfer to Cu 2 O and O 2 will reduce O 2 to • O − 2 (3), while the • O − 2 oxidize the H 2 O to form • OH (4); finally, the organics have been degraded through the formation of • OH (5) [23][24][25]. The accumulation of electron on photocatalyst will increase the rate of recombination. In Cu 2 O/Cu, the interfaces between Cu and Cu 2 O act as the sites where rapid seperation of photogenerated electrons and holes occurs. On the other hand, very high content of Cu (S5, 86 wt%) does not favor high photocatalytic activity, since Cu becomes a recombination center for electrons and holes instead [26]. Therefore, the mass fraction Journal of Nanomaterials of Cu in the nanocomposites also influences photocatalytic activity. Consider • OH +organic → Degradation products.

Conclusions
Hollow spheric Cu 2 O/Cu photocatalysts have been synthesized by following a one-pot solvent-thermal synthesis route without using any templates and additives. The reaction time and cooling rate have a strong effect on the formation of the hollow Cu 2 O/Cu nanospheres. The hollow spheric structure is formed at a reaction time in the range of 4 h to 20 h and low cooling rate 0.7 ∘ C/min. The content of Cu increases with increasing reaction time. As visible-lightdriven photocatalysts, the hollow spheric Cu 2 O/Cu exhibit better photocatalytic performance than the nanoparticles and solid spheres. Our route offers an effective way to control the synthesis of Cu 2 O/Cu hollow spheres and may shed light on the design of simple route for one-pot synthesis of metal oxide nano-heterojunction, other well defined complex nanostructures.