ABSTRACT We report a new production pathway for a variety of metal oxide nanocrystallites via submerged illumination in water: submerged photosynthesis of crystallites (SPSC). Similar to the

growth of green plants by photosynthesis, nanocrystallites shaped as nanoflowers and nanorods are hereby shown to grow at the protruded surfaces via illumination in pure, neutral water. The

process is photocatalytic, accompanied with hydroxyl radical generation via water splitting; hydrogen gas is generated in some cases, which indicates potential for application in green

technologies. Together with the aid of _ab initio_ calculation, it turns out that the nanobumped surface, as well as aqueous ambience and illumination are essential for the SPSC method.

November 2022 TAILORED SELF-ASSEMBLED PHOTOCATALYTIC NANOFIBRES FOR VISIBLE-LIGHT-DRIVEN HYDROGEN PRODUCTION Article 20 November 2020 INTRODUCTION New approaches to manufacturing the

nanocrystallites of metallic oxides are desired due to their emerging applications in a wide range of high-technology applications1,2,3,4,5,6,7,8. In the case of liquid-solid phase

crystallisation studies, the surface morphology control plays an essential role in influencing the nucleation of nanocrystallites9. Recent studies have demonstrated the role of surface

chemistry and morphology utilizing various mechanisms gained from polymeric substrates10,11. Achieving those understandings provides a powerful means to widespread reports in

nanocrystallites research. Our interest is in the easy feasible design of nanocrystallites fabrication beneficial for the nanotechnology and environment. With regard to obtaining the desired

products, we herein report a new pathway of production for variety of metal oxides nanocrystallites via SPSC. We chose various metals (Zn, W, Cu and Ce) to demonstrate the effectiveness of

the submerged photosynthesis of crystallites (SPSC) method in obtaining a variety of morphologies of metal oxide nanocrystallites (NCs). The present report primarily focuses on ZnO

nanofabrication due to its promising environmental12 applications and broad range of modern device applications, including light-emitting diodes13, photo-detectors14, gas sensors15 and solar

cells16. The functions of these semiconductive ZnO (with a wide bandgap of 3.37 eV) devices are crucially dependent on the nanostructure morphology. Hence, it is important to tune and

stabilise the syntheses parameter for improved performance. To this end, there has been a substantial increase in the number of reports on hydrothermally synthesised ZnO nanostructures17,18,

including lasing1 and the addition of metal-ion impurity19 techniques. Expanding on these efforts, this study develops a rational and environmentally benign approach to synthesise a

plethora of ZnO nanomorphologies. We employed our initial metal surface treatment based on the utilisation of the submerged liquid plasma process20,21. The reaction of plasma in an aqueous

solution facilitates the synthesis of metal oxide powder22,23. Hence, we adopted this technique for the direct (one-step) synthesis of ZnO “seeds”. Our intention was to create a

semiconductive reformed layer with protruding characteristics (nanobumps) on the material. For this purpose, a raw Zn metallic plate was used as the target material for the formation of

nanobumps. The NC growth was then completed by a “photosynthesis” reaction, where the irradiation of UV light (typically λ = 365 nm and I = 28 mWcm−2) on the nanobumps inside pure water

assisted the growth of ZnO NCs. The SPSC method is different from previous nanofabrication reports24,25, in which a hydrothermal decomposition process using UV-Vis light irradiation directed

the formation of NCs. Instead, we found that the illumination in ultrapure water induced an apical growth characteristic via water radiolysis, as will be described later. Furthermore, we

were able to demonstrate working NC fabrication at room temperature (RT) under surfactant- and contamination-free conditions by eliminating the need for organometallic or other organic

solution phases. Similar to the growth of green plants via botanical photosynthesis, our SPSC method requires only light, water and nanobumps (crystallite seeds). Interestingly, the SPSC end

products were accompanied by the generation of hydrogen gas, which gives rise to a potential application of this methodology as a green technology for energy, chemistry and nanotechnology.

RESULTS Figure 1(a) presents a scanning electron microscopy (SEM) image of ZnO nanobumps that were tailored by submerged liquid plasma treatment and depicts the metal surface having average

of two or more protrusions per 10 μm2. The protruded surface exhibits an average diameter of 1 μm or less. The higher-magnified image indicates the small ZnO seeds homogeneously localised on

the protruded surface; these seeds have an average diameter of approximately 20 nm. Here, a drastic change in the seed clustering was observed after subsequent UV irradiation in ultrapure

water and ambient temperature: widely spread ZnO NCs covered the metal substrate. The previously localised seeds grew outward to form a bunch of nanorods that formed into nanoflowers

(dandelion-like), dendrites (tree-like) and aligned nanorods (lawn grass-like) (Fig. 1(b–d), respectively). The SEM-energy-dispersive X-ray spectroscopy (EDS) analysis (Fig. 2(a,b)) and

X-ray diffraction (XRD) analysis (Fig. 2(c)) for the ZnO NCs illustrated that the NCs were synthesised on a Zn substrate, which contained Zn and O. As evidenced by the selected area electron

diffraction (SAED) pattern and high-resolution transmission electron micrograph (HRTEM) of a nanorod examined along the axis (Fig. 2(d)), the nanorods were single crystallites (a wurtzite

structure). The apical growth direction was in the c-axis <001>. This result is consistent with previous ZnO crystal growth reports24,26,27. DISCUSSION To consider the SPSC mechanism

(as illustrated in Fig. 3(a)) via dissociation of water molecules (H2O) on nanobumped ZnO surfaces, the electron density and bond-dissociation energy required to alter H2O into OH and H

radicals were calculated using _ab initio_ simulations28,29. To clarify the effect of the apical growth of NCs accompanied by the dissociation of water, the bond-dissociation energy was

calculated for the flat surface (Fig. 3(b)) and nanobumped surface (Fig. 3(c) for curvature radius, R = 0.5 nm). The high electron density appeared to be localised near the top surface of a

nanobump (Fig. 3(c)). The dissociation energy for each surface was evaluated as the difference in the total energy of the dissociated state with H and OH and that of the equilibrated bonded

state of H2O. The calculated value for the flat surface was 5.03 eV without considering the photoexcitation effect, corresponding to the experimentally measured direct dissociation energy of

a water molecule (5.1 eV)30. In contrast, the dissociation energy for the nanobumped surface model was 0.323 eV when R = 0.5 nm (subsequently, 0.409 eV for R = 1.0 nm and 0.552 eV for R = 

2.0 nm). Notably, the dissociation energy of a water molecule was lower for the nanobumped surface. Overall, the local electron density and dissociation energy reduction at the top of the NC

bumps played a key role in the SPSC process. We now suggest that the mechanism for photosynthesised NCs in water via the SPSC process (Fig. 3(a)) can, _in principle,_ be described by the

following photo-induced reactions: The mechanism starts with water splitting into ion species in the vicinity of a semiconductive (SC) surface: Hence, the water splits into ions by

photoinduction (1)–(3): The formation of transient species (H, OH, ) and other molecular byproducts (H2, H2O2) (see Fig. 3(c) for _H_ + _H_ → _H_2) can be well understood as water radiolysis

in radiation chemistry31. These reactions occur in short times of less than micro-second-order. Presumably, assisted by the aforementioned morphology effect, _H_+ and _OH_− ions are then

locally separated, e.g., _H_+ at a valley in equation (2) and _OH_− at an apical hill in equation (3) throughout a protruded surface. Otherwise, H2O will be immediately reproduced in the

reverse of equation (4). Such locality-assigned ion production gives rise to a local pH imbalance: alkaline at the hill and acidic near the valley. Therefore, one can expect NC growth at a

hill in association with hydrothermal reactions for ZnO generation in an alkaline solution26,27: The metal may resolve into an ion at the valley: Hence, the net SPSC reaction is completed

with Similarly to known hydrothermal mechanism, NC growth by equations (5)-(6), might be accompanied by aggregation and recrystallisation processes of metal oxide nanoparticles. Thus, the

SPSC is completed with three _principles_. Firstly, a photo-induced water splitting process. Secondly, separation of _H_+ and _OH_− ions due to nanobumps protruded surface. Finally,

aggregation and recrystallisation of metal oxide nanoparticles (superimposed hydrothermal reactions) result in the nanocrystallites growth. The SPSC process characteristically predicts

hydrogen gas (_H_2(_g_)) and hydroxyl radicals (OH) as intermediate products (see Fig. 4). To confirm our model, we detected H2 gas using gas chromatography (GC) after the SPSC experiment on

Zn. The ratio of H2/O2 in the collected gas was evaluated to be nearly 10. H2 gas can also be produced by a typical photocatalytic reaction12 (2_H_ + 2_e_− → _H_2), as well as via water

radiolysis (with hydrogen radicals, Fig. 3(c)) and hydrothermal reaction (equation (6)). In the present study, OH radical generation was also investigated (Fig. 4(a–d)) by monitoring the

bleaching of _p_-nitrosodimethylaniline (PNDA) as the intensity of the characteristic absorption peak at λ = 440 nm decreased32,33. These results confirm the photochemical reactions proposed

for the SPSC process, in which H2 gas and OH radicals were generated during the photo-assisted growth of ZnO nanorods. In general, hydrothermal reactions in equations (5) and (6) are known

to occur in alkaline solutions at higher temperatures18,26,27. Noting this, we tested the SPSC process at two different water temperatures (10 °C and 60 °C) other than room temperature. The

NC growth was clearly enhanced at higher water temperatures. Nonetheless, the overall SPSC process is to occur assumed in a pure, neutral water environment rather than in acidic or alkaline

aqueous solutions. However, one can observe the pH dependence or impurity additive influence on the final NC morphology. Moreover, the photocorrosion effect34, e.g., , which causes ZnO to

redissolve into Zn ions or _Zn_(_OH_)2 or (equation (7)) and (equation (6)). They may suppress the reaction processes and thus reduce the yield of SPSC in equation (7). However, the

re-dissolution effect results in the possibility of ZnO recrystallisation at the initial fine nanocrystallites to regrow into thicker and wider NCs by re-precipitation, as shown in Fig.

1(b–d). With a slight modification of reactions in equations (5, 6, 7), our SPSC method can also be applied to derive a wide variety of metal oxide NCs (e.g., metals of Cu, Ce and W, as

shown in Fig. 5). These modifications revealed the difference in the SPSC morphology, resulting in various NCs. In the present work, we typically employed the submerged liquid plasma

technique as an initial surface nanostructure treatment of natively oxidised NC seeds. Nevertheless, other possible alternative seeding methods can also be applied, including laser

processing, ion irradiation and tribological, mechanical scratching. In summary, SPSC requires _light_, ranging from UV to visible (as shown in Fig. 5(b)), to assist the apical growth of

NCs. Secondly, the use of _water_ (specifically, ultrapure water) will deliver a fine structure of NCs. Because the NC morphology is sensitive to pH changes and water impurities, the

additive effect resulted in different morphologies. For example, Si from tap water resulted in sphere-like crystallites and NaCl from natural seawater resulted in plate-like crystallites.

These results are presumably caused by the alteration of the electronic state of the apical surfaces. Finally, metal oxide surface nanobumps act as the NC _seeds_ and enclose the nucleation

for the apical growth reaction. METHODS SURFACE PRETREATMENT In the submerged liquid plasma experiment devices (Supplementary Fig. S1(a)), the anode was a φ0.5 × 1 mm platinum wire (Nilaco,

Tokyo, Japan) with purity of 99.9% arched into a hemispherical glass mesh (R = 30 mm). The cathode (target material) was a raw metal Zn plate (Nilaco, Japan, 99.5%), cut into a size of 35 × 

5 × 1 mm. A 60 mm2 contact area with a wrapped φ0.5 mm Cu wire (Nilaco, Japan, 99.9%) on the tip of the Zn plate was used to prepare the working electrode. A solution of 0.1 mol/l K2CO3 with

pH 11.5 was used as the electrolyte. Deionised water was used as the washing solution. Prior to the experiments, both of the electrodes were washed with deionised water and the electrolyte

was preheated to 90 °C. Insulation of the contact area between the Cu wire and Zn plate was achieved by a φ10 mm glass tube, ensuring that the exposed Zn plate length was approximately 25

mm. Then, both of the electrodes were immersed in the K2CO3 solution (300 ml) and separated by distance of 30 mm. A discharge voltage of 140 V (current: 1.6–1.8 A) was applied across the

electrodes using a direct current power supply (KIKUSUI, PWR1600H, Japan). The synthesis of nanobumps using submerged liquid plasma was conducted for a fixed reaction time of 10 min,

appreciating the simple and time- and cost-efficient technique. At the end of the plasma reaction, the cathode was collected and washed with deionised water and the length was cut to 25 mm.

A white film surface, confirmed to constitute of ZnO, was obtained on the electrode surface. For further experimentation and analysis, the specimen was allowed to dry at ambient temperature.

SPSC EXPERIMENT In the UV irradiation experiment (Supplementary Fig. S1(b)), the plasma-treated Zn plate was inserted into a polymethylmethacrylate (PMMA) cuvette, which was then filled

with 4 ml of ultrapure water (Wako Pure Chemical, pH 7–7.5, resistivity 18 MΩ) and capped. Prior experiments, the ultrapure water was degassed to remove the dissolved gas. A UV lamp (UVP,

B-100AP, USA) with 100 W longwave UV (λ = 365 nm, 3.4 eV) was mainly used for SPSC. Visible light irradiation (λ ≈ 500 nm) was employed for Fig. 5(b) using spot light source (Hamamatsu

LightningCure LC8, L9588, Japan). The irradiance orientation was set to the horizontal position and the distance between the specimen and UV lamp was set to 100 mm. In the typical synthesis

of nanocrystallites, the UV irradiation was performed in a dark chamber for a fixed reaction time (24 h) at room temperature. Extended UV irradiation times (48 h and 72 h) were also applied

to clarify the NC growth characteristics (Fig. 1(d), Fig. 5(c) and Supplementary Fig. S2). At the end of the UV irradiation, the specimen was collected and the ultrapure water pH change was

recorded using a pH meter (Horiba, D-51). For ZnO, the final pH of the water solution exhibited a typical increase to 8.5 in ambient temperature. The final water temperature increase was

measured to be less than 10 °C. CRYSTALLITE CHARACTERISATION The surface morphology and elemental composition analysis of the substrates were monitored using a field emission scanning

electron microscopy (FE-SEM, JEOL, JSM-7001FA). The chemical properties analysis was performed using X-ray diffraction (XRD, Rigaku, Tokyo, Japan, RINT2500HLB) with a Cu Kα line of 1.5406 Å

and a scanning field of 2.5° ≦ 2θ ≦ 100°. Peak fitting was performed in referenced to JCPDS card 4-0831 and 5-0664. TEM micrographs, SAED patterns and HRTEM micrographs for the NCs were

obtained using a double Cs-corrected-TEM (FEI, Titan cubed) operated at 300 kV. _AB INITIO_ CALCULATION The simulation models of a flat surface and a nanobumped surface were constructed

using Materials Studio® atomic simulation software (Accelrys Software Inc.). The calculations were performed based on density functional theory (DFT)35,36. The radii of curvature of the

nanobumped surface, shown in Fig. 3(c) and Supplementary Fig. S3(a) and S3(b), were set to 0.5, 1.0 and 2.0 nm, respectively. The grey, red and white spheres in these figures represent zinc,

oxygen and hydrogen atoms, respectively. Initially, two free H2O molecules were placed in positions where strong interatomic forces were not exerted on each atom. The position of each atom

in the equilibrated state was obtained using a dynamic simulated annealing method28,29. In this method, the electronic states can be calculated by solving the quantum mechanical equation. In

the actual experiment for the effect of nanobumps, the reduced dissociation energy of the water molecules can be larger than 0.323 eV because the radius of curvature of the nanobumped (or

apical) surfaces might be larger than 0.5 nm (e.g., approximately, 5 nm in Fig. 2(d)). However, that value was considered to be considerably smaller than 5.03 eV for the flat surface because

the apical radius of the curved surface was still extremely small (typically approximately 10 nm). Additionally, an illumination, e.g., a typical UV light (λ = 350 nm, 3.54 eV), further

enhanced the dissociation of water molecules on the nanobumped surface because the photon energy was considerably larger than the dissociation energy for the nanobumped surface (0.323 eV).

This energy difference resulted in the localised SPSC reaction increment via a photo-electron excitation effect, namely, the enhancement of equation (1) for the generation of additional

excited electrons. Therefore, for the dissociated state of water molecules, which was induced by illumination, followed by an equilibration process, we obtained a final state, as shown in

Fig. 3(c), in which H2 molecule (gaseous) formation was predicted. OH RADICAL ANALYSIS During the UV light irradiation of the plasma-treated Zn plate, 4 ml of PNDA with a concentration of

1.5 mg/l was used as a scavenger in OH radical detection. Based from estimated O2 production in Fig. 4(e), the greater factor of ~24 from the experiment results can neglect the dissolved gas

effect in generated radicals: photo-induced water splitting governed the OH radical production. The absorption spectra before and after UV irradiation were compared: the concentration of

PNDA was measured using a JASCO V-630 UV-Vis spectrophotometer. Then, the time vs. exponential decay was plotted and the first-order reaction rate (k) was calculated. H2 GAS ANALYSIS The gas

captured after UV120h of six plasma-treated Zn substrates was used for GC analysis. The analysis of H2 and O2 gases was performed using a Shimadzu GC 8-A (thermal conductivity detector,

molecular sieve 13X, N2 carrier for H2 and He carrier for O2). For H2 gas detection, 100% H2 gas (100 μl) was injected into the GC using a microsyringe and the calibration curve was plotted.

Then, 100 μl of the captured gas was injected into the GC and its concentration was compared with the calibration curve. The same steps were repeated when recording the O2 concentration.

The obtained result gives in the H2/O2 ratio of 10. The value is five times more than two in the case of normal water splitting. ADDITIONAL INFORMATION HOW TO CITE THIS ARTICLE: Jeem, M. _et

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was supported by the “Nanotechnology Platform” from The Ministry of Education, Culture, Sports, Science and Technology (MEXT). The authors are grateful to Professor N. Sakaguchi, Mr. K.

Ohkubo and R. Ohta for their helpful discussions and technical assistance in operating the TEM system. We also thank Mr. Yukiyasu Yamakoshi for his technical assistance in operating the gas

chromatography system. AUTHOR INFORMATION AUTHORS AND AFFILIATIONS * Graduate School of Engineering, Hokkaido University, N13, W8, Kita-ku, Sapporo, 060-8628, Hokkaido, Japan Melbert Jeem, 

Muhammad Rafiq Mirza bin Julaihi, Shigeo Yatsu, Kazumasa Okamoto, Tamaki Shibayama & Seiichi Watanabe * Faculty of Engineering, Hokkaido University, N13, W8, Kita-ku, Sapporo, 060-8628,

Hokkaido, Japan Junya Ishioka, Shigeo Yatsu, Kazumasa Okamoto, Tamaki Shibayama, Takahiko Kato & Seiichi Watanabe * Hitachi Research Laboratory, Hitachi Ltd., 7-1-1 Omika, Hitachi,

319-1292, Ibaraki, Japan Tomio Iwasaki & Takahiko Kato Authors * Melbert Jeem View author publications You can also search for this author inPubMed Google Scholar * Muhammad Rafiq Mirza

bin Julaihi View author publications You can also search for this author inPubMed Google Scholar * Junya Ishioka View author publications You can also search for this author inPubMed Google

Scholar * Shigeo Yatsu View author publications You can also search for this author inPubMed Google Scholar * Kazumasa Okamoto View author publications You can also search for this author

inPubMed Google Scholar * Tamaki Shibayama View author publications You can also search for this author inPubMed Google Scholar * Tomio Iwasaki View author publications You can also search

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can also search for this author inPubMed Google Scholar CONTRIBUTIONS M.J. and M.R.M.J. performed most of the fabrication experiments and microstructural analyses. M.R.M.J., S.Y. and K.O.

conducted the OH radical and gas analyses. T.K. performed the XRD analysis. M.J., J.I. and T.S. performed the TEM observation. T.I. and T.K. conducted the _ab initio_ calculation. S.W.

conceived and supervised the project and developed the model. M.J., J.I. and S.W. wrote the paper. All of the authors discussed the results and contributed to the manuscript. ETHICS

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Ishioka, J. _et al._ A pathway of nanocrystallite fabrication by photo-assisted growth in pure water. _Sci Rep_ 5, 11429 (2015). https://doi.org/10.1038/srep11429 Download citation *

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