出版者・発行元：Solar RRL  

Perovskite solar cells (PSCs) have undergone an unprecedentedly rapid development in both power conversion efficiency (PCE) and operational durability. However, a number of unknown challenges remain before PSC products are ready to launch. Herein, it is demonstrated that the vacuum deposition of gold (Au) onto the organic hole-transport layer (HTL) results in Au penetration into the perovskite layer. This Au penetration proves to be a limiting factor in PCE due to detrimental carrier recombination caused by the penetrated Au component inside the perovskite light absorber. To mitigate this issue, a thin molybdenum oxide (MoOx) interlayer between the organic HTL and the Au electrode is introduced, effectively reducing the Au penetration and suppressing the carrier recombination. Consequently, this MoOx introduction increases PCEs from ≈16.9% to ≈19.6% by ≈2.7%. Furthermore, using the MoOx interlayer improves the long-term durability of PSCs. These findings are crucial in elucidating a basic mechanism that limits PCE and in advancing the fabrication of PSC products with even higher performance.

DOI： 10.1002/solr.202400029

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記述言語：英語   掲載種別：研究論文（学術雑誌）   出版者・発行元：公益社団法人　電気化学会  

A dense NiO-Fe2O3 (NiFe) pellet has been developed as a potential anode-support for thin-film solid oxide fuel cells (SOFCs). However, preparation of dense NiFe is very challenging. Hole-formed NiFe pellets or porous NiFe pellets are frequently formed, which cannot be used as a support (substrate) for thin-film SOFCs. Therefore, this hole-formed NiFe support is simply wasted. In this report, we attempt to re-qualify this NiFe support to be a valuable substrate, which can be used for fabricating thin-film SOFCs. By deposition of smaller NiFe particles to cover the hole-formed NiFe support, the surface of this NiFe pellet is modified. Large holes on the surface disappear. The newly formed NiFe support can be used for fabricating a single cell with La0.9Sr0.1Ga0.8Mg0.2O3−δ as thin-film electrolyte operated at intermediate temperature. Maximum power density generated from this cell is 0.45, 0.86 and 1.28 W cm−2 at 873, 923 and 973 K, respectively. (Figure Presented).

DOI： 10.5796/electrochemistry.23-00164

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記述言語：英語   掲載種別：研究論文（学術雑誌）  

出版者・発行元：Solar RRL  

All-inorganic CsPbI2Br mixed halide perovskites show promise as wide-bandgap photoabsorbers in photovoltaics. However, the rapid crystal growth observed in solution-processed CsPbI2Br often leads to morphologies plagued by pinholes and defects, which limit device performance. This study introduces 2-Amino-5-nitrothiazole (ANT), an innovative precursor additive, to enhance film quality. ANT's selective interactions with the perovskite precursor moderate the crystal growth, resulting in a dense, flawless CsPbI2Br film characterized by superior crystallinity and coverage. Furthermore, the -NH2 group in ANT coordinates with Pb octahedra, effectively mitigating charge defects through NH=I/Br bonds. Simultaneously, S=C-N sites interact with uncoordinated Pb2+ ions, reducing defect states and nonradiative recombination. This innovation achieves an impressive device efficiency of 17.13% with a fill factor (FF) of 83.41%, surpassing the control's efficiency of 15.21% (FF of 80.45%). Notably, the champion device maintains an efficiency of 29.47% under indoor light-emitting diode lighting at 1000 lux. Additionally, the optimized perovskite solar cell demonstrates remarkable stability, retaining ≈90% of its efficiency for over 720 h at 85 °C in air, even without encapsulation.

DOI： 10.1002/solr.202300912

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掲載種別：研究論文（学術雑誌）   出版者・発行元：Applied Catalysis B: Environmental  

NH3 is an important chemical fertilizer and expecting as H2 carrier. Several methods have been investigated for eco-friendly NH3 production under mild conditions instead of Haber-Bosch process using 400 °C, 20 MPa. Here, cyanobacterial Anabaena variabilis was utilized as a nitrogenase-producing biocatalyst that converts N2/H2O to NH3 under ambient conditions. Biocatalytic reactions revealed that MV•+ can penetrate cell membrane and transfer electrons generated in inorganic photocatalyst. We first reported photobiocatalytic NH3 production of cyanobacteria and TiO2. Comparing with natural system, NH3 formation rate of the hybrid system increased 81.3 times with an initial rate of 2031.7 nmol·h−1 and turnover number of 216.8.

DOI： 10.1016/j.apcatb.2023.123431

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出版者・発行元：International Journal of Energy Research  

The processing of halide perovskites in the air significantly influences their morphology and surface coverage, often leading to the presence of numerous trap densities that adversely affect device performance. In this study, we explored the development of perovskite films using a solvent extraction method, where the temperature of the anisole antisolvent was varied. Our findings demonstrate that the hot-antisolvent strategy effectively controls nucleation, resulting in the formation of highly dense, pinhole-free, and crack-free perovskite films with reduced surface roughness. Films fabricated using this hot-antisolvent approach exhibited enhanced photoluminescence, indicating lower trap density and increased recombination resistance. They also showed slower charge carrier recombination rates and efficient charge extraction, suggesting the suppression of nonradiative recombination. Furthermore, the superior quality of perovskite films obtained through the hot-antisolvent strategy significantly enhanced the power conversion efficiency (PCE) of hot-pressed semitransparent perovskite solar cells. The PCE remarkably increased from 0.13% to an impressive 12.65% while maintaining an average visible transmittance of 26.55% and exceptional air stability for 2000 hours with no significant degradation in initial PCE. This study achieves a record-breaking light utilization efficiency of 3.36% in the realm of research on hot-press processes.

DOI： 10.1155/2024/9417829

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掲載種別：研究論文（学術雑誌）   出版者・発行元：Journal of the Electrochemical Society  

Effects of channel size in NiO-YSZ porous substrate were studied on power density in solid oxide fuel cell mode and electrolysis current in steam electrolysis mode. It was found that the cell deposited on anode substrate with larger pore diameter shows a superior performance. The LSGM cell prepared on Ni-YSZ tube with average channel diameter of ca. 2.5 μm shows the maximum power density of 0.36 W cm−2 in SOFC mode and 0.42 A cm−2 at 1.6 V in SOEC mode at 873 K. Spike potential noise which may be caused by insufficient gas diffusion in NiO-YSZ porous substrate was observed under constant current electrolysis condition in case of NiO-YSZ tube with narrow channel and the spike noise is suppressed by increasing channel size. NiO-YSZ tube with large channel size is also effective for increasing long term stability in electrolysis mode.

DOI： 10.1149/1945-7111/ad2815

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その他リンク： https://iopscience.iop.org/article/10.1149/1945-7111/ad2815/pdf

掲載種別：研究論文（学術雑誌）   出版者・発行元：Journal of Materials Chemistry C  

In this study, a hybrid photocatalyst with titanium oxide using reduced graphene nanoribbons (rGNR) was fabricated. The resulting 0.5 wt% platinum-loaded titanium oxide-supported reduced GNRs (Pt/TiO2/rGNR) exhibited an activity of 2.54 mmol h−1 g−1 which is 6.35 times higher than the 0.40 mmol h−1 g−1 of the titanium oxide photocatalyst. This activity was also higher than that of the starting material, multi-walled carbon nanotube (MWCNT)-supported titanium oxide (Pt/TiO2/MWCNT) as 0.80 mmol h−1 g−1. The resulting catalysts were characterized by X-ray photoelectron spectroscopy (XPS) and fluorescence lifetime spectroscopy, and the GNRs chemically reduced by NaBH4 (rGNR) had higher conductivity than the GNRs reduced by photogenerated electrons (pGNR) from titanium oxide. It was found using the photocatalytic reaction and photocurrent test that almost no photoresponsivity of reduced GNR character was exhibited. This result clarified that the reduced GNRs played the role of a mediator that promotes charge separation between photocatalysts and that effective hydrogen production in water was achieved.

DOI： 10.1039/d3tc03622g

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記述言語：英語   掲載種別：研究論文（学術雑誌）  

掲載種別：研究論文（学術雑誌）   出版者・発行元：Catalysis Today  

Photocatalytic hydrogen peroxide (H2O2) by oxygen and phosphorus co-doped graphitic carbon nitride (C3N4) with cobalt phosphate (CoP) cocatalyst is investigated. The photocatalyst powder of CoP-C3N4 1:n, n = 0–4, n is the weight ratio of cyanuric acid added) was synthesized by melamine cyanurate template method. Characterization of the catalyst was performed by X-ray diffraction analysis, and scanning electron microscopy, X-ray photoemission spectra, and fluorescence decay spectra. Oxygen doping was performed by the melamine and cyanuric acid template method, followed by phosphorus doping of the C3N4 backbone by the introduction of CoP. Co-doping of O and P atom facilitated charge transfer on the C3N4 backbone, while CoP facilitated charge separation at the C3N4 interface. The CoP-C3N4 (1:4) photocatalyst increased H2O2 production rate by 293 % compared to that of the cyanuric acid-free photocatalyst and also achieved the photocatalytic oxygen evolution from water. These results indicate that O,P co-doped CoP-C3N4 can perform sacrificial agent-free hydrogen peroxide under visible light irradiation.

DOI： 10.1016/j.cattod.2023.114400

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記述言語：英語   掲載種別：研究論文（学術雑誌）  

掲載種別：研究論文（学術雑誌）   出版者・発行元：Solid State Ionics  

Mullite-phase bismuth gallate (Bi2Ga4O9) was successfully synthesized with partial substitution of bismuth with alkaline-earth cation, Mg2+, Ca2+, Sr2+, and Ba2+. The effect of this substitution on the electrical conductivity was investigated. In this study, substitution with Ca2+ of Bi site was further studied for increasing the ionic conductivity as well as the phase stability in reducing atmospheres. Substitution with Ca2+ was found to be the most effective and with 12.5 mol% of Ca2+ as the optimized doping amount. Conductivity and stability in reducing atmospheres was increased down to pO2 ≤ 10−19 atm while keeping the conductivity of σ = 2.6 × 10−2 S·cm−1 at 973 K largely independent of oxygen partial pressure. Oxygen permeation analysis estimates 76% of theoretical oxygen permeation rate at 973 K suggesting main charge carrier is oxide ion. Partial electronic conductivity was measured with the ion blocking method. Oxide ion conductivity is dominated over wide pO2 range excepting for hole conduction at high pO2. Density functional theory (DFT) analysis on oxide ion diffusion route suggests oxygen hoping through lattice vacancy is main pathway for oxide ion conductivity in this doped Bi2Ga4O9. Despite the low oxide ion conductivity in Mullite-phase oxide, it was found that Ca doped Bi2Ga4O9 shows good oxide ion conductivity over wide pO2 range.

DOI： 10.1016/j.ssi.2023.116343

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出版者・発行元：Applied Surface Science  

All-inorganic α-CsPbI2Br perovskite has garnered considerable interest due to its optical bandgap (∼1.92 eV) suitable for tandem architectures and superior thermal stability. However, CsPbI2Br based perovskite solar cells (PSCs) exhibit severe energy loss due to presence of various surface defects like uncoordinated Pb2+ ions, halide ion vacancies and pinholes, which causes serious non-radiative recombination and limit the further improvement in power conversion efficiency (PCE). Surface passivation strategy is an effective approach to produce high quality α-CsPbI2Br film. Herein, we introduce fluorinated ionic liquid, 3-(Trifluoromethyl) benzylamine (CFBA), as surface passivating agent. The chemical analysis shows that the trifluoro (-CF3) and amine groups of CFBA strongly interacted with perovskite surface via forming Pb-F and H-I bonding, respectively. The high electronegative fluoride atoms of -CF3 group allow for electrostatic interaction with uncoordinated Pb2+ ions, which built a robust shield that protected against surrounding moisture as well. In addition, CFBA modification passivates the dangling bonds, enhanced crystallinity, reduced pinholes, improved the surface coverage and compactness, increased hydrophobicity, and decreased non-radiative recombination, leading to high PCE. With optimum concentration of 3 μL-CFBA, CsPbI2Br PSC revealed an impressive PCE of 17.07% with FF of 83.21% as compared to pristine device (PCE of 15.24% with FF of 79.81%). Moreover, champion device showed an excellent thermal stability by retaining ∼ 86.23% of its initial PCE, whereas pristine device maintained ∼ 48.26% of its original PCE after 1440 h aging at 85 ℃ in a dry box without any encapsulation. In addition, optimized PSC showed a decent indoor PCE of 23.24% as compared to pristine device (18.35%) under dim lighting conditions (LED, 3200 K) at 1000 lx. These results suggested that surface passivation strategy with CFBA is a promising approach for developing efficient all-inorganic CsPbI2Br outdoor/indoor PSCs with better thermal stability.

DOI： 10.1016/j.apsusc.2023.157901

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記述言語：英語   掲載種別：研究論文（学術雑誌）  

掲載種別：研究論文（学術雑誌）   出版者・発行元：Journal of Materials Chemistry A  

BODIPY (boron-dipyrromethene) compounds are extensively utilized in various applications. Typically, their activity is modified by altering the functional groups at the α-, β-, and meso-positions of the substituents. However, no systematic information has been provided regarding the effects of substituted F- positions and hydrophobicity on the activity of BODIPY sensitizers in photosensitizing chemistry. Dyes (7a-7c) with different alkyl chain lengths were synthesized and compared with the unsubstituted compound 3 to discuss the effects of -F position substituents and the hydrophobicity of BODIPY dyes on photocatalytic activity. Density functional theory (DFT) calculations showed that -F-substitution induced an intramolecular charge transfer (ICT) effect, enhancing visible-light absorption. Longer alkyl chains provided a favourable second coordination sphere reaction environment for hydrogen production. Experimentally, dye 7c demonstrated the highest activity, with a hydrogen production rate of 496.5 μmol gcat−1 h−1, which is 3 times higher than that of 3, and a 9.6 times higher turnover frequency (TOF) than that of 3. The apparent quantum yield (AQY) at 650 nm was 1.4%. This study highlights the importance of -F position substitution and optimizing hydrophobicity to enhance the photocatalytic activity of metal-free organic dyes through the creation of a new second coordination sphere.

DOI： 10.1039/d3ta03682k

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記述言語：英語   掲載種別：研究論文（学術雑誌）  

記述言語：英語   掲載種別：研究論文（学術雑誌）   出版者・発行元：Solid State Ionics  

For increasing the performance of PCFC (Protonic Ceramic Fuel Cells), it is important to prepare high-quality thin films of electrolyte materials. In this study, the preparation condition of the thin film of BaZr0.8Yb0.2O2.9 (BZYb) by pulsed laser deposition (PLD) method was optimized and the electrical conductivities of the obtained films were measured. The thin film was prepared by PLD using two kinds of BZYb targets, which were prepared by solids state reaction and Pechini method. Both thin-film samples have the single phase of the cubic perovskite-type structure, however, morphology as well as the orientation of the BZYb film was significantly different. The thin film using the target material by Pechini method is a high crystalline orientation and partially oriented [211] direction. The electrical conductivities of the obtained thin films at reduction atmosphere are dominated by proton conductivity, which is almost the same as that of the bulk sample despite [211] orientation.

DOI： 10.1016/j.ssi.2023.116240

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リポジトリ公開URL： https://hdl.handle.net/2324/7172331

掲載種別：研究論文（学術雑誌）   出版者・発行元：Applied Catalysis B: Environmental  

In the CO2 electrocatalytic reduction reaction (CO2RR) technology, high CO2 conversion rate is highly required for efficient CO2 utilization from the CO2 resource. In this study, we propose the strategy of combining UiO-66 metal organic framework (MOF) structure with Bi electrocatalyst for highly active CO2RR with selective formic acid production. The synthesized Bi/UiO-66 catalyst shows superior CO2 reduction property, 4.6 times higher current density at −0.7 V vs. reversible hydrogen electrode (RHE) than bare Bi without UiO-66 despite of low electrochemical surface area. Also, NH2 functionalized UiO-66 shows almost no effect on CO2RR as compared to without NH2 probably due to disassembled linkers during CO2RR. Various characterizations such as Fourier transform infrared (FTIR), Raman spectroscopy, X-ray photoelectron spectroscopy (XPS) indicate carbonate species captured form of CO2 at Zr-MOF site should contribute the high CO2 conversion rate. Our findings demonstrate the feasibility of Zr-MOF as a Supporting material to achieve efficient CO2 reduction.

DOI： 10.1016/j.apcatb.2023.122400

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記述言語：英語   掲載種別：研究論文（学術雑誌）   出版者・発行元：Applied Catalysis A: General  

Photobiocatalytic system has been developing as a promising approach for H2 production. Herein, the rational characteristics of biocatalysts and the role of individual components affecting the efficiency of the system were investigated. Photocatalytic studies showed that tris (2-amino-2-hydroxymethyl-1,3-propanediol) was an ideal electron donor for viologen reduction by TiO2. Biocatalytic reaction revealed that cell permeability, the redox potential of electron mediators and the cell envelope were crucial to the activity of whole-cell biocatalysts. In photobiocatalytic system, recombinant Escherichia coli with a turnover frequency of 39.43 ± 3.77 s−1 based on [FeFe]-hydrogenase activity was a more rational biocatalyst than Anabaena variabilis. A comprehensive study found that the presence of TiO2, light and biocatalysts strongly enhanced H2 production, whereas Tris and MV2+ had less influence. A maximum rate was found at 16.73 ± 1.03 μmol/min with a solar-to-H2 conversion of 1.58 ± 0.10 %. Understanding the role of each component will guide the development of high-efficient photobiocatalysis.

DOI： 10.1016/j.apcata.2022.119019

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記述言語：英語   掲載種別：研究論文（学術雑誌）  

記述言語：英語   掲載種別：研究論文（学術雑誌）   出版者・発行元：Applied Physics A: Materials Science and Processing  

Squaraine dyes are organic dyes having strong and narrow absorption properties in the near-infrared region that are widely used in photovoltaic and biomedical applications. In this work, squaraine dye (SA1) was synthesized as a dye sensitizer for a dye-sensitized photocatalytic system, which was composed of SA1 and Pt-loaded TiO2 powder photocatalyst (SA1/Pt-TiO2). The SA1/Pt-TiO2 system exhibited a good hydrogen production performance within 150 h and an apparent quantum yield of 1.4% under 800 nm monochromatic light irradiation. However, during the photocatalytic reaction, the photocatalytic activity of SA1/Pt-TiO2 decreased due to photodecomposition. Ultraviolet–visible absorption spectroscopy, 1H nuclear magnetic resonance spectroscopy, and matrix-assisted laser desorption/ionization time-of-flight mass spectrometry measurements were performed to investigate the mechanism of the decomposition of the squaraine moiety of SA1, the decomposition process, and the structure of the decomposed material. The results show that even without the Pt-loaded TiO2 powder photocatalyst, SA1 undergoes photodissociation, which cleaves the bond between the indoline moiety and the square acid. Graphical abstract: [Figure not available: see fulltext.]

DOI： 10.1007/s00339-022-06281-7

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その他リンク： https://link.springer.com/article/10.1007/s00339-022-06281-7/fulltext.html

掲載種別：研究論文（学術雑誌）   出版者・発行元：Catalysis Science and Technology  

Strained metal oxides are known to exhibit improved activity for redox and photocatalytic reactions. Here, we intentionally introduced tensile strain into rutile-type TiO2 by utilizing the difference in thermal expansion coefficients between TiO2 and Au and applied it as a solid acid catalyst. It was demonstrated that its acid catalytic activity in the acetalization of furfural was enhanced by increasing the degree of the strain introduced.

DOI： 10.1039/d2cy00736c

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記述言語：日本語   出版者・発行元：公益社団法人 石油学会  

<p>白金担持アルミナ上で，一酸化窒素（NO）を酸化剤としてメタンをシアン化水素（HCN）に変換する際の白金ナノ粒子の粒径効果について検討した。担持量と焼成温度を制御することにより，1.6〜4.1 nmの範囲で様々な平均粒子径のPt触媒を得ることができた。Pt表面サイト量はパルス法によるCO滴定で決定し，触媒活性は同一接触時間下で評価した。Pt の粒子が小さい触媒（1.6〜3.2 nm）では，NO 転化率が粒子径の大きい触媒よりも低いことが分かった。粒子径の大きな触媒（4.1〜4.2 nm）は，10 wt% Pt/Al₂O₃ において 400 ℃で 収率1.3 %（炭素ベース）で高い HCN 選択率（53.5 %）を示した。大きなPt粒子が高い活性を示す理由の一つは，金属と担体の界面で進行するHCNから二酸化炭素とアンモニアへの逐次反応を抑制したためと思われる。Pt L₃端X線吸収微細構造（XAFS）スペクトルから，反応試験後の小粒子触媒はPt–CN種で覆われていることが分かった。一方，大粒子触媒ではPt–COが主な吸着種として観測され，大粒子触媒の方がHCN脱離が容易であることが示唆された。</p>

DOI： 10.1627/jpi.65.184

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記述言語：英語   掲載種別：研究論文（学術雑誌）   出版者・発行元：Solid State Ionics  

NiO-Y2O3 stabilized ZrO2 (YSZ) tubular type cell using La0.9Sr0.1Ga0.8Mg0.2O3−δ electrolyte film was prepared by dip-coating method. Effects of Ce infiltration or Ce, Ni sequential-infiltration into NiO-YSZ substrate were studied and it was found that Ce infiltration after Ni is highly effective for increasing the cell performance and the stability in fuel cell and electrolysis mode at 873 K in spite of decrease in performance by simple Ni infiltration. Cyclic operation of the fuel cell and electrolysis of LSGM tubular cell using Ce or Ce[sbnd]Ni sequential-infiltrated NiO-YSZ substrate was measured at 873 K using 17% steam-25%H2 in Ar as fuel. After 100 cycles at ±0.1 A cm−2, OCV was almost the same with the initial value. The terminal potential in SOFC operation became slightly lower with increasing cycle number in case of simple Ce infiltration. The main reason for degradation during cyclic performance seems to be assigned to the increased fuel electrode overpotential. However, degradation rate is much decreased by Ce[sbnd]Ni sequential-infiltration.

DOI： 10.1016/j.ssi.2022.115914

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記述言語：英語   掲載種別：研究論文（学術雑誌）   出版者・発行元：Applied Catalysis A: General  

Porous boron nitride was synthesized using boric acid with urea and/or hexamethylenetetramine (HMTA) via pyrolysis method. X-ray diffraction and Fourier transform infrared measurements indicated that the synthesized boron nitride has a turbostratic structure with both amino and hydroxyl group on the surface. The synthesis using a mixture of two nitrogen-containing precursors was found to not only significantly increase the porosity, but also improve the surface functionality. X-ray photoelectron spectroscopy and B K-edge and O K-edge X-ray absorption fine structure measurements revealed that the proportion of amino and hydroxyl groups on the surface increased with increasing concentration of HMTA during synthesis. Solid-state 11B nuclear magnetic resonance spectroscopy indicated that all samples contained trigonal B-N, trigonal B-O and tetrahedral B-O sites, and that samples prepared with high concentrations of HMTA had less tetrahedral B-O sites, suppressing the formation of BOx species as byproducts. Solid base catalytic activity was evaluated through Knoevenagel condensation, and the catalytic performance was significantly improved by synthesizing boron nitride catalyst using a mixture of the two nitrogen-containing precursors. The enhancement of the activity was influenced by the development of the pore structure as well as the emergence of functional groups on the surface.

DOI： 10.1016/j.apcata.2022.118635

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記述言語：英語   掲載種別：研究論文（学術雑誌）   出版者・発行元：Journal of Materials Chemistry A  

Sillén-Aurivillius phase Bi4NbO8Cl consists of Bi2O2+/NbO3-/Bi2O2+/Cl- layers and oxide-ion conduction is expected to occur in its Bi2O2+ layer. Here, we report the influence of partial substitutions of Bi with Ca2+, Sr2+, Ba2+, La3+, Ga3+ and Sn4+ on the electrical properties. It was found that substitution with low valence cations is effective for increasing electrical conductivity, and in particular, Sr2+ substitution is the most effective for this purpose. The dependence of electrical conductivity on the oxygen partial pressure of a Sr-doped sample is quite low (PO2-0.015) and the optimized amount of Sr doping is x = 0.1 in Bi4-xSrxNbO8-δCl. The electromotive force of N2/O2 gas concentration cell is 90% of the theoretical value and the tracer diffusion constant (D) estimated by 18O2 diffusion almost corresponds with that estimated from conductivity. Considering the activation energy of the D value, oxide-ion conductivity in Sillén-Aurivillius phase Bi4NbO8Cl mainly occurs along the Bi2O22+ layer, which indicates that Bi4NbO8Cl is a new family of fast oxide-ion conductors. This journal is

DOI： 10.1039/d1ta07335d

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記述言語：英語   掲載種別：研究論文（学術雑誌）  

記述言語：その他   掲載種別：研究論文（学術雑誌）  

DOI： 10.1016/j.cej.2021.131063

記述言語：英語   掲載種別：研究論文（学術雑誌）  

記述言語：英語   掲載種別：研究論文（学術雑誌）  

記述言語：英語   掲載種別：研究論文（学術雑誌）  

DOI： 10.1016/j.apcatb.2020.119292

記述言語：その他   掲載種別：研究論文（学術雑誌）  

DOI： 10.1016/j.apcata.2020.117843

記述言語：英語   掲載種別：研究論文（学術雑誌）  

DOI： 10.1016/j.apcatb.2020.119049

記述言語：英語   掲載種別：研究論文（学術雑誌）  

DOI： 10.1063/5.0009340

記述言語：その他  

記述言語：英語   掲載種別：研究論文（学術雑誌）  

DOI： 10.1016/j.apcata.2020.117743

記述言語：英語   掲載種別：研究論文（学術雑誌）  

DOI： 10.3390/catal10050535

記述言語：英語   掲載種別：研究論文（学術雑誌）  

DOI： 10.1039/c9cc09988c

記述言語：英語   掲載種別：研究論文（学術雑誌）  

DOI： 10.1073/pnas.1918837117

記述言語：英語   掲載種別：研究論文（学術雑誌）  

DOI： 10.1021/acsenergylett.9b02511

記述言語：英語   掲載種別：研究論文（学術雑誌）  

DOI： 10.1021/acsami.9b18785

記述言語：英語  

DOI： 10.3390/catal9030224

記述言語：英語   掲載種別：研究論文（学術雑誌）  

DOI： 10.1002/ppsc.201800331

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DOI： 10.1021/acscatal.8b03520

記述言語：英語   掲載種別：研究論文（学術雑誌）  

DOI： 10.1016/j.apcatb.2018.03.071

記述言語：英語   掲載種別：研究論文（学術雑誌）  

DOI： 10.1039/c8ta01010b

記述言語：英語   掲載種別：研究論文（学術雑誌）  

DOI： 10.1039/c7nr08168e

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DOI： 10.1021/acsomega.7b00846

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DOI： 10.1039/c6ta10707a

記述言語：英語   掲載種別：研究論文（学術雑誌）  

DOI： 10.1002/aenm.201601103

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DOI： 10.1007/s13391-017-6316-1

記述言語：英語   掲載種別：研究論文（学術雑誌）  

DOI： 10.7567/JJAP.54.04DR05

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DOI： 10.7567/JJAP.53.05FZ04

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DOI： 10.1143/JJAP.51.06FL18

開催年月日： 2023年5月

記述言語：英語   会議種別：口頭発表（一般）  

国名：大韓民国  

開催年月日： 2022年6月

記述言語：日本語   会議種別：口頭発表（一般）  

開催地：オンライン   国名：日本国  

開催年月日： 2022年6月

記述言語：日本語  

開催地：オンライン   国名：日本国  

開催年月日： 2021年6月

記述言語：英語   会議種別：シンポジウム・ワークショップ パネル（公募）  

国名：大韓民国  

記述言語：英語  

国名：日本国  

記述言語：日本語  

国名：日本国