Comparison of photocatalytic and transport properties of TiO2 and ZnO nanostructures for solar-driven water splitting
文献情報
Adriano Sacco, Angelica Chiodoni, Valentina Cauda, Guido Saracco
Titanium dioxide (TiO2) and zinc oxide (ZnO) nanostructures have been widely used as photo-catalysts due to their low-cost, high surface area, robustness, abundance and non-toxicity. In this work, four TiO2 and ZnO-based nanostructures, i.e. TiO2 nanoparticles (TiO2 NPs), TiO2 nanotubes (TiO2 NTs), ZnO nanowires (ZnO NWs) and ZnO@TiO2 core–shell structures, specifically prepared with a fixed thickness of about 1.5 μm, are compared for the solar-driven water splitting reaction, under AM1.5G simulated sunlight. Complete characterization of these photo-electrodes in their structural and photo-electrochemical properties was carried out. Both TiO2 NPs and NTs showed photo-current saturation reaching 0.02 and 0.12 mA cm−2, respectively, for potential values of about 0.3 and 0.6 V vs. RHE. In contrast, the ZnO NWs and the ZnO@TiO2 core–shell samples evidence a linear increase of the photocurrent with the applied potential, reaching 0.45 and 0.63 mA cm−2 at 1.7 V vs. RHE, respectively. However, under concentrated light conditions, the TiO2 NTs demonstrate a higher increase of the performance with respect to the ZnO@TiO2 core–shells. Such material-dependent behaviours are discussed in relation with the different charge transport mechanisms and interfacial reaction kinetics, which were investigated through electrochemical impedance spectroscopy. The role of key parameters such as electronic properties, specific surface area and photo-catalytic activity in the performance of these materials is discussed. Moreover, proper optimization strategies are analysed in view of increasing the efficiency of the best performing TiO2 and ZnO-based nanostructures, toward their practical application in a solar water splitting device.
関連文献
Conjugated oligomers with alternating heterocycles from a single monomer: synthesis and demonstration of electroluminescence
Matthias Bremer, Thibault Reynaldo, Janek Buhl, Paul J. Gates, Frank D. Sönnichsen, Muriel Hissler, Martina Gerken
DOI: 10.1039/C9QO00947G
(4 + 3) cycloadditions of allenyl ether-derived oxygen-stabilized oxyallyls with furans
Xian Huang, Waygen Thor, Xiangyu Feng, Liangliang Kang, Min Yang, Chi-Sing Lee, Yuen-Kit Cheng, Shuzhong He
DOI: 10.1039/C9QO01349K
Cobalt(iii)-catalyzed ketone-directed C–H vinylation using vinyl acetate
Md Raja Sk, Modhu Sudan Maji
DOI: 10.1039/C9QO01164A
Tuning the optical properties of spiro-centered charge-transfer dyes by extending the donor or acceptor part
Jan S. Wössner, David C. Grenz, Daniel Kratzert
DOI: 10.1039/C9QO01134J
Transition-metal-free synthesis of CMe2CF3-containing chroman-4-ones via decarboxylative trifluoroalkylation
Wei Liu, Hua-Yue Wu, Yun-Bing Zhou, Qiuping Ding, Yiyuan Peng
DOI: 10.1039/C9QO01283D
The decarboxylative C–H heteroarylation of azoles catalysed by nickel catalysts to access unsymmetrical biheteroaryls
Ke Yang, Mengjie Song, Zhiyan Ma, Yi Li, Zhengyi Li, Xiaoqiang Sun
DOI: 10.1039/C9QO01073D
Copper-catalyzed synthesis of trifluoromethylated bis(indolyl)arylmethanes from 2-arylindoles and 2,2,2-trifluoroacetohydrazide
Zihang Yuan, Shouxiong Chen, Zhiqiang Weng
DOI: 10.1039/C9QO01131E
Modified diterpenoids from the tuber of Icacina oliviformis as protein tyrosine phosphatase 1B inhibitors
Junfei Zhou, Brian Guo, Meng Sun, Monday M. Onakpa, Guangmin Yao, Ming Zhao, Chun-Tao Che
DOI: 10.1039/C9QO01320B
Selectfluor™-catalyzed oxidative cyclization of ynamides enables facile synthesis of oxazolidine-2,4-diones
Guangke He, Yuan Li, Zilun Yu, Zhaoqiang Chen, Yongming Tang, Guangliang Song
DOI: 10.1039/C9QO00845D
こちらもおすすめ
噻奈普汀乙酯の物理化学的性質は何ですか?
CAS番号66981-77-9の噻奈普汀乙酯は、結晶性白色粉末であり、分子量は476.9 g/molです。この化合物は水に溶けにくく、一般的には有機溶媒で溶解し...
アミピシリン不純物Fとは何ですか?
アミピシリン不純物Fは、CAS番号124774-48-7の化合物です。これは、抗生物質アミピシリンの生産過程で生成される不純物の一つであり、(4S)-2-({[...
イリジウム(I)ヘキサフルオロフォスファートの代替品はありますか?
イリジウム(I)ヘキサフルオロフォスファートの代替品として、他の有機金属化合物や非有機金属化合物が使用されることがあります。具体的には、ダイゾニウム塩や他の金属...
含有3-(苯氧基甲基)苯硼酸频那醇酯の廃棄物はどのように処理すべきですか?
含有3-(苯氧基甲基)苯硼酸频那醇酯の廃棄物は、安全な方法で処理する必要があります。まず、廃棄物を適切な容器に収集し、避けて保管します。次に、専門の廃棄処理業者...
2-甲基辛-1-醇を取り扱う際の実験室安全事項は何ですか?
取り扱う際は、密閉のゴーグルと手袋を着用することが推奨されます。ドラフトチャンバーを使用し、漏洩時には速やかに取り扱いを中止し、適切な排気設備を使用してください...
3α-アセトキノイドコレステロールエステルはどのように保存すればよいですか?
3α-アセトキノイドコレステロールエステルは、常温から低温(0-5℃)の暗所で保存し、密閉容器に入れることで安定性を保つことが推奨されます。また、湿気や酸素から...
2-ぶンジロキシ-4-(トリフルオロメチル)フェノルビノン酸の主な用途は何ですか?
2-ぶンジロキシ-4-(トリフルオロメチル)フェノルビノン酸は、化学合成の触媒としての使用や、医薬品の合成材料としての役割があります。また、特定の合成路線で使用...
(2S,3R)-2-氨基-3-甲基丁二酸はどのように合成されますか?
(2S,3R)-2-氨基-3-甲基丁二酸は、2-ヒドロキシ-3-メチル丁酸とアミノ化反応を行うことで合成されます。触媒としてジクロロメタンが使用され、選択性と収...
1-Benzyl-2-phenyl-1H-imidazoleはどのように保存すればよいですか?
この化合物は常温で避けてください。直射日光を避け、密閉容器で保存し、湿気を防水の容器に入れて保管してください。
掲載誌
Physical Chemistry Chemical Physics

Physical Chemistry Chemical Physics (PCCP) is an international journal co-owned by 19 physical chemistry and physics societies from around the world. This journal publishes original, cutting-edge research in physical chemistry, chemical physics and biophysical chemistry. To be suitable for publication in PCCP, articles must include significant innovation and/or insight into physical chemistry; this is the most important criterion that reviewers and Editors will judge against when evaluating submissions. The journal has a broad scope and welcomes contributions spanning experiment, theory, computation and data science. Topical coverage includes spectroscopy, dynamics, kinetics, statistical mechanics, thermodynamics, electrochemistry, catalysis, surface science, quantum mechanics, quantum computing and machine learning. Interdisciplinary research areas such as polymers and soft matter, materials, nanoscience, energy, surfaces/interfaces, and biophysical chemistry are welcomed if they demonstrate significant innovation and/or insight into physical chemistry. Joined experimental/theoretical studies are particularly appreciated when complementary and based on up-to-date approaches.













![2,2'-[(Abieta-8,11,13-trien-18-ylimino)bis(2,1-ethanediyloxy)]diethanol structure 2,2'-[(Abieta-8,11,13-trien-18-ylimino)bis(2,1-ethanediyloxy)]diethanol structure](https://static.chemtradehub.com/structs/513/51344-62-8-8518.webp)
![Methyl 8-azabicyclo[3.2.1]octane-3-carboxylate hydrochloride structure Methyl 8-azabicyclo[3.2.1]octane-3-carboxylate hydrochloride structure](https://static.chemtradehub.com/structs/179/179022-43-6-77f5.webp)