Engineering 3D-printed carbon structures with atomic layer deposition coatings as photoelectrocatalysts for water splitting

Literature Information

Publication Date 2023-12-05
DOI 10.1039/D3TA04460B
Impact Factor 12.732
Authors

Siowwoon Ng, Michela Sanna, Edurne Redondo


View Original

Abstract

Three-dimensional (3D)-printing has evolved as a popular technique for producing customized parts and devices. 3D conductive structures made of metals or carbon-based materials are highly preferable in the field of electrochemistry. Compared to their metal counterparts, 3D carbon structures printed by the filament extrusion technique are readily available to end users, with the advantages of reduced electrode mass and broad compatibility with harsh environments that might be required for electrochemical applications. To elevate the applicability of 3D carbon electrodes in sensing, catalysis, energy storage, etc., surface or chemical modifications and coating of functional layers are essential. Atomic layer deposition (ALD) is an ideal deposition tool for creating coatings on geometrically complicated structures, yet the surface chemistry of the inert 3D carbon electrodes critically affects the initial growth. We performed a straightforward surface treatment, also known as ‘activation’, to improve the surface wettability and promote the ALD of TiO2, SiO2, and Al2O3 at low deposition temperatures. We applied the ALD coated electrodes for light-enhanced water splitting hydrogen and oxygen evolution reactions (HER, OER). In addition, we showed that 3D electrodes can be prepared in different geometrical shapes and sizes, as their metal counterparts. This work presents the versatility of ALD coatings on 3D carbon platforms, tunable for many other applications.

Related Literature

Polymerizability of exomethylene monomers based on adamantyl frameworks

Raita Goseki, Shogo Miyai, Satoshi Uchida, Takashi Ishizone

2021-06-02 Paper

DOI: 10.1039/D1PY00500F

Purpurin derivatives as visible-light photosensitizers for 3D printing and valuable biological applications

Pauline Sautrot-Ba, Vlasta Brezová, Jean-Pierre Malval, Annalisa Chiappone, Louise Breloy, Samir Abbad-Andaloussi, Davy-Louis Versace

2021-03-24 Paper

DOI: 10.1039/D1PY00126D

Back cover

2021-06-22 Cover

DOI: 10.1039/D1PY90087K

A quinine-based quaternized polymer: a potent scaffold with bactericidal properties without resistance

Huan-Huan Ding, Mu-Han Zhao, Le Zhai, Jian-Bin Zhen, Le-Yun Sun, Jia-Zhu Chigan, Cheng Chen, Jia-Qi Li, Han Gao, Ke-Wu Yang

2021-03-25 Paper

DOI: 10.1039/D0PY01751E

Visible light-degradable supramolecular gels comprising cross-linked polyrotaxanes capped with trithiocarbonate groups

Tae Woong Kang, Atsushi Tamura, Yoshinori Arisaka, Nobuhiko Yui

2021-06-09 Paper

DOI: 10.1039/D1PY00569C

Hollow microspherical carbazole-based conjugated polymers by photoinduced step-growth polymerization

Tugba Celiker, Ali Suerkan, Sinem Altinisik, Mert Akgun, Sermet Koyuncu

2021-07-21 Paper

DOI: 10.1039/D1PY00822F

Photo cleavable thioacetal block copolymers for controlled release

Yongjun Men, Tobias G. Brevé, Antonia G. Denkova, Rienk Eelkema

2021-06-08 Paper

DOI: 10.1039/D1PY00514F

IrAAC-based construction of dual sequence-defined polytriazoles

Xiaojun Wang, Xueyan Zhang, Yong Wang, Shengtao Ding

2021-06-21 Paper

DOI: 10.1039/D1PY00718A

Front cover

2021-03-30 Cover

DOI: 10.1039/D1PY90045E

Outstanding Reviewers for Polymer Chemistry in 2020

2021-05-25 Editorial

DOI: 10.1039/D1PY90058G

You might also like

Compound Q&A

How should waste containing 2-Ethyl-4-Methyl-1H-Imidazole-5-Carbaldehyde (CAS: 88634-80-4) be handled?

Waste containing 2-Ethyl-4-Methyl-1H-Imidazole-5-Carbaldehyde (CAS: 88634-80-4) ...

88634-80-42-Ethyl-4-Methyl-1H-...
Compound Q&A

What industries use Triethoxy(octyl)silane (CAS: 1385031-14-0)?

Triethoxy(octyl)silane (CAS: 1385031-14-0) is widely used in the pharmaceuticals...

1385031-14-0Triethoxy(octyl)sila...
Compound Q&A

Are there alternatives to 3-iodo-7-nitro-1H-indazole (CAS: 864724-64-1) in synthesis?

Several alternatives to 3-iodo-7-nitro-1H-indazole (CAS: 864724-64-1) exist in t...

864724-64-13-iodo-7-nitro-1H-in...
Compound Q&A

Are there alternatives to Benzene, bis[(trimethoxysilyl)ethyl] (CAS: 266317-71-9) in synthesis?

Yes, there are alternatives to Benzene, bis[(trimethoxysilyl)ethyl] (CAS: 266317...

266317-71-9Benzene, bis[(trimet...
Compound Q&A

Is Isothiazole-3-carbonitrile (CAS: 1452-17-1) safe?

Isothiazole-3-carbonitrile (CAS: 1452-17-1) is generally considered safe when us...

1452-17-1Isothiazole-3-carbon...
Compound Q&A

Is (3-Chlorophenyl)methanol (CAS: 873-63-2) safe?

(3-Chlorophenyl)methanol (CAS: 873-63-2) is considered low to moderately toxic. ...

873-63-2(3-Chlorophenyl)meth...
Compound Q&A

How is (2S,3S)-2-Hydroxy-3-({[(2-methyl-2-propanyl)oxy]carbonyl}amino)-3-(2-naphthyl)propanoic acid (CAS: 959583-98-3) typically synthesized?

(2S,3S)-2-Hydroxy-3-({[(2-methyl-2-propanyl)oxy]carbonyl}amino)-3-(2-naphthyl)pr...

959583-98-3(2S,3S)-2-Hydroxy-3-...
Compound Q&A

What precautions should be taken when handling Methyl 2-(bromomethyl)-5-methoxybenzoate (CAS: 788081-99-2)?

Proper handling of methyl 2-(bromomethyl)-5-methoxybenzoate requires the use of ...

788081-99-2Methyl 2-(bromomethy...
Compound Q&A

What is 6,8-Dibromoimidazo[1,2-a]pyridine-2-carboxylic acid (CAS: 904805-36-3)?

6,8-Dibromoimidazo[1,2-a]pyridine-2-carboxylic acid (CAS: 904805-36-3) is an aro...

904805-36-36,8-Dibromoimidazo[1...
Compound Q&A

Is 3-Amino-5-bromo-2-pyridinecarbonitrile (CAS: 573675-27-1) safe?

3-Amino-5-bromo-2-pyridinecarbonitrile is considered safe when handled under pro...

573675-27-13-Amino-5-bromo-2-py...

Source Journal

Journal of Materials Chemistry A

Journal of Materials Chemistry A
CiteScore: 19.5
Self-citation Rate: 4.7%
Articles per Year: 2211

Journal of Materials Chemistry A, B & C cover high quality studies across all fields of materials chemistry. The journals focus on those theoretical or experimental studies that report new understanding, applications, properties and synthesis of materials. The journals have a strong history of publishing quality reports of interest to interdisciplinary communities and providing an efficient and rigorous service through peer review and publication. The journals are led by an international team of Editors-in-Chief and Associate Editors who are all active researchers in their fields. Journal of Materials Chemistry A, B & C are separated by the intended application of the material studied. Broadly, applications in energy and sustainability are of interest to Journal of Materials Chemistry A, applications in biology and medicine are of interest to Journal of Materials Chemistry B, and applications in optical, magnetic and electronic devices are of interest to Journal of Materials Chemistry C. More than one Journal of Materials Chemistry journal may be suitable for certain fields and researchers are encouraged to submit their paper to the journal that they feel best fits for their particular article. Example topic areas within the scope of Journal of Materials Chemistry A are listed below. This list is neither exhaustive nor exclusive. Artificial photosynthesis Batteries Carbon dioxide conversion Catalysis Fuel cells Gas capture/separation/storage Green/sustainable materials Hydrogen generation Hydrogen storage Photocatalysis Photovoltaics Self-cleaning materials Self-healing materials Sensors Supercapacitors Thermoelectrics Water splitting Water treatment

Recommended Compounds

Recommended Suppliers

Disclaimer
This page provides academic journal information for reference and research purposes only. We are not affiliated with any journal publishers and do not handle publication submissions. For publication-related inquiries, please contact the respective journal publishers directly.
If you notice any inaccuracies in the information displayed, please contact us at support@chemtradehub.com. We will promptly review and address your concerns.