Photochemical water splitting mediated by a C1 shuttle

N. P. Alderman; J. M. Sommers; C. J. Viasus; C. H T Wang; V. Peneau; S. Gambarotta; B. Vidjayacoumar; K. A. Al-Bahily

doi:10.1039/C6DT03658A

Photochemical water splitting mediated by a C1 shuttle

N. P. Alderman, J. M. Sommers, C. J. Viasus, C. H T Wang, V. Peneau, S. Gambarotta, B. Vidjayacoumar, K. A. Al-Bahily

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3 Scopus citations

Abstract

The possibility of performing photochemical water splitting in a two-stage system, separately releasing the H and O components, has been probed with two separate catalysts and in combination with a formaldehyde/formate shuttling redox couple. In the first stage, formaldehyde releases hydrogen vigorously in the presence of an Na[Fe(CN)]·10HO catalyst, selectively affording the formate anion. In the second stage, the formate anion is hydro-genated back to formaldehyde by water and in the presence of a BiWO photocatalyst whilst releasing oxygen. Both stages operate at room temperature and under visible light irradiation. The two separate photocatalysts are compatible since water splitting can also be obtained in one-pot experiments with simultaneous H/O evolution.

Original language	English (US)
Pages (from-to)	49-54
Number of pages	6
Journal	Dalton Trans.
Volume	46
Issue number	1
DOIs	https://doi.org/10.1039/C6DT03658A
State	Published - 2017
Externally published	Yes

Bibliographical note

KAUST Repository Item: Exported on 2020-10-01
Acknowledgements: Saudi Basic Industry Corporation (SABIC) is gratefully acknowledged for financial support through a research grant. The authors wish to thank Dr Sharon Curtis and Dr Alexander Mommers from the John L. Homes Mass Spectrometry Facility for their help with the isotopic experiments. Parts of this study have been filed as patent applications US 15/150,680, US 62/300,175 and PCT/IB2016052676.

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title = "Photochemical water splitting mediated by a C1 shuttle",

abstract = "The possibility of performing photochemical water splitting in a two-stage system, separately releasing the H and O components, has been probed with two separate catalysts and in combination with a formaldehyde/formate shuttling redox couple. In the first stage, formaldehyde releases hydrogen vigorously in the presence of an Na[Fe(CN)]·10HO catalyst, selectively affording the formate anion. In the second stage, the formate anion is hydro-genated back to formaldehyde by water and in the presence of a BiWO photocatalyst whilst releasing oxygen. Both stages operate at room temperature and under visible light irradiation. The two separate photocatalysts are compatible since water splitting can also be obtained in one-pot experiments with simultaneous H/O evolution.",

author = "Alderman, {N. P.} and Sommers, {J. M.} and Viasus, {C. J.} and Wang, {C. H T} and V. Peneau and S. Gambarotta and B. Vidjayacoumar and Al-Bahily, {K. A.}",

note = "KAUST Repository Item: Exported on 2020-10-01 Acknowledgements: Saudi Basic Industry Corporation (SABIC) is gratefully acknowledged for financial support through a research grant. The authors wish to thank Dr Sharon Curtis and Dr Alexander Mommers from the John L. Homes Mass Spectrometry Facility for their help with the isotopic experiments. Parts of this study have been filed as patent applications US 15/150,680, US 62/300,175 and PCT/IB2016052676.",

year = "2017",

doi = "10.1039/C6DT03658A",

language = "English (US)",

volume = "46",

pages = "49--54",

journal = "Dalton Trans.",

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T1 - Photochemical water splitting mediated by a C1 shuttle

AU - Alderman, N. P.

AU - Sommers, J. M.

AU - Viasus, C. J.

AU - Wang, C. H T

AU - Peneau, V.

AU - Gambarotta, S.

AU - Vidjayacoumar, B.

AU - Al-Bahily, K. A.

N1 - KAUST Repository Item: Exported on 2020-10-01 Acknowledgements: Saudi Basic Industry Corporation (SABIC) is gratefully acknowledged for financial support through a research grant. The authors wish to thank Dr Sharon Curtis and Dr Alexander Mommers from the John L. Homes Mass Spectrometry Facility for their help with the isotopic experiments. Parts of this study have been filed as patent applications US 15/150,680, US 62/300,175 and PCT/IB2016052676.

PY - 2017

Y1 - 2017

N2 - The possibility of performing photochemical water splitting in a two-stage system, separately releasing the H and O components, has been probed with two separate catalysts and in combination with a formaldehyde/formate shuttling redox couple. In the first stage, formaldehyde releases hydrogen vigorously in the presence of an Na[Fe(CN)]·10HO catalyst, selectively affording the formate anion. In the second stage, the formate anion is hydro-genated back to formaldehyde by water and in the presence of a BiWO photocatalyst whilst releasing oxygen. Both stages operate at room temperature and under visible light irradiation. The two separate photocatalysts are compatible since water splitting can also be obtained in one-pot experiments with simultaneous H/O evolution.

AB - The possibility of performing photochemical water splitting in a two-stage system, separately releasing the H and O components, has been probed with two separate catalysts and in combination with a formaldehyde/formate shuttling redox couple. In the first stage, formaldehyde releases hydrogen vigorously in the presence of an Na[Fe(CN)]·10HO catalyst, selectively affording the formate anion. In the second stage, the formate anion is hydro-genated back to formaldehyde by water and in the presence of a BiWO photocatalyst whilst releasing oxygen. Both stages operate at room temperature and under visible light irradiation. The two separate photocatalysts are compatible since water splitting can also be obtained in one-pot experiments with simultaneous H/O evolution.

UR - http://hdl.handle.net/10754/622659

UR - http://pubs.rsc.org/en/Content/ArticleLanding/2017/DT/C6DT03658A

UR - http://www.scopus.com/inward/record.url?scp=85007020975&partnerID=8YFLogxK

U2 - 10.1039/C6DT03658A

DO - 10.1039/C6DT03658A

M3 - Article

C2 - 27841421

SN - 1477-9226

VL - 46

SP - 49

EP - 54

JO - Dalton Trans.

JF - Dalton Trans.

IS - 1

ER -

Photochemical water splitting mediated by a C1 shuttle

Abstract

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