Standard

Pivotal Impact Factors in Photocatalytic Reduction of CO2 to Value-Added C1 and C2 Products. / Cui, Y.; Labidi, A.; Liang, X.; Huang, X.; Wang, J.; Li, X.; Dong, Q.; Zhang, X.; Othman, S.I.; Allam, A.A.; Bahnemann, D.W.; Wang, C.

In: ChemSusChem, Vol. 17, No. 18, 23.09.2024.

Research output: Contribution to journalArticlepeer-review

Harvard

Cui, Y, Labidi, A, Liang, X, Huang, X, Wang, J, Li, X, Dong, Q, Zhang, X, Othman, SI, Allam, AA, Bahnemann, DW & Wang, C 2024, 'Pivotal Impact Factors in Photocatalytic Reduction of CO2 to Value-Added C1 and C2 Products', ChemSusChem, vol. 17, no. 18. https://doi.org/10.1002/cssc.202400551

APA

Cui, Y., Labidi, A., Liang, X., Huang, X., Wang, J., Li, X., Dong, Q., Zhang, X., Othman, S. I., Allam, A. A., Bahnemann, D. W., & Wang, C. (2024). Pivotal Impact Factors in Photocatalytic Reduction of CO2 to Value-Added C1 and C2 Products. ChemSusChem, 17(18). https://doi.org/10.1002/cssc.202400551

Vancouver

Cui Y, Labidi A, Liang X, Huang X, Wang J, Li X et al. Pivotal Impact Factors in Photocatalytic Reduction of CO2 to Value-Added C1 and C2 Products. ChemSusChem. 2024 Sep 23;17(18). https://doi.org/10.1002/cssc.202400551

Author

Cui, Y. ; Labidi, A. ; Liang, X. ; Huang, X. ; Wang, J. ; Li, X. ; Dong, Q. ; Zhang, X. ; Othman, S.I. ; Allam, A.A. ; Bahnemann, D.W. ; Wang, C. / Pivotal Impact Factors in Photocatalytic Reduction of CO2 to Value-Added C1 and C2 Products. In: ChemSusChem. 2024 ; Vol. 17, No. 18.

BibTeX

@article{a67505965c084f87aeb225aa874a8fc9,
title = "Pivotal Impact Factors in Photocatalytic Reduction of CO2 to Value-Added C1 and C2 Products",
abstract = "Over the past decades, CO2 greenhouse emission has been considerably increased, causing global warming and climate change. Indeed, converting CO2 into valuable chemicals and fuels is a desired option to resolve issues caused by its continuous emission into the atmosphere. Nevertheless, CO2 conversion has been hampered by the ultrahigh dissociation energy of C=O bonds, which makes it thermodynamically and kinetically challenging. From this prospect, photocatalytic approaches appear promising for CO2 reduction in terms of their efficiency compared to other traditional technologies. Thus, many efforts have been made in the designing of photocatalysts with asymmetric sites and oxygen vacancies, which can break the charge distribution balance of CO2 molecule, reduce hydrogenation energy barrier and accelerate CO2 conversion into chemicals and fuels. Here, we review the recent advances in CO2 hydrogenation to C1 and C2 products utilizing photocatalysis processes. We also pin down the key factors or parameters influencing the generation of C2 products during CO2 hydrogenation. In addition, the current status of CO2 reduction is summarized, projecting the future direction for CO2 conversion by photocatalysis processes. {\textcopyright} 2024 Wiley-VCH GmbH.",
keywords = "Asymmetric sites, CO2 reduction, Oxygen vacancies, Photocatalysis, Valuable chemicals, Global warming, Hydrogenation, Asymmetric site, CO 2 reduction, Continuous emission, Emissions into the atmosphere, Global warming and climate changes, Greenhouse emissions, Impact factor, Photocatalysis process, Photocatalytic reduction, Carbon dioxide, fuel, oxygen, article, atmosphere, climate change, dissociation, greenhouse, greenhouse effect, hydrogenation, kinetics, photocatalysis",
author = "Y. Cui and A. Labidi and X. Liang and X. Huang and J. Wang and X. Li and Q. Dong and X. Zhang and S.I. Othman and A.A. Allam and D.W. Bahnemann and C. Wang",
note = "Цитирования:3 Export Date: 19 October 2024 CODEN: CHEMI Адрес для корреспонденции: Bahnemann, D.W.; School of Environmental Science and Engineering, China; эл. почта: wangchuanyi@sust.edu.cn Адрес для корреспонденции: Wang, C.; School of Environmental Science and Engineering, China; эл. почта: cywang@ms.xjb.ac.cn Химические вещества/CAS: oxygen, 7782-44-7 Сведения о финансировании: National Natural Science Foundation of China, NSFC, 52161145409, 21976116 Сведения о финансировании: National Natural Science Foundation of China, NSFC Сведения о финансировании: 2023041004L, G2023041021L Текст о финансировании 1: . This work was supported by the National Natural Science Foundation of China ('52161145409, 21976116), SAFEA of China (\u201CBelt and Road\u201D Innovative Talent Exchange Foreign Expert Project # 2023041004L) (High\u2010end Foreign Expert Project # G2023041021L), and Alexander\u2010von\u2010Humboldt Foundation of Germany (Group\u2010Linkage Program). AOTP is thankful to the Phosagro/IUPAC/UNESCO research program in green chemistry. The authors acknowledge Princess Nourah bint Abdulrahman University Researchers Supporting Project number (PNURSP2024R5), Princess Nourah bint Abdulrahman University, Riyadh, Saudi Arabia",
year = "2024",
month = sep,
day = "23",
doi = "10.1002/cssc.202400551",
language = "Английский",
volume = "17",
journal = "ChemSusChem",
issn = "1864-5631",
publisher = "Wiley-Blackwell",
number = "18",

}

RIS

TY - JOUR

T1 - Pivotal Impact Factors in Photocatalytic Reduction of CO2 to Value-Added C1 and C2 Products

AU - Cui, Y.

AU - Labidi, A.

AU - Liang, X.

AU - Huang, X.

AU - Wang, J.

AU - Li, X.

AU - Dong, Q.

AU - Zhang, X.

AU - Othman, S.I.

AU - Allam, A.A.

AU - Bahnemann, D.W.

AU - Wang, C.

N1 - Цитирования:3 Export Date: 19 October 2024 CODEN: CHEMI Адрес для корреспонденции: Bahnemann, D.W.; School of Environmental Science and Engineering, China; эл. почта: wangchuanyi@sust.edu.cn Адрес для корреспонденции: Wang, C.; School of Environmental Science and Engineering, China; эл. почта: cywang@ms.xjb.ac.cn Химические вещества/CAS: oxygen, 7782-44-7 Сведения о финансировании: National Natural Science Foundation of China, NSFC, 52161145409, 21976116 Сведения о финансировании: National Natural Science Foundation of China, NSFC Сведения о финансировании: 2023041004L, G2023041021L Текст о финансировании 1: . This work was supported by the National Natural Science Foundation of China ('52161145409, 21976116), SAFEA of China (\u201CBelt and Road\u201D Innovative Talent Exchange Foreign Expert Project # 2023041004L) (High\u2010end Foreign Expert Project # G2023041021L), and Alexander\u2010von\u2010Humboldt Foundation of Germany (Group\u2010Linkage Program). AOTP is thankful to the Phosagro/IUPAC/UNESCO research program in green chemistry. The authors acknowledge Princess Nourah bint Abdulrahman University Researchers Supporting Project number (PNURSP2024R5), Princess Nourah bint Abdulrahman University, Riyadh, Saudi Arabia

PY - 2024/9/23

Y1 - 2024/9/23

N2 - Over the past decades, CO2 greenhouse emission has been considerably increased, causing global warming and climate change. Indeed, converting CO2 into valuable chemicals and fuels is a desired option to resolve issues caused by its continuous emission into the atmosphere. Nevertheless, CO2 conversion has been hampered by the ultrahigh dissociation energy of C=O bonds, which makes it thermodynamically and kinetically challenging. From this prospect, photocatalytic approaches appear promising for CO2 reduction in terms of their efficiency compared to other traditional technologies. Thus, many efforts have been made in the designing of photocatalysts with asymmetric sites and oxygen vacancies, which can break the charge distribution balance of CO2 molecule, reduce hydrogenation energy barrier and accelerate CO2 conversion into chemicals and fuels. Here, we review the recent advances in CO2 hydrogenation to C1 and C2 products utilizing photocatalysis processes. We also pin down the key factors or parameters influencing the generation of C2 products during CO2 hydrogenation. In addition, the current status of CO2 reduction is summarized, projecting the future direction for CO2 conversion by photocatalysis processes. © 2024 Wiley-VCH GmbH.

AB - Over the past decades, CO2 greenhouse emission has been considerably increased, causing global warming and climate change. Indeed, converting CO2 into valuable chemicals and fuels is a desired option to resolve issues caused by its continuous emission into the atmosphere. Nevertheless, CO2 conversion has been hampered by the ultrahigh dissociation energy of C=O bonds, which makes it thermodynamically and kinetically challenging. From this prospect, photocatalytic approaches appear promising for CO2 reduction in terms of their efficiency compared to other traditional technologies. Thus, many efforts have been made in the designing of photocatalysts with asymmetric sites and oxygen vacancies, which can break the charge distribution balance of CO2 molecule, reduce hydrogenation energy barrier and accelerate CO2 conversion into chemicals and fuels. Here, we review the recent advances in CO2 hydrogenation to C1 and C2 products utilizing photocatalysis processes. We also pin down the key factors or parameters influencing the generation of C2 products during CO2 hydrogenation. In addition, the current status of CO2 reduction is summarized, projecting the future direction for CO2 conversion by photocatalysis processes. © 2024 Wiley-VCH GmbH.

KW - Asymmetric sites

KW - CO2 reduction

KW - Oxygen vacancies

KW - Photocatalysis

KW - Valuable chemicals

KW - Global warming

KW - Hydrogenation

KW - Asymmetric site

KW - CO 2 reduction

KW - Continuous emission

KW - Emissions into the atmosphere

KW - Global warming and climate changes

KW - Greenhouse emissions

KW - Impact factor

KW - Photocatalysis process

KW - Photocatalytic reduction

KW - Carbon dioxide

KW - fuel

KW - oxygen

KW - article

KW - atmosphere

KW - climate change

KW - dissociation

KW - greenhouse

KW - greenhouse effect

KW - hydrogenation

KW - kinetics

KW - photocatalysis

UR - https://www.mendeley.com/catalogue/0bed81aa-bfcb-38e8-bccc-df824b19550d/

U2 - 10.1002/cssc.202400551

DO - 10.1002/cssc.202400551

M3 - статья

VL - 17

JO - ChemSusChem

JF - ChemSusChem

SN - 1864-5631

IS - 18

ER -

ID: 126385795