Please use this identifier to cite or link to this item: https://hdl.handle.net/10356/90195
Title: A spongy nickel-organic CO 2 reduction photocatalyst for nearly 100% selective CO production
Authors: Doeff, Marca M.
Koper, Marc T. M.
Niu, Kaiyang
Xu, You
Wang, Haicheng
Ye, Rong
Xin, Huolin L.
Lin, Feng
Tian, Chixia
Lum, Yanwei
Bustillo, Karen C.
Ager, Joel
Xu, Rong
Zheng, Haimei
Keywords: Catalysts
DRNTU::Engineering::Chemical engineering
Carbon Dioxide
Issue Date: 2017
Source: Niu, K., Xu, Y., Wang, H., Ye, R., Xin, H. L., Lin, F., Tian, C., et al. (2017). A spongy nickel-organic CO2 reduction photocatalyst for nearly 100% selective CO production. Science Advances, 3(7), e1700921-. doi:10.1126/sciadv.1700921
Series/Report no.: Science Advances
Abstract: Solar-driven photocatalytic conversion of CO2 into fuels has attracted a lot of interest; however, developing active catalysts that can selectively convert CO2 to fuels with desirable reaction products remains a grand challenge. For instance, complete suppression of the competing H2 evolution during photocatalytic CO2-to-CO conversion has not been achieved before. We design and synthesize a spongy nickel-organic heterogeneous photocatalyst via a photochemical route. The catalyst has a crystalline network architecture with a high concentration of defects. It is highly active in converting CO2 to CO, with a production rate of ~1.6 × 104 μmol hour−1 g−1. No measurable H2 is generated during the reaction, leading to nearly 100% selective CO production over H2 evolution. When the spongy Ni-organic catalyst is enriched with Rh or Ag nanocrystals, the controlled photocatalytic CO2 reduction reactions generate formic acid and acetic acid. Achieving such a spongy nickel-organic photocatalyst is a critical step toward practical production of high-value multicarbon fuels using solar energy.
URI: https://hdl.handle.net/10356/90195
http://hdl.handle.net/10220/47193
DOI: 10.1126/sciadv.1700921
Rights: © 2017 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works. Distributed under a Creative Commons Attribution NonCommercial License 4.0 (CC BY-NC).
Fulltext Permission: open
Fulltext Availability: With Fulltext
Appears in Collections:SCBE Journal Articles

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