TY - JOUR
T1 - Solid-Diffusion Synthesis of Single-Atom Catalysts Directly from Bulk Metal for Efficient CO 2 Reduction
AU - Zhao, Changming
AU - Wang, Yu
AU - Li, Zhijun
AU - Chen, Wenxing
AU - Xu, Qian
AU - He, Dongsheng
AU - Xi, Desheng
AU - Zhang, Qinghua
AU - Yuan, Tongwei
AU - Qu, Yunteng
AU - Yang, Jian
AU - Zhou, Fangyao
AU - Yang, Zhengkun
AU - Wang, Xiaoqian
AU - Wang, Jing
AU - Luo, Jun
AU - Li, Yafei
AU - Duan, Haohong
AU - Wu, Yuen
AU - Li, Yadong
N1 - Publisher Copyright:
© 2018 Elsevier Inc.
PY - 2019/2/20
Y1 - 2019/2/20
N2 - Electroreduction of CO 2 into value-added products is an effective approach to remit the environmental and energy issues. However, the development of an effective, accessible, and simple method for mass production of electrocatalyst is challenging. Herein, we demonstrate the solid-state diffusion between the N-doped carbon phase and bulk Ni metal can be utilized to synthesize hierarchical, self-supported, and atomistic catalyst. Strikingly, this hierarchical catalyst is programmable and scalable to meet the industrial demand and can be directly used as a binder-free electrode toward the CO 2 electroreduction, delivering a state-of-the-art current density of 48.66 mA cm −2 at −1.0 V versus reversible hydrogen electrode (RHE) and high faradic efficiency of 97% to CO. The selectivity can be retained over 90% in a wide range of working potential of −0.7 to −1.2 V versus RHE. This solid-state diffusion strategy presents great potential to produce hierarchical and atomistic catalysts at industrial levels. The excessive emission of CO 2 through massive fossil fuel consumption results in serious environmental issues. There is an urgent need to convert CO 2 into chemical fuels to mitigate atmospheric CO 2 levels and alleviate the energy crisis. Therefore, the design and synthesis of high-performance and flexible self-supported electrocatalysts for CO 2 reduction are highly desirable to realize high-efficiency practical devices. Herein, we successfully synthesize a hierarchical and atomistic catalyst through a solid-state diffusion strategy. This synthesis is initiated by the direct solid-state diffusion of Ni atoms from bulk Ni foil into the contacted carbon shell. Catalyzed by the Ni “seeds” derived from the bulk Ni, self-supported nanotube fiber-based carbon paper decorated by abundant isolated atomistic Ni sites are successfully “cultivated.” This hierarchical catalyst is programmable and scalable to meet the industrial demand for CO 2 conversion.
AB - Electroreduction of CO 2 into value-added products is an effective approach to remit the environmental and energy issues. However, the development of an effective, accessible, and simple method for mass production of electrocatalyst is challenging. Herein, we demonstrate the solid-state diffusion between the N-doped carbon phase and bulk Ni metal can be utilized to synthesize hierarchical, self-supported, and atomistic catalyst. Strikingly, this hierarchical catalyst is programmable and scalable to meet the industrial demand and can be directly used as a binder-free electrode toward the CO 2 electroreduction, delivering a state-of-the-art current density of 48.66 mA cm −2 at −1.0 V versus reversible hydrogen electrode (RHE) and high faradic efficiency of 97% to CO. The selectivity can be retained over 90% in a wide range of working potential of −0.7 to −1.2 V versus RHE. This solid-state diffusion strategy presents great potential to produce hierarchical and atomistic catalysts at industrial levels. The excessive emission of CO 2 through massive fossil fuel consumption results in serious environmental issues. There is an urgent need to convert CO 2 into chemical fuels to mitigate atmospheric CO 2 levels and alleviate the energy crisis. Therefore, the design and synthesis of high-performance and flexible self-supported electrocatalysts for CO 2 reduction are highly desirable to realize high-efficiency practical devices. Herein, we successfully synthesize a hierarchical and atomistic catalyst through a solid-state diffusion strategy. This synthesis is initiated by the direct solid-state diffusion of Ni atoms from bulk Ni foil into the contacted carbon shell. Catalyzed by the Ni “seeds” derived from the bulk Ni, self-supported nanotube fiber-based carbon paper decorated by abundant isolated atomistic Ni sites are successfully “cultivated.” This hierarchical catalyst is programmable and scalable to meet the industrial demand for CO 2 conversion.
KW - CO electroreduction
KW - self-supported electrode
KW - single-atom catalysts
KW - solid-state diffusion
UR - http://www.scopus.com/inward/record.url?scp=85061378163&partnerID=8YFLogxK
U2 - 10.1016/j.joule.2018.11.008
DO - 10.1016/j.joule.2018.11.008
M3 - Article
AN - SCOPUS:85061378163
SN - 2542-4351
VL - 3
SP - 584
EP - 594
JO - Joule
JF - Joule
IS - 2
ER -