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Liu et al. Chem Synth 2023;3:24                                 Chemical Synthesis
               DOI: 10.20517/cs.2023.13



               Research Article                                                              Open Access



               Active Pd nanoclusters supported on

               nitrogen/amino co-functionalized carbon for highly
               efficient dehydrogenation of formic acid


                                                     2
                      1,#
                                                                                1,*
                                   2,#
                                                                  1
                                             2
               Dan Liu , Cheng Zhou , Ge Wang , Yong Li , Zhimao Yang , Chuncai Kong , Ben Liu 3,*
               1
                Ministry of Education Key Laboratory for Non-equilibrium Synthesis and Modulation of Condensed Matter, Shaanxi Province
               Key Laboratory of Advanced Functional Materials and Mesoscopic Physics, School of Physics, Xi’an Jiaotong University, Xi’an
               710049, Shaanxi, China.
               2
                Beijing Institute of Control Engineering, Beijing 100190, China.
               3
                Key Laboratory of Green Chemistry and Technology of Ministry of Education, College of Chemistry, Sichuan University,
               Chengdu 610064, Sichuan, China.
               #
                Authors contributed equally.
               *Correspondence to: Prof. Ben Liu, Key Laboratory of Green Chemistry and Technology of Ministry of Education, College of
               Chemistry, Sichuan University, Wangjiang Road No. 29, Chengdu 610064, Sichuan, China. E-mail: ben.liu@scu.edu.cn; Prof.
               Chuncai Kong, Ministry of Education Key Laboratory for Non-equilibrium Synthesis and Modulation of Condensed Matter,
               Shaanxi Province Key Laboratory of Advanced Functional Materials and Mesoscopic Physics, School of Physics, Xi’an Jiaotong
               University, Xian Ning West Road No.28, Xi'an 710049, Shaanxi, China. E-mail: kongcc@xjtu.edu.cn
               How to cite this article: Liu D, Zhou C, Wang G, Li Y, Yang Z, Kong C, Liu B. Active Pd nanoclusters supported on
               nitrogen/amino co-functionalized carbon for highly efficient dehydrogenation of formic acid. Chem Synth 2023;3:24.
               https://dx.doi.org/10.20517/cs.2023.13
               Received: 1 Mar 2023  First Decision: 6 Apr 2023  Revised: 19 Apr 2023  Accepted: 27 Apr 2023  Published: 15 May 2023

               Academic Editors: Bao-Lian Su, Wei Li, Chen Wang  Copy Editor: Dong-Li Li  Production Editor: Dong-Li Li


               Abstract
               Supported noble metal catalysts have exhibited satisfactory catalytic performance in the dehydrogenation of liquid
               chemical hydrogen carriers, in which the supports play a paramount role in conditioning the nature of the active
               center and thus improving the overall reactivity. Herein, the specially designed nitrogen/amino co-functionalized
               carbon (NH -NC) supports are prepared to load active Pd nanoclusters for efficient dehydrogenation of formic acid
                         2
               (FA). The nitrogen/amino co-functionalization of carbon not only facilitates the Pd nanoclusters evenly dispersed
               with  a  mean  size  of  1.4  nm,  but  also  provides  a  beneficial  metal-support  interaction  to  promote  FA
               dehydrogenation. The as-prepared Pd@NH -NC discloses a 100% conversion of FA into CO  and H  with a
                                                   2                                         2     2
                                                             -1
                                                                                                   -1
               remarkable initial turnover frequency (TOF  ) of 4,892 h  and a low activation energy (E ) of 28.5 kJ mol  without
                                                 initial                              a
               additive at 298 K. The work proposes a co-functionalization strategy to reasonably design supports for
               heterogeneous catalysts and may be extended to develop other multi-functionalized supports with different
               compositions and nanostructures.



                           © The Author(s) 2023. Open Access This article is licensed under a Creative Commons Attribution 4.0
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