Zhang Wei, Gao Yi-Jing, Fang Qiao-Jun, Pan Jin-Kong, Zhu Xin-Cheng, Deng Sheng-Wei, Yao Zi-Hao, Zhuang Gui-Lin, Wang Jian-Guo
Institute of Industrial Catalysis, State Key Laboratory Breeding Base of Green-Chemical Synthesis Technology, College of Chemical Engineering, Zhejiang University of Technology, Hangzhou 310032, PR China.
Institute of Industrial Catalysis, State Key Laboratory Breeding Base of Green-Chemical Synthesis Technology, College of Chemical Engineering, Zhejiang University of Technology, Hangzhou 310032, PR China.
J Colloid Interface Sci. 2021 Oct;599:58-67. doi: 10.1016/j.jcis.2021.04.080. Epub 2021 Apr 21.
The electrochemical synthesis of hydrogen peroxide (HO) provides a greener and more efficient method compared with classic catalysts containing toxic metals. Herein, we used first-principles density functional theory (DFT) calculations to investigate 174 different single-atom catalysts with graphyne substrates, and conducted a three-step screening strategy to identify the optimal noble metal-free single atom catalyst. It is found that a single Ni atom loaded on γ-graphyne with carbon vacancies (Ni@V-γ-GY) displayed remarkable thermodynamic stability, excellent selectivity, and high activity with an ultralow overpotential of 0.03 V. Furthermore, based on ab-initio molecular dynamic and DFT calculations under the HO solvent, it was revealed that the catalytic performance for HO synthesis in aqueous phase was much better than that in gas phase condition, shedding light on the hydrogen bond network being beneficial to accelerate the transfer of protons for HO synthesis.
与含有毒金属的传统催化剂相比,过氧化氢(HO)的电化学合成提供了一种更绿色、更高效的方法。在此,我们使用第一性原理密度泛函理论(DFT)计算来研究174种不同的具有石墨炔基底的单原子催化剂,并采用三步筛选策略来确定最佳的无贵金属单原子催化剂。研究发现,负载在具有碳空位的γ-石墨炔上的单个镍原子(Ni@V-γ-GY)表现出显著的热力学稳定性、优异的选择性和高活性,过电位低至0.03 V。此外,基于HO溶剂下的从头算分子动力学和DFT计算,结果表明在水相中合成HO的催化性能远优于气相条件下的性能,这揭示了氢键网络有利于加速HO合成中质子的转移。