催化作用
材料科学
金属
电化学
色散(光学)
热解
碳纤维
氮气
纳米颗粒
碘化铵
化学工程
纳米技术
无机化学
电极
物理化学
化学
有机化学
复合数
冶金
物理
光学
复合材料
工程类
作者
Jianbin Liu,Jiangwen Liao,Kang Huang,Juncai Dong,Guanchao He,Zhichao Gong,Huilong Fei
标识
DOI:10.1002/adma.202211398
摘要
Metal- and nitrogen-doped nanocarbons (M-N-Cs) are promising alternatives to precious metals for catalyzing electrochemical energy conversion processes. However, M-N-Cs synthesized by high-temperature pyrolysis frequently suffer from compositional heterogeneity with the simultaneous presence of atomically dispersed M-Nx sites and crystalline metal nanoparticles (NPs), which hinders the identification of active sites and rational optimization in performance. Herein, a universal and efficient strategy is reported to obtain both precious- and nonprecious-metal-based M-N-Cs (M = Pt, Fe, Co, Ni, Mn, Cu, Zn) with exclusive atomic dispersion by making use of ammonium iodide as the etchant to remove excessive metal aggregates at high temperature. Taking Pt-N-C as a proof-of-concept demonstration, the complete removal of Pt NPs in Pt-N-C enables clarification on the contributions of the atomic Pt-Nx moieties and Pt NPs to the catalytic activity toward the hydrogen evolution reaction. Combined electrochemical measurements and theoretical calculations identify that the atomic Pt-Nx moieties by themselves possess negligible activity, but they can significantly boost the activity of the Pt NPs via the synergistic effect.
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