塔菲尔方程
过电位
析氧
纳米棒
化学工程
分解水
催化作用
氧化物
相(物质)
电化学
纳米颗粒
材料科学
电催化剂
纳米技术
电极
化学
冶金
物理化学
工程类
有机化学
光催化
生物化学
作者
Lin Tian,Xiuhui Zhai,Xiang Wang,Xinle Pang,Jun Li,Zhao Li
标识
DOI:10.1016/j.electacta.2020.135823
摘要
Abstract Engineering non-precious electrocatalysts with excellent water oxidation performance is imperative for developing renewable and clean energy. Herein, we realize the simultaneous morphology and phase transformation from α-MnO2 nanorods, large-size MnOOH nanorods to MnOOH nanoparticles by adding different content of N-CDs in the synthesizing α-MnO2 process. Benefitting from the unique structures, synergistic effect between Mn-based oxides/oxyhydroxides and N-CDs, various active oxide species and large specific surface areas, the as-prepared Mn-based oxides/oxyhydroxides@CDs with different morphologies show excellent electrocatalytic performance for oxygen evolution reaction (OER) in 1.0 M KOH. Impressively, the large-size MnOOH@CDs0.2 display high electrocatalytic performance with the overpotential of 302 mV to reach to 10 mA cm−2 along with a Tafel slope of 51.3 mA dec−1. More importantly, by coupling the MnOOH@CDs0.2 with Pt/C for overall water splitting, a cell potential of merely 1.56 V is required to reach to 10 mA cm−2. Additionally, in the process of stability studies, the key role of the (111) crystal plane in the catalytic process is established. Meanwhile, the MnOOH@CDs0.2 also shows excellent stability for continuous 72 h chronopotentiometry test. The proposed strategy showed here represents a facile and suitable method for the simultaneous transformation of the morphology and phase of Mn-based oxides/oxyhydroxides with the assistance of N-CDs for efficient energy conversion.
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