纳米片
析氧
电催化剂
过电位
材料科学
化学工程
分解水
兴奋剂
扫描电子显微镜
傅里叶变换红外光谱
氧气
介孔材料
催化作用
纳米技术
电化学
化学
物理化学
复合材料
电极
有机化学
光催化
光电子学
工程类
作者
Abdul Ghafoor Abid,Soumaya Gouadria,Rabia Yasmin Khosa,Salma Aman,Abdul Rashid,Sumaira Manzoor,Adeel Hussain Chughtai,Naseeb Ahmad,Ruimao Hua,Muhammad Naeem Ashiq
出处
期刊:Energy & Fuels
[American Chemical Society]
日期:2023-01-23
卷期号:37 (3): 2255-2261
被引量:6
标识
DOI:10.1021/acs.energyfuels.2c03263
摘要
Despite being an essential half-reaction for splitting water, the oxygen evolution reaction (OER) is rarely used in the industry because it is slow and requires expensive catalysts. Here, in the present study, the nanosheet of Co3C and carbon nano-onions (CNOs) have been prepared using an annealing process under high pressure, and Zn-doped Co3C was additionally prepared to investigate the impact of doping on Co3C nanosheet as an OER electrocatalyst. The synthesized electrocatalyst is portrayed by X-ray diffraction (XRD), scanning electron microscopy (SEM), Brunauer–Emmet–Teller (BET), and Fourier transform infrared (FTIR). The standing nanoflakes are shaped on the nanosheets of Co3C in the wake of the doping effect. The mesoporous nanoflakes Zn-Co3C@CNO have shown striking OER activity requiring 1.45 V vs RHE as the beginning potential for the OER and required a 276 mV overpotential (η) at 10 mA cm–2. Indeed, even the higher current densities of 50 and 78 mA cm–2 were achieved individually at lower η of 301 and 345 mV, respectively. The prepared electrocatalyst has shown unusual activity fit for continuous oxygen gas evolution for more than 50 h. Such excellent OER performance can be credited to doping Zn particles into the lattice structure of Co3C, along with nanoflakes like standing construction are shaped on the nanosheet of Co3C and microporosity of arranged terminals are considered as efficient for higher OER activity.
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