Yang Tingting, Zhang Zheng, Tan Fei, Liu Huayu, Li Xingyu, Wang Hongqi, Yang Qing
State Grid Chongqing Electric Power Company Material Branch, Chongqing 401120, China.
Chongqing Jie Chuang Electric Power Technology Company Ltd., Chongqing 400031, China.
Materials (Basel). 2024 Dec 31;18(1):121. doi: 10.3390/ma18010121.
The development of efficient catalysts for water electrolysis is crucial for advancing the low-carbon transition and addressing the energy crisis. This work involves the fabrication of graphene-based catalysts for the oxygen evolution reaction (OER) by integrating NiFe-LDH and PbO onto graphene using plasma treatment. The plasma process takes only 30 min. Graphene's two-dimensional structure increases the available reaction surface area and improves surface electron transport. Plasma treatment further improves catalyst performance by facilitating nanoparticle attachment and creating carbon defects and sulfur vacancies. Density functional theory (DFT) calculations at the PBE provide valuable insights into the role of vacancies in enhancing catalyst performance for OER. The catalyst's conductivity and electronic structure are greatly impacted by vacancies. While modifications to the electronic structure increase the kinetics of charge transfer, the vacancy structure can produce more active sites and improve the adsorption and reactivity of OER intermediates. This optimization of intermediate adsorption and electronic properties leads to increased overall OER activity. The catalyst NiFe-PbO/S/rGO-45, synthesized through plasma treatment, demonstrated an overpotential of 230 mV at 50 mA·cm and a Tafel slope of 44.26 mV dec, exhibiting rapid reaction kinetics and surpassing the OER activity of commercial IrO. With its excellent performance, the prepared catalyst has broad prospects in commercial applications such as water electrolysis and air batteries.
开发高效的水电解催化剂对于推进低碳转型和解决能源危机至关重要。这项工作涉及通过等离子体处理将NiFe-LDH和PbO整合到石墨烯上,制备用于析氧反应(OER)的石墨烯基催化剂。等离子体过程仅需30分钟。石墨烯的二维结构增加了可用反应表面积并改善了表面电子传输。等离子体处理通过促进纳米颗粒附着以及产生碳缺陷和硫空位进一步提高了催化剂性能。在PBE水平上的密度泛函理论(DFT)计算为空位在增强OER催化剂性能中的作用提供了有价值的见解。空位对催化剂的电导率和电子结构有很大影响。虽然电子结构的改变增加了电荷转移动力学,但空位结构可以产生更多活性位点并改善OER中间体的吸附和反应性。中间体吸附和电子性质的这种优化导致整体OER活性增加。通过等离子体处理合成的催化剂NiFe-PbO/S/rGO-45在50 mA·cm时的过电位为230 mV,塔菲尔斜率为44.26 mV dec,表现出快速的反应动力学,超过了商业IrO的OER活性。所制备的催化剂具有优异的性能,在水电解和空气电池等商业应用中具有广阔的前景。