Ziqiang Wang, Min Li, Shan Xu, Hongjie Ye, Kai Deng, You Xu, Hongjing Wang, Liang Wang
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引用次数: 0
摘要
用热力学上更有利的乙醇氧化反应(EOR)取代缓慢的氧进化反应,是一种以节能模式联合生产氢气和有价值化学品的有前途的战略。在此,我们提出了高弯曲 PdOs 双金属的合成方法,它具有高活性位点原子利用率和导电性。此外,合金效应可以调节电子结构,优化反应物的吸附能。因此,在碱性溶液条件下,PdOs 双茂钛在氢进化反应(HER)和 EOR 方面表现出卓越的性能,在 10 mA cm-2 条件下的过电位为 36 mV,质量活度为 1.51 mA μg-1Pd。在 EOR-HER 共电解系统中,PdOs 双茂钛需要 0.801 V 的低电压才能在 50 mA cm-2 的条件下同时产生氢气和醋酸盐,与传统的水电解(1.976 V)相比,大大降低了能耗。这种方法为设计双金属电催化剂提供了一种前景广阔的策略,通过用更有利的乙醇氧化反应取代迟缓的 OER,从而实现同时生成氢气和高价值化学品的节能目标。
PdOs bimetallene for energy-saving hydrogen production coupled with ethanol electro-oxidation
The replacement of sluggish oxygen evolution reaction by more thermodynamically favorable ethanol oxidation reaction (EOR) is a promising strategy for co-production of hydrogen and valuable chemicals in energy-saving mode. Here, we propose the synthesis of highly curved PdOs bimetallene, which possesses high active sites atomic utilization and conductivity. Furthermore, alloy effect can regulate electronic structure and optimize adsorption energy of reactants. Therefore, PdOs bimetallene exhibits superior performance for hydrogen evolution reaction (HER) and EOR under basic solutions, with overpotential of 36 mV at 10 mA cm-2 and mass activity of 1.51 mA μg-1Pd, respectively. In the EOR-HER co-electrolysis system, PdOs bimetallene requires low voltage of 0.801 V for concurrent production of hydrogen and acetate at 50 mA cm−2, which greatly reduces energy consumption compared to conventional water electrolysis (1.976 V). This method provides a promising strategy for designing bimetallic electrocatalysts towards simultaneous energy-saving generation of hydrogen and high-value chemicals by replacing sluggish OER with more favorable ethanol oxidation reaction.
期刊介绍:
Materials Today Energy is a multi-disciplinary, rapid-publication journal focused on all aspects of materials for energy.
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