Cu2O-Derived PtCu Nanoalloy toward Energy-Efficient Hydrogen Production via Hydrazine Electrolysis under Large Current Density

电解 联氨(抗抑郁剂) 双功能 制氢 电池电压 催化作用 阳极 材料科学 析氧 合金 电化学 化学工程 纳米技术 化学 冶金 电极 有机化学 工程类 物理化学 电解质 色谱法
作者
Shangmeng Ge,Liwen Zhang,Junrong Hou,Shuai Liu,Yongji Qin,Qian Liu,Xiaobing Cai,Zhiyong Sun,Miaosen Yang,Jun Luo,Xijun Liu
出处
期刊:ACS applied energy materials [American Chemical Society]
卷期号:5 (8): 9487-9494 被引量:66
标识
DOI:10.1021/acsaem.2c01006
摘要

Electrocatalytic overall water splitting (OWS), powered by a renewable energy source, is a promising strategy for hydrogen production. However, the OWS system usually requires large energy consumption due to the sluggish kinetics of the anodic oxygen evolution reaction. Herein, we fabricated a PtCu nanoalloy (PtCu-NA) through a template-assisted method and evaluated its bifunctional activities for both hydrogen evolution reaction (HER) in 1 M KOH and hydrazine oxidation reaction (HzOR) in 1 M KOH + 1 M hydrazine. Remarkably, the interplanar crystal spacing of PtCu-NA was larger than that of standard PtCu and closer to that of Pt, which can be attributed to the template-assisted synthesis method. Thus, the as-prepared PtCu-NA needs low overpotentials of 224 and 668 mV to drive HER and HzOR at 100 and 200 mA cm–2, respectively, which are much better than those of commercial Pt/C (453 and 1081 mV). After coupling the HER and HzOR together, the overall hydrazine splitting (OHzS) cell needs a small voltage of 0.666 V to deliver 200 mA cm–2 in 1 M KOH + 1 M hydrazine, outperforming the Pt/C (0.792 V). Impressively, the assembly OHzS cell could run stably for more than 110 h. These performances can be attributed to the regulation of the crystal structure of the PtCu alloy and the synergistic effect between Pt and Cu.
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