TY - JOUR
T1 - Cu2O-Derived PtCu Nanoalloy toward Energy-Efficient Hydrogen Production via Hydrazine Electrolysis under Large Current Density
AU - Ge, Shangmeng
AU - Zhang, Liwen
AU - Hou, Junrong
AU - Liu, Shuai
AU - Qin, Yongji
AU - Liu, Qian
AU - Cai, Xiaobing
AU - Sun, Zhiyong
AU - Yang, Miaosen
AU - Luo, Jun
AU - Liu, Xijun
N1 - Publisher Copyright:
© 2022 American Chemical Society.
PY - 2022/8/22
Y1 - 2022/8/22
N2 - 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.
AB - 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.
KW - PtCu alloy
KW - bifunctional electrocatalyst
KW - energy-efficient
KW - hydrazine-assisted hydrogen production
KW - hydrogen evolution reaction
UR - https://www.scopus.com/pages/publications/85136250935
U2 - 10.1021/acsaem.2c01006
DO - 10.1021/acsaem.2c01006
M3 - 文章
AN - SCOPUS:85136250935
SN - 2574-0962
VL - 5
SP - 9487
EP - 9494
JO - ACS Applied Energy Materials
JF - ACS Applied Energy Materials
IS - 8
ER -