TY - JOUR
T1 - Ternary PtCoSn Catalyst with Regulated Intermediates Adsorption for Efficient Ammonia Electrolysis
AU - Dai, Congfu
AU - Yuan, Xiaofen
AU - Wang, Yuxing
AU - Liu, Xinyu
AU - Ju, Chang
AU - Hu, Lin
AU - He, Shuijian
AU - Shi, Rui
AU - Liu, Yana
AU - Zhang, Jiguang
AU - Zhu, Yunfeng
AU - Wang, Jun
N1 - Publisher Copyright:
© 2025 Wiley-VCH GmbH.
PY - 2025
Y1 - 2025
N2 - Ammonia electrolysis represents a green and economical strategy for hydrogen production, yet the progress is hindered by the lack of efficient catalyst to boost the kinetically sluggish ammonia oxidation reaction (AOR). Herein, ternary PtCoSn/C catalyst prepared by a facile wet-chemical reduction method is applied for AOR, which exhibits a specific activity of 0.87 mA cmECSA−2, 3 times that of Pt/C. The highly enhanced activity is derived from the regulated intermediates adsorption on the PtCoSn/C surface, which is evidenced by in situ attenuated total reflection Fourier transform infrared measurements. The co-alloying of Co and Sn with Pt not only contributes to the weakened binding strength of *OH and *H species on Pt surface, enhancing the adsorption of NH3 and the related intermediates, but also facilitates the supply of OH− to Pt sites, compensating for the fast consumption of OH− in the double layer during AOR. Benefiting from its high activity for hydrogen evolution reaction, PtCoSn/C can be used as a bifunctional catalyst for ammonia electrolysis in a two-electrode system, which only requires 0.78 V to drive a current density of 10 mA cm−2. This work sheds light on developing efficient AOR catalysts, promoting hydrogen production from ammonia electrolysis.
AB - Ammonia electrolysis represents a green and economical strategy for hydrogen production, yet the progress is hindered by the lack of efficient catalyst to boost the kinetically sluggish ammonia oxidation reaction (AOR). Herein, ternary PtCoSn/C catalyst prepared by a facile wet-chemical reduction method is applied for AOR, which exhibits a specific activity of 0.87 mA cmECSA−2, 3 times that of Pt/C. The highly enhanced activity is derived from the regulated intermediates adsorption on the PtCoSn/C surface, which is evidenced by in situ attenuated total reflection Fourier transform infrared measurements. The co-alloying of Co and Sn with Pt not only contributes to the weakened binding strength of *OH and *H species on Pt surface, enhancing the adsorption of NH3 and the related intermediates, but also facilitates the supply of OH− to Pt sites, compensating for the fast consumption of OH− in the double layer during AOR. Benefiting from its high activity for hydrogen evolution reaction, PtCoSn/C can be used as a bifunctional catalyst for ammonia electrolysis in a two-electrode system, which only requires 0.78 V to drive a current density of 10 mA cm−2. This work sheds light on developing efficient AOR catalysts, promoting hydrogen production from ammonia electrolysis.
KW - ammonia electrolysis
KW - ammonia oxidation reaction
KW - in situ ATR-FTIR
KW - intermediates
KW - PtCoSn catalyst
UR - http://www.scopus.com/inward/record.url?scp=105004201862&partnerID=8YFLogxK
U2 - 10.1002/smll.202501582
DO - 10.1002/smll.202501582
M3 - 文章
AN - SCOPUS:105004201862
SN - 1613-6810
JO - Small
JF - Small
ER -