双金属片
塔菲尔方程
过电位
化学
催化作用
结晶学
金属
电解
密度泛函理论
分析化学(期刊)
材料科学
物理化学
电极
电化学
计算化学
电解质
有机化学
生物化学
色谱法
作者
Filipa M. Oliveira,Jan Paštika,Iva Plutnarová,Vlastimil Mazánek,Karol Strutyński,Manuel Melle‐Franco,Zdeněk Sofer,Rui Gusmão
标识
DOI:10.1002/smtd.202201358
摘要
Considerable improvements in the electrocatalytic activity of 2D metal phosphorous trichalcogenides (M2 P2 X6 ) have been achieved for water electrolysis, mostly with MII2 [P2 X6 ]4- as catalysts for hydrogen evolution reaction (HER). Herein, MI MIII P2 S6 (MI = Cu, Ag; MIII = Sc, V, Cr, In) are synthesized and tested for the first time as electrocatalysts in alkaline media, towards oxygen reduction reaction (ORR) and HER. AgScP2 S6 follows a 4 e- pathway for the ORR at 0.74 V versus reversible hydrogen electrode; CuScP2 S6 is active for HER, exhibiting an overpotential of 407 mV and a Tafel slope of 90 mV dec-1 . Density functional theory models reveal that bulk AgScP2 S6 and CuScP2 S6 are both semiconductors with computed bandgaps of 2.42 and 2.23 eV, respectively and overall similar electronic properties. Besides composition, the largest difference in both materials is in their molecular structure, as Ag atoms sit at the midpoint of each layer alongside Sc atoms, while Cu atoms are raised to a similar height to S atoms, in the external segment of the 2D layers. This structural difference probably plays a fundamental role in the different catalytic performances of these materials. These findings show that MI (Cu, Ag) together with Sc(MIII ) leads to promising achievements in MI MIII P2 S6 materials as electrocatalysts.
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