塔菲尔方程
电负性
材料科学
结晶度
电化学
催化作用
分解水
掺杂剂
无定形固体
纳米技术
化学工程
无机化学
物理化学
结晶学
化学
兴奋剂
有机化学
电极
光催化
复合材料
工程类
光电子学
作者
Yao Zhou,Wei Hao,Xiao-Kun Zhao,Jiadong Zhou,Huimei Yu,Bo Lin,Zheng Liu,Stephen J. Pennycook,Shuzhou Li,Hong Jin Fan
标识
DOI:10.1002/adma.202100537
摘要
Amorphization is an efficient strategy to activate intrinsically inert catalysts. However, the low crystallinity of amorphous catalysts often causes high solubility and poor electrochemical stability in aqueous solution. Here, a different mechanism is developed to simultaneously stabilize and activate the water-soluble amorphous MoSx Oy via a charge-balancing strategy, which is induced by different electronegativity between the co-dopants Rh (2.28) and Sn (1.96). The electron-rich Sn prefers to stabilize the unstable apical O sites in MoSx Oy through charge transfer, which can prevent the H from attacking. Meanwhile, the Rh, as the charge regulator, shifts the main active sites on the basal plane from inert Sn to active apical Rh sites. As a result, the amorphous RhSn-MoSx Oy exhibits drastic enhancement in electrochemical stability (η10 increases only by 12 mV) after 1000 cycles and a distinct activity (η10 : 26 mV and Tafel: 30.8 mV dec-1 ) for the hydrogen evolution reaction in acidic solution. This work paves a route for turning impracticably water-soluble catalysts into treasure and inspires new ideas to design high-performance amorphous electrocatalysts.
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