电催化剂
甲烷
脱氢
催化作用
材料科学
纳米技术
背景(考古学)
电化学
化学
有机化学
物理化学
电极
生物
古生物学
作者
Shuai Yuan,Yanding Li,Jiayu Peng,Ydna M. Questell‐Santiago,Karthik Akkiraju,Livia Giordano,Daniel J. Zheng,Sujay Bagi,Yuriy Román‐Leshkov,Yang Shao‐Horn
标识
DOI:10.1002/aenm.202002154
摘要
Abstract The direct partial oxidation of methane to methanol promises an energy‐efficient and environmental‐friendly utilization of natural gas. Unfortunately, current technologies confront a grand challenge in catalysis, particularly in the context of distributed sources. Research has been focused on the design of homogenous and heterogenous catalysts to improve the activation of methane under thermal and electrochemical conditions. However, the intrinsic relationship between thermal and electrochemical systems has not been exploited yet. This review intends to bridge the studies of thermal and electrochemical catalysts, in both homogenous and heterogenous systems, for methane activation from a mechanistic point of view. It is expected to provide a framework to rationalize the design of electrocatalysts beyond the state of art. First, methane activation systems reported previously are reviewed and classified into two basic mechanisms: dehydrogenation and deprotonation. Based on the mechanism types, activity and selectivity descriptors are defined to understand the performance of current catalysts and guide the design of future catalysts. Moreover, methods to enhance the activity and selectivity are discussed to emphasize the unique advantage of electrocatalysis in overcoming the limitations of traditional thermal catalysis. Finally, immense opportunities and challenges for catalyst design are discussed by unifying thermal and electrochemical catalysis.
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