材料科学
电化学
催化作用
纳米技术
碳纤维
合理设计
还原(数学)
设计要素和原则
吸附
密度泛函理论
化学工程
计算机科学
有机化学
化学
计算化学
复合材料
工程类
物理化学
几何学
软件工程
复合数
数学
电极
作者
Fuping Pan,Xiaoxuan Yang,Thomas O'Carroll,Haoyang Li,Kai‐Jie Chen,Gang Wu
标识
DOI:10.1002/aenm.202200586
摘要
Abstract Electrochemical CO 2 reduction offers a compelling route to mitigate atmospheric CO 2 concentration and store intermittent renewable energy in chemical bonds. Beyond C 1 , C 2+ feedstocks are more desirable due to their higher energy density and more significant market need. However, the CO 2 ‐to‐C 2+ reduction suffers from significant barriers of CC coupling and complex reaction pathways. Due to remarkable tunability over morphology/pore architecture along with great feasibility of functionalization to modify the electronic and geometric structures, carbon materials, serving as active components, supports, and promoters, provide exciting opportunities to tune both the adsorption properties of intermediates and the local reaction environment for the CO 2 reduction, offering effective solutions to enable CC coupling and steer C 2+ evolution. However, general design principles remain ambiguous, causing an impediment to rational catalyst refinement and application thrusts. This review clarifies insightful design principles for advancing carbon materials. First, the current performance status and challenges are discussed and effective strategies are outlined to promote C 2+ evolution. Further, the correlation between the composition, structure, and morphology of carbon catalysts and their catalytic behavior is elucidated to establish catalytic mechanisms and critical factors determining C 2+ performance. Finally, future research directions and strategies are envisioned to inspire revolutionary advancements.
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