格式化
石墨烯
钙钛矿(结构)
氧化物
卤化物
纳米晶
催化作用
氧化还原
材料科学
金属
无机化学
甲酸钠
电解质
化学
化学工程
纳米技术
物理化学
有机化学
电极
冶金
工程类
作者
Minh Tam Hoang,Chen Han,Zhipeng Ma,Xin Mao,Yang Yang,Sepideh Sadat Madani,Paul E. Shaw,Yongchao Yang,Lingyi Peng,Cui Ying Toe,Jian Pan,Rose Amal,Aijun Du,Tuquabo Tesfamichael,Zhaojun Han,Hongxia Wang
标识
DOI:10.1007/s40820-023-01132-3
摘要
Transformation of greenhouse gas (CO2) into valuable chemicals and fuels is a promising route to address the global issues of climate change and the energy crisis. Metal halide perovskite catalysts have shown their potential in promoting CO2 reduction reaction (CO2RR), however, their low phase stability has limited their application perspective. Herein, we present a reduced graphene oxide (rGO) wrapped CsPbI3 perovskite nanocrystal (NC) CO2RR catalyst (CsPbI3/rGO), demonstrating enhanced stability in the aqueous electrolyte. The CsPbI3/rGO catalyst exhibited > 92% Faradaic efficiency toward formate production at a CO2RR current density of ~ 12.7 mA cm−2. Comprehensive characterizations revealed the superior performance of the CsPbI3/rGO catalyst originated from the synergistic effects between the CsPbI3 NCs and rGO, i.e., rGO stabilized the α-CsPbI3 phase and tuned the charge distribution, thus lowered the energy barrier for the protonation process and the formation of *HCOO intermediate, which resulted in high CO2RR selectivity toward formate. This work shows a promising strategy to rationally design robust metal halide perovskites for achieving efficient CO2RR toward valuable fuels.
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