Peng Ying, Chen Shuo, Hu Zhengli, Yin Mengqi, Pei Lishun, Wei Qiaohua, Xie Zailai
Key Laboratory of Advanced Carbon-Based Functional Materials (Fujian Province University), Fuzhou University, Fuzhou 350016, Fujian, China.
Dalton Trans. 2024 Jun 10;53(23):9724-9731. doi: 10.1039/d4dt00495g.
Developing novel electrocatalysts for achieving high selectivity and faradaic efficiency in the carbon dioxide reduction reaction (CORR) poses a major challenge. In this study, a catalyst featuring a nitrogen-doped carbon shell-coated Ni nanoparticle structure is designed for efficient carbon dioxide (CO) electroreduction to carbon monoxide (CO). The optimal Ni@NC-1000 catalyst exhibits remarkable CO faradaic efficiency (FE) values exceeding 90% across a broad potential range of -0.55 to -0.9 V ( RHE), and attains the maximum FE of 95.6% at -0.75 V ( RHE) in 0.5 M NaHCO. This catalyst exhibits sustained carbon dioxide electroreduction activity with negligible decay after continuous electrolysis for 20 h. More encouragingly, a substantial current density of 200.3 mA cm is achieved in a flow cell at -0.9 V (. RHE), reaching an industrial-level current density. Fourier transform infrared spectroscopy and theoretical calculations demonstrate that its excellent catalytic performance is attributed to highly active pyrrolic nitrogen sites, promoting CO activation and significantly reducing the energy barrier for generating *COOH. To a considerable extent, this work presents an effective strategy for developing high-efficiency catalysts for electrochemical CO reduction across a wide potential window.
开发用于在二氧化碳还原反应(CORR)中实现高选择性和法拉第效率的新型电催化剂是一项重大挑战。在本研究中,设计了一种具有氮掺杂碳壳包覆镍纳米颗粒结构的催化剂,用于将二氧化碳(CO₂)高效电还原为一氧化碳(CO)。最佳的Ni@NC-1000催化剂在-0.55至-0.9 V(相对于可逆氢电极,RHE)的宽电位范围内表现出超过90%的显著一氧化碳法拉第效率(FE)值,并在0.5 M NaHCO₃中于-0.75 V(RHE)时达到95.6%的最大FE。该催化剂表现出持续的二氧化碳电还原活性,连续电解20小时后衰减可忽略不计。更令人鼓舞的是,在流动池中于-0.9 V(RHE)时实现了200.3 mA cm⁻²的可观电流密度,达到了工业级电流密度。傅里叶变换红外光谱和理论计算表明,其优异的催化性能归因于高活性的吡咯氮位点,促进了CO活化并显著降低了生成*COOH的能量壁垒。在很大程度上,这项工作提出了一种在宽电位窗口内开发用于电化学CO₂还原的高效催化剂的有效策略。