School of Chemistry and Chemical Engineering, State Key Laboratory of Materials Processing and Die & Mould Technology, Key Laboratory of Material Chemistry for Energy Conversion and Storage (Ministry of Education), Hubei Key Laboratory of Material Chemistry and Service Failure, Wuhan National Laboratory for Optoelectronics, Huazhong University of Science and Technology, Wuhan, China.
School of Chemical Sciences, University of Auckland, Auckland, New Zealand.
Nature. 2024 Feb;626(7997):86-91. doi: 10.1038/s41586-023-06917-5. Epub 2024 Jan 31.
Electrolysis that reduces carbon dioxide (CO) to useful chemicals can, in principle, contribute to a more sustainable and carbon-neutral future. However, it remains challenging to develop this into a robust process because efficient conversion typically requires alkaline conditions in which CO precipitates as carbonate, and this limits carbon utilization and the stability of the system. Strategies such as physical washing, pulsed operation and the use of dipolar membranes can partially alleviate these problems but do not fully resolve them. CO electrolysis in acid electrolyte, where carbonate does not form, has therefore been explored as an ultimately more workable solution. Herein we develop a proton-exchange membrane system that reduces CO to formic acid at a catalyst that is derived from waste lead-acid batteries and in which a lattice carbon activation mechanism contributes. When coupling CO reduction with hydrogen oxidation, formic acid is produced with over 93% Faradaic efficiency. The system is compatible with start-up/shut-down processes, achieves nearly 91% single-pass conversion efficiency for CO at a current density of 600 mA cm and cell voltage of 2.2 V and is shown to operate continuously for more than 5,200 h. We expect that this exceptional performance, enabled by the use of a robust and efficient catalyst, stable three-phase interface and durable membrane, will help advance the development of carbon-neutral technologies.
电解将二氧化碳 (CO) 还原为有用的化学物质,从原则上讲,可以为更可持续和碳中和的未来做出贡献。然而,将其开发成一种稳健的工艺仍然具有挑战性,因为高效的转化通常需要碱性条件,在这种条件下,CO 会沉淀为碳酸盐,这限制了碳的利用和系统的稳定性。物理洗涤、脉冲操作和使用偶极膜等策略可以部分缓解这些问题,但不能完全解决这些问题。因此,人们一直在探索在酸性电解质中进行 CO 电解,因为在酸性电解质中不会形成碳酸盐。在这里,我们开发了一种质子交换膜系统,该系统在源自废铅酸电池的催化剂上将 CO 还原为甲酸,其中晶格碳激活机制发挥了作用。当将 CO 还原与氢氧化偶联时,甲酸的法拉第效率超过 93%。该系统与启动/关闭过程兼容,在电流密度为 600 mA cm 和电池电压为 2.2 V 时,CO 的单程转化率接近 91%,并且已经证明可以连续运行超过 5200 小时。我们期望这种卓越的性能,得益于使用坚固高效的催化剂、稳定的三相界面和耐用的膜,将有助于推进碳中和技术的发展。