实现光电化学级联,生成甲醇这种液体太阳能燃料

Ann L., Greenaway, Thomas, Chan, Calton J. , Kong, Grace A., Rome, Darci, Collins, Alex J., King, Rajiv Ramanujam, Prabhakar, Sarah A. , Collins, Michelle S., Young, Mickey J., Wilson, Myles A., Steiner, Adele C., Tamboli, Emily L., Warren, Clifford P., Kubiak, Joel W., Ager
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摘要

生化网络使用级联反应利用太阳光的能量选择性地还原二氧化碳,但将级联方法应用于工程系统能否实现类似的选择性呢?在此,我们报告了一种液态太阳能燃料两步光电化学(PEC)级联反应的设计与实施:将 CO2 还原成 CO,再将 CO 还原成甲醇。进行还原所需的电位是通过定制的基于 III-V 的三端串联(3TT)太阳能电池产生的。固定在多壁碳纳米管(CoPc/MWCNT)上的酞菁钴催化了这两个反应。通过对电解质流动的多物理场模拟和非照明电化学测量,缩小了 CoPc/MWCNT 3TT 光电阴极的工作参数范围。冠军集成光电阴极产生甲醇的法拉第效率(FE)为 3.8 ± 0.4%,测试光电阴极的甲醇法拉第效率为 0.7-3.8%。通过核磁共振光谱和气相色谱法对产品进行了定量。受测光电阴极的电流输出高度稳定,甲醇产量可持续多次实验。甲醇产量低的原因是,当两个触点都处于激活状态时,甲醇产生子电池的 CO 通量不足,二氧化碳耗尽,而对照光电阴极的甲醇产量略高于 3TT 装置,也证明了这一点。当驱动一氧化碳还原的 3TT 子电池失活时,甲醇生产停止,这支持了级联机制的假设。导致 CoPc/MWCNT 3TT 光阴极甲醇产率低的主要因素是甲醇产生接触处的二氧化碳耗尽不足,以及使用 3TT 设计选择工作电位时的不确定性。尽管 CoPc/MWCNT 3TT 光电阴极的选择性还不高,但这项研究工作发展了 PEC 级联的基本科学原理,展示了生产碳基燃料的基于 3TT 的光电阴极的联合设计,最后讨论了利用这一概念提高产品产量的途径,包括二氧化碳供应优化和替代光电阴极和催化剂材料。
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Realization of a photoelectrochemical cascade for the generation of methanol, a liquid solar fuel
Biochemical networks use reaction cascades to selectively reduce CO2 using energy from sunlight, but can similar selectivity be achieved by applying a cascade approach to an engineered system? Here, we report the design and implementation of a two-step photoelectrochemical (PEC) cascade to a liquid solar fuel: reduction of CO2 to CO and subsequent reduction of CO to methanol. The potentials required to perform the reductions were generated using custom-made III-V-based three-terminal tandem (3TT) solar cells. Cobalt phthalocyanine immobilized on multi-walled carbon nanotubes (CoPc/MWCNT) catalyzed both reactions. Multiphysics simulations of electrolyte flow and non-illuminated electrochemical measurements were used to narrow the operating parameters for the CoPc/MWCNT 3TT photocathodes. The champion integrated photocathode produced methanol with 3.8 ± 0.4% Faradaic efficiency (FE), with tested photocathodes having 0.7-3.8% methanol FE. Products were quantified by nuclear magnetic resonance spectroscopy and gas chromatography. The current output of the tested photocathodes was highly stable, and methanol production continued over multiple experiments. The low methanol yield is attributed to insufficient CO flux to, and CO2 depletion at, the methanol-producing subcell when both contacts are active, which is supported by the observation that a control photoelectrode slightly outperformed the methanol production of the 3TT device. Methanol production ceased when the 3TT subcell driving CO reduction was deactivated, supporting the assignment of a cascade mechanism. The major factors resulting in low methanol FE by the CoPc/MWCNT 3TT photocathodes are insufficient CO2 depletion at the methanol-producing contact and uncertainty in operating potential selection using the 3TT design. Although the CoPc/MWCNT 3TT photocathode is not yet highly selective, this work develops the basic science principles underlying the PEC cascade, demonstrates the co-design of a 3TT-based photoelectrode to produce carbon-based fuels, and finally discusses routes for improving product yields with this concept, including CO2 supply optimization and alternative photoelectrode and catalyst materials.
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