Wu Yongmeng, Liu Cuibo, Wang Changhong, Yu Yifu, Shi Yanmei, Zhang Bin
Department of Chemistry, Institute of Molecular Plus, School of Science, Tianjin University, Tianjin, China.
Tianjin Key Laboratory of Molecular Optoelectronic Science, Collaborative Innovation Center of Chemical Science and Engineering, Tianjin, China.
Nat Commun. 2021 Jun 23;12(1):3881. doi: 10.1038/s41467-021-24059-y.
Electrocatalytic alkyne semi-hydrogenation to alkenes with water as the hydrogen source using a low-cost noble-metal-free catalyst is highly desirable but challenging because of their over-hydrogenation to undesired alkanes. Here, we propose that an ideal catalyst should have the appropriate binding energy with active atomic hydrogen (H*) from water electrolysis and a weaker adsorption with an alkene, thus promoting alkyne semi-hydrogenation and avoiding over-hydrogenation. So, surface sulfur-doped and -adsorbed low-coordinated copper nanowire sponges are designedly synthesized via in situ electroreduction of copper sulfide and enable electrocatalytic alkyne semi-hydrogenation with over 99% selectivity using water as the hydrogen source, outperforming a copper counterpart without surface sulfur. Sulfur anion-hydrated cation (S-K(HO)) networks between the surface adsorbed S and K in the KOH electrolyte boost the production of active H* from water electrolysis. And the trace doping of sulfur weakens the alkene adsorption, avoiding over-hydrogenation. Our catalyst also shows wide substrate scopes, up to 99% alkenes selectivity, good reducible groups compatibility, and easily synthesized deuterated alkenes, highlighting the promising potential of this method.
使用低成本无贵金属催化剂将水作为氢源电催化炔烃半加氢制烯烃是非常理想的,但具有挑战性,因为会过度加氢生成不需要的烷烃。在此,我们提出,理想的催化剂应与水电解产生的活性原子氢(H*)具有适当的结合能,且对烯烃的吸附较弱,从而促进炔烃半加氢并避免过度加氢。因此,通过硫化铜的原位电还原特意合成了表面硫掺杂和吸附的低配位铜纳米线海绵,并能够以水为氢源实现选择性超过99%的电催化炔烃半加氢,性能优于无表面硫的铜催化剂。在KOH电解质中,表面吸附的S与K之间的硫阴离子-水合阳离子(S-K(HO))网络促进了水电解产生活性H*。并且硫的微量掺杂减弱了烯烃吸附,避免了过度加氢。我们的催化剂还显示出广泛的底物范围、高达99%的烯烃选择性、良好的可还原基团兼容性以及易于合成氘代烯烃,突出了该方法的广阔前景。