Guan Qinhui, Ran Weiguang, Zhang Dapeng, Li Wenjuan, Li Na, Huang Baibiao, Yan Tingjiang
College of Chemistry and Chemical Engineering, Shaanxi University of Science and Technology, Xi'an, 710021, P. R. China.
Key Laboratory of Catalytic Conversion and Clean Energy in Universities of Shandong Province, School of Chemistry and Chemical Engineering, Qufu Normal University, Qufu, 273165, P. R. China.
Adv Sci (Weinh). 2024 Aug;11(30):e2401990. doi: 10.1002/advs.202401990. Epub 2024 Jun 13.
Photocatalytic CO reduction is considered as a promising strategy for CO utilization and producing renewable energy, however, it remains challenge in the improvement of photocatalytic performance for wide-band-gap photocatalyst with controllable product selectivity. Herein, the sulfur-doped In(OH) (In(OH)S-z) nanocubes are developed for selective photocatalytic reduction of CO to CH under simulated light irradiation. The CH yield of the optimal In(OH)S-1.0 can be enhanced up to 39 times and the CH selectivity can be regulated as high as 80.75% compared to that of pristine In(OH). The substitution of sulfur atoms for hydroxyl groups in In(OH) enhances the visible light absorption capability, and further improves the hydrophilicity behavior, which promotes the HO dissociation into protons (H) and accelerates the dynamic proton-feeding CO hydrogenation. In situ DRIFTs and DFT calculation confirm that the non-metal sulfur sites significantly weaken the over-potential of the HO oxidation and prevent the formation of ·OH radicals, enabling the stabilization of CHO intermediates and thus facilitating CH production. This work highlights the promotion effect of the non-metal doping engineering on wide-band-gap photocatalysts for tailoring the product selectivity in photocatalytic CO reduction.
光催化CO还原被认为是一种有前景的CO利用和生产可再生能源的策略,然而,对于具有可控产物选择性的宽带隙光催化剂而言,提高其光催化性能仍然是一个挑战。在此,开发了硫掺杂的In(OH)(In(OH)S-z)纳米立方体,用于在模拟光照射下将CO选择性光催化还原为CH。与原始In(OH)相比,最佳的In(OH)S-1.0的CH产率可提高至39倍,CH选择性可调节至高达80.75%。In(OH)中硫原子取代羟基增强了可见光吸收能力,并进一步改善了亲水性行为,促进了HO离解为质子(H)并加速了动态质子供料的CO加氢。原位漫反射红外傅里叶变换光谱(DRIFTs)和密度泛函理论(DFT)计算证实,非金属硫位点显著降低了HO氧化的过电位并防止了·OH自由基的形成,从而使CHO中间体得以稳定,进而促进了CH的生成。这项工作突出了非金属掺杂工程对宽带隙光催化剂在光催化CO还原中调节产物选择性的促进作用。