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Abstract Biochar, as a potential CO 2 adsorbent, is of great significance in addressing the problem of global warming. Previous studies have demonstrated that the CO 2 adsorption performance of biochar can be improved by nitrogen and sulfur doping. Co-doping can integrate the structure and function of two elements. However, the physicochemical interaction of nitrogen and sulfur during doping and the CO 2 adsorption process remains unclear in co-doped biochar. In this study, the heteroatom-doped biochar was prepared with different additives (urea, sodium thiosulfate, and thiourea) via hydrothermal carbonization, and the physicochemical interaction of nitrogen and sulfur in co-doped biochar was investigated extensively. The findings revealed that nitrogen and sulfur competed for limited doped active sites on the carbon skeleton during the co-doping process. Interestingly, thiourea retained the amino group on the surface of biochar to a great extent due to carbon–sulfur double bond breaking and bonding, which facilitated the formation of pore in the activation process. Significantly, co-doping had no significant improvement effect although nitrogen and sulfur doping separately enhanced the CO 2 adsorption performance of biochar by 11.9% and 8.5%. The nitrogen-containing and sulfur-containing functional groups in co-doped biochar exhibited mutual inhibition in the process of CO 2 adsorption. The findings of this study will have pertinent implications in the application of N/S co-doped biochar for CO 2 adsorption. Graphical Abstract
Sun et al. (Wed,) studied this question.