Photocatalytic carbon dioxide(CO_(2))to carbon monoxide(CO)offers a promising way for both alleviating the greenhouse effect and meeting the industrial demand.Herein,we constructed a Co single-atom catalyst with inten...Photocatalytic carbon dioxide(CO_(2))to carbon monoxide(CO)offers a promising way for both alleviating the greenhouse effect and meeting the industrial demand.Herein,we constructed a Co single-atom catalyst with intentional low-coordination environment design on porous ZnO(denoted as Co1/ZnO).Impressively,Co1/ZnO exhibited a remarkable activity with a CO yield rate of 22.25 mmol·g^(-1)·h^(-1) and a selectivity of 80.2%for CO_(2) photoreduction reactions under visible light.The incorporation of single Co atoms provided an additional photo-generated electron transfer channel,which suppressed the carrier recombination of photocatalysts.Moreover,the unsaturated Co active sites were capable to adsorb CO_(2) molecule spontaneously,thus facilitating the activation of CO_(2) molecule during CO_(2) reduction course.展开更多
Catalytic conversion of nitrate(NO_(3)^(-))pollutants into ammonia(NH_(3))offers a sustainable and promising route for both wastewater treatment and NH_(3)synthesis.Alkali cations are prevalent in nitrate solutions,bu...Catalytic conversion of nitrate(NO_(3)^(-))pollutants into ammonia(NH_(3))offers a sustainable and promising route for both wastewater treatment and NH_(3)synthesis.Alkali cations are prevalent in nitrate solutions,but their roles beyond charge balance in catalytic NO_(3)^(-)conversion have been generally ignored.Herein,we report the promotion effect of K^(+)cations in KNO_(3)solution for NO_(3)^(-)reduction over a TiO_(2)-supported Ni single-atom catalyst(Ni_(1)/TiO_(2)).For photocatalytic NO_(3)^(-)reduction reaction,Ni_(1)/TiO_(2)exhibited a 1.9-fold NH_(3)yield rate with nearly 100%selectivity in KNO_(3)solution relative to that in NaNO_(3)solution.Mechanistic studies reveal that the K^(+)cations from KNO_(3)gradually bonded with the surface of Ni_(1)/TiO_(2),in situ forming a K-O-Ni moiety during reaction,whereas the Na^(+)ions were unable to interact with the catalyst in NaNO_(3)solution.The charge accumulation on the Ni sites induced by the incorporation of K atom promoted the adsorption and activation of NO_(3)^(-).Furthermore,the K-O-Ni moiety facilitated the multiple proton-electron coupling of NO_(3)^(-)into NH_(3)by stabilizing the intermediates.展开更多
基金supported by the National Natural Science Foundation of China(Nos.1222508,U1932213)the Fundamental Research Funds for the Central Universities(No.WK2060000016)+1 种基金the USTC Research Funds of the Double First-Class Initiative(No.YD2310002005)the Youth Innovation Promotion Association CAS(No.2020454)。
文摘Photocatalytic carbon dioxide(CO_(2))to carbon monoxide(CO)offers a promising way for both alleviating the greenhouse effect and meeting the industrial demand.Herein,we constructed a Co single-atom catalyst with intentional low-coordination environment design on porous ZnO(denoted as Co1/ZnO).Impressively,Co1/ZnO exhibited a remarkable activity with a CO yield rate of 22.25 mmol·g^(-1)·h^(-1) and a selectivity of 80.2%for CO_(2) photoreduction reactions under visible light.The incorporation of single Co atoms provided an additional photo-generated electron transfer channel,which suppressed the carrier recombination of photocatalysts.Moreover,the unsaturated Co active sites were capable to adsorb CO_(2) molecule spontaneously,thus facilitating the activation of CO_(2) molecule during CO_(2) reduction course.
基金financial support by the National Natural Science Foundation of China(12222508,U1932213,and 22308346)the Fundamental Research Funds for the Central Universities(WK2060000016)+5 种基金the USTC Research Funds of the Double First-Class Initiative(YD2310002005 and YD9990002014)the National Key R&D Program of China(2023YFA1506304)the Youth Innovation Promotion Association CAS(2020454)Xiaomi Young Talents ProgramJoint Funds from the Hefei National Synchrotron Radiation Laboratory(KY9990000202)Natural Science Foundation of Anhui Province(2208085QB42)。
文摘Catalytic conversion of nitrate(NO_(3)^(-))pollutants into ammonia(NH_(3))offers a sustainable and promising route for both wastewater treatment and NH_(3)synthesis.Alkali cations are prevalent in nitrate solutions,but their roles beyond charge balance in catalytic NO_(3)^(-)conversion have been generally ignored.Herein,we report the promotion effect of K^(+)cations in KNO_(3)solution for NO_(3)^(-)reduction over a TiO_(2)-supported Ni single-atom catalyst(Ni_(1)/TiO_(2)).For photocatalytic NO_(3)^(-)reduction reaction,Ni_(1)/TiO_(2)exhibited a 1.9-fold NH_(3)yield rate with nearly 100%selectivity in KNO_(3)solution relative to that in NaNO_(3)solution.Mechanistic studies reveal that the K^(+)cations from KNO_(3)gradually bonded with the surface of Ni_(1)/TiO_(2),in situ forming a K-O-Ni moiety during reaction,whereas the Na^(+)ions were unable to interact with the catalyst in NaNO_(3)solution.The charge accumulation on the Ni sites induced by the incorporation of K atom promoted the adsorption and activation of NO_(3)^(-).Furthermore,the K-O-Ni moiety facilitated the multiple proton-electron coupling of NO_(3)^(-)into NH_(3)by stabilizing the intermediates.
基金supported by the Natural Science Foundation of Shandong Province(ZR2020ZD10)the National Natural Science Foundation of China(21775142)Shenzhen Natural Science Fund(20200925154115001 and JCYJ20210324115809026).
