Electronic‐State Manipulation of Surface Titanium Activates Dephosphorylation Over TiO2 Near Room Temperature

Dephosphorylation that removes a phosphate group from substrates is an important reaction for living organisms and environmental protection. Although CeO2 has been shown to catalyze this reaction, cerium is low in natural abundance and has a narrow global distribution (>90 % of these reserves are...

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Published inAngewandte Chemie International Edition Vol. 60; no. 29; pp. 16149 - 16155
Main Authors Wang, Quan, Yi, Xianfeng, Chen, Yu‐Cheng, Xiao, Yao, Zheng, Anmin, Chen, Jian Lin, Peng, Yung‐Kang
Format Journal Article
LanguageEnglish
Published Germany Wiley Subscription Services, Inc 12.07.2021
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Abstract Dephosphorylation that removes a phosphate group from substrates is an important reaction for living organisms and environmental protection. Although CeO2 has been shown to catalyze this reaction, cerium is low in natural abundance and has a narrow global distribution (>90 % of these reserves are located within six countries). It is thus imperative to find another element/material with high worldwide abundance that can also efficiently extract the phosphate out of agricultural waste for phosphorus recycle. Using para‐nitrophenyl phosphate (p‐NPP) as a model compound, we demonstrate that TiO2 with a F‐modified (001) surface can activate p‐NPP dephosphorylation at temperatures as low as 40 °C. By probe‐assisted nuclear magnetic resonance (NMR), it was revealed that the strong electron‐withdrawing effect of fluorine makes Ti atoms (the active sites) on the (001) surface very acidic. The bidentate adsorption of p‐NPP on this surface further promotes its subsequent activation with a barrier ≈20 kJ mol−1 lower than that of the pristine (001) and (101) surfaces, allowing the activation of this reaction near room temperature (from >80 °C). We demonstrate for the first time that TiO2 with a F‐modified (001) surface can activate p‐NPP dephosphorylation near room temperature. The electron‐withdrawing effect of fluorine imposed on the TiO2(001) surface strongly manipulates the electronic state of surrounding Ti5C atoms by making them very acidic, facilitating not only the bidentate adsorption of p‐NPP but also its subsequent activation.
AbstractList Dephosphorylation that removes a phosphate group from substrates is an important reaction for not only living organisms but also environmental protection. Although CeO2 has been shown to catalyze this reaction, as one of the rare earth elements, cerium is low in natural abundance and has a narrow global distribution (> 90% of these reserves are located within six countries). It is thus imperative to find another element/material with high worldwide abundance that can also efficiently extract the phosphate out of agricultural wastes for phosphorus recycle. Using para-nitrophenyl phosphate (p-NPP) as the model compound, we demonstrate herein that TiO2 with F-modified (001) surface can activate p-NPP dephosphorylation at temperature as low as 40 °C. By probe-assisted nuclear magnetic resonance (NMR), it was revealed that the strong electron withdrawing effect of fluorine makes Ti atoms (i.e., the active sites) on (001) surface very acidic. The bidentate adsorption of p-NPP on this surface further promotes its subsequent activation with barrier ~20 kJ/mol lower than that of pristine (001) and (101) surfaces, allowing the activation of this reaction at nearly room temperature (from > 80 °C).
Dephosphorylation that removes a phosphate group from substrates is an important reaction for living organisms and environmental protection. Although CeO2 has been shown to catalyze this reaction, cerium is low in natural abundance and has a narrow global distribution (>90 % of these reserves are located within six countries). It is thus imperative to find another element/material with high worldwide abundance that can also efficiently extract the phosphate out of agricultural waste for phosphorus recycle. Using para‐nitrophenyl phosphate (p‐NPP) as a model compound, we demonstrate that TiO2 with a F‐modified (001) surface can activate p‐NPP dephosphorylation at temperatures as low as 40 °C. By probe‐assisted nuclear magnetic resonance (NMR), it was revealed that the strong electron‐withdrawing effect of fluorine makes Ti atoms (the active sites) on the (001) surface very acidic. The bidentate adsorption of p‐NPP on this surface further promotes its subsequent activation with a barrier ≈20 kJ mol−1 lower than that of the pristine (001) and (101) surfaces, allowing the activation of this reaction near room temperature (from >80 °C).
Dephosphorylation that removes a phosphate group from substrates is an important reaction for living organisms and environmental protection. Although CeO2 has been shown to catalyze this reaction, cerium is low in natural abundance and has a narrow global distribution (>90 % of these reserves are located within six countries). It is thus imperative to find another element/material with high worldwide abundance that can also efficiently extract the phosphate out of agricultural waste for phosphorus recycle. Using para-nitrophenyl phosphate (p-NPP) as a model compound, we demonstrate that TiO2 with a F-modified (001) surface can activate p-NPP dephosphorylation at temperatures as low as 40 °C. By probe-assisted nuclear magnetic resonance (NMR), it was revealed that the strong electron-withdrawing effect of fluorine makes Ti atoms (the active sites) on the (001) surface very acidic. The bidentate adsorption of p-NPP on this surface further promotes its subsequent activation with a barrier ≈20 kJ mol-1 lower than that of the pristine (001) and (101) surfaces, allowing the activation of this reaction near room temperature (from >80 °C).Dephosphorylation that removes a phosphate group from substrates is an important reaction for living organisms and environmental protection. Although CeO2 has been shown to catalyze this reaction, cerium is low in natural abundance and has a narrow global distribution (>90 % of these reserves are located within six countries). It is thus imperative to find another element/material with high worldwide abundance that can also efficiently extract the phosphate out of agricultural waste for phosphorus recycle. Using para-nitrophenyl phosphate (p-NPP) as a model compound, we demonstrate that TiO2 with a F-modified (001) surface can activate p-NPP dephosphorylation at temperatures as low as 40 °C. By probe-assisted nuclear magnetic resonance (NMR), it was revealed that the strong electron-withdrawing effect of fluorine makes Ti atoms (the active sites) on the (001) surface very acidic. The bidentate adsorption of p-NPP on this surface further promotes its subsequent activation with a barrier ≈20 kJ mol-1 lower than that of the pristine (001) and (101) surfaces, allowing the activation of this reaction near room temperature (from >80 °C).
Dephosphorylation that removes a phosphate group from substrates is an important reaction for living organisms and environmental protection. Although CeO2 has been shown to catalyze this reaction, cerium is low in natural abundance and has a narrow global distribution (>90 % of these reserves are located within six countries). It is thus imperative to find another element/material with high worldwide abundance that can also efficiently extract the phosphate out of agricultural waste for phosphorus recycle. Using para‐nitrophenyl phosphate (p‐NPP) as a model compound, we demonstrate that TiO2 with a F‐modified (001) surface can activate p‐NPP dephosphorylation at temperatures as low as 40 °C. By probe‐assisted nuclear magnetic resonance (NMR), it was revealed that the strong electron‐withdrawing effect of fluorine makes Ti atoms (the active sites) on the (001) surface very acidic. The bidentate adsorption of p‐NPP on this surface further promotes its subsequent activation with a barrier ≈20 kJ mol−1 lower than that of the pristine (001) and (101) surfaces, allowing the activation of this reaction near room temperature (from >80 °C). We demonstrate for the first time that TiO2 with a F‐modified (001) surface can activate p‐NPP dephosphorylation near room temperature. The electron‐withdrawing effect of fluorine imposed on the TiO2(001) surface strongly manipulates the electronic state of surrounding Ti5C atoms by making them very acidic, facilitating not only the bidentate adsorption of p‐NPP but also its subsequent activation.
Author Chen, Yu‐Cheng
Peng, Yung‐Kang
Xiao, Yao
Chen, Jian Lin
Yi, Xianfeng
Wang, Quan
Zheng, Anmin
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Issue 29
Keywords Nuclear Magnetic Resonance
titanium dioxide
Dephosphorylation
Surface characterization
Electronic state manipulation
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Snippet Dephosphorylation that removes a phosphate group from substrates is an important reaction for living organisms and environmental protection. Although CeO2 has...
Dephosphorylation that removes a phosphate group from substrates is an important reaction for not only living organisms but also environmental protection....
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SubjectTerms Abundance
Agricultural wastes
Cerium
Cerium oxides
Dephosphorylation
electronic-state manipulation
Environmental protection
Fluorine
NMR
Nuclear magnetic resonance
Phosphorus
Room temperature
Substrates
surface characterization
Titanium
Titanium dioxide
Title Electronic‐State Manipulation of Surface Titanium Activates Dephosphorylation Over TiO2 Near Room Temperature
URI https://onlinelibrary.wiley.com/doi/abs/10.1002%2Fanie.202104397
https://www.ncbi.nlm.nih.gov/pubmed/33977664
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Volume 60
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