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Updated: Sep 19, 2025

Surface Functionalization of Metal-Organic Frameworks for Improved Moisture Resistance
Published on: September 5, 2018
Efficient surface Hydroxyl-to-Hydroxyl radical conversion on layered double hydroxide via High-Efficiency hydroxyl
Xiaoyu Li1, Yuying Wang2, Jiahong Zou2
1Engineering Research Center for Waste Oil Recovery Technology and Equipment, Ministry of Education, Chongqing Technology and Business University, Chongqing 400067, China; Analytical & Testing Center, Sichuan University, Chengdu, Sichuan 610064, China.
Abstract:
Promoting the activation of surface or edges hydroxyl groups in layered double hydroxides (LDHs) to facilitate its conversion to hydroxyl radicals (·OH) in photocatalytic process has received wider attention in research communities. However, the pristine LDHs are unable to convert surface or edges hydroxyl groups to ·OH with the energy of visible light illumination, so it is necessary to structurally modulate them to improve their conversion of surface hydroxyl groups to ·OH under light illumination. Herein, we innovatively combined nickel-iron layered double hydroxide (NiFe-LDHs, hydroxyl groups library) with bismuth carbonate oxide ((BiO)2CO3, BOC, ·OH generator), enabling a sustained and efficient transformation of hydroxyl groups on the surface or edges of NiFe-LDHs into ·OH. Mechanism studies supported by in-situ spectroscopic analyses and theoretical simulations, showed that under the visible light illumination the hot holes generated on energy band-matched BOC can capture OH- located at the surface/edge of NiFe-LDHs nanosheets and further convert them into ·OH and efficiently promoted the oxidation of NO to NO3-. The NO removal efficiency of BOC/NiFe-LDHs composite material is about 54.5%, which was 2.23 times that of the original BOC.
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One of the convenient methods for the preparation of aldehydes and ketones is via hydration of alkynes. Hydroboration-oxidation of alkynes is an indirect hydration reaction in which an alkyne is treated with borane followed by oxidation with alkaline peroxide to form an enol that rapidly converts into an aldehyde or a ketone. Terminal alkynes form aldehydes, whereas internal alkynes give ketones as the final product.

