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                  <mods:namePart>Chen, Qian-Qian</mods:namePart>
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                  <mods:namePart>Li, Qiang</mods:namePart>
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                  <mods:namePart>Hou, Chun-Chao</mods:namePart>
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                  <mods:namePart>Wang, Chuan-Jun</mods:namePart>
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                  <mods:namePart>Peng, Cheng-Yun</mods:namePart>
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               <mods:identifier type="doi">https://doi.org/10.1039/C9CY00584F</mods:identifier>
               <mods:abstract>Optimization of metal–support interactions (MSIs) is at the core of heterogeneous catalyst design. For polar
reactants, electrostatic interactions resulting from MSIs can facilitate their activation. In this work, a feasible
in situ method has been employed to control the electrostatic properties at the interface of a noblemetal-
free Cu/CoĲOH)2 nanohybrid catalyst. On the Cu/CoĲOH)2 interface, the positively charged copper
enhances the polar molecule adsorption. By varying the metal/support ratio, a highly efficient catalytic activity
for the methanolysis of ammonia borane (AB) with an initial turnover frequency (TOF) of 61.63 mol(H2)
mol(catalyst)
−1 min−1 and long-term stability at ambient temperature were observed. Theoretical analysis unravels
the role of charge transfer in promoting the reactions and the metal/support ratio in manipulating
the catalytic activity via tuning electrostatic interactions.</mods:abstract>
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                  <mods:title>Enhancing electrostatic interactions to activate polar molecules: ammonia borane methanolysis on a Cu/CoĲOH)2 nanohybrid</mods:title>
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