质子
锰
化学
无机化学
输水
传输(计算)
环境科学
计算机科学
有机化学
水资源管理
并行计算
物理
量子力学
作者
Shujiao Yang,Xialiang Li,Yifan Li,Yabo Wang,Xiaotong Jin,Lingshuang Qin,Wei Zhang,Rui Cao
标识
DOI:10.1002/anie.202215594
摘要
The effect of proton transfer on water oxidation has hardly been measurably established in heterogeneous electrocatalysts. Herein, two isomorphous manganese phosphates (NH4 MnPO4 ⋅ H2 O and KMnPO4 ⋅ H2 O) were designed to form an ideal platform to study the effect of proton transfer on water oxidation. The hydrogen-bonding network in NH4 MnPO4 ⋅ H2 O has been proven to be solely responsible for its better activity. The differences of the proton transfer kinetics in the two materials indicate a fast proton hopping transfer process with a low activation energy in NH4 MnPO4 ⋅ H2 O. In addition, the hydrogen-bonding network can effectively promote the proton transfer between adjacent Mn sites and further stabilize the MnIII -OH intermediates. The faster proton transfer results in a higher proportion of zeroth-order in [H+ ] for OER. Thus, proton transfer-affected electrocatalytic water oxidation has been measurably observed to bring detailed insights into the mechanism of water oxidation.
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