催化作用
铟
格式化
选择性
化学
产量(工程)
甲醇
原位
兴奋剂
无机化学
核化学
材料科学
有机化学
冶金
光电子学
作者
Jiawei Chen,Bohong Wu,Yan Shao,Hongwei Guo,Huanhao Chen
摘要
Abstract We describe the synthesis of CuIn/ZrO 2 catalysts via a facile mechanochemical synthesis method. In doping was demonstrated to promote the formation of strong Cu–In 2 O 3 interactions and increase the number of Cu + sites. The CuIn 0.05 /ZrO 2 catalyst shows relatively high selectivity and space–time yield of methanol (~50% and ~1.25 , respectively) at 300°C and 5 MPa, outperforming those of the Cu/ZrO 2 catalyst (~25% and ~1.12 , respectively). Time‐resolved in situ DRIFTS results acquired under various reaction conditions (typically H 2 /D 2 isotope exchange) demonstrate that the surface Cu + –bound formate was the most reactive intermediate and the subsequent hydrogenation process should be the rate‐limiting step, which was positively promoted by the inclusion of In. The strong Cu–In 2 O 3 interaction promotes a decrease in Cu 0 sites, leading to a weak interaction of the Cu 0 ‐bound CO intermediates, thus facilitating further hydrogenation of these species rather than releasing CO product.
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