锌
材料科学
无定形固体
微晶
化学工程
制氢
纳米复合材料
纳米颗粒
聚合物
配位聚合物
氧化物
异质结
纳米技术
热解
氢
化学
有机化学
冶金
光电子学
复合材料
工程类
作者
Qi Zhu,Shuai Xu,Weidong Wu,Yi Qi,Zhan Lin,Yuliang Li,Yanlin Qin
标识
DOI:10.1002/ange.202205312
摘要
Abstract Infinite coordination‐polymer particles (CPPs) are promising materials for solar energy conversion with high efficiency. However, the range of organic ligands that may be used to create CPPs is limited, as are strategies for modification, thereby hindering the applications of such material. In this paper, competitive evolution–morphological and structural change from Zn‐based crystallites to amorphous particles is described. Controlled contribution of organic linkers selectively derived six Zn‐CPPs with multivariate characters. Based on the diversity of these substructures, hollow zinc oxide particles were initially formed by self‐pyrolysis of CPPs and effectively modified by ultrathin doped nanosheets. The obtained double‐sided heterojunctions offer fully‐covered active sites, bringing together efficient light‐excited charge‐transfer nanochannels, which exhibit an excellent solar H 2 ‐releasing activity (e.g., 4512.5 μmol h −1 g −1 ) and stable cyclability.
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