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A General Polymer‐Oriented Acid‐Mediated Self‐Assembly Approach toward Crystalline Mesoporous Metal Sulfides
Author(s) -
Zhou Hongru,
Xiong Hailong,
Zhang Rui,
Zhang Liangliang,
Zhang Ling,
Li Lin,
Zhang Wei,
Zhu Zhu,
Qiao ZhenAn
Publication year - 2021
Publication title -
small
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.785
H-Index - 236
eISSN - 1613-6829
pISSN - 1613-6810
DOI - 10.1002/smll.202100428
Subject(s) - mesoporous material , materials science , metal ions in aqueous solution , chemical engineering , metal , inorganic chemistry , catalysis , chemistry , organic chemistry , metallurgy , engineering
Mesoporous metal sulfides (MMSs) with high surface areas and large pore volumes show great potential in many applications such as gas sensing, photodetection, and catalysis. However, the synthesis of MMSs is still challenging due to the uncontrollable fast precipitation between metal ions and S 2− ions and the large volume contraction during the conversion of metal precursors to sulfides. Here, a general polymer‐oriented acid‐mediated self‐assembly method to synthesize highly crystalline MMSs (e.g., ZnS, CdS, Ni 3 S 4 , CuS, and Zn x Cd 1− x S) by using polyethylenimine (PEI) as pore‐forming agent is reported. In this method, acetic acid is designed as pH regulator and coordination agent to control the interactions between inorganic precursors and PEI, and adjust the reaction kinetics of metal ions and thioacetamide. This method endows a high degree of control over crystal structure and porous structure of MMSs. The surface areas and pore volumes of obtained MMSs are as high as 157 m 2 g −1 and 1.149 cm 3 g −1 , respectively. Benefiting from the abundant mesopores and homojunctions, mesoporous Zn 0.56 Cd 0.44 S shows a superior photocatalytic H 2 generation rate of 14.3 mmol h −1 g −1 .