溶剂辅助形状依赖的MAPbI3/聚芴异质结构,具有更大的表面积,用于改善光催化H2演化†

IF 3.2 Q2 CHEMISTRY, PHYSICAL Energy advances Pub Date : 2024-10-22 DOI:10.1039/D4YA00457D
Tamal Pal, Soumalya Bhowmik, Arvin Sain Tanwar, Ameer Suhail, Nageswara Rao Peela, Chivukula V. Sastri and Parameswar Krishnan Iyer
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引用次数: 0

摘要

虽然铅基MAPbI3已被用作光催化析氢的材料,但在HI溶液中常规合成的MAPbI3的HER活性很低,析氢速率为30 μmol h−1 g−1。人们已经做了一些努力,通过标记助催化剂来提高HER性能。但目前还没有研究出改善原始MAPbI3 HER活性的有效方法。在这项工作中,通过简单的溶剂改变途径修饰了MAPbI3的形状和形态。这导致了形状和形态的实质性转变,影响了光催化和光电化学性能的各个方面。DMF辅助的原始MAPbI3的HER活性为830 μmol h−1 g−1,比典型的HI基MAPbI3高近28倍。这项工作强调了溶剂从HI到DMF的转变如何影响原始MAPbI3的形状和表面形态,从而影响其光催化和光电化学性能。为了进一步提高DMF辅助MAPbI3的HER活性,将合成的聚芴共催化剂集成在MAPbI3表面。在优化条件下,MAPbI3/聚芴复合材料的析氢量可达6200 μmol h−1 g−1。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Solvent assisted shape dependent MAPbI3/polyfluorene heterostructures with a larger surface area for improved photocatalytic H2 evolution†

Although lead based MAPbI3 has been used as a material for photocatalytic hydrogen evolution, conventionally synthesized MAPbI3 in HI solution suffers from very low HER activity with a hydrogen evolution rate of 30 μmol h−1 g−1. Several efforts have been made to boost the HER performance by tagging a co-catalyst. But no such significant approach was developed to improve the HER activity of pristine MAPbI3. In this work, the shape and morphology of MAPbI3 have been modified by a simple solvent change route. This led to substantial transformation in shape and morphology affecting various facets of photocatalytic and photoelectrochemical performance. DMF assisted pristine MAPbI3 exhibited an HER activity of 830 μmol h−1 g−1, almost 28-fold better than that of typical HI based MAPbI3. This work highlights how solvent transition from HI to DMF can influence the shape and surface morphologies which impact the photocatalytic and photoelectrochemical performances of pristine MAPbI3. To further enhance the HER activity of DMF assisted MAPbI3, the as-synthesized polyfluorene co-catalyst was integrated on the MAPbI3 surface. Under optimized conditions, the hydrogen evolution of MAPbI3/polyfluorene composites can reach up to 6200 μmol h−1 g−1.

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