纳米技术
太阳能燃料
电荷(物理)
太阳能
接受者
化学
光催化
材料科学
化学物理
工作(物理)
储能
光电子学
电池(电)
间歇性
光伏系统
光子上转换
化学能
太阳能转换
酰亚胺
作者
Rohit Mann,Ritaj Tyagi,Kaustava Bhattacharyya,Vamsee K. Voora,Deepa Khushalani
标识
DOI:10.1016/j.xcrp.2025.102812
摘要
Summary
Integrating solar energy capture and storage directly into an electrical form in a single material presents a promising strategy to address the intermittency aspect of solar power. In recent years, potassium poly-heptazine imide (K-PHI) has been showcased as having a unique ability to photo-accumulate charge, which can subsequently be utilized for dark photocatalysis and solar battery applications. However, understanding the underlying chemical and structural factors governing photo-accumulated charge (PAC) formation in K-PHI remains unclear. Here, we report a study that delves into the structural features and identifies the chemical groups that govern the formation of the PAC state in K-PHI through a combination of ex situ and in situ spectroscopic studies. Additionally, the findings suggest a donor-acceptor behavior in this extended disordered K-PHI polymer, which allows for a prolonged retention of photo-induced radicals in acceptor moieties. Importantly, this work opens avenues for exploring more precise donor-acceptor systems for photo-induced charge storage, potentially advancing materials for solar rechargeable batteries and dark photocatalytic applications.
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