Orbital Coupling–Anion Synergy in AB₂Ch₄ Semiconductors: Band Engineering for high-Performance p-Type Transparent Conductive Materials

Abstract

The scarcity of high-performance p-type transparent conductive materials (p-TCMs) stems from fundamental trade-offs between wide bandgaps and conductivity, compounded by the intrinsically constrained acceptor doping due to the valence band maximum (VBM) characteristics. Herein, we propose a "dual-track coupling–anion synergy" strategy to design ternary AB₂Ch₄ semiconductors that circumvent these limitations. Stepwise screening of 45 candidates identifies 9 high-performance p-TCMs exhibiting exceptional visible-light transparency and ultrahigh hole mobility (up to 10³ cm²/V·s). Various empirical determinations and phase-diagram-guided defect analysis confirm both intrinsic p-type conduction and enhanced dopability in the screened compounds BaGa₂Se₄ and CdAl₂Te₄. This work establishes a design-before-screening paradigm for materials discovery, enabling the efficient development of p-TCM from wide-gap systems and accelerating breakthroughs in transparent electronics, while advancing the full functionalization of semiconductor devices.

Supplementary files

Article information

Article type
Communication
Submitted
16 Dec 2025
Accepted
23 Feb 2026
First published
24 Feb 2026

J. Mater. Chem. C, 2026, Accepted Manuscript

Orbital Coupling–Anion Synergy in AB₂Ch₄ Semiconductors: Band Engineering for high-Performance p-Type Transparent Conductive Materials

J. Xia, D. Fan, Z. Liu and Q. Liu, J. Mater. Chem. C, 2026, Accepted Manuscript , DOI: 10.1039/D5TC04405G

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements