Chemical state

Semiconductor

Electrical engineering

Physics

Engineering

Nanotechnology

X-ray photoelectron spectroscopy

Thin film

Metallurgy

Materials science

Carrier lifetime

Condensed matter physics

Kesterite

Selenide

CZTS

Acceptor

Photovoltaic system

Chemical engineering

Optoelectronics

Photovoltaics

Silicon

Selenium

Advanced Materials

Kesterite‐based Cu 2 ZnSn(S,Se) 4 semiconductors are emerging as promising materials for low‐cost, environment‐benign, and high‐efficiency thin‐film photovoltaics. However, the current state‐of‐the‐art Cu 2 ZnSn(S,Se) 4 devices suffer from cation‐disordering defects and defect clusters, which generally result in severe potential fluctuation, low minority carrier lifetime, and ultimately unsatisfactory performance. Herein, critical growth conditions are reported for obtaining high‐quality Cu 2 ZnSnSe 4 absorber layers with the formation of detrimental intrinsic defects largely suppressed. By controlling the oxidation states of cations and modifying the local chemical composition, the local chemical environment is essentially modified during the synthesis of kesterite phase, thereby effectively suppressing detrimental intrinsic defects and activating desirable shallow acceptor Cu vacancies. Consequently, a confirmed 12.5% efficiency is demonstrated with a high V OC of 491 mV, which is the new record efficiency of pure‐selenide Cu 2 ZnSnSe 4 cells with lowest V OC deficit in the kesterite family by E g / q ‐ V oc. These encouraging results demonstrate an essential route to overcome the long‐standing challenge of defect control in kesterite semiconductors, which may also be generally applicable to other multinary compound semiconductors.

Defect Control for 12.5% Efficiency Cu<sub>2</sub>ZnSnSe<sub>4</sub> Kesterite Thin‐Film Solar Cells by Engineering of Local Chemical Environment

Defect Control for 12.5% Efficiency Cu2ZnSnSe4 Kesterite Thin‐Film Solar Cells by Engineering of Local Chemical Environment

Defect Control for 12.5% Efficiency Cu₂ZnSnSe₄ Kesterite Thin‐Film Solar Cells by Engineering of Local Chemical Environment