Related Experiment Video
Updated: Sep 29, 2026

Simultaneous Multi-surface Anodizations and Stair-like Reverse Biases Detachment of Anodic Aluminum Oxides in Sulfuric and Oxalic Acid Electrolyte
Published on: October 5, 2017
Unveiling a Near-Total Rear Passivation for High Performance of Ultra-Thin ACIGS
Xavier L Pinheiro1,2,3, António J N Oliveira1, André F Violas1
1INL - International Iberian Nanotechnology Laboratory, Avenida Mestre José Veiga, Braga, Portugal.
Abstract:
Thin-film Cu(In,Ga)Se2 solar cells are a key photovoltaic technology for addressing global energy and environmental challenges. Reducing absorber thickness lowers manufacturing cost and critical raw material consumption but introduces optical and electrical losses due to incomplete light absorption and increased rear interface recombination. Rear recombination can be mitigated through Ga grading and/or rear contact passivation, for example using tunnel oxide as in c-Si TOPCon technology. In this work, a full coverage plasma enhanced chemically vapor deposited 8 nm porous SiOx passivation layer was implemented in ultra-thin (Ag,Cu)(In,Ga)Se2 (ACIGS) solar cells and compared with patterned passivation layers (∼70% coverage) and an unpassivated reference. Standard current-voltage and external quantum efficiency characterization methods show that the complete passivation yielded the highest performance, achieving 16.4% efficiency, a 2% absolute improvement over the reference. Patterned samples showed enhanced performance to a lower extent. Elemental and structural analysis showed that the SiOx layers remained intact after 550°C deposition of the 700 nm ACIGS absorber. Notably, a MoSe2 interfacial layer formed between the full SiOx layer and Mo contact, likely due to Na and/or Se diffusion through SiOx pores. Combining near-complete passivation and the ohmic MoSe2 contact may explain the improved performance.
Related Concept Videos
Weak Acid Solutions
Production of Organic Acids
Acid Halides to Carboxylic Acids: Hydrolysis
As shown below, the mechanism involves a nucleophilic attack by water at the carbonyl carbon to form a tetrahedral intermediate. This is followed by the reformation of the carbon–oxygen π bond along with the departure of a halide ion. A final proton transfer step yields carboxylic acid...
Mixtures of Acids
A Mixture of a Strong Acid and a Weak Acid
In a mixture of a strong acid and a weak acid, the strong acid dissociates completely and becomes a source of almost all the hydronium ions...
Mixtures of Acids
In a strong and weak acid mixture, the strong acid dissociates completely and becomes a source of almost all the hydronium ions present in the solution. In contrast, the weak acid shows...
Esters to Carboxylic Acids: Acid-Catalyzed Hydrolysis
During hydrolysis, the ester is first activated towards nucleophilic attack through the protonation of the carboxyl oxygen atom by the acid catalyst. The protonation makes the ester carbonyl carbon more electrophilic. In the next step, water acts as a nucleophile and adds to the...

