Wet processes are gaining a renewed interest for removal of high dose ion implanted photoresist (II-PR) in front-end-of-line semiconductor manufacturing because of their excellent selectivity towards the wafer substrate and gate materials. The selection of wet chemistries is supported by an insight into the resist degradation by ion implantation. In this work, different analytical techniques have been applied for in-depth characterization of the chemical changes in 248 nm DUV PR after arsenic implantation. A radical mechanism of resist degradation is proposed involving cross-linking and chain scission reactions. The cross-linking of the resist is dominant especially for high doses and energies. It leads to significant depletion of hydrogen and formation of carbon macroradicals that recombine to form C-C cross-linked crust. Moreover, formation of ab-unsaturated ketonic and/or quinonoid structures by cross-linking reactions is suggested. In addition, the dopant species may provide rigid points in the PR matrix by chemical bonding with the resist. For higher doses and energies further dehydrogenation occurs, which leads to formation of triple bonds in the crust. Different p-conjugated structures are formed in the crust by cross-linking and dehydrogenation reactions. No presence of amorphous carbon in the crust is revealed.In the processing of integrated circuits, the source and drain of a p-type and n-type metal-oxide-semiconductor field-effect transistor (MOSFET) are defined by implantation of donor and acceptor ions respectively. During the ion implantation, a photoresist is used as a masking material. The removal of high dose ( $ >1 Â 10 15 at. cm À2 ) and low energy ion implanted photoresist (II-PR) after implantation of ultra shallow extension and halo regions is considered one of the most challenging front-end-of-line (FEOL) processing steps for 32 nm and beyond technology nodes of logic devices. This is due to the difficulties of removing the modified layer (crust) formed on top and the sidewalls of the PR during the ion implantation in combination with the compatibility towards shallow implanted substrates, novel metal gate and high k-materials. Commonly used resist strip processes such as fluorine-based dry plasma ash and hot sulfuric/peroxide mixtures induce unacceptable levels of oxidation and material loss. 1-4 Alternative cleans are being developed for removal of II-PR. [5][6][7][8][9][10][11][12][13][14][15] In order to design approaches for selective stripping of II-PR a more profound insight into the resist degradation induced by ion implantation is needed.The degradation of photoresist by ion bombardment is a complex phenomenon, which is discussed in few reports. 15-22 Some of them seem even contradictory or difficult to compare, mainly because the results are obtained on different resist systems (resist chemical structure) and/or implantation conditions such as ion species, ion energy, ion dose etc. The chemical modifications in high energy ( $ > 100 keV) and high dose implanted novolak based resis...