Researcher profile

Bin Wang

Bin Wang contributes to research discovery and scholarly infrastructure.

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Published work

2 published item(s)

preprint2026arXiv

BadSKP: Backdoor Attacks on Knowledge Graph-Enhanced LLMs with Soft Prompts

Recent knowledge graph (KG)-enhanced large language models (LLMs) move beyond purely textual knowledge augmentation by encoding retrieved subgraphs into continuous soft prompts via graph neural networks, introducing a graph-conditioned channel that operates alongside the standard text interface. However, existing backdoor attacks are largely designed for the textual channel, and their effectiveness against this dual-channel architecture remains unclear. We show that this architecture creates a robustness gap: text-channel backdoor attacks that readily compromise textual KG prompting systems become largely ineffective against soft-prompt-based counterparts. We interpret this gap through semantic anchoring, whereby graph-derived soft prompts bias the generation-driving hidden state toward query-consistent semantics and suppress surface-level malicious instructions. Because this anchoring effect is itself induced by the graph channel, an attacker who manipulates graph-level representations can in turn redirect it toward adversarial semantics. To demonstrate this risk, we propose BadSKP, a backdoor attack that targets the graph-to-prompt interface through a multi-stage optimization strategy: it constructs adversarial target embeddings, optimizes poisoned node embeddings to steer the induced soft prompt, and approximates the optimized representations with fluent adversarial node attributes. Experiments on two soft-prompt KG-enhanced LLMs across four datasets show that BadSKP achieves high attack success under both frozen and trojaned settings, while text-only attacks remain unreliable even under perplexity-based defenses.

preprint2026arXiv

MolRecBench-Wild: A Real-World Benchmark for Optical Chemical Structure Recognition

Optical Chemical Structure Recognition (OCSR) aims to translate molecular diagrams in scientific literature into machine-readable formats, but current systems remain unreliable on real-world images due to substantial visual and chemical complexity. We introduce MOSAIC, a dual-dimensional difficulty framework with 37 fine-grained labels that jointly characterize visual interference and chemical semantic challenges in molecular diagrams. Based on this framework, we construct MolRecBench-Wild, a benchmark of 5,029 structures from 820 recent chemistry papers, covering the full difficulty spectrum observed in real publications. To enable faithful semantic evaluation beyond SMILES and MolFile, we propose CARBON, a representation language capable of expressing valence variations, icon-based groups, and other non-standard chemical semantics. We further adopt a dual-track evaluation protocol supporting both CARBON and SMILES outputs for broad model compatibility. Comprehensive experiments over 18 OCSR-capable models reveal severe performance degradation on MolRecBench-Wild, exposing a large gap between previous patent benchmarks and real-world academic scenarios.